A series of pregnancies in women with inherited metabolic disease

Journal of Inherited Metabolic Disease

Volumn 35, Issue 3, 2012, Pages 419-424

  Langendonk, Janneke G ^a   Roos, Jonathan C P ^b   Angus, Lindsay ^a   Williams, Monique ^a   Karstens, François P J ^a   De Klerk, Johannes B C ^a   Maritz, Charlé ^b   Ben Omran, Tawfeg ^c   Williamson, Catherine ^d   Lachmann, Robin H ^b   Murphy, Elaine ^b  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^c WEILL CORNELL MEDICAL COLLEGE   (Qatar)

^d Institute of Reproductive and Developmental Biology   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXY 3 METHYLGLUTARIC COENZYME A LYASE DEFICIENCY; ADULT; ARTICLE; CLINICAL ARTICLE; DELIVERY; FEMALE; FETUS OUTCOME; GLUTARIC ACIDEMIA TYPE 1; HOMOCYSTINURIA; HUMAN; INBORN ERROR OF METABOLISM; MATERNAL MORTALITY; METHYLMALONIC ACIDEMIA; ORNITHINE TRANSCARBAMYLASE DEFICIENCY; PREGNANCY; PROPIONIC ACIDEMIA; PUERPERIUM;

ADULT; DELIVERY, OBSTETRIC; FEMALE; HUMANS; METABOLIC DISEASES; OBSTETRICS; ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY DISEASE; OXO-ACID-LYASES; PREGNANCY; PREGNANCY COMPLICATIONS; PREGNANCY OUTCOME; RISK; TIME FACTORS; TREATMENT OUTCOME;

EID: 84863337153     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-011-9389-2     Document Type: Article

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