Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 56

1.

Diagnosis of Alport syndrome--search for proteomic biomarkers in body fluids.

Pohl M, Danz K, Gross O, John U, Urban J, Patzer L, Habbig S, Feldkötter M, Witzke O, Walther M, Rhode H.

Pediatr Nephrol. 2013 Nov;28(11):2117-23. doi: 10.1007/s00467-013-2533-5. Epub 2013 Jun 23.

PMID:
23793922
2.

Preclinical Alterations in the Serum of COL(IV)A3(-)/(-) Mice as Early Biomarkers of Alport Syndrome.

Muckova P, Wendler S, Rubel D, Büchler R, Alert M, Gross O, Rhode H.

J Proteome Res. 2015 Dec 4;14(12):5202-14. doi: 10.1021/acs.jproteome.5b00814. Epub 2015 Nov 3.

PMID:
26487288
3.

Proteome analysis of gelatin-bound urinary proteins from patients with bladder cancers.

Saito M, Kimoto M, Araki T, Shimada Y, Fujii R, Oofusa K, Hide M, Usui T, Yoshizato K.

Eur Urol. 2005 Nov;48(5):865-71.

PMID:
15964125
4.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
5.

An update on the pathomechanisms and future therapies of Alport syndrome.

Noone D, Licht C.

Pediatr Nephrol. 2013 Jul;28(7):1025-36. doi: 10.1007/s00467-012-2272-z. Epub 2012 Aug 18. Review.

PMID:
22903660
6.

Angiotensin converting enzyme inhibitor therapy in children with Alport syndrome: effect on urinary albumin, TGF-beta, and nitrite excretion.

Adler L, Mathew R, Futterweit S, Frank R, Gauthier BG, Kashtan CE, Trachtman H.

BMC Nephrol. 2002 Feb 14;3:2.

7.

[Alport syndrome in 23-year-old woman].

Finke D, Bilińska W, Kałuzyński A, Nowicki M.

Pol Merkur Lekarski. 2008;24 Suppl 4:22-4. Polish.

PMID:
18924495
8.

Study of diabetic nephropathy in the proteomic era.

Thongboonkerd V.

Contrib Nephrol. 2011;170:172-83. doi: 10.1159/000325657. Epub 2011 Jun 9. Review.

PMID:
21659770
9.

Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.

Marcocci E, Uliana V, Bruttini M, Artuso R, Silengo MC, Zerial M, Bergesio F, Amoroso A, Savoldi S, Pennesi M, Giachino D, Rombolà G, Fogazzi GB, Rosatelli C, Martinhago CD, Carmellini M, Mancini R, Di Costanzo G, Longo I, Renieri A, Mari F.

Nephrol Dial Transplant. 2009 May;24(5):1464-71. doi: 10.1093/ndt/gfn681. Epub 2009 Jan 7.

10.

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. doi: 10.1043/1543-2165-133.2.224. Review.

PMID:
19195966
11.
12.

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.

14.

Alport syndrome: clinical experience with 21 paediatric patients.

Barten S, Proesmans W.

Eur J Pediatr. 1996 Jan;155(1):49-52.

PMID:
8750811
15.

Diagnosis of Alport syndrome without biopsy?

Gubler MC.

Pediatr Nephrol. 2007 May;22(5):621-5. Epub 2006 Dec 2.

PMID:
17143627
16.

Proteomic biomarkers for the diagnosis and risk stratification of polycystic ovary syndrome: a systematic review.

Atiomo W, Khalid S, Parameshweran S, Houda M, Layfield R.

BJOG. 2009 Jan;116(2):137-43. doi: 10.1111/j.1471-0528.2008.02041.x. Review.

17.

Searching for novel biomarkers and new therapeutic targets of diabetic nephropathy using proteomics approaches.

Thongboonkerd V.

Contrib Nephrol. 2008;160:37-52. doi: 10.1159/000125928. Review.

PMID:
18401160
18.

Proteomic approaches in the search for biomarkers of liver fibrosis.

Cowan ML, Rahman TM, Krishna S.

Trends Mol Med. 2010 Apr;16(4):171-83. doi: 10.1016/j.molmed.2010.01.006. Epub 2010 Mar 19. Review.

PMID:
20304704
19.

Low molecular weight protein enrichment on mesoporous silica thin films for biomarker discovery.

Fan J, Gallagher JW, Wu HJ, Landry MG, Sakamoto J, Ferrari M, Hu Y.

J Vis Exp. 2012 Apr 17;(62). pii: 3876. doi: 10.3791/3876.

20.

Alport disease: a review of the diagnostic difficulties.

Meleg-Smith S.

Ultrastruct Pathol. 2001 May-Jun;25(3):193-200. Review.

PMID:
11465475

Supplemental Content

Support Center