Experience with NTBC therapy in hereditary tyrosinaemia type I: an alternative to liver transplantation

By Joshi S.N.   Venugopalan P.  

Annals of Tropical Paediatrics, Vol. 24, Iss. 3, 2004-09 ,pp. : 259-265

Maney Publishing

Access to resources Recommend Favorite

Tyrosinemia type 1 and Angelman syndrome due to paternal uniparental isodisomy 15

By Ferrer-Bolufer Irene   Dalmau Jaime   Quiroga Ramiro   Oltra Silvestre   Orellana Carmen   Monfort Sandra   Roselló Mónica   Osa Alberto   Martinez Francisco  

Journal of Inherited Metabolic Disease, Vol. 32, Iss. 1, 2009-12 ,pp. : 349-353

Springer Publishing Company

Access to resources Recommend Favorite

Severe neurological impairment in hereditary methaemoglobinaemia type 2

By Toelle Sandra   Boltshauser Eugen   Mössner Ekkehard   Zurbriggen Karin   Eber Stefan  

European Journal of Pediatrics, Vol. 163, Iss. 4-5, 2004-04 ,pp. : 207-209

Springer Publishing Company

Access to resources Recommend Favorite

Hyperinsulinism in tyrosinaemia type I

By Baumann U.   Preece M.   Green A.   Kelly D.   McKiernan P.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 2, 2005-04 ,pp. : 131-135

Springer Publishing Company

Access to resources Recommend Favorite

Variation by ethnicity in incidence of diabetes type 1 and clinical condition at onset in the Netherlands

By Wouwe Jacobus   Verkerk Paul   Mattiazzo Gemma   Mokadem Nayet   HiraSing Remy  

European Journal of Pediatrics, Vol. 161, Iss. 10, 2002-10 ,pp. : 559-560

Springer Publishing Company

Access to resources Recommend Favorite