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F Scaglia

Showing results (1-10 of 25) with videos related to

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Seminars in Perinatology|May 20, 1999
Primary and secondary alterations of neonatal carnitine metabolismF Scaglia, N Longo
Lancet (London, England)|November 7, 1999
Sublingual therapy for cobalamin deficiencyO A Bodamer, F Scaglia
Archives of Biochemistry and Biophysics|March 24, 1999
Functional characterization of the carnitine transporter defective in primary carnitine deficiencyF Scaglia, Y Wang, N Longo
American Journal of Physiology. Cell Physiology|March 14, 2001
Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblastsN Longo, F Scaglia, Y Wang
Journal of Inherited Metabolic Disease|February 22, 2000
Psychiatric symptoms of inherited metabolic diseaseY Estrov, F Scaglia, O A Bodamer
Pediatric Nephrology (Berlin, Germany)|August 25, 1999
Minimal change nephrotic syndrome: a possible complication of ehrlichiosisF Scaglia, L B Vogler, L C Hymes, et al.
Gene|July 3, 2013
A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorptionN Diop-Bove, M Jain, F Scaglia, et al.
Nutrition & Metabolism|April 9, 2005
Exogenous recombinant human growth hormone effects during suboptimal energy and zinc intakeRussell Rising, Julio F Scaglia, Conrad Cole, et al.
Annals of Neurology|January 5, 2002
Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvementK Inoue, H Tanaka, F Scaglia, et al.
American Journal of Medical Genetics|April 5, 2000
Deletion (9) (p13.1 p21.1)F Scaglia, O A Bodamer, S A Berend, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Seminars in Perinatology|May 20, 1999
Primary and secondary alterations of neonatal carnitine metabolismF Scaglia, N Longo
Lancet (London, England)|November 7, 1999
Sublingual therapy for cobalamin deficiencyO A Bodamer, F Scaglia
Archives of Biochemistry and Biophysics|March 24, 1999
Functional characterization of the carnitine transporter defective in primary carnitine deficiencyF Scaglia, Y Wang, N Longo
American Journal of Physiology. Cell Physiology|March 14, 2001
Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblastsN Longo, F Scaglia, Y Wang
Journal of Inherited Metabolic Disease|February 22, 2000
Psychiatric symptoms of inherited metabolic diseaseY Estrov, F Scaglia, O A Bodamer
Pediatric Nephrology (Berlin, Germany)|August 25, 1999
Minimal change nephrotic syndrome: a possible complication of ehrlichiosisF Scaglia, L B Vogler, L C Hymes, et al.
Gene|July 3, 2013
A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorptionN Diop-Bove, M Jain, F Scaglia, et al.
Nutrition & Metabolism|April 9, 2005
Exogenous recombinant human growth hormone effects during suboptimal energy and zinc intakeRussell Rising, Julio F Scaglia, Conrad Cole, et al.
Annals of Neurology|January 5, 2002
Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvementK Inoue, H Tanaka, F Scaglia, et al.
American Journal of Medical Genetics|April 5, 2000
Deletion (9) (p13.1 p21.1)F Scaglia, O A Bodamer, S A Berend, et al.
Pageof 3