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International Journal of Neonatal Screening
|
September 26, 2021
The Editor's Choice for Issue 2, Volume 7
Can Ficicioglu
The New England Journal of Medicine
|
December 30, 2025
Breaking Barriers in Mucopolysaccharidosis Type II
Can 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 1
Can Ficicioglu
Pediatrics
|
December 5, 2006
3-Methylcrotonyl-CoA carboxylase deficiency: metabolic decompensation in a noncompliant child detected through newborn screening
Can 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 Deficiency
Alanna 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 screening
Reena Jethva, Can Ficicioglu
Pediatric Neurology
|
October 18, 2011
Isolated neonatal seizures: when to suspect inborn errors of metabolism
Can Ficicioglu, David Bearden
Pediatrics
|
August 27, 2009
Failure to thrive: when to suspect inborn errors of metabolism
Can Ficicioglu, Kristina An Haack
Clinical Pediatrics
|
April 14, 2012
Severe metabolic acidosis in a newborn with an abnormal newborn screen
Samantha A Schrier, Can Ficicioglu
Page
of 11
Search research articles
Search
Showing results (1-10 of 110) with videos related to
Sort By:
Page
of 11
International Journal of Neonatal Screening
|
September 26, 2021
The Editor's Choice for Issue 2, Volume 7
Can Ficicioglu
The New England Journal of Medicine
|
December 30, 2025
Breaking Barriers in Mucopolysaccharidosis Type II
Can 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 1
Can Ficicioglu
Pediatrics
|
December 5, 2006
3-Methylcrotonyl-CoA carboxylase deficiency: metabolic decompensation in a noncompliant child detected through newborn screening
Can 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 Deficiency
Alanna 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 screening
Reena Jethva, Can Ficicioglu
Pediatric Neurology
|
October 18, 2011
Isolated neonatal seizures: when to suspect inborn errors of metabolism
Can Ficicioglu, David Bearden
Pediatrics
|
August 27, 2009
Failure to thrive: when to suspect inborn errors of metabolism
Can Ficicioglu, Kristina An Haack
Clinical Pediatrics
|
April 14, 2012
Severe metabolic acidosis in a newborn with an abnormal newborn screen
Samantha A Schrier, Can Ficicioglu
Page
of 11