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W Rhead

Showing results (1-10 of 18) with videos related to

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The Journal of Prosthetic Dentistry|May 1, 1983
An intraoral nighttime feeding attachment for patients with glycogen storage disease, types I and IIIW E LaVelle, W Rhead
Pediatric Research|December 1, 1980
Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblastsW Rhead, S Mantagos, K Tanaka
Progress in Clinical and Biological Research|January 1, 1990
Riboflavin responsive glutaric aciduria type IIN Gregersen, W Rhead, E Christensen
European Journal of Pediatrics|November 19, 1997
Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyW Sperl, R Geiger, W Lehnert, et al.
Pediatric Research|February 1, 1993
Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblastsW Rhead, V Roettger, T Marshall, et al.
American Journal of Medical Genetics|January 1, 1987
Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormalityV Ionasescu, S Patil, M Hart, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal ultrasound findings in hydrolethalus: continuing difficulties in diagnosisM Norgard, J Yankowitz, W Rhead, et al.
Nucleic Acids Research|July 11, 1989
Purified U5 small nuclear ribonucleoprotein can relieve the inhibition of spliceosome assembly and splicing by snRNP-free nuclear proteinsJ Tazi, J Temsamani, C Alibert, et al.
Molecular Genetics and Metabolism|August 11, 2007
Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiencyM A Chiong, K G Sim, K Carpenter, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
The Journal of Prosthetic Dentistry|May 1, 1983
An intraoral nighttime feeding attachment for patients with glycogen storage disease, types I and IIIW E LaVelle, W Rhead
Pediatric Research|December 1, 1980
Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblastsW Rhead, S Mantagos, K Tanaka
Progress in Clinical and Biological Research|January 1, 1990
Riboflavin responsive glutaric aciduria type IIN Gregersen, W Rhead, E Christensen
European Journal of Pediatrics|November 19, 1997
Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyW Sperl, R Geiger, W Lehnert, et al.
Pediatric Research|February 1, 1993
Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblastsW Rhead, V Roettger, T Marshall, et al.
American Journal of Medical Genetics|January 1, 1987
Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormalityV Ionasescu, S Patil, M Hart, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal ultrasound findings in hydrolethalus: continuing difficulties in diagnosisM Norgard, J Yankowitz, W Rhead, et al.
Nucleic Acids Research|July 11, 1989
Purified U5 small nuclear ribonucleoprotein can relieve the inhibition of spliceosome assembly and splicing by snRNP-free nuclear proteinsJ Tazi, J Temsamani, C Alibert, et al.
Molecular Genetics and Metabolism|August 11, 2007
Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiencyM A Chiong, K G Sim, K Carpenter, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
Pageof 2