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

102 related items for PubMed ID: 1549981

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

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

  • 3. Brugada syndrome and sudden cardiac death in children.
    Priori SG, Napolitano C, Giordano U, Collisani G, Memmi M.
    Lancet; 2000 Mar 04; 355(9206):808-9. PubMed ID: 10711933
    [Abstract] [Full Text] [Related]

  • 4. Autosomal dominant Lewy-body Parkinson's disease.
    Golbe LI, Miller DC, Duvoisin RC.
    Adv Neurol; 1990 Mar 04; 53():287-92. PubMed ID: 2173372
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Variable onset of adult inherited focal dystonia: a problem for genetic studies.
    Micheli S, Fernández-Pardal M, Quesada P, Brannan T, Obeso JA.
    Mov Disord; 1994 Jan 04; 9(1):64-8. PubMed ID: 8139606
    [No Abstract] [Full Text] [Related]

  • 7. [Genic diseases and chromosome diseases].
    Robert JM, Cordier MP.
    Soins; 1983 Apr 04; (403):3-6. PubMed ID: 6553367
    [No Abstract] [Full Text] [Related]

  • 8. Familial distal dysautonomia.
    Robinson B, Johnson R, Abernethy D, Holloway L.
    J Neurol Neurosurg Psychiatry; 1989 Nov 04; 52(11):1281-5. PubMed ID: 2592970
    [Abstract] [Full Text] [Related]

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

  • 10.
    ; . PubMed ID:
    [No 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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Autosomal dominant polycystic renal disease: a study of 5 familial cases].
    Puche López N, González López E, Yébenes Díaz G, Kloppe Villegas P, Rubio Benito E.
    Aten Primaria; 1990 Oct 04; 7(9):570-4. PubMed ID: 2103812
    [Abstract] [Full Text] [Related]

  • 17. [Hypo-/aplasia of the nasal bones--an autosomal dominant inherited anomaly].
    Ernst M, Schilbach U.
    HNO; 1987 Nov 04; 35(11):478-81. PubMed ID: 3692934
    [Abstract] [Full Text] [Related]

  • 18. [Familial idiopathic atrial fibrillation with bradyarrhythmia].
    Beyer F, Paul T, Luhmer I, Bertram H, Kallfelz HC.
    Z Kardiol; 1993 Nov 04; 82(11):674-7. PubMed ID: 8291288
    [Abstract] [Full Text] [Related]

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

  • 20. Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.
    Chakrabarti A, Pearce JM.
    J Neurol Neurosurg Psychiatry; 1981 Dec 04; 44(12):1146-52. PubMed ID: 7334411
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.