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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

193 related items for PubMed ID: 8293160

  • 21. X-linked infantile spinal muscular atrophy.
    Greenberg F, Fenolio KR, Hejtmancik JF, Armstrong D, Willis JK, Shapira E, Huntington HW, Haun RL.
    Am J Dis Child; 1988 Feb; 142(2):217-9. PubMed ID: 3341327
    [Abstract] [Full Text] [Related]

  • 22. Atrial Septal Defect, Neuromuscular Junction and Skeletal Abnormalities in Spinal Muscular Atrophy Type III.
    Luan XH, Liu J.
    Chin Med J (Engl); 2017 Oct 05; 130(19):2382-2383. PubMed ID: 28937047
    [No Abstract] [Full Text] [Related]

  • 23. Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q.
    Dubowitz V, Daniels RJ, Davies KE.
    Neuromuscul Disord; 1995 Jan 05; 5(1):25-9. PubMed ID: 7719137
    [No Abstract] [Full Text] [Related]

  • 24. [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 05; 138(3):157-9. PubMed ID: 2352537
    [Abstract] [Full Text] [Related]

  • 25. Spinal muscular atrophies.
    Lancet; 1990 Aug 04; 336(8710):280-1. PubMed ID: 1973974
    [No Abstract] [Full Text] [Related]

  • 26. [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 Aug 04; 16(2):125-8. PubMed ID: 8078785
    [Abstract] [Full Text] [Related]

  • 27. [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].
    THIEFFRY S, ARTHUIS M, BARGETON E.
    Rev Neurol (Paris); 1955 Oct 04; 93(4):621-44. PubMed ID: 13298385
    [No Abstract] [Full Text] [Related]

  • 28. 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 04; 19(3):550-2. PubMed ID: 9541317
    [Abstract] [Full Text] [Related]

  • 29. Peripheral nerve involvement in Werdnig-Hoffmann disease.
    Chien YY, Nonaka I.
    Brain Dev; 1989 Mar 04; 11(4):221-9. PubMed ID: 2774090
    [Abstract] [Full Text] [Related]

  • 30. [Usefulness of ECG in the early diagnosis of infantile spinal muscular dystrophy].
    Carboni P, Porro G.
    Minerva Pediatr; 1988 Jun 04; 40(6):321-5. PubMed ID: 3185431
    [No Abstract] [Full Text] [Related]

  • 31. Brain atrophy in Werdnig-Hoffmann disease.
    Yohannan M, Patel P, Kolawole T, Malabarey T, Mahdi A.
    Acta Neurol Scand; 1991 Nov 04; 84(5):426-8. PubMed ID: 1776391
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
    Hahnen E, Forkert R, Marke C, Rudnik-Schöneborn S, Schönling J, Zerres K, Wirth B.
    Hum Mol Genet; 1995 Oct 04; 4(10):1927-33. PubMed ID: 8595417
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. 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 04; 7(4):347-53. PubMed ID: 1469240
    [Abstract] [Full Text] [Related]

  • 36. Statistical considerations in the study of spinal muscular atrophy. Dallas-Cincinnati-Newington Spinal Muscular Atrophy (DCN-SMA) Study Group.
    Buncher CR, Samaha F, Iannaccone ST, Russman BS, Cook JD, White M, McLaughlin C.
    Muscle Nerve; 1990 Oct 04; 13 Suppl():S45-8. PubMed ID: 2233886
    [No Abstract] [Full Text] [Related]

  • 37. Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophy.
    Paul DA, Goldsmith LS, Miles DK, Moser AB, Spiro AJ, Grover WD.
    Pediatr Neurol; 1993 Oct 04; 9(6):496-7. PubMed ID: 7605563
    [Abstract] [Full Text] [Related]

  • 38. Congenital autosomal dominant distal spinal muscular atrophy.
    Adams C, Suchowersky O, Lowry RB.
    Neuromuscul Disord; 1998 Aug 04; 8(6):405-8. PubMed ID: 9713859
    [Abstract] [Full Text] [Related]

  • 39. Pontocerebellar hypoplasia type 1 for the neuropediatrician: Genotype-phenotype correlations and diagnostic guidelines based on new cases and overview of the literature.
    Ivanov I, Atkinson D, Litvinenko I, Angelova L, Andonova S, Mumdjiev H, Pacheva I, Panova M, Yordanova R, Belovejdov V, Petrova A, Bosheva M, Shmilev T, Savov A, Jordanova A.
    Eur J Paediatr Neurol; 2018 Jul 04; 22(4):674-681. PubMed ID: 29656927
    [Abstract] [Full Text] [Related]

  • 40. Spinal Muscular Atrophy: Autopsy Based Neuropathological Demonstration.
    Thirunavukkarasu B, Gupta K, Bansal A, Dhanasekaran N, Baranwal A.
    Neurol India; 2020 Jul 04; 68(4):882-885. PubMed ID: 32859833
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.