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F Scaglia

Showing results (11-20 of 25) with videos related to

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Clinical Endocrinology|November 6, 2007
Prevalence of metabolic syndrome (MS) in children and adolescents with varying degrees of obesityV Calcaterra, C Klersy, T Muratori, et al.
Journal of Endocrinological Investigation|September 13, 2007
Pregnancy in a woman with Turner syndrome and celiac diseaseV Calcaterra, L Lanzarini, B Guerci, et al.
The Neuroradiology Journal|November 12, 2013
The brain-heart connection in mitochondrial respiratory chain diseasesM Cordeiro, F Scaglia, S Lopes Da Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiencyF Scaglia, Y Wang, R H Singh, et al.
Journal of Child Neurology|April 9, 2001
Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduriaF Scaglia, V R Sutton, O A Bodamer, et al.
Molecular Genetics and Metabolism Reports|September 6, 2018
Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong KongS C Chong, P Lo, C W Chow, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|February 27, 2024
Aspirin delays the metabolic clock of gestation in women at risk of preeclampsia: abridged secondary publicationC Y L Poon, T Y Leung, C C Wang, et al.
Journal of Medical Genetics|February 6, 2004
MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutationK Szigeti, L-J C Wong, C-L Perng, et al.
Journal of Medical Genetics|April 5, 2005
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephalyS A Yatsenko, S W Cheung, D A Scott, et al.
Clinical Genetics|September 14, 2007
Identification of proximal 1p36 deletions using array-CGH: a possible new syndromeS-H L Kang, A Scheffer, Z Ou, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Clinical Endocrinology|November 6, 2007
Prevalence of metabolic syndrome (MS) in children and adolescents with varying degrees of obesityV Calcaterra, C Klersy, T Muratori, et al.
Journal of Endocrinological Investigation|September 13, 2007
Pregnancy in a woman with Turner syndrome and celiac diseaseV Calcaterra, L Lanzarini, B Guerci, et al.
The Neuroradiology Journal|November 12, 2013
The brain-heart connection in mitochondrial respiratory chain diseasesM Cordeiro, F Scaglia, S Lopes Da Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiencyF Scaglia, Y Wang, R H Singh, et al.
Journal of Child Neurology|April 9, 2001
Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduriaF Scaglia, V R Sutton, O A Bodamer, et al.
Molecular Genetics and Metabolism Reports|September 6, 2018
Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong KongS C Chong, P Lo, C W Chow, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|February 27, 2024
Aspirin delays the metabolic clock of gestation in women at risk of preeclampsia: abridged secondary publicationC Y L Poon, T Y Leung, C C Wang, et al.
Journal of Medical Genetics|February 6, 2004
MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutationK Szigeti, L-J C Wong, C-L Perng, et al.
Journal of Medical Genetics|April 5, 2005
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephalyS A Yatsenko, S W Cheung, D A Scott, et al.
Clinical Genetics|September 14, 2007
Identification of proximal 1p36 deletions using array-CGH: a possible new syndromeS-H L Kang, A Scheffer, Z Ou, et al.
Pageof 3