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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]
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]
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]
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]