Zobrazeno 1 - 10
of 292
pro vyhledávání: '"J, Cledes"'
Autor:
B. Whebe, Isabelle Quéré, A. Carre, R Perrichot, Claude Férec, B. Mercier, J. Cledes, P.M. Simon
Publikováno v:
European Journal of Human Genetics. 8:353-359
Autosomal dominant polycystic kidney disease (ADPKD) exhibits a genetically heterogeneous transmission involving at least three different genes. PKD1 gene linked mutations are responsible for the disease in about 85% of ADPKD cases. The search for mu
Autor:
Yair Levy, J. Cledes, Jacob George, Sylvie Polak-Charcon, Yehuda Shoenfeld, H Amital, Boris Gilburd, L. Ziporen, P Youinou
Publikováno v:
Human Antibodies. 7:91-96
Primary antiphospholipid syndrome (PAPS) is a recently recognized clinical entity encompassing the combination of thromboembolic phenomena, thrombocytopenia and recurrent abortions in the presence of antiphospholipid antibodies. We present a patient
Autor:
Hiroshi Oda, E. Bullorsky, Takashi Wada, Salvatore Badalamenti, Stephan R. Lederer, Tomoko Gomi, Hiroshi Nakajima, Shin-ichi Takeda, George J. Schwartz, E. Galperin, D. Modai, D. Oz, Masako Ohnishi, J. Weissgarten, Kouji Matsushima, Hitoshi Yokoyama, Alois Sellmayer, Yoshio Uehara, Silvia Santostasi, M. Cohn, Minoru Yamakado, Morito Endo, Sonja Mandl-Weber, J. Schropp, Hiroshi Kida, L. de Parscau, Kumiko Hamano, L. Lysenko, Norihiko Sakai, Reinhard Schinzel, Hideho Gomi, Yasunori Iwata, Kousuke Seiki, Giorgio Graziani, Tatsuo Hosoya, O. Marcus, E. Freixas, Keiichi Yoshimoto, Isao Ohsawa, H. Trimarchi, P.M. Simon, Masao Takagi, H. Pereyra, I. Bobkova, Miho Shimizu, L. Polyantseva, Teizo Fujita, J. Cledes, Z. Averbukh, Kengo Furuichi, Yoshihiro Urade, B. Mercier, Hirotsugu Hayashi, Fuad S. Shihab, Yasuo Totsuka, Bettina Haslinger, Jorge Isaac, Thomas Sitter, Hideaki Okabe, Noriaki Imanishi, August Heidland, Misao Matsushita, R.A. Perrichot, O. Rabinovich, Shinichiro J. Tojo, Kazuya Takasawa, Naomi Eguchi, Takayuki Fujita, Z. Chen Levy, Toshio Ikeda, Iwao Ohno, Kimiyoshi Ichida, Guillermo A. Herrara, C. Ferec, Gerald Münch, Nobuhito Hirawa, Ken-ichi Kobayashi, Claudio Angelini, Miho Hikita, I. Tareyeva, Hiroyuki Ohi, Katharina Sebekova, V. Dishi
Publikováno v:
Nephron. 87:381-383
Autor:
Roscoe M. Moore, Marinus H. de Keijzer, Alison MacLeod, Chris E. Kaufman, Shigeaki Muto, Hikaru Koide, A. Oliet, Giorgio Annessi, R. Romero, M. Segasothy, Ronald G. Kaczmarek, P. Ronco, A. Notarbartolo, Sali Caglar, C.M. Barbagallo, Paola Omedè, William E. Nelson, Egidio Lusvarghi, Julie Piper, E. Barrio, Mayer Brezis, Iren B. Kovacs, L. Campanacci, Osman Özcebe, Stanford Hamburger, Gianna Mazzucco, Angela Recker, Shuichi Ishii, Tohru Yamaji, F. Mignon, C. Michel, J.L. Mahe, Neva E. Haites, M.A. Morel, Francesco Paolo Schena, Geoffrey M. Berlyne, Gobi Engler-Blum, J. Cledes, Eduardo H. Garin, Massimo Massaia, Teut Risler, Renate Klauser, J. Forteza, Ko Okumura, Cetin Turgan, Serafettin Kirazli, Giovanna Zambruno, S.R. Stella, Anthony E.G. Raine, Oktay Özdemir, Carlo Feletti, Antonio Amoroso, John Simpson, Kurt Widhalm, M. Bardelli, Freek J. Zijlstra, Monika Pergande, J.C. Bigot, Cristiana Rollino, Samuel N. Heyman, Yasushi Asano, Laurence R.I. Baker, S. Tomé Martínez de Rituerto, Anne Dieny, Beatriz Tucker, E. Vijaykumar, P.H. Ong, Semra Dündar, P. Dosquet, Dario Roccatell, Giuseppe Aimo, Stanley A. McMillan, Giuseppe Piccoli, Nicole Pinel, E. Hernández, Yoshihisa Itoh, J. Goffinet, Tadashi Kawai, Jean-Marc Weinstein, Erich Pohanka, Reinhold Deppisch, Vincenzo Montinaro, Claudia A. Müller, Teruyo Ozaki, Leopoldo Baldrati, A. Baraldi, M.I. Rodriguez, Martina Franz, Gerhard A. Müller, Mark Gruber, Claudia Capponcini, Nick Corontzes, Alan N. Charney, F. Fischetti, L. Furci, R. Carretta, M C Jones, Adalbert Bohle, Klaus Jung, O. Traindl, Josef Kovarik, V.E.R. Melhado, Peggy Hamilton, F. Vran, David A. Power, Fujiro Sendo, A. Vigil, Turgay Arinsoy, Rosanna Coppo, Bruno Watschinger, William Dickey, M.Y. Norazlina, Silvano Battaglio, V. Scafidi, Kyuzi Kamoi, Ryuta Okutani, Jean-Charles Renversez, Helmut Reichel, Daniel Cordonnier, Miyuki Ishibashi, L.G. Bardou, B. Mougenot, Wolfgang Kühn, C. Versolato, Hans Pidlich, Abraham P. Provoost, M. Jamil, S. Raziuddin, D. Sanchez-Guisande, A. Vasile, Ünal Yasavul, Prabir Roy-Chaudhury, A. Galione, Yasuhiko Tomino, Susan Reading, L.A. Moura, P. Gallar, Yutaka Yaguchi, Eberhard Ritz, Gina Mazzola, Kenneth G. Porter, M.-A. Bernard, Simon D. Roger, E.N. Wardle, Dino Docci, M.A. Boim, M.R. Averna, B. Viron, Thomas Kahn, N. Schor, S. Muiesan, Loreto Gesualdo, Elke Stier, D. Novoa, B. Fabris, Elisabetta Rubbiani, Jasmina Markovic-Lipkovski, François Le Marc’hadour, Claire M. Hill, Nurol Arik, Mario Boccadoro
Publikováno v:
Nephron. 62:I-VI
Publikováno v:
Journal of Internal Medicine. 230:187-191
Sjogren's syndrome (SS) is an autoimmune exocrinopathy that develops into systemic autoimmune disease in 25% of patients, leading to general complications, one of which is kidney involvement. It presents mainly as interstitial nephritis, disclosed by
Autor:
A. Gentric, J. Cledes
Publikováno v:
Nephrology Dialysis Transplantation. 6:86-90
Acute renal failure (ARF) is particularly frequent in the elderly. A few studies have reviewed immediate prognosis of ARF in older patients, but these do not allow any conclusion on long-term renal prognosis. Our retrospective study included 46 patie
Autor:
M, Decoster, J C, Bigot, J L, Carre, J F, Morin, J L, Mahé, T, Tanquerel, J, Cledes, H H, Floch
Publikováno v:
Presse medicale (Paris, France : 1983). 31(3)
An epidemiologic study of urinary calculi (N = 1843) was conducted in Western France: distribution according to the main chemical compounds, age and sex. Comparison with the results of a study with national recruitment (N = 10,617) and a study with r
Publikováno v:
Nephron. 87(4)
Autosomal/dominant polycystic kidney disease (ADPKD) exhibits a high inter- and intrafamilial heterogeneity partly explained by the involvement of at least 3 different genes in the disorder transmission. PKD1, the major locus, is located on chromosom
Publikováno v:
Geriatric Nephrology and Urology. 2:143-145
In clinical practice, the Cockcroft and Gault formula (CG) is used to evaluate creatinine clearance from serum creatinine in the elderly. Its validity in a very old nondebilitated population over 80 years of age has not been investigated. In our stud