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 *

119 related articles for article (PubMed ID: 3334783)

  • 1. Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study.
    Micaglio G; Fardin P; Battilana M; Lombardi A; Mostacciuolo ML; Danieli GA; Angelini C
    Adv Neurol; 1988; 48():209-19. PubMed ID: 3334783
    [No Abstract]   [Full Text] [Related]  

  • 2. DNA probes in Charcot-Marie-Tooth neuropathy.
    Nicholson GA; Griffiths LR; McLeod JG
    Aust Paediatr J; 1988; 24 Suppl 1():90-1. PubMed ID: 3202739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic linkage of the autosomal dominant form of Charcot-Marie-Tooth amyotrophy and 3 genetic markers on chromosome 1].
    Ferák V; Kádasi L; Hrubisko M; Siváková D; Véghová E
    Cesk Neurol Neurochir; 1989 May; 52(3):200-7. PubMed ID: 2582521
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
    Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM
    Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. [X-linked recessively inherited peroneal muscular atrophy].
    Wang DS
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):139-40, 190. PubMed ID: 2591266
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci.
    Kochanski A; Kennerson M; Kawulak M; Ryniewicz B; Rowinska-Marcinska K; Walizada G; Nowakowski A; Hausmanowa-Petrusewicz I; Nicholson GA
    Neurology; 2005 Feb; 64(3):533-5. PubMed ID: 15699389
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD; Ott J; Giblett ER; Chance PF; Sumi SM; Kraft GH
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N; Mihatov I
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies.
    Ionasescu VV; Ionasescu R; Searby C
    Muscle Nerve; 1993 Nov; 16(11):1232-8. PubMed ID: 8413376
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR
    Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary motor and sensory neuropathy: evolution of the concept and present status.
    Thomas PK
    Electroencephalogr Clin Neurophysiol Suppl; 1987; 39():115-20. PubMed ID: 2820690
    [No Abstract]   [Full Text] [Related]  

  • 14. Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form.
    Rossi A; Paradiso C; Cioni R; Rizzuto N; Guazzi G
    J Neurol; 1985; 232(2):91-8. PubMed ID: 4020397
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study.
    Ionasescu VV; Burns TL; Searby C; Ionasescu R
    Muscle Nerve; 1988 Nov; 11(11):1154-6. PubMed ID: 3226432
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.
    Barraquer-Bordas L; Navarro C; Salisachs P
    Acta Neurol Latinoam; 1981; 27(3-4):177-89. PubMed ID: 6965173
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease.
    Lance JW; Durke D; Pollard J
    Clin Exp Neurol; 1979; 16():49-56. PubMed ID: 550956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked Charcot-Marie-Tooth disease with myokymia: report of a family.
    Chakravarty A; Ghosh B; Sengupta S; Mukhopadhyay S
    Neurol India; 2003 Sep; 51(3):385-7. PubMed ID: 14652447
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K; Kyriakides T; Puls I; Nicholson GA; Funalot B; Antonellis A; Sambuughin N; Christodoulou K; Beggs JL; Zamba-Papanicolaou E; Ionasescu V; Dalakas MC; Green ED; Fischbeck KH; Goldfarb LG
    Brain; 2005 Oct; 128(Pt 10):2304-14. PubMed ID: 16014653
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
    Othmane KB; Johnson E; Menold M; Graham FL; Hamida MB; Hasegawa O; Rogala AD; Ohnishi A; Pericak-Vance M; Hentati F; Vance JM
    Genomics; 1999 Dec; 62(3):344-9. PubMed ID: 10644431
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.