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S M Willi

Showing results (11-20 of 24) with videos related to

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The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
Journal of Medical Genetics|November 1, 1996
Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocationM Joseph, E S Cantú, G S Pai, et al.
Clinical Chemistry|February 1, 1992
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, A Bhala, S F Poirier, et al.
Pediatric Research|February 1, 1997
A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiencyS M Willi, Y Zhang, J B Hill, et al.
Pediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.
Cancer|October 11, 1992
The effects of adjuvant chemotherapy on growth in children with medulloblastomaJ S Olshan, J Gubernick, R J Packer, et al.
Pediatric Obesity|March 31, 2012
Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trialS M Willi, K Hirst, R Jago, et al.
The Journal of Pediatrics|November 1, 1995
Neurocognitive deficits in morbidly obese children with obstructive sleep apneaS K Rhodes, K C Shimoda, L R Waid, et al.
American Journal of Medical Genetics|December 31, 1997
Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional familiesJ D Marshall, M D Ludman, S E Shea, et al.
The Journal of Clinical Investigation|October 14, 1998
Effects of mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetesG Argyropoulos, A M Brown, S M Willi, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
Journal of Medical Genetics|November 1, 1996
Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocationM Joseph, E S Cantú, G S Pai, et al.
Clinical Chemistry|February 1, 1992
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, A Bhala, S F Poirier, et al.
Pediatric Research|February 1, 1997
A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiencyS M Willi, Y Zhang, J B Hill, et al.
Pediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.
Cancer|October 11, 1992
The effects of adjuvant chemotherapy on growth in children with medulloblastomaJ S Olshan, J Gubernick, R J Packer, et al.
Pediatric Obesity|March 31, 2012
Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trialS M Willi, K Hirst, R Jago, et al.
The Journal of Pediatrics|November 1, 1995
Neurocognitive deficits in morbidly obese children with obstructive sleep apneaS K Rhodes, K C Shimoda, L R Waid, et al.
American Journal of Medical Genetics|December 31, 1997
Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional familiesJ D Marshall, M D Ludman, S E Shea, et al.
The Journal of Clinical Investigation|October 14, 1998
Effects of mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetesG Argyropoulos, A M Brown, S M Willi, et al.
Pageof 3