Your browser doesn't support javascript.
loading
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx.
Calvo, P L; Pagliardini, S; Baldi, M; Pucci, A; Sturiale, L; Garozzo, D; Vinciguerra, T; Barbera, C; Jaeken, J.
Affiliation
  • Calvo PL; Department of Pediatric Gastroenterology, University of Turin, Regina Margherita Hospital, Piazza Polonia 94, 10126, Turin, Italy. pierluigi.calvo@fastwebnet.i
J Inherit Metab Dis ; 31 Suppl 2: S437-40, 2008 Dec.
Article in En | MEDLINE | ID: mdl-19067230
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspartate Aminotransferases / Congenital Disorders of Glycosylation / Alanine Transaminase / Clinical Enzyme Tests Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: J Inherit Metab Dis Year: 2008 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspartate Aminotransferases / Congenital Disorders of Glycosylation / Alanine Transaminase / Clinical Enzyme Tests Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: J Inherit Metab Dis Year: 2008 Document type: Article Affiliation country: Country of publication: