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Results 1 - 10 of 12 for Kimura disease
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  1. MKKS gene 
    ... Kitamura A, Oda Y, Morito D, Okawa K, Kimura H, Cyr DM, Kubota H, Nagata K. MKKS is a centrosome-shuttling protein degraded by disease-causing mutations via CHIP-mediated ubiquitination. Mol Biol ...
    https://medlineplus.gov/genetics/gene/mkks - Genetics
  2. COVID-19 Symptoms and Complementary Approaches: What You Need To Know From the National Institutes of Health (National Center for Complementary and Integrative Health)  
    COVID-19 (Coronavirus Disease 2019)/Treatments and Therapies ... COVID-19 (Coronavirus Disease 2019) ... Information about complementary and integrative health approaches ...
    https://www.nccih.nih.gov/...entary-approaches-what-you-need-to-know - External Health Links
  3. Familial hypertrophic cardiomyopathy 
    ... WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar;5(3):158-68. doi: 10.1038/ncpcardio1110. Epub 2008 Jan 29. Citation on PubMed Kimura A. Molecular genetics and pathogenesis of cardiomyopathy. J ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  4. SMCHD1 gene 
    ... Shibata S, Shirai N, Nozaki N, Sado T, Kimura H, Obuse C. Human inactive X ... SMCHD1 is a modifier of disease severity in families affected by FSHD1. Am J ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
  5. RETREG1 gene 
    ... 18. Citation on PubMed Mochida K, Oikawa Y, Kimura Y, Kirisako ... Disease mechanisms in hereditary sensory and autonomic neuropathies. Neurobiol ...
    https://medlineplus.gov/genetics/gene/retreg1 - Genetics
  6. Myoclonic epilepsy with ragged-red fibers 
    ... Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J. A novel point mutation in the ... presentation of mitochondrial disease due to a mutation in the tRNA(His) ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  7. NKX2-1 gene 
    ... VH, Fuccillo MV, Hjerling-Leffler J, Miyoshi G, Kimura S, Fishell G. The ... interstitial lung disease in "Brain-Lung-Thyroid Syndrome". Hum Mutat. 2010 ...
    https://medlineplus.gov/genetics/gene/nkx2-1 - Genetics
  8. Congenital nephrotic syndrome 
    ... Tsuruya K, Furuichi K, Hoshino J, Watanabe Y, Kimura K, Matsuo S. Evidence-based ... Mar 9. Citation on PubMed
    https://medlineplus.gov/.../condition/congenital-nephrotic-syndrome - Genetics
  9. White sponge nevus 
    ... this phenomenon is called reduced penetrance. ... on PubMed or Free article on PubMed Central Kimura M, Nagao T, Machida J, Warnakulasuriya S. Mutation ...
    https://medlineplus.gov/genetics/condition/white-sponge-nevus - Genetics
  10. CACNA1C gene 
    ... Ohno S, Ding WG, Toyoda F, Itoh H, Kimura H, Makiyama T, Ito M, Matsuura H, ... HG, Zacher P; Undiagnosed Diseases Network; Rush E, Pitt GS, Au PYB, Shashi ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
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