Similar articles for PMID: 26621952

Year	Number of Results
1984	1
1985	1
1989	2
1990	2
1991	1
1993	1
1994	2
1997	3
1998	2
1999	1
2001	4
2002	3
2003	2
2004	3
2005	5
2006	2
2007	6
2008	5
2009	4
2010	2
2011	1
2012	2
2013	5
2014	5
2015	4
2016	6
2017	3
2018	5
2019	7
2020	9
2021	4
2022	1
2023	5
2024	2

1

Isolated microscopic haematuria of glomerular origin: clinical significance and diagnosis in the 21st century.

Chan MM, Gale DP. Chan MM, et al. Clin Med (Lond). 2015 Dec;15(6):576-80. doi: 10.7861/clinmedicine.15-6-576. Clin Med (Lond). 2015. PMID: 26621952 Free PMC article.

2

Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.

Imafuku A, Nozu K, Sawa N, Hasegawa E, Hiramatsu R, Kawada M, Hoshino J, Tanaka K, Ishii Y, Takaichi K, Fujii T, Ohashi K, Iijima K, Ubara Y. Imafuku A, et al. Nephrology (Carlton). 2018 Oct;23(10):940-947. doi: 10.1111/nep.13115. Nephrology (Carlton). 2018. PMID: 28704582 Free PMC article.

3

Thin basement membrane nephropathy.

Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY. Savige J, et al. Kidney Int. 2003 Oct;64(4):1169-78. doi: 10.1046/j.1523-1755.2003.00234.x. Kidney Int. 2003. PMID: 12969134 Free article. Review.

4

Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members.

Savige J. Savige J. Pediatr Nephrol. 2020 Jan;35(1):59-66. doi: 10.1007/s00467-018-4121-1. Epub 2018 Nov 30. Pediatr Nephrol. 2020. PMID: 30506145 Review.

5

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.

Haas M. Haas M. Arch Pathol Lab Med. 2009 Feb;133(2):224-32. doi: 10.5858/133.2.224. Arch Pathol Lab Med. 2009. PMID: 19195966 Free article. Review.

6

Alport Syndrome.

Kashtan CE. Kashtan CE. 2001 Aug 28 [updated 2019 Feb 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2001 Aug 28 [updated 2019 Feb 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301386 Free Books & Documents. Review.

7

Thin basement membrane nephropathy and IgA glomerulonephritis: can they be distinguished without renal biopsy?

Packham DK. Packham DK. Nephrology (Carlton). 2007 Oct;12(5):481-6. doi: 10.1111/j.1440-1797.2007.00813.x. Nephrology (Carlton). 2007. PMID: 17803472

8

Renal biopsy diagnosis in children presenting with haematuria.

Piqueras AI, White RH, Raafat F, Moghal N, Milford DV. Piqueras AI, et al. Pediatr Nephrol. 1998 Jun;12(5):386-91. doi: 10.1007/s004670050471. Pediatr Nephrol. 1998. PMID: 9686957

9

[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. Endreffy E, et al. Orv Hetil. 2005 Dec 25;146(52):2647-53. Orv Hetil. 2005. PMID: 16468607 Hungarian.

10

Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.

Vizjak A, Ferluga D. Vizjak A, et al. Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:323-6. doi: 10.2298/sarh08s4323v. Srp Arh Celok Lek. 2008. PMID: 20804103 Free article. Review.

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