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Stereotyped Upper Limb Movement in MECP2 Duplication Syndrome.
Wakabayashi, Tomohiro; Fukumura, Shinobu; Takahashi, Satoru; Kurosawa, Kenji; Miyamoto, Shuichi; Tsuchida, Kosuke; Kato, Shinsuke; Tsugawa, Takeshi; Sakai, Yoshiyuki; Kawasaki, Yukihiko.
Afiliação
  • Wakabayashi T; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Fukumura S; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Takahashi S; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Kurosawa K; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Miyamoto S; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Tsuchida K; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Kato S; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Tsugawa T; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Sakai Y; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
  • Kawasaki Y; From the Department of Pediatrics (T.W., S.F., K.T., S.K., T.T., Y.K.), Sapporo Medical University School of Medicine; Department of Pediatrics (S.T.), Asahikawa Medical University, Hokkaido; Division of Medical Genetics (K.K.), Kanagawa Children's Medical Center; and Departments of Gastroenterology
Neurology ; 97(2): 92-94, 2021 07 13.
Article em En | MEDLINE | ID: mdl-33931529
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Estereotipado / Extremidade Superior / Deficiência Intelectual Ligada ao Cromossomo X Limite: Adult / Humans / Male Idioma: En Revista: Neurology Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Estereotipado / Extremidade Superior / Deficiência Intelectual Ligada ao Cromossomo X Limite: Adult / Humans / Male Idioma: En Revista: Neurology Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos