Myasthenia Gravis
What's New
Last Posted: Mar 07, 2023
- Short-term outcome prediction for myasthenia gravis: an explainable machine learning model.
Huahua Zhong et al. Therapeutic advances in neurological disorders 2023 1617562864231154976 - Familial autoimmunity in patients with idiopathic inflammatory myopathies.
Che Weng Ian et al. Journal of internal medicine 2022 - Human Leukocyte Antigen Class II associations in late-onset Myasthenia Gravis.
Spagni Gregorio et al. Annals of clinical and translational neurology 2021 Feb - Familial associations for Addison disease and between Addison disease and other autoimmune diseases.
Thomsen Hauke et al. Endocrine connections 2020 Oct - Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America.
Green Joshua D et al. BMJ open 2020 Sep 10(9) e037909 - CLINGEN Actionability Report for Wilson Disease - ATP7B
ClinGen Actionability Working Group - Familial risk of Sjögren's syndrome and co-aggregation of autoimmune diseases in affected families: A nationwide population study.
Kuo Chang-Fu et al. 2015 May 4. - Myasthenia gravis
From NCATS Genetic and Rare Diseases Information Center - Myasthenia gravis congenital
From NCATS Genetic and Rare Diseases Information Center - Myasthenia gravis, limb-girdle
From NCATS Genetic and Rare Diseases Information Center
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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