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


193 related items for PubMed ID: 1595709

  • 21. Alport's syndrome in monozygotic twins.
    Wang AY, Lai KN, Lai FM, Leung CB, Li PK.
    Am J Kidney Dis; 1996 Feb; 27(2):267-9. PubMed ID: 8659504
    [Abstract] [Full Text] [Related]

  • 22. Alport's syndrome and achalasia.
    Leichter HE, Vargas J, Cohen AH, Ament M, Salusky IB.
    Pediatr Nephrol; 1988 Jul; 2(3):312-4. PubMed ID: 3153032
    [Abstract] [Full Text] [Related]

  • 23. Alport syndrome misdiagnosed with IgA nephropathy from familial history: a case report and brief review.
    Rahimzadeh H, Ajlou S, Nili F, Razeghi E.
    BMC Nephrol; 2023 Apr 15; 24(1):97. PubMed ID: 37059980
    [Abstract] [Full Text] [Related]

  • 24. Thin basement membrane disease in patients with familial IgA nephropathy.
    Frascá GM, Soverini L, Gharavi AG, Lifton RP, Canova C, Preda P, Vangelista A, Stefoni S.
    J Nephrol; 2004 Apr 15; 17(6):778-85. PubMed ID: 15593051
    [Abstract] [Full Text] [Related]

  • 25. [RETINAL CHANGES IN ALPORT'S SYNDROME (HEREDITARY NEPHROPATHY WITH INNER EAR DEAFNESS)].
    UNGER HH, ROTHER K.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1964 Apr 15; 65():293-8. PubMed ID: 14260538
    [No Abstract] [Full Text] [Related]

  • 26. Familial IgA nephropathy and sensorineural deafness.
    Bizzarri D, Duranti E, Sasdelli M, Casanova S.
    Contrib Nephrol; 1990 Apr 15; 80():113-7. PubMed ID: 2282808
    [No Abstract] [Full Text] [Related]

  • 27. Glomerular morphometry II: familial and nonfamilial haematuria.
    Yoshikawa N, Cameron AH, White RH.
    Histopathology; 1981 May 15; 5(3):251-6. PubMed ID: 7239446
    [Abstract] [Full Text] [Related]

  • 28. HEREDITARY NEPHROPATHY (ALPORT'S SYNDROME). A CAUSE OF HEMATURIA IN CHILDHOOD.
    ELLIS JG, YAFFE SJ.
    Calif Med; 1964 Apr 15; 100(4):289-93. PubMed ID: 14165881
    [No Abstract] [Full Text] [Related]

  • 29. Hereditary nephritis associated with low-tone sensorineural hearing difficulty: a case report.
    Motoyama O, Ohshima M, Shigetomi Y, Ohara T, Nagai Y, Kawamura S, Iitaka K.
    Nihon Jinzo Gakkai Shi; 1996 May 15; 38(5):233-7. PubMed ID: 8699614
    [Abstract] [Full Text] [Related]

  • 30. Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds.
    Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN, Gupta A, Gupta KL.
    Nephrol Dial Transplant; 1993 May 15; 8(8):690-5. PubMed ID: 8414153
    [Abstract] [Full Text] [Related]

  • 31. [Alport's syndrome (heredo-familial glomerulonephritis with deafness and eye abnormalities)].
    Genova R.
    Clin Pediatr (Bologna); 1971 Sep 15; 53(9):301-13. PubMed ID: 5004353
    [No Abstract] [Full Text] [Related]

  • 32. Thin basement membrane nephropathy: is there genetic predisposition to more severe disease?
    Deltas C.
    Pediatr Nephrol; 2009 Apr 15; 24(4):877-9. PubMed ID: 19018577
    [No Abstract] [Full Text] [Related]

  • 33. Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach.
    Lubec G, Balzar E, Weissenbacher G, Syré G.
    Arch Dis Child; 1978 May 15; 53(5):401-6. PubMed ID: 666354
    [Abstract] [Full Text] [Related]

  • 34. Familial hereditary nephropathy (Alport's syndrome).
    Purriel P, Drets M, Pascale E, Sánchez Cestau R, Borrás A, Ferreira WA, de Lucca A, Fernández L.
    Am J Med; 1970 Dec 15; 49(6):753-73. PubMed ID: 5006614
    [No Abstract] [Full Text] [Related]

  • 35. Alport's syndrome of hereditary nephritis and deafness.
    Crawfurd MD, Toghill PJ.
    Q J Med; 1968 Oct 15; 37(148):563-76. PubMed ID: 5696367
    [No Abstract] [Full Text] [Related]

  • 36. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
    Hinglais N, Grünfeld JP, Bois E.
    Lab Invest; 1972 Nov 15; 27(5):473-87. PubMed ID: 4653971
    [No Abstract] [Full Text] [Related]

  • 37. [3 cases of Alport's syndrome with different clinical and morphologic manifestations].
    Bechcińska B, Danilewicz M, Kałuzyński A, Marek K, Wagrowska-Danilewicz M.
    Patol Pol; 1989 Nov 15; 40(1):123-8. PubMed ID: 2477788
    [Abstract] [Full Text] [Related]

  • 38. Hereditary nephropathy with nerve deafness (Alport's syndrome). Electron microscopic studies on the renal glomerulus.
    Sessa A, Cioffi A, Conte F, D'Amico G.
    Nephron; 1974 Nov 15; 13(5):404-15. PubMed ID: 4431551
    [No Abstract] [Full Text] [Related]

  • 39. Auditory manifestations of Alport's disease syndrome.
    Rintelmann W.
    Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol; 1976 Nov 15; 82(3 Pt 1):375-87. PubMed ID: 960411
    [No Abstract] [Full Text] [Related]

  • 40. [Epidemiological study in 4 family units with Alport's syndrome].
    García-Delgado C, Gordillo-Paniagua G.
    Bol Med Hosp Infant Mex; 1981 Nov 15; 38(6):887-902. PubMed ID: 7317143
    [Abstract] [Full Text] [Related]


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