BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 2249464)

  • 1. An unusual neurologic problem: Werdnig-Hoffmann disease.
    Barden C; Lee R; Parchment Y; Dempsey RM
    Crit Care Nurse; 1990; 10(10):60-7. PubMed ID: 2249464
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [Werdnig-Hoffmann's congenital spinal atrophy in nursing infants].
    Kutafin IuF; Osipov SM; Osipov ES
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):15-8. PubMed ID: 1646528
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Spinal muscular atrophy in young infants].
    Smit LM; Hageman EG
    Tijdschr Kindergeneeskd; 1989 Jun; 57(3):102-6. PubMed ID: 2799798
    [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. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
    Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R
    Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861
    [No Abstract]   [Full Text] [Related]  

  • 7. Histochemistry and morphometry of Werdnig-Hoffmann disease.
    Artacho Pérula E; Roldán Villalobos R; Vaamonde Lemos R
    Histol Histopathol; 1989 Jul; 4(3):265-70. PubMed ID: 2485193
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Morphological and morphometrical study of human muscle spindles in Werdnig-Hoffmann disease (infantile spinal muscular atrophy type I).
    Kararizou E; Manta P; Kalfakis N; Gkiatas K; Vassilopoulos D
    Acta Histochem; 2006; 108(4):265-9. PubMed ID: 16730053
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
    Feng J; Toshiyuki Y
    Chin Med J (Engl); 2003 May; 116(5):673-5. PubMed ID: 12875676
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes.
    Stipoljev F; Sertić J; Latin V; Rukavina-Stavljenić A; Kurjak A
    Croat Med J; 1999 Sep; 40(3):433-7. PubMed ID: 10411975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.
    Melki J; Abdelhak S; Burlet P; Raclin V; Kaplan J; Spiegel R; Gilgenkrantz S; Philip N; Chauvet ML; Dumez Y
    J Med Genet; 1992 Mar; 29(3):171-4. PubMed ID: 1348092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Progressive spinal amyotrophy type I or Werdnig-Hoffman disease. Apropos of 5 cases in Dakar (Senegal)].
    Ndiaye O; Sall G; Sylla A; Diouf S; Diagne I; Kuakuvi N
    Bull Soc Pathol Exot; 2002 Jun; 95(2):81-2. PubMed ID: 12145964
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. [The men behind the syndrome: Werdnig and Hoffmann. They classified spinal muscular atrophies].
    Fogström B; Bui TH
    Lakartidningen; 1993 Jan; 90(4):275-6. PubMed ID: 8433609
    [No Abstract]   [Full Text] [Related]  

  • 19. [Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood].
    Distefano G; Sciacca P; Parisi MG; Parano E; Smilari P; Marletta M; Fiumara A
    Pediatr Med Chir; 1994; 16(2):125-8. PubMed ID: 8078785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Two cases of Werdnig-Hofmann disease].
    Palmer-Morales Y; Pacheco-Flores G; Ames-Guevara Y; Gaxiola-Apodaca M; Gaspar-Franco D; Landavazo-Acuña G; Hernández-Rocha F
    Rev Med Inst Mex Seguro Soc; 2010; 48(3):317-9. PubMed ID: 21192906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.