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Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.
Horinouchi, Tomoko; Nozu, Kandai; Yamamura, Tomohiko; Minamikawa, Shogo; Omori, Takashi; Nakanishi, Keita; Fujimura, Junya; Ashida, Akira; Kitamura, Mineaki; Kawano, Mitsuhiro; Shimabukuro, Wataru; Kitabayashi, Chizuko; Imafuku, Aya; Tamagaki, Keiichi; Kamei, Koichi; Okamoto, Kenjirou; Fujinaga, Shuichiro; Oka, Masafumi; Igarashi, Toru; Miyazono, Akinori; Sawanobori, Emi; Fujimaru, Rika; Nakanishi, Koichi; Shima, Yuko; Matsuo, Masafumi; Ye, Ming Juan; Nozu, Yoshimi; Morisada, Naoya; Kaito, Hiroshi; Iijima, Kazumoto.
Afiliação
  • Horinouchi T; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan; nozu@med.kobe-u.ac.jp.
  • Yamamura T; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Minamikawa S; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Omori T; Clinical and Translational Research Center, Kobe University Hospital, Kobe, Japan.
  • Nakanishi K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Fujimura J; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Ashida A; Department of Pediatrics, Osaka Medical College, Osaka, Japan.
  • Kitamura M; Department of Nephrology, Nagasaki University Hospital, Nagasaki, Japan.
  • Kawano M; Department of Rheumatology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.
  • Shimabukuro W; Department of Pediatrics, Japan Community Health Care Organization Kyushu Hospital, Sapporo, Hokkaido, Japan.
  • Kitabayashi C; Department of Nephrology and Hypertension, Osaka City General Hospital, Osaka, Japan.
  • Imafuku A; Department of Nephrology, Toranomon Hospital, Tokyo, Japan.
  • Tamagaki K; Department of Nephrology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kamei K; Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
  • Okamoto K; Department of Urology, Ehime Prefectural Central Hospital, Ehime, Japan.
  • Fujinaga S; Division of Nephrology, Saitama Children's Medical Center, Saitama, Japan.
  • Oka M; Department of Pediatrics, Faculty of Medicine Saga University, Saga, Japan.
  • Igarashi T; Department of Pediatrics, Nippon Medical School, Tokyo, Japan.
  • Miyazono A; Department of Pediatrics, Faculty of Medicine Kagoshima University, Kagoshima, Japan.
  • Sawanobori E; Department of Pediatrics, University of Yamanashi, Yamanashi, Japan.
  • Fujimaru R; Department of Pediatrics, Osaka General Hospital, Osaka, Japan.
  • Nakanishi K; Department of Child Health and Welfare (Pediatrics), Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
  • Shima Y; Department of Pediatrics, Wakayama Medical University, Wakayama, Japan; and.
  • Matsuo M; Department of Physical Therapy, Faculty of Rehabilitation, Kobe Gakuin University, Kobe, Japan.
  • Ye MJ; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nozu Y; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Morisada N; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Kaito H; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
J Am Soc Nephrol ; 29(8): 2244-2254, 2018 08.
Article em En | MEDLINE | ID: mdl-29959198
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação Puntual / Predisposição Genética para Doença / Colágeno Tipo IV / Estudos de Associação Genética / Nefrite Hereditária Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male País/Região como assunto: Asia Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação Puntual / Predisposição Genética para Doença / Colágeno Tipo IV / Estudos de Associação Genética / Nefrite Hereditária Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male País/Região como assunto: Asia Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão