These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


150 related items for PubMed ID: 31983616

  • 1. Acute rhabdomyolysis following viral infection with coxsackie A4 in a 50-day-old infant with Fukuyama congenital muscular dystrophy.
    Yamaguchi H, Taniguchi-Ikeda M, Nagase H, Ito Y, Tokumoto S, Toyoshima D, Enkhjargal S, Nishiyama M, Awano H, Kurosawa H, Kasai M, Maruyama A, Iijima K.
    J Infect Chemother; 2020 May; 26(5):516-519. PubMed ID: 31983616
    [Abstract] [Full Text] [Related]

  • 2. Rhabdomyolysis associated with human parvovirus B19 infection in a patient with Fukuyama-type congenital muscular dystrophy.
    Ishikawa A, Yoto Y, Ohya K, Tsugawa T, Tsutsumi H.
    J Child Neurol; 2014 Jul; 29(7):977-9. PubMed ID: 23594821
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Severe muscle damage following viral infection in patients with Fukuyama congenital muscular dystrophy.
    Murakami T, Ishigaki K, Shirakawa S, Ikenaka H, Sakauchi M, Osawa M.
    Brain Dev; 2012 Apr; 34(4):293-7. PubMed ID: 21726969
    [Abstract] [Full Text] [Related]

  • 6. National registry of patients with Fukuyama congenital muscular dystrophy in Japan.
    Ishigaki K, Ihara C, Nakamura H, Mori-Yoshimura M, Maruo K, Taniguchi-Ikeda M, Kimura E, Murakami T, Sato T, Toda T, Kaiya H, Osawa M.
    Neuromuscul Disord; 2018 Oct; 28(10):885-893. PubMed ID: 30220444
    [Abstract] [Full Text] [Related]

  • 7. Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients.
    Yang H, Kobayashi K, Wang S, Jiao H, Xiao J, Toda T, Wu X, Xiong H.
    Brain Dev; 2015 Oct; 37(9):880-6. PubMed ID: 25814170
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Severe rhabdomyolysis and acute renal failure following recent Coxsackie B virus infection.
    Fodili F, van Bommel EF.
    Neth J Med; 2003 May; 61(5):177-9. PubMed ID: 12916546
    [Abstract] [Full Text] [Related]

  • 12. Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patient.
    Xiong H, Wang S, Kobayashi K, Jiang Y, Wang J, Chang X, Yuan Y, Liu J, Toda T, Fukuyama Y, Wu X.
    Am J Med Genet A; 2009 Nov; 149A(11):2403-8. PubMed ID: 19842201
    [Abstract] [Full Text] [Related]

  • 13. Novel mutation in the fukutin gene in an Egyptian family with Fukuyama congenital muscular dystrophy and microcephaly.
    Ismail S, Schaffer AE, Rosti RO, Gleeson JG, Zaki MS.
    Gene; 2014 Apr 15; 539(2):279-82. PubMed ID: 24530477
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy.
    Yamamoto T, Taniguchi-Ikeda M, Awano H, Matsumoto M, Lee T, Harada R, Imanishi T, Hayashi N, Sakai Y, Morioka I, Takeshima Y, Iijima K, Saegusa J, Toda T.
    Brain Dev; 2017 Nov 15; 39(10):861-868. PubMed ID: 28578814
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.