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 *

158 related articles for article (PubMed ID: 2614795)

  • 21. [Werdnig-Hoffmann amyotrophy in a 7-month-old child].
    Kutafin IuF; Osipov SM
    Pediatriia; 1990; (4):91-3. PubMed ID: 2371136
    [No Abstract]   [Full Text] [Related]  

  • 22. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R; Hagmann A; Boltshauser E; Moser H
    Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].
    Cneude F; Sukno S; Boidein F; Dehouck MB; Bourlet A; Vittu G
    Rev Neurol (Paris); 1999 Sep; 155(8):589-91. PubMed ID: 10486849
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Early diaphragmatic paralysis. In infants with genetic disorders.
    Sivan Y; Galvis A
    Clin Pediatr (Phila); 1990 Mar; 29(3):169-71. PubMed ID: 2407409
    [TBL] [Abstract][Full Text] [Related]  

  • 25. MR findings of Werdnig-Hoffmann disease in two infants.
    Hsu CF; Chen CY; Yuh YS; Chen YH; Hsu YT; Zimmerman RA
    AJNR Am J Neuroradiol; 1998 Mar; 19(3):550-2. PubMed ID: 9541317
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.
    Melki J; Abdelhak S; Sheth P; Bachelot MF; Burlet P; Marcadet A; Aicardi J; Barois A; Carriere JP; Fardeau M
    Nature; 1990 Apr; 344(6268):767-8. PubMed ID: 1970420
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Werdnig-Hoffmann disease. The first prenatal diagnosis in Cuba].
    Acevedo-López AM; Zaldívar-Vaillant T; Hernández-Chico C; Moreno F; Rosich-Capablanca G; Guerra-Badía R
    Rev Neurol; 1999 Dec 16-31; 29(12):1172-5. PubMed ID: 10652743
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].
    Ben Hamida M; Hentati F; Chebbi N; Mhiri C; Ayed K; Hamzaoui K
    Rev Neurol (Paris); 1988; 144(11):737-47. PubMed ID: 3231963
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transient cytoplasmic bodies in muscle of three infants with Werdnig-Hoffmann disease.
    Buchino JJ; Bove KE; Iannaccone ST
    Pediatr Pathol; 1990; 10(4):563-73. PubMed ID: 2164661
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K
    J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The effect of peripheral nerve injury on immature motor and sensory neurons and on muscle fibres. Possible relation to the histogenesis of Werdnig-Hoffmann disease.
    Schmalbruch H
    Rev Neurol (Paris); 1988; 144(11):721-9. PubMed ID: 3231961
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Acute respiratory insufficiency as the initial clinical manifestation of spinal muscular atrophy].
    Poets C; Heyer R; von der Hardt H; Walter GF
    Monatsschr Kinderheilkd; 1990 Mar; 138(3):157-9. PubMed ID: 2352537
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
    Appelbaum JS; Roos RP
    Muscle Nerve; 1993 Dec; 16(12):1416. PubMed ID: 8232401
    [No Abstract]   [Full Text] [Related]  

  • 34. [Results of neonatal screening for spinal muscular atrophy in Hungary in 2023].
    Mikos B; Molnár MJ; Szatmári I; Monostori P; Bereczki C; Szabó AJ; Szabó L; Csősz K; Muzsik B; Velkey GJ
    Orv Hetil; 2024 Jul; 165(29):1122-1129. PubMed ID: 39033493
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
    Camu W; Billiard M
    J Neurol Sci; 1994 Jul; 124 Suppl():88-9. PubMed ID: 7807154
    [No Abstract]   [Full Text] [Related]  

  • 36. [Case of Werdnig-Hoffman's disease in an infant].
    LUKASZEWICZ-DANCOWA D; WALENTYNOWICZ-STANCZYK R
    Pediatr Pol; 1956 Sep; 31(9):1031-4. PubMed ID: 13407985
    [No Abstract]   [Full Text] [Related]  

  • 37. Cerebellar hypoplasia in Werdnig-Hoffmann disease.
    NORMAN RM
    Arch Dis Child; 1961 Feb; 36(185):96-101. PubMed ID: 13729575
    [No Abstract]   [Full Text] [Related]  

  • 38. [Electromyogram and Werdnig-Hoffmann disease].
    GAUDIER B; MILBLED G; RAMEZ T
    J Radiol Electrol Med Nucl; 1962; 43():426-8. PubMed ID: 13897277
    [No Abstract]   [Full Text] [Related]  

  • 39. Ubiquitin and phosphorylated neurofilament epitopes in ballooned neurons of the extraocular muscle nuclei in a case of Werdnig-Hoffmann disease.
    Kato S; Hirano A
    Acta Neuropathol; 1990; 80(3):334-7. PubMed ID: 1698008
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High incidence of acute infantile spinal atrophy in Hungary.
    Czeizel A
    Hum Genet; 1991 Mar; 86(5):539. PubMed ID: 2016096
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.