Results 21 to 30 of about 1,452 (154)
La enfermedad de Addison en el Síndrome de Schmidt
Galicia Clínica, 2022 Autoimmune polyglandular syndromes are rare conditions distinguished by the coexistence of at least two autoimmune glandular diseases. Autoimmune polyendocrine syndrome type II, also known as Schmidt syndrome is characterized by Addison's disease ...
Maria João Palavras +1 more
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Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1 [PDF]
Proceedings of the National Academy of Sciences, 2007 Autoimmune polyendocrine syndrome type 1 (APS1) is a rare autosomal recessive disorder caused by mutations in the autoimmune regulator ( AIRE ) gene. High titer autoantibodies (Aabs) toward intracellular enzymes are a hallmark for APS1 and serve as diagnostic markers and predictors for ...
Bensing, Sophie +11 more
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Journal of Diabetes Investigation, 2021 Anti‐N‐methyl‐D‐aspartate receptor (NMDA‐R) encephalitis is an autoimmune disorder in which autoantibodies in the limbic system bind to GluN1 subunits of NMDA‐Rs in the brain.
Akira Kurozumi +3 more
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Autoimmune polyendocrine syndrome type 1 (APS‐1) as a model for understanding autoimmune polyendocrine syndrome type 2 (APS‐2) [PDF]
Journal of Internal Medicine, 2009 Abstract.Autoimmune polyendocrine syndromes type 1 and 2 (APS‐1 and APS‐2) are diverse in regards to their component diseases and immunologic features of pathogenesis. Animal models and human studies highlight the importance of alleles of HLA (human leukocyte antigen)‐like molecules determining tissue specific targeting that with the loss of tolerance ...
A W, Michels, G S, Eisenbarth
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Frontiers in Neuroscience, 2023 Fahr’s syndrome, also known as bilateral striopallidodendate calcinosis, is a rare inherited neurodegenerative illness characterized by abnormal calcium deposition in several areas of the brain, resulting in a wide range of neuropsychological symptoms ...
Ahmad Nawaz +5 more
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BMC Pediatrics, 2020 Background Auto-immune polyendocrinopathy syndrome type I is a rare genetic disease, usually revealed by chronic superficial candidiasis and autoimmune endocrine dysfunction in childhood. Cases presentation We report the cases of 2 children, a 4 years-11
Basilice Mireille Minka +3 more
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Autoimmune Polyendocrine Syndromes: Clues to Type 1 Diabetes Pathogenesis [PDF]
Immunity, 2010 Autoimmune diseases such as type 1 diabetes are complex in their pathogenesis. One approach to improving our understanding of type 1 diabetes is the study of diseases that represent more extreme examples of autoimmunity. Autoimmune polyendocrine syndromes (APS) are relatively rare diseases that often include type 1 diabetes as part of the disease ...
Husebye, Eystein S., Anderson, Mark S.
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Autoimmune polyglandular syndrome type 1 and eye damage
Acta Biomedica Scientifica, 2021 Autoimmune polyendocrine syndrome type 1 (APS type 1) is a disease characterized by a variety of clinical manifestations resulting from the involvement of multiple endocrine and non-endocrine organs in the pathological process.
L. Yu. Khamnueva +3 more
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Insights into type 1 diabetes from the autoimmune polyendocrine syndromes [PDF]
Current Opinion in Endocrinology, Diabetes & Obesity, 2013 Advances in human genetics and investigations in animal models of autoimmune disease have allowed insight into the basic mechanisms of immunologic tolerance. These advances allow us to understand the pathogenesis of type 1 diabetes and other autoimmune diseases as never before.
Cheng, Mickie H, Anderson, Mark S
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Alʹmanah Kliničeskoj Mediciny, 2020 Rationale: In Russia, assessment of anti-P450c21 antibodies (AB) in the diagnosis of autoimmune adrenal insufficiency (AAI) has not been commonly used, and the disease screening has not been implemented.Aims: 1) To determine the sensitivity and ...
N. F. Nuralieva +4 more
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