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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 7139106)

  • 61. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Serum enzymes in peroneal muscular atrophy (Charcot-Marie-Tooth disease).
    Switala KJ; Robinson N; Sances A; Larson S; Evans SM; Pintar K
    Wis Med J; 1977 Jan; 76(1):S4-6. PubMed ID: 835307
    [No Abstract]   [Full Text] [Related]  

  • 64. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K; Sobue G; Takahashi A; Mitsuma T
    Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775
    [No Abstract]   [Full Text] [Related]  

  • 65. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D; Dan H; Mo J
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr; 34(2):77-80. PubMed ID: 12764852
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [Family with hereditary polyneuropthy assoicated with pyramidal signs].
    Doi H; Shibasaki H; Goto I; Kuroiwa Y; Ohta M
    Rinsho Shinkeigaku; 1976 Sep; 16(9):642-8. PubMed ID: 1034548
    [No Abstract]   [Full Text] [Related]  

  • 67. Cochleosaccular degeneration of the inner ear and progressive cataracts inherited as an autosomal dominant trait.
    Nadol JB; Burgess B
    Laryngoscope; 1982 Sep; 92(9 Pt 1):1028-37. PubMed ID: 7121157
    [TBL] [Abstract][Full Text] [Related]  

  • 68. [Trophic disorders in Charcot-Marie-Tooth disease].
    Deceuninck FG
    Ned Tijdschr Geneeskd; 1972 Jun; 116(24):997-1001. PubMed ID: 5028775
    [No Abstract]   [Full Text] [Related]  

  • 69. A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
    Kochanski A; Drac H; Kabzińska D; Hausmanowa-Petrusewicz I
    Neuromuscul Disord; 2004 Mar; 14(3):229-32. PubMed ID: 15036333
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J
    Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
    [TBL] [Abstract][Full Text] [Related]  

  • 71. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
    Xia J; Deng H; Feng Y; Zhang H; Pan Q; Dai H; Long Z; Tang B; Deng H; Chen Y; Zhang R; Zheng D; He Y; Xia K
    J Hum Genet; 2002; 47(12):635-40. PubMed ID: 12522684
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)].
    Sadaba Garay F; Franco Vicario R; Miguel de la Villa F; Ibarmia Lahuerta J; Bustamante Murga V
    Med Clin (Barc); 1980 Oct; 75(6):240-6. PubMed ID: 7421358
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Controversy in genetic disorders.
    Sybert VP
    Arch Dermatol; 1981 Jul; 117(7):380-1. PubMed ID: 6455091
    [No Abstract]   [Full Text] [Related]  

  • 74. [The importance of studying stimulation parameters in amyotrophic lateral sclerosis and Charcot-Marie-Tooth neural amyotrophy].
    Kyral V; Pára F
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1980; 23(4):415-22. PubMed ID: 6971479
    [No Abstract]   [Full Text] [Related]  

  • 75. [Charcot-Marie-Tooth disease and glomerular nephropathy].
    Deniau F; Guillot M; Plus A; Leveque C; Gubler MC; Broyer M; Aicardi J; Lechevalier B
    Arch Fr Pediatr; 1986 Dec; 43(10):791-3. PubMed ID: 3827511
    [TBL] [Abstract][Full Text] [Related]  

  • 76. A family with Charcot-Marie-Tooth's disease, showing a probable X-linked incompletely dominant inheritance.
    Iselius L; Grimby L
    Hereditas; 1982; 97(1):157-8. PubMed ID: 6890052
    [No Abstract]   [Full Text] [Related]  

  • 77. [Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example].
    Berg RL; Kryshova NA; Ozeretskovskaia NG; Artemchuk NL; Begzhanov KB
    Genetika; 1973 Oct; 9(10):127-38. PubMed ID: 4807104
    [No Abstract]   [Full Text] [Related]  

  • 78. [Early diagnosis and differentiation of Charcot-Marie neural atrophy].
    Lobzin VS; Saĭkova LA; Poliakova LA; Kosachev VD
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1601-5. PubMed ID: 6524176
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Conduction system disease and Charcot-Marie-Tooth syndrome].
    Rosselot E; Brinck G
    Rev Med Chil; 1989 Aug; 117(8):914-7. PubMed ID: 2519453
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Rare variants in methionyl- and tyrosyl-tRNA synthetase genes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy.
    Hyun YS; Park HJ; Heo SH; Yoon BR; Nam SH; Kim SB; Park CI; Choi BO; Chung KW
    Clin Genet; 2014 Dec; 86(6):592-4. PubMed ID: 24354524
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.