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Relevant bibliographies by topics / Radiologically Isolated Syndrom

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Academic literature on the topic 'Radiologically Isolated Syndrom'

Author: Grafiati

Published: 11 January 2025

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Journal articles on the topic "Radiologically Isolated Syndrom"

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Okuda, Darin T. "Radiologically Isolated Syndrome." Neuroimaging Clinics of North America 27, no. 2 (2017): 267–75. http://dx.doi.org/10.1016/j.nic.2016.12.008.

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Fazekas, F., N. De Stefano, M. Filippi, F. Barkhof, and A. Rovira. "Radiologically isolated syndrome." Journal of the Neurological Sciences 357 (October 2015): e462-e463. http://dx.doi.org/10.1016/j.jns.2015.09.166.

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Filippi, Massimo. "Radiologically isolated syndrome and clinically isolated syndrome." Journal of the Neurological Sciences 429 (October 2021): 118003. http://dx.doi.org/10.1016/j.jns.2021.118003.

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Niino, Masaaki, and Yusei Miyazaki. "Radiologically isolated syndrome and clinically isolated syndrome." Clinical and Experimental Neuroimmunology 8 (January 2017): 24–32. http://dx.doi.org/10.1111/cen3.12346.

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Lebrun, C. "The radiologically isolated syndrome." Revue Neurologique 171, no. 10 (2015): 698–706. http://dx.doi.org/10.1016/j.neurol.2015.05.001.

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El Helou, Jeanine. "Traitement du Radiologically isolated syndrome." Revue Neurologique 177 (April 2021): S150. http://dx.doi.org/10.1016/j.neurol.2021.02.053.

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Makhani, Naila, Christine Lebrun, Aksel Siva, et al. "Radiologically isolated syndrome in children." Neurology - Neuroimmunology Neuroinflammation 4, no. 6 (2017): e395. http://dx.doi.org/10.1212/nxi.0000000000000395.

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Objective:To describe clinical and radiologic outcomes of children with incidental findings on neuroimaging suggestive of CNS demyelination (termed “radiologically isolated syndrome” or RIS).Methods:Clinical and radiologic data were obtained from a historical cohort of children with no symptoms of demyelinating disease who had MRI scans that met the 2010 MRI criteria for dissemination in space for MS.Results:We identified 38 children (27 girls and 11 boys) with RIS now being prospectively followed at 16 sites in 6 countries. The mean follow-up time was 4.8 ± 5.3 years. The most common reason f

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Yeh, E. Ann. "Radiologically isolated syndrome in children." Neurology - Neuroimmunology Neuroinflammation 4, no. 6 (2017): e411. http://dx.doi.org/10.1212/nxi.0000000000000411.

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Cummings, A., and J. Chataway. "Negotiating the radiologically isolated syndrome." British Journal of Hospital Medicine 75, no. 10 (2014): 552–57. http://dx.doi.org/10.12968/hmed.2014.75.10.552.

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Joly, Héloise, Emilie Gerbier, Margaux Zerlini, et al. "Alexithymia in radiologically isolated syndrome." Multiple Sclerosis and Related Disorders 91 (November 2024): 105905. http://dx.doi.org/10.1016/j.msard.2024.105905.

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Dissertations / Theses on the topic "Radiologically Isolated Syndrom"

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Landes-Chateau, Cassandre. "Identification et caractérisation de marqueurs prédictifs d'inflammation et de neurodégénérescence chez les personnes présentant un syndrome radiologique isolé." Electronic Thesis or Diss., Université Côte d'Azur, 2024. https://theses.hal.science/tel-04867716.

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Le Syndrome Radiologique Isolé (RIS pour Radiologically Isolated Syndrome) représente la phase pré-clinique de la sclérose en plaques (SEP), et correspond à la découverte fortuite d'anomalies de la substance blanche évocatrices de SEP de par leur localisation, leur taille et leur forme, sur une Imagerie par Résonance Magnétique (IRM) pratiquée pour une autre raison que pour une suspicion de maladie démyélinisante chez des sujets sans histoire de symptôme neurologique et présentant un examen clinique neurologique strictement normal. Les critères diagnostiques de RIS ont été décrits la première

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Silva, Joana Almada. "Síndrome Radiológica Isolada em idade pediátrica: o modelo clínico ideal para o estudo da remielinização?" Master's thesis, 2021. http://hdl.handle.net/10316/98549.

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Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de Medicina<br>A Síndrome Radiológica Isolada (RIS) corresponde a uma situação clínica em que são identificadas em exames de imagem, nomeadamente de ressonância magnética (RM), lesões de características desmielinizantes consideradas típicas de esclerose múltipla (EM), sem que o indivíduo tenha tido, em algum momento, qualquer manifestação clínica a elas atribuível. Por este motivo, é a RIS habitualmente considerada como uma fase pré-sintomática da EM, o que a torna um alvo de investigação extremamente apetecível, no senti

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Books on the topic "Radiologically Isolated Syndrom"

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Freedman, Mark S., and Mohammad Abdoli. The Importance and Utility of Cerebrospinal Fluid Evaluation in the Diagnosis of Central Demyelinating Diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199341016.003.0008.

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This chapter aims to highlight the diagnostic and prognostic value of cerebrospinal fluid (CSF) findings in multiple sclerosis with a special consideration of distinguishing it from neuromyelitis optica (NMO) and NMO spectrum disorder. Interpretation of CSF findings in daily clinical practice in patients with MS is thoroughly explained. New advances in CSF analysis and recently identified biomarkers may be helpful for diagnosis, help elucidate disease subtype and activity, or aid in prognosis and monitoring of the response to treatment. Characteristics of CSF changes in different subtypes of m

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Thompson, Jonathan P. Anaesthesia for vascular surgery. Edited by Philip M. Hopkins. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0058.

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Vascular surgical patients are at higher risk of cardiovascular morbidity and mortality than other surgical patients, and perioperative care remains challenging. However, vascular surgical practice is changing, with the expanding use of endovascular techniques to treat patients with vascular disease, improvements in medical therapy, and the evolution of evidence-based approaches to preoperative assessment. Preoperative assessment should concentrate on identifying and optimizing potentially correctable medical conditions, in particular cardiovascular disease. Successful outcomes depend on good

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Book chapters on the topic "Radiologically Isolated Syndrom"

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DeStefano, Katherine, and Naila Makhani. "Radiologically Isolated Syndrome." In Pediatric Demyelinating Diseases of the Central Nervous System and Their Mimics. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61407-6_8.

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Wingerchuk, Dean M. "Lesions Found by Chance." In Mayo Clinic Cases in Neuroimmunology, edited by Andrew McKeon, B. Mark Keegan, and W. Oliver Tobin. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197583425.003.0009.

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A healthy 26-year-old woman with a history of episodic migraine without aura since age 12 years had a first-ever event of transient visual impairment. She reported to her neurologist that she “lost vision” for 15 minutes and described a “black blob” with a bright jagged border that moved across her binocular visual field and resolved without sequelae. Minutes later, one of her typical migraine headaches developed. Given the patient’s history of typical episodic migraine, the new visual event’s clinical characteristics were highly consistent with a migraine aura. Because of the new transient visual symptoms, the neurologist ordered brain magnetic resonance imaging, which showed several periventricular white matter lesions, including some that involved the corpus callosum and were oriented perpendicular to the septocallosal surface. The patient was counseled about the magnetic resonance imaging findings and expressed the desire to fully evaluate her risk of multiple sclerosis. The patient was diagnosed with radiologically isolated syndrome. The patient was counseled regarding the relevance of the magnetic resonance imaging findings and risk of future development of multiple sclerosis. She was not prescribed a disease-modifying therapy for multiple sclerosis. This patient has radiologically isolated syndrome —incidentally found magnetic resonance imaging lesions consistent with demyelination in a patient with no symptoms or signs suggestive of multiple sclerosis.

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Butler, Gary, and Jeremy Kirk. "The pituitary and hypopituitarism." In Paediatric Endocrinology and Diabetes. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198786337.003.0003.

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• The pituitary is formed of two anatomically and embryologically distinct lobes: ◦ anterior pituitary: which secretes growth hormone (GH), gonadotropins (luteinizing hormone (LH) and follicle-stimulating hormone (FSH)), adrenocorticotropic hormone (ACTH), thyroid-stimulating hormone (TSH), and prolactin ◦ posterior pituitary: which secretes vasopressin and oxytocin. • Hypopituitarism is deficiency of one or more pituitary hormones. Some hormones, e.g. GH (LH/FSH), are more likely to present with isolated deficiencies, while others, e.g. TSH, ACTH, are more often found as part of multiple pituitary hormone deficiency (MPHD). • Deficiencies may be congenital (including genetic) or acquired; secondary to tumour, trauma, infiltration, infection, or irradiation. • GH deficiency: ◦ diagnosed using a combination of clinical, radiological, and biochemical assessment (including GH stimulation testing) ◦ treatment is with GH (including if necessary into adulthood). • LH/FSH deficiency: ◦ If acquired, often one of the first anterior pituitary hormones to be lost. ◦ Congenital forms: ■ present with cryptorchidism and/or micropenis in males ■ may occur in isolation, or in association with anosmia (Kallmann and CHARGE syndromes). ◦ Treatment: sex steroid therapy to induce secondary sexual characteristics, and recombinant FSH/LH to induce fertility potential. • ACTH deficiency: ◦ Unlike primary adrenal problems, hyperpigmentation does not occur. ◦ Although mineralocorticoid production is preserved, hyponatraemia may still occur. ◦ Treatment is with hydrocortisone. • TSH deficiency: ◦ TSH may be low, normal, or raised (but inappropriate for free thyroxine level). ◦ Treatment is with thyroxine. • Vasopressin deficiency: ◦ produces cranial diabetes insipidus ◦ treatment is with DDAVP (orally or nasally). • Prolactin and oxytocin deficiency rarely produce clinical problems.

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Conference papers on the topic "Radiologically Isolated Syndrom"

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Gunduz, Tuncay, Irem Ciftci, Bilge Piri Cinar, et al. "Comparative Analysis of Diagnostic Criteria for Radiologically Isolated Syndrome (S31.009)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000203730.

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Schneider, Raphael, Koroboshka Brand-Arzamendi, Timothy Lim, et al. "Plasma glial fibrillary acidic protein levels correlate with unfavourable imaging measures in Radiologically Isolated Syndrome (P1-3.003)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000202516.

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Borri, Juliana Baleki, and Hilton Mariano da Silva Junior. "Red Ear Syndrome: um relato de caso sobre uma síndrome rara associada a cefaleia." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.124.

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Context: The Red Ear Syndrome” (RES) is a rare condition characterized by ear hyperemia associated with burning pain. This syndrome is classified into secondary and idiopathic forms, which pathophysiological mechanisms are still unclear. Idiopathic forms occur isolated or associated with primary headaches and secondary forms are associated to cervical disorders. The aim of this study is to report a case of RES related to migraine, the new published cases make this syndrome earn more attention and investigation. Case report: A 31-year-old woman presented with acute pain, edema and marked erythe

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Keane, Connor, Poljanka Johnson, Joshua Lee, et al. "Using Myelin Water Imaging to Investigate Myelin Damage and its Association with Clinical Outcomes in Radiologically Isolated Syndrome (S27.005)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000202254.

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Oh, Jiwon, Timothy Lim, Suradech Suthiphosuwan, et al. "Paramagnetic rim lesions predict the development of clinical MS in radiologically isolated syndrome: results from a prospective cohort study (S27.003)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000203626.

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Oliveira, Jefferson Borges de, Caroline Berthier Zanin, Gustavo Carreira Henriques, et al. "Pallister-Hall Syndrome - case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.575.

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In 1980, Hall et all described a syndrome characterized by “hamartoblastoma”, hypopituitarism, unperfurated anus, polydactyly postaxial and numerous visceral anomalies, today known as Pallister-Hall Syndrome. On the study, Hall et all reported six cases of children with that malformation syndrome - lethal on neonatal period. None of the newborns had anterior hypophysis and the hypothalamic tumor was apparent in the inferior part of the brain, going from the optic chiasm to the interpeduncular fossa. Besides, other anomalies were found, such as: laryngeal split, abnormal pulmonary lobation, ren

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