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Journal Abstract Search

519 related items for PubMed ID: 16924012

  • 21.
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  • 23. Charcot-Marie-tooth disease.
    Casasnovas C, Cano LM, Albertí A, Céspedes M, Rigo G.
    Foot Ankle Spec; 2008 Dec; 1(6):350-4. PubMed ID: 19825739
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  • 25. Charcot-Marie-Tooth disease type 4C in Japan: report of a case.
    Iguchi M, Hashiguchi A, Ito E, Toda K, Urano M, Shimizu Y, Takeuchi C, Saito K, Takashima H, Uchiyama S.
    Muscle Nerve; 2013 Feb; 47(2):283-6. PubMed ID: 23281072
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  • 27. Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
    Gabreëls-Festen A, van Beersum S, Eshuis L, LeGuern E, Gabreëls F, van Engelen B, Mariman E.
    J Neurol Neurosurg Psychiatry; 1999 May; 66(5):569-74. PubMed ID: 10209165
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  • 28. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 31. X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic study.
    Ionasescu VV, Trofatter J, Haines JL, Summers AM, Ionasescu R, Searby C.
    Muscle Nerve; 1992 Mar; 15(3):368-73. PubMed ID: 1557086
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  • 32. Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot-Marie-Tooth disease reveals a varied and unusual phenotypic spectrum.
    Kontogeorgiou Z, Nikolaou K, Kartanou C, Breza M, Panas M, Karadima G, Koutsis G.
    J Peripher Nerv Syst; 2019 Mar; 24(1):125-130. PubMed ID: 30653784
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  • 34. Compound heterozygous mutations of SH3TC2 in Charcot-Marie-Tooth disease type 4C patients.
    Lee AJ, Nam SH, Park JM, Kanwal S, Choi YJ, Lee HJ, Lee KS, Lee JE, Park JS, Choi BO, Chung KW.
    J Hum Genet; 2019 Sep; 64(9):961-965. PubMed ID: 31227790
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  • 35. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ, Jensen AD, Brandt CA, Bisgård C.
    Ugeskr Laeger; 1995 Jun 19; 157(25):3613-8. PubMed ID: 7652980
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  • 40. Phenotypic variability in a large Czech family with a dynamin 2-associated Charcot-Marie-Tooth neuropathy.
    Haberlová J, Mazanec R, Ridzoň P, Baránková L, Nürnberg G, Nürnberg P, Sticht H, Huehne K, Seeman P, Rautenstrauss B.
    J Neurogenet; 2011 Dec 19; 25(4):182-8. PubMed ID: 22091729
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