BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 3022527)

  • 1. Heterogeneity of hereditary motor and sensory neuropathy type I (HMSN I): electroneurographical findings, visual evoked potentials and blood group markers in a family with Charcot-Marie-Tooth disease (CMT).
    Leblhuber F; Reisecker F; Mayr WR; Deisenhammer E
    Acta Neurol Scand; 1986 Aug; 74(2):145-9. PubMed ID: 3022527
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Heterogeneity of neural muscular atrophies].
    Leblhuber F; Reisecker F; Mayr WR; Deisenhammer E
    Nervenarzt; 1986 Jul; 57(7):419-21. PubMed ID: 3462518
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy.
    Raeymaekers P; De Jonghe P; Swerts L; Muylle L; Gheuens J; Martin JJ; Van Broeckhoven C; Vandenberghe A
    J Neurol Sci; 1988 Dec; 88(1-3):145-50. PubMed ID: 3225617
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.
    De Jonghe P; Timmerman V; Nelis E; De Vriendt E; Löfgren A; Ceuterick C; Martin JJ; Van Broeckhoven C
    Arch Neurol; 1999 Oct; 56(10):1283-8. PubMed ID: 10520946
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ; Thomas PK; Contreras M; Armitage S; Schwarz G; Sedgwick EM
    J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):669-74. PubMed ID: 7130990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markers.
    Chance PF; Murray JC; Bird TD; Kochin RS
    Neurology; 1987 Feb; 37(2):325-9. PubMed ID: 3468376
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pattern reversal visual evoked potentials. Studies in Charcot-Marie-Tooth hereditary neuropathy.
    Bird TD; Griep E
    Arch Neurol; 1981 Dec; 38(12):739-41. PubMed ID: 7316837
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I).
    Ionasescu V; Murray JC; Burns TL; Ionasescu R; Ferrell R; Searby C; Chirgwin J
    J Neurol Sci; 1987 Aug; 80(1):73-8. PubMed ID: 3302118
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).
    Raeymaekers P; Timmerman V; De Jonghe P; Swerts L; Gheuens J; Martin JJ; Muylle L; De Winter G; Vandenberghe A; Van Broeckhoven C
    Am J Hum Genet; 1989 Dec; 45(6):953-8. PubMed ID: 2589322
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
    Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M
    Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
    Bird TD
    Neurol Clin; 1989 Feb; 7(1):9-23. PubMed ID: 2646524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.
    Bird TD; Ott J; Giblett ER
    Am J Hum Genet; 1982 May; 34(3):388-94. PubMed ID: 6952764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree.
    Timmerman V; Raeymaekers P; Nelis E; De Jonghe P; Muylle L; Ceuterick C; Martin JJ; Van Broeckhoven C
    J Neurol Sci; 1992 May; 109(1):41-8. PubMed ID: 1517763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.
    Nicholson G; Nash J
    Neurology; 1993 Dec; 43(12):2558-64. PubMed ID: 8255457
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.
    Defesche JC; Hoogendijk JE; de Visser M; de Visser O; Bolhuis PA
    Neurology; 1990 Sep; 40(9):1450-3. PubMed ID: 2392234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system.
    Hisama FM; Lee HH; Vashlishan A; Tekumalla P; Russell DS; Auld E; Goldstein JM
    Arch Neurol; 2001 Nov; 58(11):1891-6. PubMed ID: 11709000
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I.
    Dyck PJ; Ott J; Moore SB; Swanson CJ; Lambert EH
    Mayo Clin Proc; 1983 Jul; 58(7):430-5. PubMed ID: 6865476
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [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]  

    [Next]    [New Search]
    of 8.