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A L Gropman

Showing results (1-10 of 15) with videos related to

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Current Neurology and Neuroscience Reports|March 20, 2002
Diagnosis and treatment of childhood mitochondrial diseasesA L Gropman
Case Reports in Genetics|May 7, 2020
Late Onset Ornithine Transcarbamylase Deficiency Triggered by an Acute Increase in Protein Intake: A Review of 10 Cases Reported in the LiteratureE Barkovich, A L Gropman
Journal of Inherited Metabolic Disease|November 27, 2007
Neurological implications of urea cycle disordersA L Gropman, M Summar, J V Leonard
Lancet (London, England)|September 12, 1998
Wernicke's encephalopathy due to self starvation in a childA L Gropman, W D Gaillard, P Campbell, et al.
AJNR. American Journal of Neuroradiology|May 22, 2010
Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiencyA L Gropman, B Gertz, K Shattuck, et al.
Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Molecular Syndromology|November 1, 2012
High Intellectual Function in Individuals with Mutation-Positive Microform HoloprosencephalyB D Solomon, D E Pineda-Alvarez, A L Gropman, et al.
Neuropediatrics|August 1, 1997
Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patientsA L Gropman, A J Barkovich, L G Vezina, et al.
Neurology|February 8, 2012
So what? Does the test lead to improved health outcomes?D J Michelson, M I Shevell, E H Sherr, et al.
Molecular Syndromology|November 4, 2010
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in HumansR F Arauz, B D Solomon, D E Pineda-Alvarez, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Current Neurology and Neuroscience Reports|March 20, 2002
Diagnosis and treatment of childhood mitochondrial diseasesA L Gropman
Case Reports in Genetics|May 7, 2020
Late Onset Ornithine Transcarbamylase Deficiency Triggered by an Acute Increase in Protein Intake: A Review of 10 Cases Reported in the LiteratureE Barkovich, A L Gropman
Journal of Inherited Metabolic Disease|November 27, 2007
Neurological implications of urea cycle disordersA L Gropman, M Summar, J V Leonard
Lancet (London, England)|September 12, 1998
Wernicke's encephalopathy due to self starvation in a childA L Gropman, W D Gaillard, P Campbell, et al.
AJNR. American Journal of Neuroradiology|May 22, 2010
Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiencyA L Gropman, B Gertz, K Shattuck, et al.
Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Molecular Syndromology|November 1, 2012
High Intellectual Function in Individuals with Mutation-Positive Microform HoloprosencephalyB D Solomon, D E Pineda-Alvarez, A L Gropman, et al.
Neuropediatrics|August 1, 1997
Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patientsA L Gropman, A J Barkovich, L G Vezina, et al.
Neurology|February 8, 2012
So what? Does the test lead to improved health outcomes?D J Michelson, M I Shevell, E H Sherr, et al.
Molecular Syndromology|November 4, 2010
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in HumansR F Arauz, B D Solomon, D E Pineda-Alvarez, et al.
Pageof 2