Search Results - Ferreira, Carlos
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Clinical and biochemical footprints of congenital disorders of glycosylation: proposed nosology by Ng, Bobby (Author) , Freeze, Hudson H. (Author) , Himmelreich, Nastassja (Author) , Blau, Nenad (Author) , Ferreira, Carlos R. (Author) ,
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International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): diagnosis, follow-up, and management by Altassan, Ruqaiah (Author) , Radenkovic, Silvia (Author) , Edmondson, Andrew C. (Author) , Barone, Rita (Author) , Brasil, Sandra (Author) , Cechova, Anna (Author) , Coman, David (Author) , Donoghue, Sarah (Author) , Falkenstein, Kristina (Author) , Ferreira, Vanessa (Author) , Ferreira, Carlos (Author) , Fiumara, Agata (Author) , Francisco, Rita (Author) , Freeze, Hudson (Author) , Grunewald, Stephanie (Author) , Honzik, Tomas (Author) , Jaeken, Jaak (Author) , Krasnewich, Donna (Author) , Lam, Christina (Author) , Lee, Joy (Author) , Lefeber, Dirk (Author) , Marques-da-Silva, Dorinda (Author) , Pascoal, Carlota (Author) , Quelhas, Dulce (Author) , Raymond, Kimiyo M. (Author) , Rymen, Daisy (Author) , Seroczynska, Malgorzata (Author) , Serrano, Mercedes (Author) , Sykut-Cegielska, Jolanta (Author) , Thiel, Christian (Author) , Tort, Frederic (Author) , Vals, Mari-Anne (Author) , Videira, Paula (Author) , Voermans, Nicol (Author) , Witters, Peter (Author) , Morava, Eva (Author) ,
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Clinical and biochemical footprints of inherited metabolic diseases: III. psychiatric presentations by Horvath, Gabriela Ana (Author) , Stowe, Robert M. (Author) , Ferreira, Carlos R. (Author) , Blau, Nenad (Author) ,
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4
Metabolic evaluation of epilepsy: a diagnostic algorithm with focus on treatable conditions by Karnebeek, Clara D. M. van (Author) , Sayson, Bryan (Author) , Lee, Jessica J. Y. (Author) , Tseng, Laura A. (Author) , Blau, Nenad (Author) , Horvath, Gabriella A. (Author) , Ferreira, Carlos R. (Author) ,
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Aggressive behavior
Anxiety
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CDG
Depression
Glycans
Glycoproteins
Glycosaminoglycans
Glycosphingolipids
Glycosylphosphatidylinositol
Hyperactivity
IEMbase
Inborn errors of metabolism
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PGM1-CDG
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congenital disorder of glycosylation
d-galactose
diagnostic algorithm
inborn errors of metabolism
management guidelines
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phosphoglucomutase 1 deficiency
seizures
treatment