Grünfeld JP - Search Results

1

Hereditary nephritis with macrothrombocytopenia: phenotypic variety and the genotypic defect.

Basile C, Schiavone P, Heidet L, Grünfeld JP. Basile C, et al. Among authors: grunfeld jp. J Nephrol. 2002 May-Jun;15(3):320-3. J Nephrol. 2002. PMID: 12113606

2

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations.

Temme J, Peters F, Lange K, Pirson Y, Heidet L, Torra R, Grunfeld JP, Weber M, Licht C, Müller GA, Gross O. Temme J, et al. Among authors: grunfeld jp. Kidney Int. 2012 Apr;81(8):779-83. doi: 10.1038/ki.2011.452. Epub 2012 Jan 11. Kidney Int. 2012. PMID: 22237748 Free article.

3

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes.

Arrondel C, Vodovar N, Knebelmann B, Grünfeld JP, Gubler MC, Antignac C, Heidet L. Arrondel C, et al. Among authors: grunfeld jp. J Am Soc Nephrol. 2002 Jan;13(1):65-74. doi: 10.1681/ASN.V13165. J Am Soc Nephrol. 2002. PMID: 11752022

4

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

Gross O, Licht C, Anders HJ, Hoppe B, Beck B, Tönshoff B, Höcker B, Wygoda S, Ehrich JH, Pape L, Konrad M, Rascher W, Dötsch J, Müller-Wiefel DE, Hoyer P; Study Group Members of the Gesellschaft für Pädiatrische Nephrologie; Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, Heidet L, Lebbah S, Torra R, Friede T, Lange K, Müller GA, Weber M. Gross O, et al. Among authors: grunfeld jp. Kidney Int. 2012 Mar;81(5):494-501. doi: 10.1038/ki.2011.407. Epub 2011 Dec 14. Kidney Int. 2012. PMID: 22166847 Free article.

5

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

Boye E, Mollet G, Forestier L, Cohen-Solal L, Heidet L, Cochat P, Grünfeld JP, Palcoux JB, Gubler MC, Antignac C. Boye E, et al. Among authors: grunfeld jp. Am J Hum Genet. 1998 Nov;63(5):1329-40. doi: 10.1086/302106. Am J Hum Genet. 1998. PMID: 9792860 Free PMC article.

6

Renal prognosis in women with hereditary nephritis.

Grünfeld JP, Noël LH, Hafez S, Droz D. Grünfeld JP, et al. Clin Nephrol. 1985 Jun;23(6):267-71. Clin Nephrol. 1985. PMID: 4028523

7

Hereditary nephritis with macrothrombocytopenia: no longer an Alport syndrome variant.

Knebelmann B, Fakhouri F, Grünfeld JP. Knebelmann B, et al. Among authors: grunfeld jp. Nephrol Dial Transplant. 2001 Jun;16(6):1101-3. doi: 10.1093/ndt/16.6.1101. Nephrol Dial Transplant. 2001. PMID: 11390704 No abstract available.

8

[Renal arterial thrombosis complicating nephrotic syndrome].

Pochet JM, Bobrie G, Basile C, Grunfeld JP. Pochet JM, et al. Among authors: grunfeld jp. Presse Med. 1988 Nov 12;17(40):2139. Presse Med. 1988. PMID: 2974147 French. No abstract available.

9

The glomerular basement membrane defect in Alport-type hereditary nephritis: absence of cationic antigenic components.

van den Heuvel LP, Savage CO, Wong M, Price RG, Noel L, Grunfeld JP, Lockwood CM. van den Heuvel LP, et al. Among authors: grunfeld jp. Nephrol Dial Transplant. 1989;4(9):770-5. Nephrol Dial Transplant. 1989. PMID: 2483255

10

Pregnancy in women with impaired renal function.

Jungers P, Chauveau D, Choukroun G, Moynot A, Skhiri H, Houillier P, Forget D, Grünfeld JP. Jungers P, et al. Among authors: grunfeld jp. Clin Nephrol. 1997 May;47(5):281-8. Clin Nephrol. 1997. PMID: 9181274

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