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

84 related items for PubMed ID: 1144845

  • 21. De-novo COL4A5 gene mutations in Alport's syndrome.
    Massella L, Rizzoni G, De Blasis R, Barsotti P, Faraggiana T, Renieri A, Seri M, Galli L, De Marchi M.
    Nephrol Dial Transplant; 1994; 9(10):1408-11. PubMed ID: 7816253
    [Abstract] [Full Text] [Related]

  • 22. Hereditary nephritis and deafness. Report of a family.
    Shani M, Fine LG.
    Isr J Med Sci; 1970; 6(4):544-8. PubMed ID: 5472337
    [No Abstract] [Full Text] [Related]

  • 23. [Hereditary nephritis (Alport's syndrome). Clinical, histological, ultrastructural and immunohistological study].
    Imbasciati E, Gaboardi F, Limido D, Tarantino A, Chiccoli C.
    Minerva Nefrol; 1973; 20(3):148-61. PubMed ID: 4586688
    [No Abstract] [Full Text] [Related]

  • 24. [Various types of glomerulonephritis. Hereditary nephritis].
    Tanaka C, Kitagawa T.
    Nihon Rinsho; 1988 Jun; 46(6):1300-4. PubMed ID: 3418898
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. [Nephropathy and deafness (Alport syndrome) without positive family history (author's transl)].
    Rüdiger HW, Gaertner U, Klapdor R, Neumann OG.
    Med Klin; 1975 Feb 21; 70(8):337-40. PubMed ID: 1124046
    [Abstract] [Full Text] [Related]

  • 27. Familial hematuria: a clinical, ultrastructural and morphometric study.
    Schärer K, Waldherr R, Müller-Möhlis TC, Tariverdian G.
    Prog Clin Biol Res; 1989 Feb 21; 305():173-7. PubMed ID: 2762351
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Renal biopsy and family studies in 65 children with isolated hematuria.
    Schröder CH, Bontemps CM, Assmann KJ, Schuurmans Stekhoven JH, Foidart JM, Monnens LA, Veerkamp JH.
    Acta Paediatr Scand; 1990 Feb 21; 79(6-7):630-6. PubMed ID: 2386054
    [Abstract] [Full Text] [Related]

  • 31. Hereditary nephropathy with hearing loss. "Alport's syndrome".
    Iversen UM.
    Acta Paediatr Scand Suppl; 1974 Feb 21; (245):1-23. PubMed ID: 4617477
    [No Abstract] [Full Text] [Related]

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

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 35. Hereditary glomerulonephritis of non-Alport type.
    Doherty CC, Middleton DT, Hill CM.
    Proc Eur Dial Transplant Assoc; 1983 Feb 21; 19():575-81. PubMed ID: 6878256
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J.
    Ophthalmic Genet; 2000 Dec 21; 21(4):217-25. PubMed ID: 11135492
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. [Alport's syndrome].
    Knotková V, Stejskal J, Voldrich L, Beran M, Straková M, Tomásek R.
    Sb Lek; 1973 Jun 21; 75(6):169-76. PubMed ID: 4709456
    [No Abstract] [Full Text] [Related]

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