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 *

148 related articles for article (PubMed ID: 7246142)

  • 1. Hereditary neurologic disorders, characterized by ataxia. Immunological in vitro parameters and HLA.
    Pedersen L; Platz P; Raun NE
    Acta Pathol Microbiol Scand C; 1980 Dec; 88(6):281-6. PubMed ID: 7246142
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hereditary spastic paraplegia associated with peroneal muscular atrophy].
    Laso FJ; Cacho J; Díez Jarilla JL; González Macías J
    Med Clin (Barc); 1982 Apr; 78(8):329-31. PubMed ID: 7087602
    [No Abstract]   [Full Text] [Related]  

  • 3. Nosology, genetics, and epidemiology of hereditary ataxias, with particular reference to the epidemiology to these disorders in western Norway.
    Refsum S; Skre H
    Adv Neurol; 1978; 19():497-508. PubMed ID: 369332
    [No Abstract]   [Full Text] [Related]  

  • 4. HLA in Charcot-Marie-Tooth disease.
    Williams LL
    Ann Neurol; 1980 Oct; 8(4):452. PubMed ID: 7436389
    [No Abstract]   [Full Text] [Related]  

  • 5. [HLA antigens in certain hereditary diseases of the central nervous system].
    Fedrunova VS; Nazarova EK; Pevnitskiĭ LA; Ivanova-Smolenskaia IA; Alieva LM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(11):1500-3. PubMed ID: 160174
    [No Abstract]   [Full Text] [Related]  

  • 6. Neurological approaches to the inherited ataxias.
    Refsum S; Skre H
    Adv Neurol; 1978; 21():1-13. PubMed ID: 367114
    [No Abstract]   [Full Text] [Related]  

  • 7. Hereditary ataxias. Occurrence and clinical features.
    Werdelin L
    Acta Neurol Scand Suppl; 1986; 106():1-124. PubMed ID: 3460301
    [No Abstract]   [Full Text] [Related]  

  • 8. A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia.
    Pedersen L; Platz P; Ryder LP; Lamm LU; Dissing J
    Hum Genet; 1980; 54(3):371-83. PubMed ID: 6772543
    [No Abstract]   [Full Text] [Related]  

  • 9. Computed tomography in hereditary ataxias.
    Gyldensted C; Pedersen L
    Neuroradiology; 1978; 16():327-8. PubMed ID: 745705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary spastic paraplegia: a clinical and genetic study of cases in the north-east of England.
    Livingstone IR; Roberts DF
    J Genet Hum; 1983 Dec; 31(4):295-305. PubMed ID: 6582228
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Computerized tomography in hereditary ataxias.
    Pedersen L; Gyldensted C
    Acta Neurol Scand; 1978 Aug; 58(2):81-8. PubMed ID: 707041
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. [Clinical characteristics of hereditary ataxia].
    Sidorova OP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(3):13-8. PubMed ID: 3381607
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Troyer syndrome: a recessively inherited form of spastic paraplegia with distal muscle wasting.
    Cross HE
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):211-3. PubMed ID: 5173362
    [No Abstract]   [Full Text] [Related]  

  • 16. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.
    Erichsen AK; Koht J; Stray-Pedersen A; Abdelnoor M; Tallaksen CM
    Brain; 2009 Jun; 132(Pt 6):1577-88. PubMed ID: 19339254
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Roussy-Levy hereditary areflexic dystasis presenting as Charcot-Marie-Tooth syndrome.
    Murdoch JL; Beighton PH
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):106-7. PubMed ID: 5173115
    [No Abstract]   [Full Text] [Related]  

  • 18. The hereditary ataxias.
    Skre H; Haugstad TS; Berg K
    Prog Med Genet; 1985; 6():123-240. PubMed ID: 2425393
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Hereditary spastic paraplegia (a review of two families with eight case reports).
    Rath RN; Das RK; Panda RK; Santhalia RR
    J Assoc Physicians India; 1978 Jun; 26(6):535-40. PubMed ID: 721758
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.