Propionic acidemia is a rare autosomal recessive inherited metabolic disorder that can inhibit the synthesis of N-acetylglutamate, the obligatory activator in urea synthesis, leading to hyperammonemia. N-carbamyl...
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Medicine by Alexandros G.Sfakianakis,Anapafseos 5 Agios Nikolaos,Crete 72100,Greece,tel :00302841026182 & 00306932607174
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Ετικέτες
Κυριακή 22 Απριλίου 2018
Long-term continuous N-carbamylglutamate treatment in frequently decompensated propionic acidemia: a case report
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