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Utility of genetic testing in children with leukodystrophy.
Zerem, Ayelet; Libzon, Stephanie; Ben Sira, Liat; Meirson, Hadas; Hausman-Kedem, Moran; Haviv, Noam; Yosovich, Keren; Mory, Adi; Baris Feldman, Hagit; Lev, Dorit; Lerman-Sagie, Tally; Fattal-Valevski, Aviva; Hacohen, Yael; Marom, Daphna.
Afiliación
  • Zerem A; Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: ayeletze@tlvmc.gov.il.
  • Libzon S; Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Magen Rare Disease Center, Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel.
  • Ben Sira L; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Pediatric Radiology, Department of Radiology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Meirson H; Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Hausman-Kedem M; Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Haviv N; Statistical Advisor and Senior Lecturer, The Ashkelon Academic College, Israel.
  • Yosovich K; Magen Rare Disease Center, Genetics Institute, Wolfson Medical Center, Holon, Israel.
  • Mory A; Genetics Institute and Genomic Center, Tel Aviv Sourasky Medical Center, Israel.
  • Baris Feldman H; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Genetics Institute and Genomic Center, Tel Aviv Sourasky Medical Center, Israel.
  • Lev D; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Magen Rare Disease Center, Genetics Institute, Wolfson Medical Center, Holon, Israel.
  • Lerman-Sagie T; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Magen Rare Disease Center, Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel.
  • Fattal-Valevski A; Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Hacohen Y; Queen Square MS Centre, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, United Kingdom; Department of Neurology, Great Ormond Street Hospital for Children, London, United Kingdom.
  • Marom D; Sackler Faulty of Medicine, Tel Aviv University, Tel Aviv, Israel; Genetics Institute and Genomic Center, Tel Aviv Sourasky Medical Center, Israel.
Eur J Paediatr Neurol ; 45: 29-35, 2023 Jul.
Article en En | MEDLINE | ID: mdl-37267771
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido