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Phenylketonuria is an inherited metabolic disorder that occurs when patients cannot convert the essential amino acid phenylalanine into tyrosine. Since the phenylalanine is not broken down in these patients, it accumulates in the body and, most importantly, in the brain, leading to severe cognitive impairment. Serwet Demirdas’s research aimed at optimising psychosocial and nutritional care for patients with phenylketonuria.

Event details of Optimal care of patients with phenylketonuria
Date 11 September 2015
Time 14:00
Location Agnietenkapel
Room Location

Ms S. Demirdas: Phenylketonuria: Optimizing Care

Supervisor

Prof. F. A. Wijburg

Co-supervisor

Dr A.M. Bosch

Agnietenkapel

Room Location

Oudezijds Voorburgwal 229 - 231
1012 EZ Amsterdam