185 related articles for article (PubMed ID: 37059980)
1. 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; 24(1):97. PubMed ID: 37059980
[TBL] [Abstract][Full Text] [Related]
2. IgA nephropathy suspected to be combined with Fabry disease or Alport syndrome: a case report.
Hao W; Ao L; Zhang C; Zhu L; Xie D
J Int Med Res; 2020 Mar; 48(3):300060519891290. PubMed ID: 31840555
[TBL] [Abstract][Full Text] [Related]
3. Tale of two nephropathies; co-occurring Alport syndrome and IgA nephropathy, a case report.
Bhattacharyya A; Huang Y; Khan SH; Drachenberg CB; Malone LC
BMC Nephrol; 2021 Oct; 22(1):358. PubMed ID: 34717572
[TBL] [Abstract][Full Text] [Related]
4. Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.
Haas M
Arch Pathol Lab Med; 2009 Feb; 133(2):224-32. PubMed ID: 19195966
[TBL] [Abstract][Full Text] [Related]
5. Pediatric glomerular hematuria: a clinicopathological study.
Moustafa FE; Eid R; Hamdy N
Clin Exp Nephrol; 2020 Jul; 24(7):613-621. PubMed ID: 32198715
[TBL] [Abstract][Full Text] [Related]
6. Thin basement membrane nephropathy.
Savige J; Rana K; Tonna S; Buzza M; Dagher H; Wang YY
Kidney Int; 2003 Oct; 64(4):1169-78. PubMed ID: 12969134
[TBL] [Abstract][Full Text] [Related]
7. A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome.
Vischini G; Kapp ME; Wheeler FC; Hopp L; Fogo AB
Hum Pathol; 2018 Nov; 81():229-234. PubMed ID: 29530752
[TBL] [Abstract][Full Text] [Related]
8. [Genetic variants of familial hematuria associated genes in three families with hematuria with probands initially diagnosed as IgA nephropathy].
Liu JW; Wang P; Huang J; Nie XJ; Zhao F; Chen LZ; Li Z; Yu ZH
Zhonghua Er Ke Za Zhi; 2019 Sep; 57(9):674-679. PubMed ID: 31530352
[No Abstract] [Full Text] [Related]
9. Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome.
Ishiko S; Tanaka A; Takeda A; Hara M; Hamano N; Koizumi M; Ueno T; Hayashi H; Kondo A; Nagai S; Aoto Y; Sakakibara N; Nagano C; Horinouchi T; Yamamura T; Ninchoji T; Shima Y; Nakanishi K; Yoshikawa N; Iijima K; Nozu K
Clin Exp Nephrol; 2021 Jul; 25(7):779-787. PubMed ID: 33743099
[TBL] [Abstract][Full Text] [Related]
10. Thin basement membrane nephropathy: is there genetic predisposition to more severe disease?
Deltas C
Pediatr Nephrol; 2009 Apr; 24(4):877-9. PubMed ID: 19018577
[No Abstract] [Full Text] [Related]
11. A novel frameshift mutation of COL4A5 in a Chinese family with presumed IgA nephropathy and chronic glomerulonephritis.
Zhu Q; Zhou C; Wang J
J Clin Lab Anal; 2020 Dec; 34(12):e23558. PubMed ID: 32893410
[TBL] [Abstract][Full Text] [Related]
12. [Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].
Endreffy E; Ondrik Z; Kemény E; Vas Z; Maróti Z; Lencse G; Bereczki C; Haszon I; Túri S; Iványi B
Orv Hetil; 2005 Dec; 146(52):2647-53. PubMed ID: 16468607
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndrome.
Li Z; Zhu P; Huang H; Pan Y; Han P; Cui H; Kang Z; Xun M; Zhang Y; Liu S; Wang J; Wu J
Sci China Life Sci; 2019 Dec; 62(12):1572-1579. PubMed ID: 31209800
[TBL] [Abstract][Full Text] [Related]
14. Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
Papazachariou L; Papagregoriou G; Hadjipanagi D; Demosthenous P; Voskarides K; Koutsofti C; Stylianou K; Ioannou P; Xydakis D; Tzanakis I; Papadaki A; Kallivretakis N; Nikolakakis N; Perysinaki G; Gale DP; Diamantopoulos A; Goudas P; Goumenos D; Soloukides A; Boletis I; Melexopoulou C; Georgaki E; Frysira E; Komianou F; Grekas D; Paliouras C; Alivanis P; Vergoulas G; Pierides A; Daphnis E; Deltas C
Clin Genet; 2017 Nov; 92(5):517-527. PubMed ID: 28632965
[TBL] [Abstract][Full Text] [Related]
15. [Clinicopathological study of patients presenting hematuria and proteinuria by renal biopsy].
Shinohara Y; Mitsui H; Nasu T; Hayashida S
Nihon Hinyokika Gakkai Zasshi; 1991 Jan; 82(1):72-9. PubMed ID: 2046202
[TBL] [Abstract][Full Text] [Related]
16. Familial hematuria: A review.
Plevová P; Gut J; Janda J
Medicina (Kaunas); 2017; 53(1):1-10. PubMed ID: 28236514
[TBL] [Abstract][Full Text] [Related]
17. Hematuria and risk for end-stage kidney disease.
Vivante A; Calderon-Margalit R; Skorecki K
Curr Opin Nephrol Hypertens; 2013 May; 22(3):325-30. PubMed ID: 23449218
[TBL] [Abstract][Full Text] [Related]
18. [Thin glomerular basement membrane disease].
Frascà GM; Balestra E; Fanciulli E; Freddi P; Mazzucchelli R; Montironi R; D'Arezzo M; Sagripanti S
G Ital Nefrol; 2008; 25(1):49-56. PubMed ID: 18264918
[TBL] [Abstract][Full Text] [Related]
19. Study of asymptomatic microscopic hematuria in potential living related kidney donors.
Sobh MA; Moustafa FE; el-Din Saleh MA; Tawfik A; Ghoneim MA
Nephron; 1993; 65(2):190-5. PubMed ID: 8247179
[TBL] [Abstract][Full Text] [Related]
20. [Alport syndrome: Hereditary nephropathy associated with mutations in genes coding for type IV collagen chains].
Heidet L; Gubler MC
Nephrol Ther; 2016 Dec; 12(7):544-551. PubMed ID: 27816395
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
