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 *

112 related articles for article (PubMed ID: 5801822)

  • 1. Heritable spinal muscular atrophies.
    Zellweger H; Schneider HJ; Schuldt DR; Mergner W
    Helv Paediatr Acta; 1969 Feb; 24(1):92-105. PubMed ID: 5801822
    [No Abstract]   [Full Text] [Related]  

  • 2. [Arthogryposis multiplex congenita with neurogenic atrophy and brachydactyly (author's transl)].
    Eckel U; Spranger J; Klein H
    Klin Padiatr; 1979 May; 191(3):325-9. PubMed ID: 572450
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Arthrogryposis accompanying congenital spinal-type muscular atrophy.
    Besser M; Behar A
    Arch Dis Child; 1967 Dec; 42(226):666-70. PubMed ID: 6073835
    [No Abstract]   [Full Text] [Related]  

  • 4. Spinal muscular atrophy.
    Hausmanowa-Petrusewicz I
    Neurologija; 1979; 27(1-4):75-94. PubMed ID: 262022
    [No Abstract]   [Full Text] [Related]  

  • 5. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)].
    Fujimori N; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1980 Jun; 20(6):423-9. PubMed ID: 7408341
    [No Abstract]   [Full Text] [Related]  

  • 6. A family with Kugelberg-Welander sydrome. Hereditary proximal spinal muscul atrophy--some additional features.
    Almog C; Tal E
    Confin Neurol; 1968; 30(5):313-24. PubMed ID: 5729137
    [No Abstract]   [Full Text] [Related]  

  • 7. [Progressive muscular spinal atrophy of Werdnig-Hoffmann].
    Galimberti A; Graziano L; Airò R
    Folia Hered Pathol (Milano); 1968; ():113-26. PubMed ID: 5760545
    [No Abstract]   [Full Text] [Related]  

  • 8. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN; Sushcheva GP; Viatkina SIa; Novikova NP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):321-30. PubMed ID: 6326437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A contribution to the pathogenesis of arthrogryposis multiplex congenita].
    Kozik M; Wróblewski T
    Reumatologia; 1968; 6(4):315-9. PubMed ID: 5714612
    [No Abstract]   [Full Text] [Related]  

  • 10. [Proximal spinal muscular atrophies].
    Magalov ShI
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):18-22. PubMed ID: 7180297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-progressive proximal and generalized spinal muscular atrophy in siblings.
    Kessler GB
    Bull Los Angeles Neurol Soc; 1968 Jan; 33(1):21-5. PubMed ID: 5651700
    [No Abstract]   [Full Text] [Related]  

  • 12. Autosomal recessive disease.
    Szwabowska-Orzeszko E; Jóźwiak S; Michałowicz R
    Acta Neurol Scand; 1993 May; 87(5):428. PubMed ID: 8333249
    [No Abstract]   [Full Text] [Related]  

  • 13. [Spinal muscular atrophies].
    Emery AE
    Recenti Prog Med; 1973 Mar; 54(3):262-73. PubMed ID: 4740195
    [No Abstract]   [Full Text] [Related]  

  • 14. [Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy].
    Parnitzke C; Hagen EM
    Z Arztl Fortbild (Jena); 1981 Jul; 75(13):577-81. PubMed ID: 7314671
    [No Abstract]   [Full Text] [Related]  

  • 15. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype.
    Johnson WG; Wigger HJ; Karp HR; Glaubiger LM; Rowland LP
    Trans Am Neurol Assoc; 1981; 106():215-8. PubMed ID: 7348998
    [No Abstract]   [Full Text] [Related]  

  • 16. [Clinicopathology of neuromuscular diseases].
    Tokuomi H
    Rinsho Byori; 1969 Jan; 17(1):6-14. PubMed ID: 5814289
    [No Abstract]   [Full Text] [Related]  

  • 17. Juvenile motor neuron diseases--the sex influence in benign juvenile pseudodystrophic spinal muscular atrophy.
    Hausmanowa-Petrusewicz I; Borkowska J; Zaremba J
    Adv Neurol; 1982; 36():131-7. PubMed ID: 7180679
    [No Abstract]   [Full Text] [Related]  

  • 18. Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.
    Bürglen L; Amiel J; Viollet L; Lefebvre S; Burlet P; Clermont O; Raclin V; Landrieu P; Verloes A; Munnich A; Melki J
    J Clin Invest; 1996 Sep; 98(5):1130-2. PubMed ID: 8787675
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Sporadic distal myopathy].
    Il'ina NA; Aver'ianov IuN; Nechkina NP; Potomskaia LZ; Sokolina NA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1620-3. PubMed ID: 6675357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant late adult spinal muscular atrophy, type Finkel.
    Richieri-Costa A; Rogatko A; Levisky R; Finkel N; Frota-Pessoa O
    Am J Med Genet; 1981; 9(2):119-28. PubMed ID: 7258225
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.