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

148 related items for PubMed ID: 2030350

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Congenital muscular dystrophy with cerebral involvement--report of a case of "occidental type cerebromuscular dystrophy"?
    Topaloglu H, Yalaz K, Kale G, Ergin M.
    Neuropediatrics; 1990 Feb; 21(1):53-4. PubMed ID: 2314559
    [Abstract] [Full Text] [Related]

  • 4. Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy.
    Tachi N, Tachi M, Sasaki K, Nagata N, Chiba S.
    Pediatr Neurol; 1990 Feb; 6(4):265-8. PubMed ID: 2206159
    [Abstract] [Full Text] [Related]

  • 5. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods].
    Wagner M, Diedrich U, Pozsàr C, Becker PE, Reiss J.
    Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder].
    Castro-Gago M, Novo-Rodríguez MI, Pintos-Martínez E, Alonso-Martín A, Morales-Redondo R, Eirís-Puñal J.
    Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.
    Leyten QH, ter Laak HJ, Gabreëls FJ, Renier WO, Renkawek K, Sengers RC.
    Acta Neuropathol; 1993 Sep; 86(4):386-92. PubMed ID: 8256590
    [Abstract] [Full Text] [Related]

  • 15. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images.
    Yoshioka M, Kuroki S, Mizue H.
    Brain Dev; 1987 Sep; 9(3):316-8. PubMed ID: 3661912
    [Abstract] [Full Text] [Related]

  • 16. Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency.
    Reed UC, Marie SK, Vainzof M, Salum PB, Levy JA, Zatz M, Diament A.
    Brain Dev; 1996 Sep; 18(1):53-8. PubMed ID: 8907344
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.