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

Journal Abstract Search


70 related items for PubMed ID: 651413

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

  • 2. [Epstein syndrome].
    Niimura F.
    Ryoikibetsu Shokogun Shirizu; 1997; (17 Pt 2):503-6. PubMed ID: 9277978
    [No Abstract] [Full Text] [Related]

  • 3. [Chronic hereditary nephropathy with deafness and ocular lesions].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630
    [No Abstract] [Full Text] [Related]

  • 4. [Dialysis treatment in hereditary nephritis (Alport's syndrome)].
    Koall W, Mampel E.
    Z Urol Nephrol; 1976 Jul 18; 69(7):465-70. PubMed ID: 998012
    [No Abstract] [Full Text] [Related]

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

  • 6. [Late hereditary degenerative sensorineural hearing loss associated with IgA mesangial glomerulonephritis of probable autosomal dominant heredity].
    de Serdio JL, Chahin J, Gil-Curbelo JA, Perera A, Saavedra JA.
    Acta Otorrinolaringol Esp; 1993 Jul 18; 44(6):447-54. PubMed ID: 8155361
    [Abstract] [Full Text] [Related]

  • 7. Alport's syndrome (progressive hereditary nephritis).
    Gaboardi F, Edefonti A, Imbasciati E, Tarantino A, Mihatsch MJ, Zollinger HU.
    Clin Nephrol; 1974 Jul 18; 2(4):143-56. PubMed ID: 4603152
    [No Abstract] [Full Text] [Related]

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

  • 9. [Clinical and genetic characteristics of a family with Alport's syndrome (author's transl)].
    García Delgado C, Gordillo-Paniagua G.
    Rev Invest Clin; 1980 Jul 18; 32(4):471-7. PubMed ID: 7221237
    [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. [The syndrome of familial hereditary nephropathy with hearing disorders of the inner ear (Alport's syndrome)].
    Just L, Schieche M, Weigl E.
    Med Welt; 1967 Oct 07; 40():2340-4. PubMed ID: 5605789
    [No Abstract] [Full Text] [Related]

  • 14. [Hereditary nephropathy. II. Hearing loss in childhood].
    Pellant A, Pellantová Z, Frank M.
    Cesk Otolaryngol; 1987 Nov 07; 36(6):335-9. PubMed ID: 3442833
    [No Abstract] [Full Text] [Related]

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

  • 16. 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 07; 21(4):217-25. PubMed ID: 11135492
    [Abstract] [Full Text] [Related]

  • 17. [Combination of the nephrotic syndrome and hereditary nephritis with hearing disorder].
    Fokeeva, Degtiareva EM, Klembovskiĭ AI, Kabanova SA, Kovtun GV.
    Vopr Okhr Materin Det; 1974 Oct 07; 19(10):79-82. PubMed ID: 4446457
    [No Abstract] [Full Text] [Related]

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

  • 19. [A case of familial hematuria. (A contribution to Alport's syndrome)].
    Jończyk K, Kobierska-Szczepańska A.
    Wiad Lek; 1970 Dec 01; 23(23):2139-42. PubMed ID: 5496021
    [No Abstract] [Full Text] [Related]

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


    Page: [Next] [New Search]
    of 4.