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Laurence Heidet
Laurence Heidet
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Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy
O Gross, C Licht, HJ Anders, B Hoppe, B Beck, B Tönshoff, B Höcker, ...
Kidney international 81 (5), 494-501, 2012
3812012
Early glomerular filtration defect and severe renal disease in podocin-deficient mice
S Roselli, L Heidet, M Sich, A Henger, M Kretzler, MC Gubler, C Antignac
Molecular and cellular biology, 2004
3452004
Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases
L Heidet, S Decramer, A Pawtowski, V Moriniere, F Bandin, ...
Clinical Journal of the American Society of Nephrology 5 (6), 1079-1090, 2010
3082010
Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group
CE Kashtan, J Ding, G Garosi, L Heidet, L Massella, K Nakanishi, K Nozu, ...
Kidney international 93 (5), 1045-1051, 2018
3012018
COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome
I Longo, P Porcedda, F Mari, D Giachino, I Meloni, C Deplano, A Brusco, ...
Kidney international 61 (6), 1947-1956, 2002
2882002
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes
C Arrondel, N Vodovar, B Knebelmann, JP Gru, MC Gubler, C Antignac, ...
Journal of the American Society of Nephrology 13 (1), 65-74, 2002
2402002
Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome
L Heidet, C Arrondel, L Forestier, L Cohen-Solal, G Mollet, B Gutierrez, ...
Journal of the American Society of Nephrology 12 (1), 97-106, 2001
2322001
Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation
FTL Van Der Loop, L Heidet, EDJ Timmer, BJC Van Den Bosch, ...
Kidney international 58 (5), 1870-1875, 2000
1842000
Improving mutation screening in familial hematuric nephropathies through next generation sequencing
V Morinière, K Dahan, P Hilbert, M Lison, S Lebbah, A Topa, ...
Journal of the American Society of Nephrology 25 (12), 2740-2751, 2014
1822014
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis
M Konrad, S Saunier, L Heidet, F Silbermann, F Benessy, J Calado, ...
Human molecular genetics 5 (3), 367-371, 1996
1791996
Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative
CE Kashtan, J Ding, M Gregory, O Gross, L Heidet, B Knebelmann, ...
Pediatric nephrology 28, 5-11, 2013
1772013
Evidence of digenic inheritance in Alport syndrome
MA Mencarelli, L Heidet, H Storey, M van Geel, B Knebelmann, C Fallerini, ...
Journal of medical genetics 52 (3), 163-174, 2015
1762015
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome
E Boye, G Mollet, L Forestier, L Cohen-Solal, L Heidet, P Cochat, ...
The American Journal of Human Genetics 63 (5), 1329-1340, 1998
1751998
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes
C Rohr, J Prestel, L Heidet, H Hosser, W Kriz, RL Johnson, C Antignac, ...
The Journal of clinical investigation 109 (8), 1073-1082, 2002
1742002
Mutations in theCOL4A4 and COL4A3 genes cause familial benign hematuria
M Praga, B Tazón, L Heidet, C Arrondel, A Armengol, A Andrés, ...
Journal of the American Society of Nephrology 13 (5), 1248-1254, 2002
1662002
Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations
J Temme, F Peters, K Lange, Y Pirson, L Heidet, R Torra, JP Grunfeld, ...
Kidney international 81 (8), 779-783, 2012
1562012
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus‐specific database
M Bower, R Salomon, J Allanson, C Antignac, F Benedicenti, E Benetti, ...
Human mutation 33 (3), 457-466, 2012
1542012
Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations
G Bollée, K Dahan, M Flamant, V Moriniere, A Pawtowski, L Heidet, ...
Clinical Journal of the American Society of Nephrology 6 (10), 2429-2438, 2011
1512011
The renal lesions of Alport syndrome
L Heidet, MC Gubler
Journal of the American Society of Nephrology 20 (6), 1210-1215, 2009
1472009
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ...
New England Journal of Medicine 376 (8), 742-754, 2017
1452017
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