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The Journal of Pediatrics
|
June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency
A 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 translocation
M 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 deficiency
M 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 deficiency
S M Willi, Y Zhang, J B Hill, et al.
Pediatric Research
|
July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disorders
C A Stanley, G T Berry, M J Bennett, et al.
Cancer
|
October 11, 1992
The effects of adjuvant chemotherapy on growth in children with medulloblastoma
J 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 trial
S M Willi, K Hirst, R Jago, et al.
The Journal of Pediatrics
|
November 1, 1995
Neurocognitive deficits in morbidly obese children with obstructive sleep apnea
S 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 families
J 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 diabetes
G Argyropoulos, A M Brown, S M Willi, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
The Journal of Pediatrics
|
June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency
A 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 translocation
M 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 deficiency
M 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 deficiency
S M Willi, Y Zhang, J B Hill, et al.
Pediatric Research
|
July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disorders
C A Stanley, G T Berry, M J Bennett, et al.
Cancer
|
October 11, 1992
The effects of adjuvant chemotherapy on growth in children with medulloblastoma
J 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 trial
S M Willi, K Hirst, R Jago, et al.
The Journal of Pediatrics
|
November 1, 1995
Neurocognitive deficits in morbidly obese children with obstructive sleep apnea
S 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 families
J 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 diabetes
G Argyropoulos, A M Brown, S M Willi, et al.
Page
of 3