Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Testuro, Nagashima"'
46,XY Phenotypic Male with Focal Segmental Glomerulosclerosis Caused by the WT1 Splice Site Mutation
Autor:
Testuro Nagashima, Yayoi Tanaka, Katsuya Nonomura, Toshihiro Tajima, Kenji Fujieda, Hiroyuki Kusunoki, Satoshi Sasaki
Publikováno v:
Hormone Research in Paediatrics. 60:302-305
Objective: Frasier syndrome is characterized by progressive glomerulopathy due to nonspecific focal and segmental glomerulosclerosis (FSGS), 46,XY sex reversal and the development of gonadoblastoma from dysgenetic gonads. Donor splice site heterozygo
Autor:
Andreas Pfaff, Omar Villaroel, Hiroyuki Kusunoki, Han-Wook Yoo, Katsuya Nonomura, Gu-Hwan Kim, P.M. Braillon, Kenji Fujieda, Raja Brauner, Mariela Paoli, Young-Lim Shin, Michael B. Ranke, Shih-Yi Lin, Tsai-Sung Tai, Satoshi Sasaki, Theodor H. Lippert, M. Fonseca, Sung-Su Kim, Young Ho Kim, Jean-Claude Souberbielle, Christine Trivin, Roberto Lanes, E. Lawson-Body, Tae-Ue Kim, Anselmo Palacios, Alfred O. Mueck, Testuro Nagashima, Yayoi Tanaka, Eduardo Carrillo, Wayne Huey-Herng Sheu, V. Giacobbi, Toshihiro Tajima, Harald Seeger
Publikováno v:
Hormone Research in Paediatrics. 60:306-308
Autor:
Young Ho Kim, Omar Villaroel, Wayne Huey-Herng Sheu, M. Fonseca, Alfred O. Mueck, V. Giacobbi, Harald Seeger, Jean-Claude Souberbielle, Sung-Su Kim, Michael B. Ranke, Christine Trivin, Raja Brauner, Eduardo Carrillo, P.M. Braillon, Tae-Ue Kim, Satoshi Sasaki, Mariela Paoli, Han-Wook Yoo, Theodor H. Lippert, Anselmo Palacios, Gu-Hwan Kim, Kenji Fujieda, Hiroyuki Kusunoki, Katsuya Nonomura, Testuro Nagashima, Yayoi Tanaka, Roberto Lanes, E. Lawson-Body, Andreas Pfaff, Tsai-Sung Tai, Young-Lim Shin, Toshihiro Tajima, Shih-Yi Lin
Publikováno v:
Hormone Research in Paediatrics. 60:313-315
46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation
Autor:
Toshihiro, Tajima, Satoshi, Sasaki, Yayoi, Tanaka, Hiroyuki, Kusunoki, Testuro, Nagashima, Katsuya, Nonomura, Kenji, Fujieda
Publikováno v:
Hormone research. 60(6)
Frasier syndrome is characterized by progressive glomerulopathy due to nonspecific focal and segmental glomerulosclerosis (FSGS), 46,XY sex reversal and the development of gonadoblastoma from dysgenetic gonads. Donor splice site heterozygous mutation
Autor:
Wayne Huey-Herng Sheu, Christine Trivin, Raja Brauner, Satoshi Sasaki, E. Lawson-Body, Jean-Claude Souberbielle, Andreas Pfaff, Tsai-Sung Tai, Hiroyuki Kusunoki, Sung-Su Kim, Toshihiro Tajima, Roberto Lanes, Shih-Yi Lin, Tae-Ue Kim, P.M. Braillon, Young-Lim Shin, Mariela Paoli, Theodor H. Lippert, V. Giacobbi, Harald Seeger, Testuro Nagashima, Yayoi Tanaka, Katsuya Nonomura, Han-Wook Yoo, Gu-Hwan Kim, Kenji Fujieda, Alfred O. Mueck, Eduardo Carrillo, Young Ho Kim, Anselmo Palacios, Omar Villaroel, Michael B. Ranke, M. Fonseca
Publikováno v:
Hormone Research in Paediatrics. 60:311-312