99 related articles for article (PubMed ID: 7868500)
41. Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
Ilan T; Shohat T; Tobar A; Magal N; Yahav M; Halpern GJ; Rechavi G; Shohat M
Isr Med Assoc J; 2001 Jul; 3(7):488-91. PubMed ID: 11791413
[TBL] [Abstract][Full Text] [Related]
42. [Clinical and genetics aspects of Alport syndrome].
Golshayan D; Venetz JP; Cachat F; Fellmann F; Moll S; Burnier M; Barbey F
Rev Med Suisse; 2006 Mar; 2(55):593-8. PubMed ID: 16562603
[TBL] [Abstract][Full Text] [Related]
43. Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.
Yoshioka K; Hino S; Takemura T; Maki S; Wieslander J; Takekoshi Y; Makino H; Kagawa M; Sado Y; Kashtan CE
Am J Pathol; 1994 May; 144(5):986-96. PubMed ID: 8178947
[TBL] [Abstract][Full Text] [Related]
44. Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome.
Nagel M; Nagorka S; Gross O
Hum Mutat; 2005 Jul; 26(1):60. PubMed ID: 15954103
[TBL] [Abstract][Full Text] [Related]
45. Evaluation of hematuria in children.
Meyers KE
Urol Clin North Am; 2004 Aug; 31(3):559-73, x. PubMed ID: 15313065
[TBL] [Abstract][Full Text] [Related]
46. Asymptomatic microscopical haematuria.
White RH
Br Med J (Clin Res Ed); 1986 Jun; 292(6535):1599. PubMed ID: 3087534
[No Abstract] [Full Text] [Related]
47. Familial and nonfamilal benign hematuria.
McConville JM; McAdams AJ
J Pediatr; 1966 Aug; 69(2):207-14. PubMed ID: 5949931
[No Abstract] [Full Text] [Related]
48. Persistent microscopic haematuria without proteinuria.
Flinter FA
Pediatr Nephrol; 1993 Apr; 7(2):150. PubMed ID: 8476708
[No Abstract] [Full Text] [Related]
49. Alpha 5 COLIV chain distribution in glomerular basement membrane in a male with X-linked Alport syndrome and thin basement membrane.
Rizzoni G; Massella L; Muda AO
Pediatr Nephrol; 2000 Dec; 15(3-4):325. PubMed ID: 11149132
[No Abstract] [Full Text] [Related]
50. Epstein's syndrome: case report and survey of the literature.
Standen GR; Saunders J; Michael J; Bloom AL
Postgrad Med J; 1987 Jul; 63(741):573-5. PubMed ID: 3309919
[TBL] [Abstract][Full Text] [Related]
51. [Case report: a case with Alport syndrome lacking hypoacusis diagnosed at 41 years of age].
Kudo K; Miyoshi K; Nagao T; Jotoku M; Enomoto D; Irita J; Okura T; Higaki J
Nihon Naika Gakkai Zasshi; 2013 Jan; 102(1):140-2. PubMed ID: 23777124
[No Abstract] [Full Text] [Related]
52. Alport's syndrome.
Oni AO; Eweka AO; Otuaga PO; Odia JO
Saudi J Kidney Dis Transpl; 2009 Nov; 20(6):1087-9. PubMed ID: 19861880
[No Abstract] [Full Text] [Related]
53. Renal transplantation in patients with Alport syndrome.
Kashtan CE
Pediatr Transplant; 2006 Sep; 10(6):651-7. PubMed ID: 16911486
[TBL] [Abstract][Full Text] [Related]
54. de-novo Alport syndrome: for the diagnosis of inherited glomerulonephritis with neither any family history nor extrarenal manifestation.
Fukushima T; Nomura S; Kawai S; Osawa G
Clin Nephrol; 1997 Aug; 48(2):134-5. PubMed ID: 9285155
[No Abstract] [Full Text] [Related]
55. Consultation with the specialist. Familial nephritis/Alport syndrome.
Fouser L
Pediatr Rev; 1998 Aug; 19(8):265-7. PubMed ID: 9707716
[No Abstract] [Full Text] [Related]
56. Is genetic testing of healthy pre-symptomatic children with possible Alport syndrome ethical?
Copelovitch L; Kaplan BS
Pediatr Nephrol; 2006 Apr; 21(4):455-6. PubMed ID: 16491420
[No Abstract] [Full Text] [Related]
57. Benign familial haematuria.
Lancet; 1988 Sep; 2(8610):549-50. PubMed ID: 2900928
[No Abstract] [Full Text] [Related]
58. [Mathematical analysis in the differential diagnosis of hereditary and acquired nephritis in children].
Ignatova MS; Skripkina LA; Bosin VIu; Degtiareva EM; Korshun GN
Sov Med; 1977 Nov; (11):55-60. PubMed ID: 607455
[No Abstract] [Full Text] [Related]
59. [A case of autosomal recessive Alport syndrome with nephrotic syndrome as initial symptom].
Ding J; Luan J; Wang X
Zhonghua Er Ke Za Zhi; 2015 Sep; 53(9):712-3. PubMed ID: 26757974
[No Abstract] [Full Text] [Related]
60. [Progress in diagnosis and treatment of kidney diseases. III. Hereditary kidney diseases and others. 2. Alport syndrome].
Harada T; Nomura S; Naito I
Nihon Naika Gakkai Zasshi; 1996 Oct; 85(10):1681-7. PubMed ID: 8999061
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
