Grünfeld, Jean-Pierre
Grünfeld, Jean-Pierre, 1939-...., néphrologue
Grünfeld, Jean-Pierre, 1939-
Jean-Pierre Grünfeld
Grünfeld, J.-P.
Grünfeld, J.-P. (Jean-Pierre)
VIAF ID: 46762047 (Personal)
Permalink: http://viaf.org/viaf/46762047
Preferred Forms
- 200 _ | ‡a Grünfeld ‡b Jean-Pierre ‡f 1939-....
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- 100 1 0 ‡a Grünfeld, Jean-Pierre
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- 100 1 _ ‡a Grünfeld, Jean-Pierre, ‡d 1939-...., ‡c néphrologue
- 100 1 _ ‡a Grünfeld, J.-P.
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- 100 1 0 ‡a Grünfeld, Jean-Pierre
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- 100 1 _ ‡a Grünfeld, Jean-Pierre
- 100 1 _ ‡a Grünfeld, Jean-Pierre
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- 100 0 _ ‡a Jean-Pierre Grünfeld
4xx's: Alternate Name Forms (11)
Works
Title | Sources |
---|---|
Actualités d'hypertension artérielle de l'Hôpital Necker pharmacologie et thérapeutique | |
Advances in nephrology : from the Necker Hospital | |
AMYLOSE AL SYSTEMIQUE : EXPERIENCE CHEZ 20 PATIENTS | |
Anderson-Fabry disease: its place among other genetic causes of renal disease. | |
Angiotensin-converting enzyme inhibitors for secondary erythrocytosis | |
Anti-hormones and blood pressure, 1988: | |
Circulation médullaire rénale | |
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome | |
COMPARAISON DE DEUX TRAITEMENTS : APPORT DE L'ANALYSE SPECTRALE, APPLICATION AU RYTHME DES TEMPERATURES CHEZ L'HEMODIALYSE CHRONIQUE | |
Comparison between siblings and twins supports a role for modifier genes in ADPKD. | |
Congenital/inherited kidney diseases: how to identify them early and how to manage them | |
Conséquences métaboliques nutritionnelles et endocriniennes de l'insuffisance rénale chronique | |
Crystals from fat. Acute oxalate nephropathy | |
Cyclosporin therapy in patients with Alport syndrome. | |
DETECTION DES CELLULES PROSTATIQUES CIRCULANTES AU COURS DE L'ADENOCARCINOME PROSTATIQUE : MISE AU POINT ET APPLICATIONS DE LA RT-PCR PSM | |
Dictionnaire de médecine Flammarion | |
Dictionnaire des difficultés du français médical | |
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy | |
ETUDE DE L'ANOMALIE GENETIQUE RESPONSABLE D'UN SYNDROME D'ALPORT | |
The expanding spectrum of renal diseases associated with antiphospholipid syndrome | |
Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. | |
GLOMERULAR AND TUBULAR FUNCTION IN EARLY INSULIN-DEPENDENT DIABETES. | |
HEMANGIOBLASTOME ET MALADIE DE VON HIPPEL-LINDAU : UNE HISTOIRE DE FAMILLE ? | |
Hématologie et maladies rénales : La Baule, 20-21 septembre 1991 | |
HEMATURIE ET ANOMALIE DU DRAINAGE VEINEUX RENAL PAR COMPRESSION DE LA VEINE RENALE DANS LA PINCE AORTO-MESENTERIQUE OU LE NUTCRACKER SYNDROME | |
HEMODIALYSE CHRONIQUE AU COURS DU MYELOME MULTIPLE | |
Heterogeneous histologic and clinical evolution in 3 cases of dense deposit disease with long-term follow-up | |
Hormone parathyroïdienne et hyperparathyroïdie : Hépatite virale en milieu néphrologique : Acquisitions récentes en transplantation et dialyse | |
Inherited disorders of the kidney investigation and management | |
Insuffisance rénale : diagnostics et suivis biologiques | |
Insuffisance rénale, dialyse et transplantation dans les maladies rénales héréditaires | |
Interprétation des désordres hydro-électrolytiques et acido-basiques | |
Jin no kozo to kino. | |
Kidney failure: aims for the next 10 years and barriers to success | |
Late-onset nephropathic cystinosis: clinical presentation, outcome, and genotyping | |
Lithium-induced nephropathy: Rate of progression and prognostic factors | |
Lithium nephrotoxicity revisited | |
Localized amyloidosis of the genitourinary tract: report of 5 new cases and review of the literature | |
LA MALADIE DE CASTLEMAN : REVUE DE LA LITTERATURE A PROPOS DE TROIS CAS D'INSUFFISANCE RENALE ASSOCIEE | |
Maladies kystiques rénales héréditaires : du phénotype au génotype | |
Médecine de la femme enceinte | |
Monitoring of glomerular filtration rate in lithium-treated outpatients--an ambulatory laboratory database surveillance | |
Monogenic renal diseases: a clinical introduction | |
MUTATIONS DU GENE VHL DANS LES CANCERS DU REIN SPORADIQUES DE L'ADULTE | |
Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis | |
Mutations in the hepatocyte nuclear factor-1beta, cystic kidney diease, type 5 maturity-onset diabetes of the young and chromophobe renal carcinoma | |
Nefrología | |
Néphrologie | |
Paraganglioma of the bladder in a kidney transplant recipient: A case report | |
La pathologie médicale / Urologie | |
Physiopathologie rénale de l'hypertension artérielle : conférences rein et hypertension artérielle, jeudi 28 janvier 1988 | |
POLYKYSTOSE RENALE AUTOSOMIQUE DOMINANTE ET ANEVRYSMES INTRACRANIENS : A PROPOS DE SIX CAS, DISCUSSION ET REVUE DE LA LITTERATURE | |
La pression artérielle chez l'urémique | |
Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome | |
Rare inherited disorders with renal involvement-approach to the patient | |
Recommandations pour le plan cancer 2009-2013 pour un nouvel élan rapport au président de la République | |
Rein, cœur et vaisseaux | |
Le rein du sujet âgé | |
Renal and thymic pathology in thymoma-associated nephropathy: report of 21 cases and review of the literature | |
Renal involvement in cystic fibrosis: diseases spectrum and clinical relevance | |
Renal involvement in monoclonal (type I) cryoglobulinemia: two cases associated with IgG3 kappa cryoglobulin | |
Renoprotection by enzyme replacement therapy | |
The risk of developing end-stage renal disease in patients with type 2 diabetes and nephropathy: the RENAAL study | |
Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: a case report | |
ROLE DE L'HORMONE PARATHYROIDIENNE ET DU PEPTIDE ATRIAL NATRIURETIQUE DANS LA REPONSE RENALE A UNE EXPANSION VOLEMIQUE AIGUE | |
Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN). | |
Screening for intracranial aneurysms in autosomal dominant polycystic kidney disease is cost-effective. | |
The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation | |
Structure and function of the kidney | |
textes réunis par J.-P. [Dr Jean-Pierre] Grünfeld | |
Traité de médecine hospitalière | |
Tubulointerstitial nephritis and Fanconi syndrome in primary biliary cirrhosis | |
Urinary procollagen III aminoterminal propeptide (PIIINP): a fibrotest for the nephrologist. | |
腎の構造と機能 |