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 *

210 related articles for article (PubMed ID: 8352229)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. Acute onset spinal muscular atrophy in siblings.
    Robb SA; McShane MA; Wilson J; Payan J
    Neuropediatrics; 1991 Feb; 22(1):45-6. PubMed ID: 2038428
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pictorial essay of Werdnig-Hoffman disease.
    Poggiani C; Ferrari D; Parati S; Torresani P
    Minerva Pediatr; 2009 Apr; 61(2):237-8. PubMed ID: 19322128
    [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. Nerve conduction velocity in severe childhood spinal muscular atrophy (SMA type I).
    Ignatius J
    Neurol Neurochir Pol; 1996; 30 Suppl 3():91-4. PubMed ID: 9153014
    [No 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. [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]  

  • 10. [Diagnostic progress in spinal muscular atrophy].
    Gergont A; Kaciński M; Steczkowska-Klucznik M
    Przegl Lek; 2001; 58(11):989-91. PubMed ID: 11987841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. A clinical and genetic study of spinal muscular atrophy.
    Mishra VN; Kalita J; Kesari A; Mitta B; Shankar SK; Misra UK
    Electromyogr Clin Neurophysiol; 2004; 44(5):307-12. PubMed ID: 15378871
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A predominantly cervical form of spinal muscular atrophy.
    Goutières F; Bogicevic D; Aicardi J
    J Neurol Neurosurg Psychiatry; 1991 Mar; 54(3):223-5. PubMed ID: 2030349
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
    Haliloglu G; Chattopadhyay A; Skorodis L; Manzur A; Mercuri E; Talim B; Akçören Z; Renda Y; Muntoni F; Topaloğlu H
    Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Spinal muscular atrophy.
    Wessel HB
    Pediatr Ann; 1989 Jul; 18(7):421-7. PubMed ID: 2666923
    [No Abstract]   [Full Text] [Related]  

  • 18. [Contribution of the electromyogram in the diagnosis of infantile spinal muscular atrophy in the neonatal period].
    Renault F; Chartier JP; Harpey JP
    Arch Pediatr; 1996 Apr; 3(4):319-23. PubMed ID: 8762951
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease).
    Kang PB; Krishnamoorthy KS; Jones RM; Shapiro FD; Darras BT
    Neuromuscul Disord; 2006 Aug; 16(8):492-4. PubMed ID: 16797181
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Two cases of a proximal spinal muscular atrophy (Werdnig-Hoffmann's disease) in one family].
    Nurbekova UA
    Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(10):106-7. PubMed ID: 25591528
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.