Showing results (601-610 of 4,287) with videos related to
Sort By:
Pageof 429
Journal of Inherited Metabolic Disease|September 10, 2005
Dihydropyrimidine dehydrogenase deficiency presenting at birthN A Al-Sanna'a, A B P Van Kuilenburg, T M Atrak, et al.Journal of Inherited Metabolic Disease|September 10, 2005
Body composition in young adults with inborn errors of protein metabolism--a pilot studyG Wilcox, B J G Strauss, D E M Francis, et al.Journal of Inherited Metabolic Disease|November 13, 2007
Molecular screening of Smith-Lemli-Opitz syndrome in pregnant women from the Czech RepublicI Blahakova, E Makaturova, L Kotrbova, et al.Journal of Inherited Metabolic Disease|November 13, 2007
Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 casesE H Davies, A Erikson, T Collin-Histed, et al.Journal of Inherited Metabolic Disease|October 25, 2007
Classic and late-onset neurological disease in two siblings with glutaryl-CoA dehydrogenase deficiencyE López-Laso, J García-Villoria, E Martín, et al.Journal of Inherited Metabolic Disease|August 19, 2007
Direct comparison of enzyme measurements from dried blood and leukocytes from male and female Fabry disease patientsZ Lukacs, R Hartung, M Beck, et al.Journal of Inherited Metabolic Disease|August 19, 2007
Structures for clinical follow-up: newborn screeningR Rodney Howell, Gilian EngelsonJournal of Inherited Metabolic Disease|August 19, 2007
Newborn screening in Latin America at the beginning of the 21st centuryG J C BorrajoJournal of Inherited Metabolic Disease|August 19, 2007
Quality performance of newborn screening systems: strategies for improvementD WebsterJournal of Inherited Metabolic Disease|August 21, 2007
Three successful pregnancies through dietary management of fructose-1,6-bisphosphatase deficiencyV Krishnamurthy, K Eschrich, A Boney, et al.Pageof 429