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Showing results (131-140 of 137) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|September 25, 2001
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter studyM Bonamico, P Mariani, H M Danesi, et al.
Human Mutation|May 25, 1999
Cystathionine beta-synthase mutations in homocystinuriaJ P Kraus, M Janosík, V Kozich, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statementT M Cox, J M F G Aerts, G Andria, et al.
Neurology|September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
JAMA|June 11, 1997
Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action ProjectI M Graham, L E Daly, H M Refsum, et al.
Journal of Medical Genetics|August 16, 2003
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wideB Wilcken, F Bamforth, Z Li, et al.
Pageof 14

Showing results (131-140 of 137) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 137 results.
Journal of Pediatric Gastroenterology and Nutrition|September 25, 2001
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter studyM Bonamico, P Mariani, H M Danesi, et al.
Human Mutation|May 25, 1999
Cystathionine beta-synthase mutations in homocystinuriaJ P Kraus, M Janosík, V Kozich, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statementT M Cox, J M F G Aerts, G Andria, et al.
Neurology|September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
JAMA|June 11, 1997
Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action ProjectI M Graham, L E Daly, H M Refsum, et al.
Journal of Medical Genetics|August 16, 2003
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wideB Wilcken, F Bamforth, Z Li, et al.
Pageof 14