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 *

103 related articles for article (PubMed ID: 2249464)

  • 41. Transition to adult care: another view.
    Minicozzi A
    Pediatr Nurs; 2000; 26(4):411-2. PubMed ID: 12026477
    [No Abstract]   [Full Text] [Related]  

  • 42. Brain atrophy in Werdnig-Hoffmann disease.
    Yohannan M; Patel P; Kolawole T; Malabarey T; Mahdi A
    Acta Neurol Scand; 1991 Nov; 84(5):426-8. PubMed ID: 1776391
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype.
    Dubowitz V
    Eur J Paediatr Neurol; 1999; 3(2):49-51. PubMed ID: 10700538
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Interpretation of a familial case of Werdnig-Hoffmann disease].
    GEDDA L; ALFIERI A; GENTILE R
    Minerva Med; 1959 Dec; 50():4287-93. PubMed ID: 13827049
    [No Abstract]   [Full Text] [Related]  

  • 45. Malignant ventricular arrhythmia in a case of adult onset of spinal muscular atrophy (Kugelberg-Welander disease).
    Roos M; Sarkozy A; Chierchia GB; De Wilde P; Schmedding E; Brugada P
    J Cardiovasc Electrophysiol; 2009 Mar; 20(3):342-4. PubMed ID: 19175839
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [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]  

  • 47. [Intestinal pseudo-obstruction secondary to systemic neuropathies and myopathies].
    García Aroca J; Sanz N; Alonso JL; de Mingo L; Rollán V
    Cir Pediatr; 1994 Jul; 7(3):115-20. PubMed ID: 7999513
    [TBL] [Abstract][Full Text] [Related]  

  • 48. CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.
    NORMAN RM; KAY JM
    Arch Dis Child; 1965 Jun; 40(211):302-8. PubMed ID: 14294750
    [No Abstract]   [Full Text] [Related]  

  • 49. [Oppenheim-Werdnig-Hoffmann disease].
    FULLADOSA A; MAGGI R
    Arch Pediatr Urug; 1962 Oct; 33():654-5. PubMed ID: 13960221
    [No Abstract]   [Full Text] [Related]  

  • 50. [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].
    THIEFFRY S; ARTHUIS M; BARGETON E
    Rev Neurol (Paris); 1955 Oct; 93(4):621-44. PubMed ID: 13298385
    [No Abstract]   [Full Text] [Related]  

  • 51. [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]  

  • 52. [Infantile spinal muscular atrophy. An unusual disease with various differential diagnoses].
    Solders G
    Lakartidningen; 1993 Jan; 90(4):268-9. PubMed ID: 8433607
    [No Abstract]   [Full Text] [Related]  

  • 53. A hungarian study on Werdnig-Hoffmann disease.
    Czeizel A; Hamula J
    J Med Genet; 1989 Dec; 26(12):761-3. PubMed ID: 2614795
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Myatonia congenita Oppenheim, with special reference to its relation to Werdnig-Hoffmann disease].
    FUKUYAMA Y
    Sogo Igaku; 1961 Oct; 18():671-82. PubMed ID: 13895848
    [No Abstract]   [Full Text] [Related]  

  • 55. Modern management of spinal muscular atrophy.
    Iannaccone ST
    J Child Neurol; 2007 Aug; 22(8):974-8. PubMed ID: 17761652
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Amyotonia congenita syndrome, with the report of a case of Werdnig-Hoffmann disease.
    SINGH R; PRASAD R; MATHUR GP; KALRA K
    Indian J Pediatr; 1963 Apr; 30():118-21. PubMed ID: 13977661
    [No Abstract]   [Full Text] [Related]  

  • 57. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
    Brunialti AL; Poirier C; Schmalbruch H; Guénet JL
    Genomics; 1995 Sep; 29(1):131-5. PubMed ID: 8530062
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Clinical and genetic study of spinal muscular atrophies in Oman.
    Koul R; Al Futaisi A; Chacko A; Rao V; Simsek M; Muralitharan S; Ganguly SS; Bayoumi R
    J Child Neurol; 2007 Oct; 22(10):1227-30. PubMed ID: 17940251
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Werdnig-Hoffmann disease in a Nigerian infant.
    Pelleboer RA; Maaswinkel-Mooy PD; Gelderen HH
    Trop Geogr Med; 1989 Jul; 41(3):282-4. PubMed ID: 2595812
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and III.
    Kroksmark AK; Beckung E; Tulinius M
    Eur J Paediatr Neurol; 2001; 5(5):191-8. PubMed ID: 11585107
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.