Transferrin hypoglycosylation in hereditary fructose intolerance: Using the clues and avoiding the pitfalls

Author： Adamowicz M.   Płoski R.   Rokicki D.   Morava E.   Giżewska M.   Mierzewska H.   Pollak A.   Lefeber D.   Wevers R.   Pronicka E.  

Publisher： Springer Publishing Company

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.30, Iss.3, 2007-06, pp. : 407-407

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

HEREDITARY AND FAMILIAL SYNDROMES OF BONE AND BLOOD. GENETIC PATHWAYS, DIAGNOSTIC PITFALLS

By Rossbach Hans-Christoph  

Fetal and Pediatric Pathology, Vol. 26, Iss. 1, 2007-01 ,pp. : 1-16

Informa Healthcare

Access to resources Recommend Favorite

Transferrin Microheterogeneity in Fetal Blood

By  

Neonatology, Vol. 86, Iss. 2, 2004-08 ,pp. : 98-103

Karger

Access to resources Recommend Favorite

Avoiding sedation in pediatric radiology

By Koch Bernadette  

Pediatric Radiology, Vol. 38, Iss. 2, 2008-05 ,pp. : 225-226

Springer Publishing Company

Access to resources Recommend Favorite

Increased NO production in lysinuric protein intolerance

By Mannucci L.   Emma F.   Markert M.   Bachmann C.   Boulat O.   Carrozzo R.   Rizzoni G.   Dionisi-Vici C.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 2, 2005-04 ,pp. : 123-129

Springer Publishing Company

Access to resources Recommend Favorite

Pitfalls in the approach to pica

By Fotoulaki Maria   Panagopoulou Paraskevi   Efstratiou Ioannis   Nousia-Arvanitakis Sanda  

European Journal of Pediatrics, Vol. 166, Iss. 6, 2007-06 ,pp. : 623-624

Springer Publishing Company

Access to resources Recommend Favorite