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 *

119 related articles for article (PubMed ID: 8433609)

  • 41. 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]  

  • 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. [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]  

  • 44. [Werdnig-Hoffmann disease type I with progressive ophthalmoplegia and ptosis].
    Ohkura M; Mitsudome A; Yasumoto S; Ogawa A
    No To Hattatsu; 1996 Jul; 28(4):332-5. PubMed ID: 8753133
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Significant dates and anniversaries of neuropathology and psychiatry in 1986].
    Shereshevskiĭ AM; Rokhlina ML; Tom A
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(1):109-20. PubMed ID: 3513466
    [No Abstract]   [Full Text] [Related]  

  • 46. Arnold-Chiari malformation.
    Arnett B
    Arch Neurol; 2003 Jun; 60(6):898-900. PubMed ID: 12810499
    [No Abstract]   [Full Text] [Related]  

  • 47. [The woman behind the syndrome. Lucja Frey. Famous for her description of gustatory facial sweating].
    Hakulinen E
    Lakartidningen; 1992 Jan; 89(4):211-2. PubMed ID: 1734154
    [No Abstract]   [Full Text] [Related]  

  • 48. [Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy].
    Heber U; Müller CR
    Klin Padiatr; 1994; 206(1):30-5. PubMed ID: 8152204
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Electrophysiological findings in childhood spinal muscular atrophies.
    Hausmanowa-Petrusewicz I
    Rev Neurol (Paris); 1988; 144(11):716-20. PubMed ID: 3231960
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [The man behind the syndrome--Adolf Wallenberg].
    Hydén D; Norrving B
    Lakartidningen; 2004 Sep; 101(36):2735-6. PubMed ID: 15455638
    [No Abstract]   [Full Text] [Related]  

  • 51. Prevalence of type I spinal muscular atrophy in North Dakota.
    Burd L; Short SK; Martsolf JT; Nelson RA
    Am J Med Genet; 1991 Nov; 41(2):212-5. PubMed ID: 1785637
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. [The men behind the syndrome: Eugen Bamberger and Pierre Marie. They developed the theses of Hippocrates on lung disease as a cause of skeletal changes].
    Johansen I; Nilsson F; Hansen BU
    Lakartidningen; 1992 Jul; 89(30-31):2519-20. PubMed ID: 1507984
    [No Abstract]   [Full Text] [Related]  

  • 54. The spinal muscular atrophies.
    Gordon N
    Dev Med Child Neurol; 1991 Oct; 33(10):934-8. PubMed ID: 1743421
    [No Abstract]   [Full Text] [Related]  

  • 55. [Changes in the motor apparatus of the bronchial cilia. Comparative study of two types of myopathies: nemaline myopathy and the Werdnig-Hoffmann syndrome].
    Calì A; Berni Canani M; De Luca L; Terraciano L; Foggia L; Corradino G; Berni Canani R; Chiummariello S
    Pediatr Med Chir; 1991; 13(4):345-8. PubMed ID: 1754465
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Nineteenth century neurology/psychiatry.
    Troncale JA
    J Med Assoc State Ala; 1982 Aug; 52(2):29-30, 32-5. PubMed ID: 6752323
    [No Abstract]   [Full Text] [Related]  

  • 57. 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]  

  • 58. 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]  

  • 59. [Type I spinal atrophy (Werdnig-Hoffman disease). Case report].
    Collado-Ortiz MA; Shkurovich-Bialik P; González-De Leo S; Arch-Tirado E
    Cir Cir; 2007; 75(2):119-22. PubMed ID: 17511908
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [From the past of the Cracow neurology. The history of neurological and psychiatric publications].
    Gaertner H
    Neurol Neurochir Pol; 1991; 25(6):833-42. PubMed ID: 1811193
    [No Abstract]   [Full Text] [Related]  

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