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 *

91 related articles for article (PubMed ID: 5912249)

  • 21. [Werdnig-Hoffmann disease: report of two cases?].
    Forties-Rêgo J
    Arq Neuropsiquiatr; 1976 Dec; 34(4):387-93. PubMed ID: 985151
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Ultrastructural findings and characterization of isoenzymes in the muscle in case of Werdnig-Hoffmann disease].
    Ferreli A; Cao A; Onnis C
    Arch De Vecchi Anat Patol; 1967 Dec; 50(3):629-44. PubMed ID: 5634345
    [No Abstract]   [Full Text] [Related]  

  • 23. [The Werdnig-Hoffmann disease].
    Nagy L; Bodosi M
    Orv Hetil; 1969 Oct; 110(43):2497-501. PubMed ID: 5358757
    [No Abstract]   [Full Text] [Related]  

  • 24. Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease.
    Steiman GS; Rorke LB; Brown MJ
    Ann Neurol; 1980 Sep; 8(3):317-24. PubMed ID: 7436375
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [ELECTROMYOGRAPHIC FINDINGS IN WERDNIG-HOFFMANN AMYOTROPHY].
    MONACELLI G
    Lattante; 1964 Feb; 35():65-82. PubMed ID: 14138492
    [No Abstract]   [Full Text] [Related]  

  • 26. Spinal muscular atrophy: the natural course of disease.
    Russman BS; Melchreit R; Drennan JC
    Muscle Nerve; 1983; 6(3):179-81. PubMed ID: 6855803
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Imaging case of the month: Werdnig-Hoffman disease.
    Giacoia GP
    Am J Perinatol; 1987 Jul; 4(3):271-2. PubMed ID: 3606762
    [No Abstract]   [Full Text] [Related]  

  • 28. Vitamin E deficiency in Werdnig-Hoffmann disease.
    Shapira Y; Amit R; Rachmilewitz E
    Ann Neurol; 1981 Sep; 10(3):266-8. PubMed ID: 7294734
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. Congenital cervical spinal atrophy.
    Darwish H; Sarnat H; Archer C; Brownell K; Kotagal S
    Muscle Nerve; 1981; 4(2):106-10. PubMed ID: 7207500
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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]  

  • 32. Is Kugelberg-Welander spinal muscular atrophy a fetal defect?
    Hausmanowa-Petrusewicz I; Fidziańska A; Niebrój-Dobosz I; Strugalska MH
    Muscle Nerve; 1980; 3(5):389-402. PubMed ID: 7421874
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Preservation of the phrenic motoneurons in Werdnig-Hoffmann disease.
    Kuzuhara S; Chou SM
    Ann Neurol; 1981 May; 9(5):506-10. PubMed ID: 7271245
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Werdnig-Hoffmann disease.
    Mamvura CB
    Cent Afr J Med; 1980 May; 26(5):107-11. PubMed ID: 7397774
    [No Abstract]   [Full Text] [Related]  

  • 35. [CLINICAL CONTRIBUTION TO THE STUDY OF WERDNIG-HOFFMANN MUSCULAR AMYOTROPHY].
    CIULLA M
    Boll Soc Med Chir Cremona; 1963; 17():141-8. PubMed ID: 14109627
    [No Abstract]   [Full Text] [Related]  

  • 36. Pathological cases of the month. Type 1 spinal muscular atrophy (Werdnig-Hoffman disease).
    Miles JM; Gilbert-Barness E
    Am J Dis Child; 1993 Aug; 147(8):907-8. PubMed ID: 8352229
    [No Abstract]   [Full Text] [Related]  

  • 37. Werdnig-Hoffmann disease with congenital hypothyroidism.
    Gunes T; Akcakus M; Cetin N; Kurtoğlu S; Kumandaş S
    Ann Trop Paediatr; 2003 Dec; 23(4):301-4. PubMed ID: 14738578
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. 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]  

  • 40. Electromyography and biopsy correlation with suggested protocol for evaluation of the floppy infant.
    David WS; Jones HR
    Muscle Nerve; 1994 Apr; 17(4):424-30. PubMed ID: 8170489
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.