Relevant bibliographies by topics / Skin associated

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Skin associated'

Author: Grafiati
Published: 25 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Skin associated"

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Liu, Jesse, and Jesse Veenstra. "COVID-19 Associated Onychomadesis." SKIN The Journal of Cutaneous Medicine 5, no. 3 (May 17, 2021): 286–88. http://dx.doi.org/10.25251/skin.5.3.11.

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Goldberger, David, Kristin McCloskey, Ryan Surmaitis, and Dilan Patel. "Skin necrosis associated with cocaine “skin popping”." Visual Journal of Emergency Medicine 6 (January 2017): 41–42. http://dx.doi.org/10.1016/j.visj.2016.08.007.

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Zambito, Jeanette R., Pooja R. Shah, Glynis A. Scott, Andrew Evans, and Lisa A. Beck. "CVID-associated Granulomatous Dermatosis Resembling Sarcoidosis." SKIN The Journal of Cutaneous Medicine 3, no. 4 (July 8, 2019): 253–57. http://dx.doi.org/10.25251/skin.3.4.4.

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Common variable immunodeficiency (CVID) is a disorder of the adaptive immune system predominantly characterized by hypogammaglobulinemia and variable T-cell abnormalities. Patients classically present with recurrent sinopulmonary infections, but interstitial lung disease, autoimmunity, and lymphoproliferative disorders are also common. Approximately 10% of CVID patients are reported to have noncaseating granulomatous disease that is indistinguishable from sarcoidosis on pathology; it most commonly affects the lungs, lymph nodes, and liver.We present the case of a 75-year-old male with known CVID who presented with granulomatous dermatosis on the trunk and extremities in the setting of progressive cognitive impairment, new-onset cough with ground glass opacities on chest computed tomography in the setting of stable mediastinal lymphadenopathy, and the presence of granulomas on prior bone marrow biopsy, initially suggesting the diagnosis of sarcoidosis. Though clinically and histologically similar, it is important to make the distinction between CVID-associated granulomatous disease and sarcoidosis in order to select appropriate treatment.
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Millichap, J. Gordon. "Lamotrigine-Associated Skin Rash." Pediatric Neurology Briefs 13, no. 8 (August 1, 1999): 61. http://dx.doi.org/10.15844/pedneurbriefs-13-8-8.

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Lee, Jeong Deuk. "Cold-associated skin disorders." Journal of the Korean Medical Association 62, no. 4 (2019): 193. http://dx.doi.org/10.5124/jkma.2019.62.4.193.

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Alessi, Elvio. "HIV-associated skin conditions." Current Opinion in Infectious Diseases 6, no. 5 (October 1993): 668–77. http://dx.doi.org/10.1097/00001432-199310000-00009.

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Gray, Mikel, Joyce M. Black, Mona M. Baharestani, Donna Z. Bliss, Janice C. Colwell, Margaret Goldberg, Karen L. Kennedy-Evans, Susan Logan, and Catherine R. Ratliff. "Moisture-Associated Skin Damage." Journal of Wound, Ostomy and Continence Nursing 38, no. 3 (2011): 233–41. http://dx.doi.org/10.1097/won.0b013e318215f798.

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Blaise, Géraldine, Arjen F. Nikkels, Trihn Hermanns-Lê, Nazli Nikkels-Tassoudji, and Gérald E. Piérard. "Corynebacterium-associated skin infections." International Journal of Dermatology 47, no. 9 (September 2008): 884–90. http://dx.doi.org/10.1111/j.1365-4632.2008.03773.x.

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McCoy, Christopher M. "Leflunomide-Associated Skin Ulceration." Annals of Pharmacotherapy 36, no. 6 (June 2002): 1009–11. http://dx.doi.org/10.1345/aph.1a347.

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OBJECTIVE: To report a case of skin ulceration as a result of treatment with leflunomide for rheumatoid arthritis. CASE SUMMARY: A 78-year-old white woman developed bilateral leg ulcers after 6 months of treatment with leflunomide for rheumatoid arthritis. A history of leg ulcers after methotrexate therapy had been documented. Serologic and diagnostic tests did not support an alternate process. Other medications prescribed were oral ethinyl estradiol 0.05 mg/d, felodipine 5 mg/d, and paroxetine 20 mg/d, for which no documented correlation with the skin breakdown could be made. DISCUSSION: This is the first published case describing a possible relationship between the use of the immunosuppressant agent leflunomide and skin ulceration. CONCLUSIONS: Skin breakdown and ulceration is a recognized adverse effect of drugs with immunosuppressant activity such as methotrexate. Leflunomide, a newer agent prescribed in the treatment of rheumatoid arthritis, may now be listed among the drugs in this category associated with this adverse drug effect.
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Akgül, Baki, James C. Cooke, and Alan Storey. "HPV-associated skin disease." Journal of Pathology 208, no. 2 (2005): 165–75. http://dx.doi.org/10.1002/path.1893.

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Dissertations / Theses on the topic "Skin associated"

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Martínez, Gutiérrez Alfredo. "Regulation of Sirtuin-dependent skin cell Senescence by dermatology-associated compounds." Doctoral thesis, Universitat de Barcelona, 2019. http://hdl.handle.net/10803/668801.

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One of the main causal factors of skin aging is ultraviolet radiation as part of sun exposure. This radiation induces many changes at the molecular level that alter the proper function of skin biological processes, being cellular senescence one characteristic process included in this group. Senescence is a cellular state in which the cells enters an irreversible cell cycle arrest and develops a proinflammatory phenotype that contributes to tissue damage and aging. In this context, the aim of this thesis was to find compounds that both activate sirtuins and protect against UV-induced cellular senescence in human dermal fibroblasts. Among the 30 compounds tested, 8 compounds induced sirtuin activation, while 2 compounds protected against UV-induced senescence. Only one of these compounds had positive effects on both processes. Further charaterization of the compound revealed that the protection exerted by this compound against cellular senescence was mediated by SIRT1 activation. Besides, we observed that this compound activates autophagy, one of the stress response pathways of the cell linked to increased longevity and regulated by SIRT1, among other factors. In conclusion, the caracterized compound has proven to be a good candidate as skin anti aging compound through its action on autophagy, sirtuins and senescence.
Uno de los principales factores causantes del envejecimiento de la piel es la radiación ultravioleta procedente del sol. Esta radiación induce una serie de cambios que alteran la correcta función biológica de la piel, entre los que destaca la senescencia celular, un proceso en el cual las células dejan de proliferar y desarrollan un fenotipo inflamatorio que incrementa el daño en el tejido. En este contexto, el objetivo de esta tesis era encontrar compuestos que fueran capaces de activar las sirtuínas y de proteger frente a la senescencia inducida por daño ultravioleta en fibroblastos de piel humana. Del total de 30 compuestos testados, 8 fueron capaces de inducir la activación de las sirtuínas, mientras que 2 fueron capaces de proteger frente a la senescencia inducida por ultravioleta. De todos estos compuestos, sólo uno fue capaz de tener un efecto positivo en ambos procesos. En posteriores ensayos para caracterizar la acción de este compuesto, observamos que la protección del éste frente a la senescencia inducida por ultravioleta era mediada por SIRT1. Además, observamos que este compuesto era capaz de activar la autofagia en estas células, una de las respuestas a estrés en la célula que promueve la longevidad celular y esta controlada por SIRT1, entre otros factores. En conclusión, el compuesto caracterizado ha demostrado ser un buen candidato para su uso en la prevención del envejecimiento de la piel a través de su acción sobre sirtuínas, autofagia y protección de la senescencia.
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Azzarello, Lora M. "Psychological Factors Associated with Skin Cancer Detection Behaviors in Individuals with a Family History of Melanoma." [Tampa, Fla.] : University of South Florida, 2003. http://purl.fcla.edu/fcla/etd/SFE0000174.

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Al-Myouf, Abdullah Abdulaziz. "Cadherins, catenins and associated proteins in normal epidermis, basal cell carcinoma and other cutaneous tumours : an immunohistochemical study." Thesis, University of Glasgow, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341723.

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West, Julie Ann. "Factors Associated With Tuberculin Skin Test Positivity Prevalence in U.S. Medical Laboratory Microbiologists." Thesis, Walden University, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3607454.

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Prior research has indicated that healthcare personnel (HCP) who work in areas where Mycobacterium tuberculosis poses an occupational hazard are at high risk of tuberculin skin test (TST) positivity and subsequent conversion to active tuberculosis (TB). U.S. medical laboratory microbiologists confront similar hazards but have not been studied outside of the HCP aggregate. The purpose of this study was to fill this gap by examining the relationships between the predictor variables of self-reported history of bacille Calmette-Guérin (BCG) immunization, place of birth, and years of laboratory experience and the outcomes of self-reported lifetime TST positivity, preventive treatment noninitiation, and barriers to treatment adherence for this subgroup. This quantitative, cross-sectional study was guided by the epidemiologic triad model. A researcher-designed self-administered questionnaire including Part A of the Brief Medication Questionnaire was mailed to 4,335 U.S. microbiologist members of the American Society for Clinical Pathology. From the 1,628 eligible respondents, results showed that prevalence of positive TSTs (17.0%) and treatment noninitiation (9.8%) was low. Multivariate analysis identified BCG and foreign birth, as well as age, nonoccupational exposure, history of TB, work in mycobacteriology, and work outside of microbiology as predictors of a positive TST; foreign birth was a predictor of treatment noninitiation. Additional research is needed to identify other laboratorian groups at increased risk for developing TB. These results enhance positive social change by helping to inform recommendations in the global fight to stop the spread of TB, as well as improve allocation of resources among this specific group of HCP.

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Wu, Ling. "A HYPER TH17 RESPONSE CONNECTS THE PSORIASIS-ASSOCIATED ACT1 VARIANT TO SKIN INFLAMMATION." Case Western Reserve University School of Graduate Studies / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=case1409866338.

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Large, Juliette. "Characterisation of Staphylococci associated with atopic eczema and chronic plaque psoriasis." Thesis, Aston University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341358.

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Arnold, Long Mary Caroleen. "Building Expert Consensus on Including Indicators of Moisture-Associated Skin Damagein The National Database of Nursing Quality Indicators (NDNQI)." Otterbein University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=otbn1461076119.

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Tawadros, Fady, Sakshi Singal, Maria Zayko, and Devapiran Jaishankar. "Mucosal Associated Lymphoid tissue of the Skin, A Common Entity in a Rare Location." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/55.

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Marginal zone (MZ) lymphomas (MZLs) represent a group of lymphomas originating from B lymphocytes of the “marginal zone” which is the external part of the secondary lymphoid follicles. The WHO classifies MZL into 3 entities; extranodal MZL, splenic MZL and nodal MZL. Extranodal marginal zone lymphoma (EMZL) can arise in different tissues, including the stomach, salivary gland, lung, small bowel, thyroid, ocular adnexa and skin. We present a 25 years old female with a history of angioedema and chronic cutaneous eczema who developed an unusual EMZL. Patient presented with a history of rapidly enlarging skin nodule on her left elbow that had been present for almost one year. Over a period of 2-3 weeks she felt the nodule rapidly changed in size and shape. Excisional biopsy of the mass revealed a lymphoid infiltrate based in the reticular dermis and focally extending into the subcutaneous adipose tissue with formation of disrupted lymphoid follicles positive for CD20, CD23 and BCL2 but negative for CD10, Cyclin D1 and SOX11. Diagnosis was consistent with extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma). Patient on presentation did not have any B symptoms other cutaneous lesions, lymphadenopathy or hepatosplenomegaly. PET scan revealed no evidence of abnormal uptake leading to a final Stage IE definition. Patient initiated definitive radiation therapy. EMZL accounts for 5 -10 % of non-Hodgkin lymphoma. It has been described often in organs that are normally devoid of germinal centers. It may arise in reactive lymphoid tissue induced by chronic inflammation in extranodal sites. Primary cutaneous marginal zone lymphoma (PCMZL) is associated with infectious etiologies such as Borrelia burgdorferi and less commonly with viral infections or in relation to autoimmune disorders. Autoimmune disorders, specifically Sjögren's syndrome is associated with a 30-fold increased risk of marginal zone lymphoma. Localized disease can be treated by local radiotherapy, intralesional injections or excision. Widespread skin disease is usually treated with a CD20 directed monoclonal antibody-Rituximab. Patients with PCMZL usually have an indolent clinical course. Extracutaneous dissemination of MALT Lymphoma is uncommon and happens in 6-8 % of patients. The 5 years overall survival is between 98-100%. Family physicians and dermatologists should have a high index of suspicion for this rare lymphoma subtype especially in patients with inflammatory chronic skin conditions and atopy.
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Medina, Lopez Daniel Christofer. "Assessing Diversity, Culturability and Context-dependent Function of the Amphibian Skin Microbiome." Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/84855.

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Emergent infectious diseases are a major driver of the accelerated rates of biodiversity loss that are being documented around the world. Global losses of amphibians provide evidence of this, especially those associated with chytridiomycosis, a lethal skin disease caused by the fungus Batrachochytrium dendrobatidis (Bd). Amphibian skin can harbor diverse bacterial communities that, in some cases, can inhibit the growth of Bd. Thus, there is interest in using skin bacteria as probiotics to mitigate Bd infections in amphibians. However, experiments testing this conservation approach have yielded mixed results, suggesting a lack of understanding about the ecology of these microbial communities. My dissertation research aimed to assess basic ecological questions in microbial ecology and to contribute to the development of probiotics using amphibian skin bacteria. First, to assess whether environmental conditions influence the function of amphibian skin bacterial communities, I conducted a field survey across low and high elevation populations of an amphibian host to assess their skin bacterial communities and metabolite profiles. I found that similar bacterial communities produced different metabolites at different locations, implying a potential functional plasticity. Second, since culturing is critical for characterizing bacteria, I aimed to identify the culture media (low vs high nutrient concentration) that recovers the most representative fraction of the amphibian skin bacterial community. I found that media with low nutrient concentrations cultured a higher diversity and recovered a more representative fraction of the diversity occurring on amphibian skin. I also determined that sampling more individuals is critical to maximize culture collections. Third, I assessed the diversity of the amphibian skin fungal community in relation to Bd infection across eight amphibian species. I determined that amphibian species was the most important predictor of fungal diversity and community structure, and that Bd infection did not have a strong impact. My dissertation highlights the importance of environmental conditions in the function of amphibian skin bacteria, expands our knowledge of the understudied fungal component of the amphibian skin microbiome, and complements current efforts in amphibian conservation.
Ph. D.
In light of the global losses of amphibian diversity due to, in part, the skin disease chytridiomycosis (caused by the fungus Batrachochytrium dendrobatidis [Bd]); the discovery that some amphibian-skin bacteria can inhibit Bd growth provides hope for amphibian conservation via their use as probiotics to control Bd infections. However, experiments testing these bacteria have yielded inconsistent results, suggesting a limited understanding about the factors influencing the diversity of amphibian-skin microbes and their ability to inhibit Bd. Also, efforts to identify effective candidates for probiotic therapy are still premature. Thus, my dissertation had an ecological emphasis and focused on complementing conservation efforts focused on probiotics. First, I assessed whether environmental conditions influence bacteriallyproduced products, which can have antifungal properties. Specifically, I surveyed low and highelevation populations of an amphibian species to assess the skin-bacteria and their products. I determined that, while skin bacterial communities were similar across an environmental gradient, their products differed, suggesting potential different antifungal properties. Second, I assessed the ability of different culture media types (low vs high nutrient concentrations) to grow a high portion and most representative fraction of the amphibian-skin bacteria. I found that culture media with low nutrient concentrations allowed the growth of a higher diversity of the bacteria occurring on the amphibian-skin, including the abundant members, and also determined that including a large number of amphibians is the best way to improve culture collections. Third, I assessed the fungal diversity occurring in the skin of different amphibian species and how it might response to Bd infections, and examined whether skin-fungi interact with co-occurring bacteria. I found that the amphibian species was the most important driver of the fungal diversity, and that Bd infection did not influence the diversity of these communities. Moreover, I identified the most diverse fungal phyla occurring in the amphibian-skin and determined that these fungi might interact with co-occurring bacteria. My dissertation contributes to our understanding about the influence of the environmental conditions in the amphibian-skin bacteria, expands our limited knowledge on the amphibian-skin fungi, and complement current amphibian conservation efforts.
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Wax, Noah David. "Comparative genomics of bacteria from amphibian skin associated with inhibition of an amphibian fungal pathogen Batrachochytrium dendrobatidis." Thesis, Virginia Tech, 2021. http://hdl.handle.net/10919/103961.

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Chytridiomycosis is a fungal skin disease in amphibians that is primarily caused by Batrachochytrium dendrobatidis (Bd). We analyzed whole genome sequences of 40 bacterial isolates that had been previously cultured from the skin of four amphibian species from Virginia, USA, and tested for their ability to inhibit Bd growth via an in vitro challenge assay. These 40 isolates spanned 11 families and 13 genera. The aim of this study was to identify genomic differences among the amphibian skin bacterial isolates and generate hypotheses about possible differences that could contribute to variation in their ability to inhibit the growth of Bd. We identified sixty-five gene families that were present in all 40 isolates. We also looked for the presence of biosynthetic gene clusters. While this set of isolates contained a wide variety of biosynthetic gene clusters, the two most abundant clusters with potential anti-fungal activity were siderophores (N=17) and Type III polyketide synthases (N=20). We then analyzed the isolates belonging to the phylum Proteobacteria in more detail. We identified 197 gene families that were present in all 22 Proteobacteria. We examined various subsets of the Proteobacteria for genes for specific compounds with known activity against fungi, including chitinase and violacein. We identified a difference in the number, as well as amino acid sequences, of predicted chitinases found in two isolates belonging to the genus Agrobacterium that varied in their inhibition of Bd. After examining the annotated genomes, we identified a predicted chitinase in a Sphingomonas isolate that inhibited the growth of Bd that was absent from the five Sphingomonas isolates that did not inhibit Bd growth. The genes vioA, vioB, vioC, vioD and vioE are necessary to produce violacein, a compound which inhibits the growth of Bd. Differences in these genes were identified in three out of the four Janthinobacterium isolates. Of these three isolates, two showed strong inhibition of Bd growth, while the third inhibited Bd growth to a lesser extent. Using comparative genomics, we generated several testable hypotheses about differences among bacterial isolates that could contribute to variation in ability to inhibit Bd growth. Further work is necessary to test the various mechanisms utilized by amphibian skin bacterial isolates to inhibit Bd.
Master of Science
Many amphibian population declines around the world have been caused by chytridiomycosis, a skin disease. This disease is caused by the fungus Batrachochytrium dendrobatidis (Bd). The skin of amphibians is also home to many bacteria that can provide important functions for the amphibian host, like preventing infection by Bd. To understand how these bacteria might provide protection, we examined the entire genomes of 40 bacterial isolates that reside on the skin of four amphibian species from Virginia, USA. These bacteria were previously tested for their ability to prevent Bd growth and 40 of them were chosen for sequencing based on selecting closely related isolates that varied in their ability to inhibit Bd growth. This allowed us to compare their genomes and generate hypotheses about possible genomic differences that could contribute to the variation in Bd growth inhibition. We identified sixty-five gene families that were present in all 40 bacteria. We also looked for sets of genes (biosynthetic gene clusters) that are known to produce secondary metabolites, which are compounds that can include antifungals. The two most abundant clusters we identified that had the potential to produce compounds that inhibit fungal growth were siderophores and Type III polyketide synthases. We then looked for genes that were not part of biosynthetic gene clusters that could produce specific compounds that can inhibit Bd growth, such as chitinase and violacein. We found variation in chitinase genes in several isolates that seemed to be associated with the ability to inhibit Bd growth. In addition, there were some differences in violacein genes that should be examined more in future studies. Overall, we suggest that using comparative genomic approaches can be valuable for identifying key bacterial functions in the microbiome.
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Books on the topic "Skin associated"

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Rhein, Linda D. Skin, hair and nail structure and function and associated diseases. [New York]: Society of Cosmetic Chemists, 1997.

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Reflexology and associated aspects of health: A practitioner's guide. Berkeley, Calif: North Atlantic Books, 2005.

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Song, Young-Ho. The targeting of phospholipid liposomes to oral and skin-associated bacteria and their use forbactericide delivery. Manchester: University of Manchester, 1994.

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Sanderson, Neil Michael. Interaction of cationic liposomes with the skin-associated bacteria Staphylococcus epidermis for the delivery of antibacterial agents. Manchester: University of Manchester, 1996.

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Great Britain. Associate Parliamentary Group on Skin. Report on the enquiry into skin diseases in elderly people: A report of the Associate Parliamentary Group on Skin. London: Great Britain, Associate Parliamentary Group on Skin, 2000.

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Foundation, Mammoth Lakes, and Mammoth Ski Museum, eds. Tracks of passion: Eastern Sierra skiing, Dave McCoy, and Mammoth Mountain : a photo essay. Mammoth Lakes, CA: Mammoth Lakes Foundation, 2008.

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Estwanik, Joseph J. Sportsmedicine for the combat arts. Charlotte, NC: Boxergenics Press, 1996.

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Bundy, Christine. Visible Difference Associated With Disease: Skin Conditions. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780199580521.013.0029.

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Eluri, Swathi. Catheter-Associated Infections. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0020.

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Catheter-associated infections, which often present as sepsis, include primary bloodstream infections that occur in the presence of intravascular catheters. They are not related to an infection at another site and are defined as a primary bloodstream infection with documented colonization of the device and microbiologically proven, device-related bloodstream infection. Multiple hospitals have started to implement standardized quality control interventions to minimize catheter-related bloodstream infections. Ultrasound-guided line placement results in a decrease in mechanical complication and the number of attempts, which in turn reduces the risk of infection. Preparing the skin with 0.5% chlorhexidine or alcohol containing chlorhexidine solutions has been shown to reduce line-related infections. Antimicrobial lock solutions should be used in patients with recurrent catheter-associated infections and high-risk groups, such as those on total parenteral nutrition, dialysis, or oncologic patients. The preservation of skin integrity surrounding the device decreases the risk of infection.
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Shaibani, Aziz. Skin Signs. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0027.

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Many neuromuscular diseases are expressed by skin manifestations such as dermatomyositis. Skin changes of dermatomyositis can be of many types and be subtle in dark skin. They include heliotropes, periungual telangiectasia, and thickening and fissuring of the skin. Unlike SLE rash, dermatomyositis rash affects the knuckles. Many systemic inflammatory diseases are associated with neuromuscular disease, such as vasculitis, systemic lupus erythematosus (SLE), and scleroderma. Steroids may lead to acne like skin lesions that should be differentiated from the rash of the underlying disease. This chapter provides examples of skin signs that are associated with neuromuscular diseases.
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Book chapters on the topic "Skin associated"

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Rayan, Ghazi M., and Joseph Upton III. "Congenital Skin Dysplasia." In Congenital Hand Anomalies and Associated Syndromes, 477–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-54610-5_37.

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Deliveliotou, Aikaterini E. "Gynaecological Problems Associated with Menopause." In Skin, Mucosa and Menopause, 199–208. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44080-3_16.

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Grewal, Parbeer S., Walter P. Maksymowych, and Alain Brassard. "Inflammatory Bowel-Associated Spondyloarthropathy." In Skin Manifestations in Rheumatic Disease, 127–32. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7849-2_15.

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Gattorno, Marco. "Cryopyrin-Associated Periodic Syndromes." In Skin Manifestations in Rheumatic Disease, 363–71. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7849-2_44.

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Steinbrink, K., and V. Raker. "SALT (»skin-associated lymphoid tissue«)." In Allergologie, 127–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-37203-2_12.

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Mokhtar, Doaa M. "Skin and Associated Sense Structures." In Fish Histology, 99–136. 2nd ed. 2nd edition.: Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003097419-7.

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Buckley, David. "Skin Problems Associated with Diabetes." In Textbook of Primary Care Dermatology, 489–93. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-29101-3_52.

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Rose, Sharon, Shivani B. Kaushik, and Mark Lebwohl. "Skin Diseases Associated with Biologic Therapies." In Skin Diseases in the Immunosuppressed, 155–65. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-68790-2_8.

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Ladizinski, Barry, Marigdalia Ramirez-Fort, Megan Shelton, and Aisha Sethi. "Skin Diseases Associated with HIV Disease." In Skin Diseases in the Immunosuppressed, 53–71. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-68790-2_3.

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Tolkachjov, Stanislav N., and Jerry D. Brewer. "Skin Cancers Associated with Lymphoid Malignancies." In Skin Diseases in the Immunosuppressed, 139–53. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-68790-2_7.

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Conference papers on the topic "Skin associated"

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Meng, Zhaokai, and Vladislav V. Yakovlev. "Brillouin spectroscopy characterizes microscopic viscoelasticity associated with skin injury." In SPIE BiOS, edited by E. Duco Jansen. SPIE, 2015. http://dx.doi.org/10.1117/12.2079692.

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Alım, Bülent, Fahrettin Bostancı, M. Alperen Servi, Sinan Çetinel, and M. Ozan Bingöl. "Unexpected complication associated with balneotherapy: Skin and soft tissue infection." In II. INTERNATIONAL CONFERENCE ON ADVANCES IN NATURAL AND APPLIED SCIENCES: ICANAS 2017. Author(s), 2017. http://dx.doi.org/10.1063/1.4981765.

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Titova, Lyubov V., Ayesheshim K. Ayesheshim, David Purschke, Andrey Golubov, Rocio Rodriguez-Juarez, Rafal Woycicki, Frank A. Hegmann, and Olga Kovalchuk. "Effect of intense THz pulses on expression of genes associated with skin cancer and inflammatory skin conditions." In SPIE BiOS, edited by E. Duco Jansen, Robert J. Thomas, Gerald J. Wilmink, and Bennett L. Ibey. SPIE, 2014. http://dx.doi.org/10.1117/12.2044167.

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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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Khosravi-Hafshejani, T., M. Ghoreishi, A. Kariminia, S. Kalia, A. Avina-Zubieta, J. Reynolds, and JP Dutz. "217 Prior sun exposure and skin-specific auto-antibodies are associated with skin disease in systemic lupus erythematosus." In LUPUS 2017 & ACA 2017, (12th International Congress on SLE &, 7th Asian Congress on Autoimmunity). Lupus Foundation of America, 2017. http://dx.doi.org/10.1136/lupus-2017-000215.217.

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Hwang, DannyP, and Tom Biesiadny. "Experimental evaluation of penalty associated with micro-blowing for reducing skin friction." In 36th AIAA Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1998. http://dx.doi.org/10.2514/6.1998-677.

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Sousa-Neves, J., M. Cerqueira, D. Santos-Faria, J. Leite Silva, C. Afonso, and F. Teixeira. "FRI0394 Neuropathic pain is associated with skin thickness in systemic sclerosis patients." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.5288.

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Telenga, Eef, Hajo Jongepier, Leslie A. Lange, Dirkje S. Postma, Maarten van den Berge, and Gerard Koppelman. "Glucocorticoid Skin Responsiveness Is Associated With Level Of FEV1 In Asthma Families." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3122.

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Becker, Sid, and Andrey Kuznetsov. "The Importance od the Composite Skin Model in Numerical Investigations of the Thermal Response Associated with In Vivo Skin Electroporation." In 9th AIAA/ASME Joint Thermophysics and Heat Transfer Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2006. http://dx.doi.org/10.2514/6.2006-2939.

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Chan, Jeremy Soon Kiat, Ming Keat Sng, Zi Qiang Teo, and Nguan Soon Tan. "Abstract 3369: Nuclear hormone receptor profiling of skin cancer-associated fibroblasts for targeted pharmacological modulation of skin squamous cell carcinoma." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-3369.

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