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 *

180 related articles for article (PubMed ID: 4749680)

  • 1. Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease.
    Pearn JH; Wilson J
    Arch Dis Child; 1973 Oct; 48(10):768-74. PubMed ID: 4749680
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical picture and genetics of Werdnig-Hoffman spinal amyotrophy in childhood].
    Mazaeva IV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1452-6. PubMed ID: 5139405
    [No Abstract]   [Full Text] [Related]  

  • 3. Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy.
    Pearn JH; Wilson J
    Arch Dis Child; 1973 Jun; 48(6):425-30. PubMed ID: 4712772
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. [Werdnig-Hoffmann spinal amyotrophy in twins].
    Mazaeva IV; Lipovetskaia NG; Balashova EG
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(10):1491-5. PubMed ID: 4795172
    [No Abstract]   [Full Text] [Related]  

  • 6. Fetal movements and Werdnig-Hoffmann disease.
    Pearn JH
    J Neurol Sci; 1973 Apr; 18(4):373-9. PubMed ID: 4699429
    [No Abstract]   [Full Text] [Related]  

  • 7. [Infantile progressive spinal muscular atrophy. Werdnig-Hoffmann disease].
    Mohr W; Olischläger A; Carl H
    Med Welt; 1971 Aug; 35():1317-9. PubMed ID: 5564452
    [No Abstract]   [Full Text] [Related]  

  • 8. Spinal muscular atrophy.
    McLeod JG; Williams IM
    Minn Med; 1971 Jun; 54(6):457-61. PubMed ID: 5559368
    [No Abstract]   [Full Text] [Related]  

  • 9. The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.
    Pearn JH
    J Med Genet; 1973 Sep; 10(3):260-5. PubMed ID: 4774536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Respiratory distress as the initial manifestation of Werdnig-Hoffmann disease.
    Mellins RB; Hays AP; Gold AP; Berdon WE; Bowdler JD
    Pediatrics; 1974 Jan; 53(1):33-40. PubMed ID: 4809192
    [No Abstract]   [Full Text] [Related]  

  • 11. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
    Fried K; Emery AE
    Clin Genet; 1971; 2(4):203-9. PubMed ID: 5146579
    [No Abstract]   [Full Text] [Related]  

  • 12. [Increased occurrence of "sporadic" spinal progressive muscular atrophy in infancy].
    Beckmann R; Manz F; Moser R
    Monatsschr Kinderheilkd (1902); 1970 Feb; 118(2):41-4. PubMed ID: 5526771
    [No Abstract]   [Full Text] [Related]  

  • 13. [Neurogenic muscular atrophy in children].
    Hainaut H; Chapelle P; Hariga J
    Acta Paediatr Belg; 1969; 23(5):261-74. PubMed ID: 5398928
    [No Abstract]   [Full Text] [Related]  

  • 14. Editorial: Diagnosis of childhood spinal muscular atrophy.
    Br Med J; 1973 Oct; 4(5883):2-3. PubMed ID: 4755211
    [No Abstract]   [Full Text] [Related]  

  • 15. Ultrastructure of chromatolytic motoneurons in a case of Werdnig-Hoffmann disease.
    Chou SM; Fakadej AV
    Neurology; 1970 Apr; 20(4):381. PubMed ID: 4104901
    [No Abstract]   [Full Text] [Related]  

  • 16. An unusual inheritane pattern for spinal muscular atrophy.
    White NR; Blaw ME
    Dev Med Child Neurol; 1971 Oct; 13(5):621-4. PubMed ID: 5119919
    [No Abstract]   [Full Text] [Related]  

  • 17. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy].
    Raimbault J; Laget P
    Pathol Biol (Paris); 1972 Mar; 20(5):287-96. PubMed ID: 4556213
    [No Abstract]   [Full Text] [Related]  

  • 18. Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease.
    Hausmanowa-Petrusewicz I; Fidzianska A
    Bull N Y Acad Med; 1974 Dec; 50(11):1157-72. PubMed ID: 4529631
    [No Abstract]   [Full Text] [Related]  

  • 19. [Variant of childhood spinal amyotrophy].
    Savel'eva-Vasil'eva
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1456-61. PubMed ID: 5139406
    [No Abstract]   [Full Text] [Related]  

  • 20. Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.
    Ghetti B; Amati A; Turra MV; Pacini A; Del Vecchio M; Guazzi GC
    Acta Genet Med Gemellol (Roma); 1971 Jan; 20(1):43-58. PubMed ID: 5568110
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.