Your browser doesn't support javascript.
loading
A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age.
Eltan, Mehmet; Alavanda, Ceren; Yavas Abali, Zehra; Ergenekon, Pinar; Yalindag Ozturk, Nilufer; Sakar, Mustafa; Dagcinar, Adnan; Kirkgoz, Tarik; Kaygusuz, Sare Betul; Gokdemir, Yasemin; Elcioglu, Huriye Nursel; Guran, Tulay; Bereket, Abdullah; Ata, Pinar; Turan, Serap.
Afiliação
  • Eltan M; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Alavanda C; Department of Medical Genetics, Marmara University School of Medicine, Istanbul, Turkey.
  • Yavas Abali Z; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Ergenekon P; Department of Pediatric Chest Disease, Marmara University School of Medicine, Istanbul, Turkey.
  • Yalindag Ozturk N; Department of Pediatric Intensive Care Unit, Marmara University School of Medicine, Istanbul, Turkey.
  • Sakar M; Department of Pediatric Neurosurgery, Marmara University School of Medicine, Istanbul, Turkey.
  • Dagcinar A; Department of Pediatric Neurosurgery, Marmara University School of Medicine, Istanbul, Turkey.
  • Kirkgoz T; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Kaygusuz SB; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Gokdemir Y; Department of Pediatric Chest Disease, Marmara University School of Medicine, Istanbul, Turkey.
  • Elcioglu HN; Department of Pediatric Genetics, Marmara University School of Medicine, Istanbul, Turkey.
  • Guran T; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Bereket A; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Ata P; Department of Medical Genetics, Marmara University School of Medicine, Istanbul, Turkey.
  • Turan S; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey. serap.turan@marmara.edu.tr.
Calcif Tissue Int ; 107(1): 96-103, 2020 07.
Article em En | MEDLINE | ID: mdl-32337609

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteosclerose / Exoftalmia / Fissura Palatina / Hipofosfatemia / Microcefalia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteosclerose / Exoftalmia / Fissura Palatina / Hipofosfatemia / Microcefalia Idioma: En Ano de publicação: 2020 Tipo de documento: Article