Relevant bibliographies by topics / Skin pathologies

Academic literature on the topic 'Skin pathologies'

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Published: 30 May 2022
Last updated: 31 May 2022

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Journal articles on the topic "Skin pathologies"

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Snarskaya, Elena Sergeevna, Olga Yurievna Olisova, Alexander Davidovich Makatsariya, Nikolai Georgievich Kochergin, Lyudmila Radetskaya, Viktoriya Bitsadze, and Jamilya Khizroeva. "Skin pathologies in pregnancy." Journal of Perinatal Medicine 47, no. 4 (May 27, 2019): 371–80. http://dx.doi.org/10.1515/jpm-2018-0338.

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Abstract Progesterone is a hormone responsible for pregnancy maintenance and the amount of progesterone increases in a woman’s body during pregnancy, as well as the level of female sex hormones, estrogens are also upregulated. Due to these changes the cutaneous sensitivity to external stimuli (meteorological factors, bacteria, etc.) increases. In general, all skin changes during pregnancy can be divided into three groups: physiological changes (hormone-associated), nonspecific or dermatoses that existed before pregnancy or were triggered by it, and specific pregnancy-related dermatoses, which appear during pregnancy and resolve in the postpartum period. In this brief review, we describe the dermatoses commonly seen in pregnancy and present our own clinical examples. We hope the review will be of some practical help for dermatologists and obstetricians.
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Bongiovanni, Laura, Eliane J. Müller, and Leonardo Della Salda. "Survivin in skin pathologies." Experimental Dermatology 20, no. 6 (May 18, 2011): 457–63. http://dx.doi.org/10.1111/j.1600-0625.2011.01273.x.

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Cobo, Ramón, Jorge García-Piqueras, Juan Cobo, and José A. Vega. "The Human Cutaneous Sensory Corpuscles: An Update." Journal of Clinical Medicine 10, no. 2 (January 10, 2021): 227. http://dx.doi.org/10.3390/jcm10020227.

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Sensory corpuscles of human skin are terminals of primary mechanoreceptive neurons associated with non-neuronal cells that function as low-threshold mechanoreceptors. Structurally, they consist of an extreme tip of a mechanosensory axon and nonmyelinating peripheral glial cells variably arranged according to the morphotype of the sensory corpuscle, all covered for connective cells of endoneurial and/or perineurial origin. Although the pathologies of sensitive corpuscles are scarce and almost never severe, adequate knowledge of the structure and immunohistochemical profile of these formations is essential for dermatologists and pathologists. In fact, since sensory corpuscles and nerves share a basic structure and protein composition, a cutaneous biopsy may be a complementary method for the analysis of nerve involvement in peripheral neuropathies, systemic diseases, and several pathologies of the central nervous system. Thus, a biopsy of cutaneous sensory corpuscles can provide information for the diagnosis, evolution, and effectiveness of treatments of some pathologies in which they are involved. Here, we updated and summarized the current knowledge about the immunohistochemistry of human sensory corpuscles with the aim to provide information to dermatologists and skin pathologists.
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Cobo, Ramón, Jorge García-Piqueras, Juan Cobo, and José A. Vega. "The Human Cutaneous Sensory Corpuscles: An Update." Journal of Clinical Medicine 10, no. 2 (January 10, 2021): 227. http://dx.doi.org/10.3390/jcm10020227.

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Sensory corpuscles of human skin are terminals of primary mechanoreceptive neurons associated with non-neuronal cells that function as low-threshold mechanoreceptors. Structurally, they consist of an extreme tip of a mechanosensory axon and nonmyelinating peripheral glial cells variably arranged according to the morphotype of the sensory corpuscle, all covered for connective cells of endoneurial and/or perineurial origin. Although the pathologies of sensitive corpuscles are scarce and almost never severe, adequate knowledge of the structure and immunohistochemical profile of these formations is essential for dermatologists and pathologists. In fact, since sensory corpuscles and nerves share a basic structure and protein composition, a cutaneous biopsy may be a complementary method for the analysis of nerve involvement in peripheral neuropathies, systemic diseases, and several pathologies of the central nervous system. Thus, a biopsy of cutaneous sensory corpuscles can provide information for the diagnosis, evolution, and effectiveness of treatments of some pathologies in which they are involved. Here, we updated and summarized the current knowledge about the immunohistochemistry of human sensory corpuscles with the aim to provide information to dermatologists and skin pathologists.
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Stolbova, O. "SKIN DISEASES OF DIFFERENT ETIOLOGY IN DOGS." THEORY AND PRACTICE OF PARASITIC DISEASE CONTROL, no. 22 (May 19, 2021): 504–8. http://dx.doi.org/10.31016/978-5-6046256-1-3.2021.22.504-508.

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Currently, skin pathologies in animals are of close attention by veterinary practitioners, since the qualities of service dogs are reduced against their background, as well as natural resistance is decreased, which contributes to the emergence of skin diseases of different etiology. In this regard, a goal was set to study and analyze the occurrence of skin diseases of different etiology in dogs. To study skin pathologies in dogs, animals were examined from 2010–2018. According to the results of the data obtained, we found that skin diseases were widespread. Among skin pathologies, diseases of parasitic etiology, allergic diseases, infectious skin diseases, diseases caused by formation of neoplasms, as well as endocrine dermopathy were recorded. At the same time, the taxonomic composition of parasites in dogs was represented by 8 species, of which the class Arachnida, Cuvier, 1812 by five species of parasites, and the class Insécta, Linnaeus, 1758 by three representatives. For skin pathologies of infectious nature, representatives of these classes are Bacillales Erenberg, 1835 (Staphylococcus Rosenbach, 1884; Streptococcus Rosenbach, 1884) and the class Eurotiomycetes Microsporum Gruby 1843; Trichophyton verrucosum (Boden, 1902).
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Morales-Avalos, Rodolfo, and Priscila Madelein Requena-Araujo. "The Dynamic Microanatomy of skin and fascia. From the deep fascia to the skin surface." Dermatology and Dermatitis 2, no. 2 (May 23, 2018): 01–05. http://dx.doi.org/10.31579/2578-8949/024.

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The study of the structure of the skin and fascia in recent years has made important advances with respect to the "dynamic anatomy" that they present, that is, the anatomical relationships and tissue interconnections that you share through different tissues. In the same way fascias have been recognized as important sources of origin of different pathologies in the last years, so the greater knowledge of their function and structure is indispensable. The aim of this article is to review the last advances in the anatomic terminology of the soft superficial tissues as advances and recent anatomical discoveries.
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Esposito, Elisabetta, Claudio Nastruzzi, Maddalena Sguizzato, and Rita Cortesi. "Nanomedicines to Treat Skin Pathologies with Natural Molecules." Current Pharmaceutical Design 25, no. 21 (September 26, 2019): 2323–37. http://dx.doi.org/10.2174/1381612825666190709210703.

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The skin and mucous membranes are subjected to many disorders and pathological conditions. Nature offers a wide range of molecules with antioxidant activity able to neutralize, at least in part, the formation of free radicals and therefore to counteract the phenomena of cellular aging. Since synthetic drugs for the treatment of skin diseases can induce resistance, it is particularly interesting to use compounds of plant origin, transporting them in pharmaceutical forms capable of controlling their release and absorption. This review provides an overview of new findings about the use of lipid-based nanosystems for the delivery of natural molecules useful on the topical treatment of skin disorders. Several natural molecules encapsulated in lipid nanosystems have been considered in the treatment of some skin pathologies or diseases. Particularly, the use of rosemary and eucalyptus essential oil, saffron derivatives, curcumin, eugenol, capsaicin, thymol and lycopene has been reported. The molecules have been alternatively encapsulated in viscous systems, such as the organogels, or in liquid systems, such as ethosomes, transferosomes, solid lipid nanoparticles and monoolein based dispersions thickened by inclusion in carbomer gels. The nanostructured forms have been in vitro and in vivo investigated for the treatment of skin disorders due to dehydration, inflammation, melanoma, wound healing, fungal infections or psoriasis. The data reported in the different studies have suggested that the cutaneous application of lipid nanosystems allows a deep interaction between lipid matrix and skin strata, promoting a prolonged release and efficacy of the loaded natural molecules. This review suggests that the application of natural molecules onto the skin by lipid-based nanosystems can provide numerous clinician benefits in dermatology and cosmetics.
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Bratchenko, I. A., M. V. Alonova, O. O. Myakinin, A. A. Moryatov, S. V. Kozlov, and V. P. Zakharov. "Hyperspectral visualization of skin pathologies in visible region." Computer Optics 40, no. 2 (January 1, 2016): 240–48. http://dx.doi.org/10.18287/2412-6179-2016-40-2-240-248.

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Gieringer, Matthias, Ramin Naim, Karl Hormann, Katherine Elliott, Alexander Sauter, and Jan Gosepath. "Angiogenesis in Different Types of the Skin: Pathologies." Otolaryngology–Head and Neck Surgery 141, no. 2_suppl (September 2009): P34—P35. http://dx.doi.org/10.1016/j.otohns.2009.06.099.

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Bristow, Ivan. "Non-ulcerative skin pathologies of the diabetic foot." Diabetes/Metabolism Research and Reviews 24, S1 (2008): S84—S89. http://dx.doi.org/10.1002/dmrr.818.

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Dissertations / Theses on the topic "Skin pathologies"

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Isaeva, O. A., O. G. Avrunin, and О. Г. Аврунін. "Basic skin pathologies and the possibilities of their diagnosis." Thesis, Дніпро, 2019, 2019. http://openarchive.nure.ua/handle/document/9954.

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Isaieva, O. A., and О. Г. Аврунін. "Video dermoscopy study of the skin." Thesis, Liverpool, United Kingdom, 2019. http://openarchive.nure.ua/handle/document/10265.

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The work is devoted to the study of the main pathologies of the skin, the possibility of diagnosing them using video dermatoscopy. Determining the differences between digital dermoscopy and video dermoscopy. The difference between the diagnosis of common skin diseases from malignant and tumors is considered. The science of fluorescent technology is being studied. The diagnostic capabilities of digital dermatoscopy are discussed.
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Damato, Elaine. "Automated analysis in reflectance confocal microscopy images of skin anatomy and pathologies." Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/automated-analysis-in-reflectance-confocal-microscopy-images-of-skin-anatomy-and-pathologies(6bff8c67-0b66-4f5e-9f3e-7e885df92977).html.

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This thesis contributes to knowledge by developing algorithms that automatically detect and quantify structures of clinical interest in reflectance confocal microscopy (RCM) images, captured in-vivo and from excised skin tissue. The first part of the thesis presents an algorithm that detects the dermalepidermal junction (DEJ), characterised by papillae, in cubes of RCM images of in-vivo skin. A cube of images is a number of mosaic images captured at different depths parallel to the skin surface. A classifier, which makes use of texture and anatomical-based features was designed. The anatomical-based features are parameters that quantify the absence and presence of papillae across different images of the cube. The second part of the thesis analyses RCM images of excised tissue collected during Mohs surgery. These tissue samples include basal cell carcinoma (BCC) and non-diseased samples. An algorithm was developed to differentiate between (i) cancerous regions, (ii) regions of inflammation, and (iii) non-diseased regions. A classifier based on texture and nuclei-concentration features was designed. The nuclei concentration in cancerous sites is different from that in nondiseased sites and thus can be used to distinguish the two. The third part of the thesis analyses RCM video sequences of in-vivo skin imaged at the level of the DEJ. The boundaries of superficial skin capillaries can be delineated by visually observing the highly reflective red blood cells (RBCs) passing through the capillaries. An algorithm that automatically detects skin capillaries in RCM video sequences was developed. Additionally, an algorithm that quantifies the velocity of RBCs in cross-sectionally imaged capillaries is devised. The change in total capillary area (per unit frame area), individual capillary parameters and RBC velocity due to incremental ultra-violet radiation (UVR) doses are analysed in both fair and dark skinned volunteers. The work presented in this thesis has the potential to increase the acceptance of RCM in the dermatology clinic, both for diagnosis and for assessing treatment response of skin conditions located at (or above) the DEJ. Additionally, the thesis enhances the potential of using RCM images of excised samples instead of preparing the tissue for histological examinations during surgery.
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Thévenet, Annick. "Modalités de la cicatrisation de plaies expérimentales et spontanées de la peau embryonnaire de poulet." Grenoble 1, 1986. http://www.theses.fr/1986GRE10039.

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Wyndham-Thomas, Chloe. "Screening for latent M. tuberculosis infection in HIV-positive patients residing in low tuberculosis incidence settings: Investigation of the current practices and identification of clinical- and immune-based strategies for improvement." Doctoral thesis, Universite Libre de Bruxelles, 2016. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/241270.

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Tuberculosis (TB) remains the main cause of death in people living with HIV (PLHIV). Indeed, PLHIV have a 20-30% greater risk of developing TB compared to HIV-uninfected subjects and have lower TB treatment success rates. In 2014, among the 9.6 million incident cases of TB reported worldwide, 12% occurred in PLHIV and 0.4 million deaths from HIV-associated TB were recorded.Mycobacterium tuberculosis is the main etiological agent for TB. For a majority of individuals, the immune response upon infection by M. tuberculosis is sufficient to prevent the development of disease, but insufficient to clear the bacteria. This leads to the persistence of viable M. tuberculosis in diverse cells with no resulting clinical manifestations, an entity known as latent tuberculosis infection (LTBI). The resulting reservoir of M. tuberculosis is vast, and an estimated one third of the world population is concerned. For subjects with LTBI, the life-time risk of reactivation and progression to TB lies between 5 and 10%. However, if co-infected with HIV, the risk is much greater and reaches 10% per year. According to a Cochrane review in 2010, the screening and treatment of LTBI in PLHIV reduces this risk by 30-60%. This prevention strategy is therefore widely recommended. However, the implementation of LTBI screening and treatment into standard HIV-care has been limited. In this work, three different approaches have been used to understand and address this issue, focusing on a low TB-incidence and high-income setting.The first approach was to assess the implementation of LTBI screening in HIV-care across Belgium and identify its barriers as perceived by the caregivers on the field. Raising awareness to this issue was an indirect objective of the study. A multi-choice questionnaire was sent to 55 physicians working in a Belgian AIDS reference center or satellite clinic. A response rate of 62% was obtained. Only 20% of participants performed LTBI screening on all their patients and notable variations in the screening methods used were observed. A large majority of participants were in favor of targeting LTBI screening to HIV-infected patients at highest risk of TB rather than a systematic screening of all PLHIV. These results have been communicated to the Belgian LTBI working group, currently updating the national LTBI screening guidelines. Indeed, targeting screening to those at highest risk of TB is an attractive strategy in low-TB incidence countries and is already recommended in the United Kingdom. However, to date, no score assessing the risk of TB in PLHIV has been validated. Among the barriers to LTBI screening identified by the participants of this first study, the most frequently reported were lack of sensitivity of screening tools, risk associated to polypharmacy and toxicity of treatment. Improving the sensitivity of LTBI screening was the cornerstone of the second approach. The available screening tools for LTBI are the tuberculin skin test (TST) and two Interferon-gamma release assays (IGRAs): the QuantiFERON-TB Gold-IT (QFT-GIT) and the T-SPOT.TB®. All three lack sensitivity in PLHIV. Various strategies to discover superior LTBI screening tools are therefore being explored, including the development of IGRAs in response to alternative M. tuberculosis antigens to those used in the QFT-GIT or T-SPOT.TB®. A potential candidate is the native Heparin-Binding Haemagglutin (nHBHA), a methylated M. tuberculosis protein regarded as a latency-associated antigen. An in-house IGRA based on nHBHA (nHBHA-IGRA) has been shown to be a promising LTBI screening tool both in immunocompetent adults and in hemodialysed patients. The contribution of this nHBHA-IGRA to the detection of M. tuberculosis in PLHIV was therefore investigated. Treatment-naïve HIV-infected subjects were recruited from 4 Brussels-based hospitals. Subjects underwent screening for latent TB using the nHBHA-IGRA in parallel to the classical method consisting of medical history, chest X-ray, TST and QFT-GIT. Prospective clinical and biological follow-up ensued, with repeated testing with nHBHA-IGRA. Among 48 candidates enrolled for screening, 9 were diagnosed with LTBI by combining the TST and QFT-GIT results (3 TST+/QFT-GIT+, 1 TST+/QFT-GIT- and 5 TST-/QFT-GIT+). All 3 TST+/QFT-GIT+ patients, the TST+/QFT-GIT- patient as well an additional 3 subjects screened positive with the nHBHA-IGRA. These 3 additional patients had known M. tuberculosis exposure risks compatible with LTBI. During follow-up (median 14 months) no case of TB was reported and nHBHA-IGRA results remained globally constant. Multiplex analysis confirmed IFN- as the best read-out for the assay. From this study, we concluded that the nHBHA-IGRA appears complementary to the QFT-GIT for the screening of LTBI in PLHIV and the combination of the two tests may increase the sensitivity of screening. A large-scale study is however necessary to determine whether combining nHBHA-IGRA and QFT-GIT offers sufficient sensitivity to dismiss TST, as suggested by our results. In the same study, a group of HIV-infected adults with clinical suspicion of active TB were also recruited and tested with nHBHA-IGRA. Contrary to results in HIV-uninfected subjects, the nHBHA-IGRA could not discriminate between LTBI and active TB in PLHIV. This is an important caveat as HIV-infected subjects may present subclinical TB.A different angle was used for the third approach to the problem of LTBI in PLHIV. Systemic immune activation (SIA) is one of the principal driving forces in the natural course of HIV-infection. Despite long-term viral suppression by combination antiretroviral treatment (cART), a low-level SIA persists and is associated with an early-onset of age-associated disorders such as cardiovascular disease, dementia and osteoporosis. Causes of SIA in PLHIV are multiple and certain chronic infections appear to be implicated. A recent study in South Africa found that LTBI in PLHIV was associated with an increase in circulating activated CD8+ T-cells. If LTBI should contribute to the persistence of SIA, its screening and treatment could have an additional benefit on the clinical outcome of PLHIV. To investigate this theory, the expression of T-cell activation markers (CD38 and HLADR) as well as the level of plasmatic markers of immune activation (IL-6, sCD14, D-Dimers) were compared between subjects presenting active TB, subjects with LTBI and M. tuberculosis-free persons, with and without HIV-infection. In accordance with previous studies, active TB was associated with higher levels of SIA biomarkers in both HIV-infected and -uninfected groups. Among the HIV-uninfected subjects, no significant difference in biomarker level was found between those presenting LTBI and those with no evidence of M. tuberculosis. The effect of LTBI on activation biomarkers in the HIV-infected groups remained inconclusive because of the small number of individuals in the HIV+/LTBI group. Further investigation is therefore warranted. Interestingly, it was found that plasmatic markers may have a greater sensitivity for the detection of M. tuberculosis-associated SIA than the T-cell activation markers, an important result for future studies.Overall, LTBI in PLHIV is a challenging topic, in particular because of the lack of a gold-standard for the diagnosis of LTBI. Despite suboptimal tools, the evident clinical impact of LTBI screening and treatment in PLHIV on TB incidence justifies its implementation in standard HIV-care. In low TB-incidence countries, who, when and how to screen for LTBI in PLHIV remains unclear. This work offers an overview on the subject with particular focus on possible measures for improvement in the field.
Doctorat en Sciences médicales (Médecine)
info:eu-repo/semantics/nonPublished
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Djeldjellani, Mohamed. "Étude d'un applicateur destiné à la mesure des propriétés diélectriques de la peau par réflectométrie temporelle." Besançon, 1989. http://www.theses.fr/1989BESA2019.

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Appareil de mesure de la permittivite de la peau "in vivo" en haute frequence (0,1 a 10 ghz). Variations de la dispersion dielectrique dues a l'hydratation, la vascularisation, a l'epaisseur du tissu sous-cutane
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Dauchel, Hélène. "Le système du complément et la cellule endothéliale : biosynthèse in vitro des protéines de la voie alterne et activation pathologique au cours des vascularités leucocytoclasiques." Rouen, 1993. http://www.theses.fr/1993ROUES032.

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Ce travail est consacré à l'analyse des relations existant entre la cellule endothéliale et le complément au cours de l'inflammation. Une première approche a consisté en une étude in vitro de la synthèse constitutive et de sa régulation, sous l'influence de cytokines pro-inflammatoires et d'un agent pharmacologique anti-inflammatoire, par les cellules endothéliales, de protéines essentielles de la voie alterne: les protéines activatrices C3 et facteur B et les protéines inhibitrices facteur H et facteur I. Les résultats suggèrent que, in vivo, les cellules endothéliales seraient orientées, dans des conditions physiologiques normales, vers une fonction inhibitrice de l'activation spontanée du complément par la voie alterne, c'est-a-dire vers une fonction anti-inflammatoire. Cytokines et corticoïdes influenceraient les synthèses dans un sens, qui respectivement, favoriserait l'activation locale du complément ou au contraire renforcerait son inactivation constitutive. L'existence de ces synthèses locales hautement régulées des protéines de la voie alterne du complément constituerait de nouveaux éléments dans les processus d'activation de l'endothélium au cours de l'inflammation et d'inactivation de l'endothélium au cours de glucocorticothérapie. La deuxième approche est une étude clinique de l'implication du complément au cours de pathologies inflammatoires de l'endothélium à complexes immuns: les vascularités leucocytoclasiques cutanées. Elle a permis de démontrer: i) l'intérêt, dans l'exploration clinique du complément au cours de ces maladies, de nouveaux dosages plasmatiques des marqueurs d'activation initiale et finale, le fragment C3d,g et le complexe d'attaque membranaire (CAM); ii) l'implication de l'intégralité de la cascade, jusqu'à formation du CAM  à la surface de l'endothélium, dans la genèse des lésions vasculaires; iii) la responsabilité potentielle prépondérante des immunoglobulines A dans l'activation pathologique du complément; iv) l'intervention d'un processus de contrôle de l'activation par les protéines régulatrices du complément. A la fois source et cible du complément, l'endothélium pourrait potentialiser le processus inflammatoire local, mais aussi subir les dommages consécutifs à son activation pathologique
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Thibault, Jacky. "Contribution a l'etude des moyens de prevention de l'escarre de position assise : developpement d'une plateforme de mesure des pressions et deplacements au niveau de l'assise et mise au point d'une aide technique a la prevention, active et personnlisee, geree par microprocesseur." Poitiers, 1987. http://www.theses.fr/1987POIT2288.

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Aouidet, Abdallah. "L'installation et le devenir de l'athérome chez le singe Cynomolgus (Macacus fascicularis) soumis à un régime hypercholestérolémique : étude des parois aortiques et coronariennes, des paramètres sériques et cutanés." Toulouse 3, 1987. http://www.theses.fr/1987TOU30237.

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Hanauer, André. "Le chromosome x humain : recherche de sequences exprimees et localisation genique de deux loci correspondanta des maladies." Université Louis Pasteur (Strasbourg) (1971-2008), 1989. http://www.theses.fr/1989STR13010.

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Caracterisation d'expressions geniques liees au chromosome x, de 6 sequences genomiques humaines liees au chromosome x; localisation du syndrome coffin-lowry par analyse de linkage et de la dysplasie ectodermique anhidrotique
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Books on the topic "Skin pathologies"

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The skin collector. Rearsby, Leicester: WF Howes Ltd, 2015.

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Essential skin pathology. London: Mosby, 1999.

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1957-, Swanson Paul E., ed. Cutaneous adnexal tumors: A guide to pathologic diagnosis. Chicago: ASCP Press, 1991.

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J, Herzberg Arlene, ed. Atlas of dermatopathology. Philadelphia: Saunders, 1996.

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J, Honig Paul, and Jaworsky Christine, eds. Pediatric dermatopathology: Clinical and pathologic correlations. Boston: Butterworth-Heinemann, 1994.

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A concise atlas of dermatopathology. London: Gower Medical Pub., 1993.

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1936-, Ackerman A. Bernard, Sison-Torre Evita Q, Gelmetti Carlo, and Annessi Giorgio, eds. Pediatric dermatology and dermatopathology: A text and atlas. Philadelphia: Lea & Febiger, 1990.

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Caputo, Ruggero. Pediatric dermatology and dermatopathology: A concise atlas. London: Martin Dunitz, 2002.

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Cascarini, Luke, Clare Schilling, Ben Gurney, and Peter Brennan. In the clinic. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198767817.003.0005.

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This chapter discusses oral and maxillofacial surgery in the clinic, including, Mandible fractures, Orbital floor fractures, Zygoma fractures, Maxillary fractures, Nose, naso-ethmoidal, and frontal bone fractures, Face and scalp soft tissue injuries, Dento-alveolar: assessment for extractions, Dento-alveolar: impacted teeth, Dento-alveolar: jaw pathologies, Temporomandibular joint problems, Oral and facial pain, Management of oral lesions, Management of neck lumps, Skin tumours, Work-up for major head and neck oncoplastic surgery, Reviewing head and neck cancer patients, Salivary gland diseases, Orthognathic patients, and Miscellaneous conditions in the clinic
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Skin Pathology. Churchill Livingstone, 2002.

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Book chapters on the topic "Skin pathologies"

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Eissa, Azza, and Eleftherios P. Diamandis. "Kallikrein Protease Involvement in Skin Pathologies Supports a New View of the Origin of Inflamed Itchy Skin." In Proteases and Their Receptors in Inflammation, 51–71. Basel: Springer Basel, 2011. http://dx.doi.org/10.1007/978-3-0348-0157-7_3.

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Roughley, Mark. "Pores, Pimples and Pathologies: 3D Capture and Detailing of the Human Skin for 3D Medical Visualisation and Fabrication." In Advances in Experimental Medicine and Biology, 141–60. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47483-6_8.

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Richardson, Sunil, and Rakshit Vijay Sinai Khandeparker. "Cleft Rhinoplasty." In Oral and Maxillofacial Surgery for the Clinician, 1703–32. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-1346-6_76.

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AbstractCleft rhinoplasty is one of the most difficult and challenging aesthetic surgeries to carry out and bears a significant impact on the overall nasal aesthetics and function. Two reasons understood for this are the simultaneous involvement of all the layers of the nose including the skin, cartilage, skeleton and vestibular lining (this being the principal reason) and the significant scarring that is the consequence of multiple previous surgical interventions. There is a mention of numerous techniques for ultimate correction of unilateral and bilateral cleft nasal deformities but no single technique has till date provided a definite solution for correction of all the problems that accompany these deformities. There is a revised interest in performing primary rhinoplasties at the time of lip repair with or without presurgical orthopedics but these procedures may still warrant definitive rhinoplasty at a later date. The purpose of this chapter is to provide a comprehensive review of cleft rhinoplasty in the most systematic manner beginning with the pathologic anatomy followed by surgical timing, pre-operative evaluation and surgical correction. The chapter also discusses the use of various grafts in a typical cleft rhinoplasty case as well as treatment strategy for management of both, unilateral and bilateral cleft nasal deformities. The outcomes as well as complications and a note on further revisions have also been presented.
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AlBastaki, Usama M., and Claude Pierre-Jerome. "The skin: anatomy and pathologies in diabetes." In The Essentials of Charcot Neuroarthropathy, 287–98. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-323-99352-4.00007-3.

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Zhang, Guolong, Peiru Wang, and Xiuli Wang. "Skin Ageing and Cancer." In The Role of Matrix Metalloproteinase in Human Body Pathologies. InTech, 2017. http://dx.doi.org/10.5772/intechopen.70266.

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Tüting, T., and E. Gaffal. "Regulatory Role of Cannabinoids for Skin Barrier Functions and Cutaneous Inflammation." In Handbook of Cannabis and Related Pathologies, 543–49. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800756-3.00067-3.

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Hakim, Alan J., Gavin P. R. Clunie, and Inam Haq. "Rheumatological emergencies." In Oxford Handbook of Rheumatology, 609–25. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199587186.003.0024.

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Septic arthritis 610 Infections in patients taking biologic therapy 614 Acute systemic lupus erythematosus 616 Systemic vasculitis 622 Scleroderma crises 624 Methotrexate-induced pneumonitis 625 For acute skin and cardiac pathologies see b Chapter 4, p 193. For vertebral fracture see b Chapter 20, p 525...
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Rabe, Eberhard, and Felizitas Pannier. "Epidemiology and classification of venous disease." In ESC CardioMed, 2805–6. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0669.

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Chronic venous diseases are frequent pathologies in the general population. The most common chronic venous pathologies are varicose veins and chronic venous insufficiency including post-thrombotic syndrome. In the general adult population, varicose veins are present in up to 25% of people with an increasing prevalence with age. Risk factors include advanced age, genetic predisposition, female sex, and multiparity. The term chronic venous insufficiency summarizes the clinical signs of chronic venous disease with oedema, skin changes, or venous ulcers. More than 15% of the population is affected by chronic venous insufficiency. Risk factors include advanced age, obesity, and prolonged sitting.
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Vardasca, Ricardo, and Carolina Magalhaes. "Towards an Effective Imaging-Based Decision Support System for Skin Cancer." In Advances in Healthcare Information Systems and Administration, 354–82. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-7709-7.ch021.

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The usage of expert systems to aid in medical decisions has been employed since 1980s in distinct applications. With the high demands of medical care and limited human resources, these technologies are required more than ever. Skin cancer has been one of the pathologies with higher growth, which suffers from lack of dermatology experts in most of the affected geographical areas. A permanent record of examination that can be further analyzed are medical imaging modalities. Most of these modalities were also assessed along with machine learning classification methods. It is the aim of this research to provide background information about skin cancer types, medical imaging modalities, data mining and machine learning methods, and their application on skin cancer imaging, as well as the disclosure of a proposal of a multi-imaging modality decision support system for skin cancer diagnosis and treatment assessment based in the most recent available technology. This is expected to be a reference for further implementation of imaging-based clinical support systems.
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Yokozeki, Hiroo. "New Pathologies of Skin Disorders Identified from the History of Perspiration Research." In Perspiration Research, 1–6. S. Karger AG, 2016. http://dx.doi.org/10.1159/000446750.

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Conference papers on the topic "Skin pathologies"

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Gavrilov, Dmitriy, Lyubov Lazarenko, and Emil Zakirov. "AI Recognition in Skin Pathologies Detection." In 2019 International Conference on Artificial Intelligence: Applications and Innovations (IC-AIAI). IEEE, 2019. http://dx.doi.org/10.1109/ic-aiai48757.2019.00017.

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Lihachev, Alexey, Emilija Vija Plorina, Alexander Derjabo, Marta Lange, and Ilze Lihacova. "Evaluation of skin pathologies by RGB autofluorescence imaging." In The Second International Conference "Biophotonics-Riga 2017", edited by Janis Spigulis. SPIE, 2017. http://dx.doi.org/10.1117/12.2297007.

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Anand, Suresh, Riccardo Cicchi, Alessandro Cosci, Susanna Rossari, Dimitrios Kapsokalyvas, Enrico Baria, Vincenza Maio, et al. "Fluorescence ratiometric classifier for the detection of skin pathologies." In European Conference on Biomedical Optics. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/ecbo.2015.95371r.

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Lihacova, Ilze, Aleksandrs Derjabo, and Janis Spigulis. "A multispectral imaging approach for diagnostics of skin pathologies." In European Conferences on Biomedical Optics, edited by Volker Deckert and Nirmala Ramanujam. SPIE, 2013. http://dx.doi.org/10.1117/12.2032491.

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Anand, Suresh, Riccardo Cicchi, Alessandro Cosci, Susanna Rossari, Dimitrios Kapsokalyvas, Enrico Baria, Vincenza Maio, et al. "Fluorescence ratiometric classifier for the detection of skin pathologies." In European Conferences on Biomedical Optics, edited by J. Quincy Brown and Volker Deckert. SPIE, 2015. http://dx.doi.org/10.1117/12.2183786.

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Seviaryna, Inna, Shizuka Nakada, Sachiko Yoshida, Naohiro Hozumi, and Roman G. Maev. "Multi-layered phantoms mimicking skin pathologies for high-resolution ultrasound." In Ultrasonic Imaging and Tomography, edited by Nicole V. Ruiter and Brett C. Byram. SPIE, 2020. http://dx.doi.org/10.1117/12.2549833.

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Putintseva, Maria, Ekaterina Korneeva, and Elena Velichko. "New approach to detect skin pathologies with polarimetric detection and processing." In Saratov Fall Meeting 2018: Optical and Nano-Technologies for Biology and Medicine, edited by Valery V. Tuchin and Elina A. Genina. SPIE, 2019. http://dx.doi.org/10.1117/12.2523344.

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Yanina, Irina Y., Viktor V. Nikolaev, Аleksey A. Markelov, Maksim B. Miroshnichenko, Evgeniy E. Buyko, Vladimir V. Ivanov, Vyacheslav I. Kochubey, and Valery V. Tuchin. "THz spectroscopy of skin pathologies associated with water migration and content." In Fourth International Conference on Terahertz and Microwave Radiation: Generation, Detection, and Applications, edited by Oleg A. Romanovskii and Yurii V. Kistenev. SPIE, 2020. http://dx.doi.org/10.1117/12.2581719.

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Sharikova, M. O. "Hyperspectral imaging of human skin pathologies: tasks to be solved and equipment used." In Акустооптические и радиолокационные методы измерений и обработки информации. Москва: Научно-технологический центр уникального приборостроения РАН, 2021. http://dx.doi.org/10.25210/armimp-2021-21.

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Strąkowska, M., M. Strzelecki, A. Kaszuba, and B. Więcek. "Thermal parameter extraction for screening procedure of skin pathologies based on the cold provocation." In 2016 Quantitative InfraRed Thermography. QIRT Council, 2016. http://dx.doi.org/10.21611/qirt.2016.125.

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