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World Journal of Cardiology
|
November 28, 2014
Infant with cardiomyopathy: When to suspect inborn errors of metabolism?
Stephanie L Byers, Can Ficicioglu
International Journal of Neonatal Screening
|
October 24, 2022
Addition of MPS-II to the Recommended Uniform Screening Panel in the United States
David S Millington, Can Ficicioglu
Journal of Inherited Metabolic Disease
|
January 29, 2010
Genotype-phenotype correlations: sudden death in an infant with very-long-chain acyl-CoA dehydrogenase deficiency
Curtis R Coughlin, Can Ficicioglu
Molecular Genetics and Metabolism
|
January 27, 2005
Galactitol and galactonate in red blood cells of children with the Duarte/galactosemia genotype
Can Ficicioglu, Claire Yager, Stanton Segal
Clinical Chemistry
|
January 16, 2010
Newborn screening for galactosemia: a review of 5 years of data and audit of a revised reporting approach
Dennis E Freer, Can Ficicioglu, David Finegold
Pediatrics
|
July 4, 2008
A false-positive newborn screening result: goat's milk acidopathy
Kimberly A Chapman, Jaya Ganesh, Can Ficicioglu
Orphanet Journal of Rare Diseases
|
February 26, 2020
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Amanda Barone Pritchard, Alanna Strong, Can Ficicioglu
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 2, 2019
Response to Neeleman et al
Jeffrey M Chinsky, Can Ficicioglu, C Ronald Scott
European Journal of Pediatrics
|
June 8, 2007
Effect of galactose free formula on galactose-1-phosphate in two infants with classical galactosemia
Can Ficicioglu, Christie Hussa, Claire Yager, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
April 25, 2015
Adolescent presentations of inborn errors of metabolism
Rebecca C Ahrens-Nicklas, Gail Slap, Can Ficicioglu
Page
of 11
Search research articles
Search
Showing results (11-20 of 110) with videos related to
Sort By:
Page
of 11
World Journal of Cardiology
|
November 28, 2014
Infant with cardiomyopathy: When to suspect inborn errors of metabolism?
Stephanie L Byers, Can Ficicioglu
International Journal of Neonatal Screening
|
October 24, 2022
Addition of MPS-II to the Recommended Uniform Screening Panel in the United States
David S Millington, Can Ficicioglu
Journal of Inherited Metabolic Disease
|
January 29, 2010
Genotype-phenotype correlations: sudden death in an infant with very-long-chain acyl-CoA dehydrogenase deficiency
Curtis R Coughlin, Can Ficicioglu
Molecular Genetics and Metabolism
|
January 27, 2005
Galactitol and galactonate in red blood cells of children with the Duarte/galactosemia genotype
Can Ficicioglu, Claire Yager, Stanton Segal
Clinical Chemistry
|
January 16, 2010
Newborn screening for galactosemia: a review of 5 years of data and audit of a revised reporting approach
Dennis E Freer, Can Ficicioglu, David Finegold
Pediatrics
|
July 4, 2008
A false-positive newborn screening result: goat's milk acidopathy
Kimberly A Chapman, Jaya Ganesh, Can Ficicioglu
Orphanet Journal of Rare Diseases
|
February 26, 2020
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Amanda Barone Pritchard, Alanna Strong, Can Ficicioglu
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 2, 2019
Response to Neeleman et al
Jeffrey M Chinsky, Can Ficicioglu, C Ronald Scott
European Journal of Pediatrics
|
June 8, 2007
Effect of galactose free formula on galactose-1-phosphate in two infants with classical galactosemia
Can Ficicioglu, Christie Hussa, Claire Yager, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
April 25, 2015
Adolescent presentations of inborn errors of metabolism
Rebecca C Ahrens-Nicklas, Gail Slap, Can Ficicioglu
Page
of 11