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 *

93 related articles for article (PubMed ID: 702182)

  • 21. Selective type II muscle fiber hypertrophy in severe infantile spinal muscular atrophy.
    Kingma DW; Feeback DL; Marks WA; Bobele GB; Leech RW; Brumback RA
    J Child Neurol; 1991 Oct; 6(4):329-34. PubMed ID: 1940135
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [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]  

  • 23. 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]  

  • 24. Spinal muscular atrophy: new thoughts on the pathogenesis and classification schema.
    Russman BS; Iannacone ST; Buncher CR; Samaha FJ; White M; Perkins B; Zimmerman L; Smith C; Burhans K; Barker L
    J Child Neurol; 1992 Oct; 7(4):347-53. PubMed ID: 1469240
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Expression of developmentally regulated cytoskeleton and cell surface proteins in childhood spinal muscular atrophies.
    Soubrouillard C; Pellissier JF; Lepidi H; Mancini J; Rougon G; Figarella-Branger D
    J Neurol Sci; 1995 Nov; 133(1-2):155-63. PubMed ID: 8583219
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Spinal muscular atrophy: the natural course of disease.
    Russman BS; Melchreit R; Drennan JC
    Muscle Nerve; 1983; 6(3):179-81. PubMed ID: 6855803
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Animal model of human disease: Werdnig-Hoffmann disease (infantile spinal muscular atrophy).
    Leestma JE
    Am J Pathol; 1980 Sep; 100(3):821-4. PubMed ID: 7416238
    [No Abstract]   [Full Text] [Related]  

  • 28. [Werdnig-Hoffmann disease].
    Perentes E; Donati F
    Rev Med Suisse Romande; 1981 Sep; 101(9):685-96. PubMed ID: 7302452
    [No Abstract]   [Full Text] [Related]  

  • 29. [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]  

  • 30. Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease.
    Goebel HH; Zeman W; DeMyer W
    Neuropadiatrie; 1976 May; 7(2):182-95. PubMed ID: 183171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spinal muscular atrophy: survival pattern and functional status.
    Chung BH; Wong VC; Ip P
    Pediatrics; 2004 Nov; 114(5):e548-53. PubMed ID: 15492357
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Infantile spinal muscular atrophy (morbus Werdnig-Hoffmann) causing neonatal asphyxia.
    Kyllerman M
    Neuropadiatrie; 1977 Feb; 8(1):53-6. PubMed ID: 576732
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN gene.
    Lohkamp LN; von Au K; Goebel HH; Kress W; Grieben U; Drossel K; Garbes L; Wirth B; Heppner FL; Stenzel W
    J Child Neurol; 2014 Feb; 29(2):254-9. PubMed ID: 24334346
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
    Brzustowicz LM; Mérette C; Kleyn PW; Lehner T; Castilla LH; Penchaszadeh GK; Das K; Munsat TL; Ott J; Gilliam TC
    Hum Hered; 1993; 43(6):380-7. PubMed ID: 7904586
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Spinal muscular atrophy : Time for newborn screening?].
    Vill K; Blaschek A; Schara U; Kölbel H; Hohenfellner K; Harms E; Olgemöller B; Walter MC; Müller-Felber W
    Nervenarzt; 2017 Dec; 88(12):1358-1366. PubMed ID: 29101527
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.
    Higgs EJ; McClaren BJ; Sahhar MA; Ryan MM; Forbes R
    J Paediatr Child Health; 2016 Jan; 52(1):40-6. PubMed ID: 26437687
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy.
    Bertini E; Gadisseux JL; Palmieri G; Ricci E; Di Capua M; Ferriere G; Lyon G
    Am J Med Genet; 1989 Jul; 33(3):328-35. PubMed ID: 2801766
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [Role of signs of fetal hypokinesia in the diagnosis of spinal muscular atrophy of neonatal onset].
    González De Dios J; Martínez Frías ML; Arroyo Carrera I; Fondevilla Saucí J; Sanchís Calvo A; Hernández Ramón F; Martínez Guardia N; García González MM
    An Esp Pediatr; 2002 Mar; 56(3):233-40. PubMed ID: 11864521
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan.
    Okamoto K; Fukuda M; Saito I; Urate R; Maniwa S; Usui D; Motoki T; Jogamoto T; Aibara K; Hosokawa T; Konishi Y; Arakawa R; Mori K; Ishii E; Saito K; Nishio H
    Brain Dev; 2019 Jan; 41(1):36-42. PubMed ID: 30093179
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.