BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 13466409)

  • 1. [Progressive spinal muscular atrophy (Werdnig-Hoffman disease); clinical study, pathological anatomy, electromyography & genetics in 15 cases].
    DE CORDOVA A; ESTRADA R; DE LA ARENA JF
    Rev Cubana Pediatr; 1957 Jun; 29(6):291-328. PubMed ID: 13466409
    [No Abstract]   [Full Text] [Related]  

  • 2. [Genetic aspects of primary myopathies, infantile progressive spinal atrophy (Werdnig-Hoffman atrophy) and neural atrophy (Charcot-Marie-Tooth disease)].
    HANHART E
    Acta Neurol Psychiatr Belg; 1954 Feb; 54(2):91-119. PubMed ID: 13157965
    [No Abstract]   [Full Text] [Related]  

  • 3. [Study of the clinical aspects of infantile spinal progressive muscular atrophy of the Werdnig-Hoffman type].
    SCHMID PC
    Z Kinderheilkd; 1958; 81(1):13-25. PubMed ID: 13604538
    [No Abstract]   [Full Text] [Related]  

  • 4. [An association of Werdnig-Hoffman disease and pregnancy: apropos of an unusual case].
    Laffargue F; Boulot P; Lafont L; Jonquet O; Hedon B; Viala JL
    J Gynecol Obstet Biol Reprod (Paris); 1990; 19(3):321-3. PubMed ID: 2345274
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [A congenital form of progressive spinal muscular atrophy of the Werdnig-Hoffman type].
    HOFMAN H; KOWALCZYK Z; ZELMAN I
    Pol Tyg Lek; 1962 Nov; 17():1761-3. PubMed ID: 13963967
    [No Abstract]   [Full Text] [Related]  

  • 7. Urodynamics in a patient with Werdnig-Hoffman disease.
    Han Kr KR; Glazier DB; Gazi MA; Cummings KB; Barone JG
    Can J Urol; 1999 Feb; 6(1):706-708. PubMed ID: 11178590
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)].
    HORSTMANN W
    Z Kinderheilkd; 1959; 82():649-67. PubMed ID: 13848453
    [No Abstract]   [Full Text] [Related]  

  • 10. Werdnig-Hoffmann's progressive muscular atrophy. Creatine excretion following vitamin E treatment and muscle radiography.
    FRANTZELL A; HAGBERG B; SODERHJELM L
    Acta Soc Med Ups; 1951; 56(5-6):209-23. PubMed ID: 14902615
    [No Abstract]   [Full Text] [Related]  

  • 11. Rapidly progressive spinal muscular atrophy in an ambulatory 2-year-old male.
    Lin J; da Silva RJ; Grillo E
    Pediatr Neurol; 2005 Jul; 33(1):72-4. PubMed ID: 15993324
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Spinal muscular atrophy associated with olivopontocerebellar hypoplasia. A case report].
    Serra-Ortega A; Torres A; Segreo M
    Rev Neurol; 2005 Jan 16-31; 40(2):90-2. PubMed ID: 15712162
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinal muscular atrophy combined with sporadic olivopontocerebellar atrophy.
    Luo W; Ouyang Z; Guo Y; Chen Y; Ding M
    Clin Neurol Neurosurg; 2008 Sep; 110(8):855-8. PubMed ID: 18667265
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A comparison of gait in spinal muscular atrophy, type II and Duchenne muscular dystrophy.
    Armand S; Mercier M; Watelain E; Patte K; Pelissier J; Rivier F
    Gait Posture; 2005 Jun; 21(4):369-78. PubMed ID: 15886126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Progressive muscular atrophy; its electromyographic diagnosis].
    THIEBAUT F; ISCH F; ISCH-TREUSSARD C
    Rev Neurol (Paris); 1953; 89(5):333-55. PubMed ID: 13167909
    [No Abstract]   [Full Text] [Related]  

  • 16. [Electromyography in distal atrophy of the upper limbs with segmental spinal muscular atrophy: Hirayama's disease].
    García-Solana MI; García-Rodríguez V; Rodrigo-Sesma A; Lloret-Alcañiz MA; Medrano-Tovar L; Mora-Rodríguez E
    Rev Neurol; 2006 May 1-15; 42(9):570-2. PubMed ID: 16676281
    [No Abstract]   [Full Text] [Related]  

  • 17. [Neonatal muscular spinal atrophy: a case report].
    Pavone P; Velardita M; Trigilia T; Luca G; Lucenti C; Romeo G; Falsaperla R
    Pediatr Med Chir; 2004; 26(2):139-41. PubMed ID: 15700740
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nerve, muscle or bone disease? Look before you leap.
    Muthukrishnan J; Harikumar KV; Sangeeta J; Singh MK; Modi K
    Singapore Med J; 2009 Aug; 50(8):e293-4. PubMed ID: 19710962
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Spinal amyotonia-amyotrophy (Werdnig-Hoffman disease) on the basis of observation of 40 cases].
    Lesný I; Kocura P; Jirásek A; Krahulec B
    Cesk Neurol Neurochir; 1980 Jan; 43(1):26-31. PubMed ID: 7357655
    [No Abstract]   [Full Text] [Related]  

  • 20. Spinal muscular atrophy type I mimicking critical illness neuropathy in a paediatric intensive care neonate: electrophysiological features.
    Fernández-Torre JL; Teja JL; Castellanos A; Figols J; Obeso T; Arteaga R
    Brain Dev; 2008 Oct; 30(9):599-602. PubMed ID: 18384992
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.