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Can Ficicioglu

Showing results (1-10 of 110) with videos related to

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International Journal of Neonatal Screening|September 26, 2021
The Editor's Choice for Issue 2, Volume 7Can Ficicioglu
The New England Journal of Medicine|December 30, 2025
Breaking Barriers in Mucopolysaccharidosis Type IICan Ficicioglu
Cold Spring Harbor Molecular Case Studies|May 11, 2017
New tools and approaches to newborn screening: ready to open Pandora's box?Can Ficicioglu
Therapeutics and Clinical Risk Management|August 30, 2008
Review of miglustat for clinical management in Gaucher disease type 1Can Ficicioglu
Pediatrics|December 5, 2006
3-Methylcrotonyl-CoA carboxylase deficiency: metabolic decompensation in a noncompliant child detected through newborn screeningCan Ficicioglu, Irma Payan
Journal of Pediatric Gastroenterology and Nutrition|May 16, 2022
Lessons Learned From the Long-Term Use of Enzyme Replacement Therapy in the Treatment of Lysosomal Acid Lipase DeficiencyAlanna Strong, Can Ficicioglu
Molecular Genetics and Metabolism|October 28, 2008
Clinical outcomes of infants with short-chain acyl-coenzyme A dehydrogenase deficiency (SCADD) detected by newborn screeningReena Jethva, Can Ficicioglu
Pediatric Neurology|October 18, 2011
Isolated neonatal seizures: when to suspect inborn errors of metabolismCan Ficicioglu, David Bearden
Pediatrics|August 27, 2009
Failure to thrive: when to suspect inborn errors of metabolismCan Ficicioglu, Kristina An Haack
Clinical Pediatrics|April 14, 2012
Severe metabolic acidosis in a newborn with an abnormal newborn screenSamantha A Schrier, Can Ficicioglu
Pageof 11

Showing results (1-10 of 110) with videos related to

Sort By:
Pageof 11
International Journal of Neonatal Screening|September 26, 2021
The Editor's Choice for Issue 2, Volume 7Can Ficicioglu
The New England Journal of Medicine|December 30, 2025
Breaking Barriers in Mucopolysaccharidosis Type IICan Ficicioglu
Cold Spring Harbor Molecular Case Studies|May 11, 2017
New tools and approaches to newborn screening: ready to open Pandora's box?Can Ficicioglu
Therapeutics and Clinical Risk Management|August 30, 2008
Review of miglustat for clinical management in Gaucher disease type 1Can Ficicioglu
Pediatrics|December 5, 2006
3-Methylcrotonyl-CoA carboxylase deficiency: metabolic decompensation in a noncompliant child detected through newborn screeningCan Ficicioglu, Irma Payan
Journal of Pediatric Gastroenterology and Nutrition|May 16, 2022
Lessons Learned From the Long-Term Use of Enzyme Replacement Therapy in the Treatment of Lysosomal Acid Lipase DeficiencyAlanna Strong, Can Ficicioglu
Molecular Genetics and Metabolism|October 28, 2008
Clinical outcomes of infants with short-chain acyl-coenzyme A dehydrogenase deficiency (SCADD) detected by newborn screeningReena Jethva, Can Ficicioglu
Pediatric Neurology|October 18, 2011
Isolated neonatal seizures: when to suspect inborn errors of metabolismCan Ficicioglu, David Bearden
Pediatrics|August 27, 2009
Failure to thrive: when to suspect inborn errors of metabolismCan Ficicioglu, Kristina An Haack
Clinical Pediatrics|April 14, 2012
Severe metabolic acidosis in a newborn with an abnormal newborn screenSamantha A Schrier, Can Ficicioglu
Pageof 11