Early neurological complications in children with classical galactosemia and p.gln188arg mutation

Author:

Özgün Nezir1,Celik Muhittin2,Akdeniz Osman3,Ozbek Mehmet Nuri4,Bulbul Ali5,Anlar Banu6

Affiliation:

1. M.D. Specialist in Pediatric NeurologyDepartment of PediatricsDivision of Pediatric NeurologyDiyarbakir Children's HospitalDiyarbakirTurkey

2. M.D. Specialist in NeonatologyDepartment of PediatricsDivision of NeonatologyDiyarbakir Children's HospitalDiyarbakirTurkey

3. M.D. Specialist in Pediatric CardiologyDepartment of PediatricsDivision of Pediatric CardiologyDiyarbakir Children's HospitalDiyarbakirTurkey

4. Prof. Dr. Specialist in Pediatrics EndocrineMetabolism Diyarbakır Gazi Yaşargil Education and Research HospitalDiyarbakirTurkey

5. Prof. Dr. Specialist in NeonatologyDepartment of PediatricsDivision of NeonatologySisli Hamidiye Etfal Research HospitalIstanbulTurkey

6. Prof. Dr. Specialist in Pediatric NeurologyDepartment of PediatricsDivision of Pediatric NeurologyHacettepe University Children's HospitalAnkaraTurkey

Publisher

Wiley

Subject

Developmental Biology,Developmental Neuroscience

Reference47 articles.

1. Late neurologic complications of galactosemia: study of 3 cases;Bohu P.A.;Rev. Neurol.,1995

2. Living With Classical Galactosemia: Health-Related Quality of Life Consequences

3. Galactosemia, a Single Gene Disorder With Epigenetic Consequences

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