Zobrazeno 1 - 10
of 322
pro vyhledávání: '"collagen disorder"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 09, Pp 03-05 (2024)
Systemic sclerosis or scleroderma is an uncommon autoimmune condition with a global incidence of 8 to 56 new cases per million per year, which commences from skin and progresses to affect multiple systems in the body. It is marked by abnormalities in
Externí odkaz:
https://doaj.org/article/9ba78f3657644c269c2230fb5276d969
Autor:
David F. Gaieski
Publikováno v:
Journal of Emergencies, Trauma and Shock, Vol 17, Iss 2, Pp 53-57 (2024)
Introduction: Scurvy, the disease state caused by ascorbic acid deficiency, was once an extremely common disease but is now thought to be a rare disease in postmodern societies. Physicians are not trained to consider scurvy as a possible diagnosis in
Externí odkaz:
https://doaj.org/article/6f35faca292a4101a1478d301ac40f18
Publikováno v:
Indian Journal of Ophthalmology, Vol 71, Iss 6, Pp 2385-2398 (2023)
Collagen vascular disorders (CVDs), also known as connective tissue diseases (CTDs), are a heterogeneous group of entities that affect the connective tissues and are capable of causing end-organ damage to multiple systems, primarily cardiopulmonary a
Externí odkaz:
https://doaj.org/article/6443648e656d4039ac501ebf06a39b67
Akademický článek
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Akademický článek
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Akademický článek
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Autor:
Katarina Stefanovic, Laurent Létourneau-Guillon, David Bergeron, Michel W. Bojanowski, Behzad Farzin, Chiraz Chaalala
Publikováno v:
World Neurosurgery. 157:e264-e270
Background Aneurysms of spinal arteries not associated with any known predisposing condition are referred to as isolated spinal aneurysms (SAs). In our series, an SA was found in 2 patients during the postpartum period. The goal of this study is to d
Publikováno v:
The Journal of Dermatology. 48:1817-1826
A special kind of scar, keloid, sometimes grows huge, disturbing patients in different ways. We discussed the pathogenesis of keloids and found researches about fibroblasts and collagen disorders, with little emphasis on immunity. Coupled with few ef
Publikováno v:
Contemporary Clinical Dentistry, Vol 6, Iss 2, Pp 233-236 (2015)
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatoses characterized by deposition of amorphous hyaline material in different parts of the body, especially the skin, mucous membranes of the upper aerodigestive tract, and internal organs
Externí odkaz:
https://doaj.org/article/a3848d83f449456bad8e6d3d06dd25f3
Autor:
Gillian Morven Belbin, Jacqueline Odgis, Elena P Sorokin, Muh-Ching Yee, Sumita Kohli, Benjamin S Glicksberg, Christopher R Gignoux, Genevieve L Wojcik, Tielman Van Vleck, Janina M Jeff, Michael Linderman, Claudia Schurmann, Douglas Ruderfer, Xiaoqiang Cai, Amanda Merkelson, Anne E Justice, Kristin L Young, Misa Graff, Kari E North, Ulrike Peters, Regina James, Lucia Hindorff, Ruth Kornreich, Lisa Edelmann, Omri Gottesman, Eli EA Stahl, Judy H Cho, Ruth JF Loos, Erwin P Bottinger, Girish N Nadkarni, Noura S Abul-Husn, Eimear E Kenny
Publikováno v:
eLife, Vol 6 (2017)
Achieving confidence in the causality of a disease locus is a complex task that often requires supporting data from both statistical genetics and clinical genomics. Here we describe a combined approach to identify and characterize a genetic disorder
Externí odkaz:
https://doaj.org/article/2d12ca3f02f1483fbfe397e1124b87d3