Zobrazeno 1 - 10
of 22
pro vyhledávání: '"S. Verhaart"'
Publikováno v:
American Journal of Medical Genetics. 86:420-426
Spinal muscular atrophy (SMA) is an autosomal recessive disorder occurring at a rate of between 1/5,000 and 1/10,000 births in most European countries. The phenotype results from the degeneration of the anterior horn cells of the spinal cord, resulti
Autor:
F. J. Gainza, A.M. Pollock, Ignacio Minguela, Musa Bali, Ünal Yasavul, Takashi Harada, T. Naruse, Yoshiyuki Ozono, Naoto Kawamura, P. H. Whiting, F. Strutz, M. Buemi, Trevor H. Thomas, Kuniyoshi Kojima, Wen-Yu Chang, Sumio Takahashi, K. Kawasaki, M. K. Almond, Shinn-Cherng Chen, Koichi Yamaguchi, Kazuya Higashino, A. Maezawa, Oleg Eremin, Michel Aparicio, V.I. Kirpatovsky, Kazutaka Murakami, Turgay Arinsoy, Sukru Sindel, Tzu-Chao Hsu, R. Musolino, José Portolés, A. M. Meyers, Peter Rutherford, I. Lampreabe, J. Ortuño, Marie-Christine Delmas-Beauvieux, C. Aloisi, W. A. Wadee, Y. Fukushima, Shirou Kawashima, F. Locatelli, Hiroshi Hassegawa, J.P. van Hooff, Shraga Shany, F. Fabrizi, Masanori Hara, M.J. Raftery, Wan-Long Chuang, M.J.A.P. Daemen, P. Marai, Emeterio Pina, G. Bacchini, Zafer Akcali, G. Erba, Hung-Chun Chen, Toshiyuki Yanai, Franciszek Kokot, Cetin Turgan, P.P. De Deyn, A.M. Chumakov, Rachel Levy, Toshio Yanagihara, Ana Sánchez-Fructuoso, Michel Clerc, Sofía Zárraga, R. Wijnen, Beril Cakir, Marie-Annette Carbonneau, Örner Uluoğlu, Sigemi Tomiyama, E.A. Sevrukov, Sali Caglar, Valery Wajsbrot, S. Yano, Y. Tsukada, Liliane Dubourg, Minoru Ohara, I. A. Qureshi, N.V. Nikiforova, Yunus Erdem, Tsuneo Takada, Evelyne Peuchant, F. Tripodi, Uğur Yalcin, Valérie de Precigout, J. Przedlacki, Masahiko Shikano, Steven D. Heys, Antonio Torralbo, Kelvin K.K.L. Ho, Yuji Moriwaki, Akira Yoshizumi, Akira Tatematsu, A.F. Darenkov, Michio Suda, J.P. Kooman, J.L. Sastre, L. P. Margolius, S. Verhaart, F. Di Maria, Tadashi Yamamoto, Kenji Maeda, S. Dhillon, Midori Hasegawa, Andrzej Wiecek, Lazaro Gotloib, Hideo Yoshizumi, Wojciech Marcinkowski, I. Guarnori, Tetsuya Yamamoto, K. Huttunen, Yung-Hsiung Lai, K. Hiromura, M. Vanasse, H. Kanai, Naohito Takeda, Koichi Niimura, Juei-Hsiung Tsai, Kohei Hara, Robert Wilkinson, Toshimitsu Niwa, Chi-Yuan Yang, G. A. Müller, Hideki Katsumata, Itaru Kihara, S. Fan, Michio Itoh, J. Manelius, L. Raffaele, J.F. Navarro, P. Robitaille, F. Liaño, B. Marescau, M.J Verluyten-Goessens, Cidio Chaimovitz, K.M.L. Leunissen, Avshalom Shostak, Alberto Barrientos, Makoto Tomita, M Fernández Lucas, Yuuichi Adachi, M. Molinaro, Oktay Oymak, Takashi Miyazaki, N. T. Levy, Christian Combe, Raisa Kuschnier, Jinn-Yuh Guh, S.P. Darenkov, C. Quereda
Publikováno v:
Nephron. 69:I-VIII
Publikováno v:
European Journal of Pediatric Surgery. 9:331-333
A case of massive true thymic hyperplasia in a child of eleven months is described. This rare disorder must be included in the differential diagnosis of a mediastinal mass in children. Diagnosis and management are discussed and the relevant literatur
Publikováno v:
Pediatric nephrology (Berlin, Germany). 13(2)
We report the response of ten patients (6 male, 4 female) with steroid-resistant focal segmental glomerulosclerosis (FSGS) to treatment with intravenous pulse cyclophosphamide (IVCP) together with oral prednisone. All patients had been treated with 6
Publikováno v:
Nephron. 69(4)
Hereditary interstitial nephritides are a heterogeneous group of disorders comprising medullary cystic disease, several varieties of Alport's syndrome and also one familial disorder with a distinct clinical syndrome and without characteristic ultrast
Autor:
Yoshiyuki Ozono, G. Bacchini, F. Strutz, Shinn-Cherng Chen, A. Maezawa, Michel Aparicio, Wojciech Marcinkowski, Trevor H. Thomas, W. A. Wadee, Toshio Yanagihara, V.I. Kirpatovsky, A.M. Chumakov, Örner Uluoğlu, Y. Tsukada, Akira Yoshizumi, A. M. Meyers, Masanori Hara, Makoto Tomita, M Fernández Lucas, Yuuichi Adachi, Koichi Yamaguchi, Steven D. Heys, Antonio Torralbo, K. Kawasaki, I. A. Qureshi, J.P. Kooman, Rachel Levy, Toshimitsu Niwa, Kenji Maeda, Ignacio Minguela, Marie-Christine Delmas-Beauvieux, Raisa Kuschnier, M.J. Raftery, Tsuneo Takada, Koichi Niimura, A.M. Pollock, Hiroshi Hassegawa, Wan-Long Chuang, G. Erba, M. Vanasse, B. Marescau, Kuniyoshi Kojima, Wen-Yu Chang, Sumio Takahashi, Uğur Yalcin, Peter Rutherford, F. Locatelli, Zafer Akcali, Toshiyuki Yanai, Franciszek Kokot, M.J.A.P. Daemen, Tetsuya Yamamoto, Ünal Yasavul, Valery Wajsbrot, S. Dhillon, Marie-Annette Carbonneau, Chi-Yuan Yang, P. H. Whiting, N.V. Nikiforova, Kohei Hara, Oleg Eremin, P.P. De Deyn, José Portolés, T. Naruse, Sali Caglar, M. K. Almond, Ana Sánchez-Fructuoso, C. Quereda, G. A. Müller, Cetin Turgan, Kazutaka Murakami, Hideki Katsumata, J. Manelius, Sigemi Tomiyama, F. J. Gainza, M. Buemi, P. Marai, Emeterio Pina, J.F. Navarro, E.A. Sevrukov, I. Lampreabe, Beril Cakir, Y. Fukushima, Musa Bali, H. Kanai, Jinn-Yuh Guh, Yunus Erdem, J. Przedlacki, S. Fan, Valérie de Precigout, Takashi Harada, P. Robitaille, Shirou Kawashima, Itaru Kihara, Naohito Takeda, F. Liaño, Michio Itoh, J.P. van Hooff, Andrzej Wiecek, Michio Suda, L. Raffaele, S. Verhaart, M.J Verluyten-Goessens, Tadashi Yamamoto, Kelvin K.K.L. Ho, Masahiko Shikano, C. Aloisi, F. Di Maria, Avshalom Shostak, Yuji Moriwaki, Lazaro Gotloib, Midori Hasegawa, Sukru Sindel, Michel Clerc, I. Guarnori, Tzu-Chao Hsu, K. Huttunen, Naoto Kawamura, J. Ortuño, Yung-Hsiung Lai, K. Hiromura, Hideo Yoshizumi, Kazuya Higashino, J.L. Sastre, Minoru Ohara, R. Musolino, A.F. Darenkov, L. P. Margolius, Juei-Hsiung Tsai, Akira Tatematsu, Liliane Dubourg, Turgay Arinsoy, Shraga Shany, F. Fabrizi, Sofía Zárraga, R. Wijnen, Robert W. Wilkinson, M. Molinaro, Oktay Oymak, F. Tripodi, S. Yano, Evelyne Peuchant, Hung-Chun Chen, Cidio Chaimovitz, K.M.L. Leunissen, Alberto Barrientos, Takashi Miyazaki, N. T. Levy, Christian Combe, S.P. Darenkov
Publikováno v:
Nephron. 69:495-496
Publikováno v:
Ultrastructural pathology. 11(1)
A tumor from a 52–year-old Albino male had the ultrastructural features of an anemone cell tumor. Evidence of squamous differentiation was seen by electron microscopy and immunohistochemistry. “Anemone cell” tumors have been shown to be classif
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