Search research articles
Contact Us
Filters
Showing results (1-10 of 68) with videos related to
Page
of 7
Sort By:
Pediatric Research
|
August 24, 2002
Answers to missing mtDNA found at last
Annette Feigenbaum
Molecular Genetics and Metabolism Reports
|
January 9, 2023
Challenges of managing ornithine transcarbamylase deficiency in female heterozygotes
Annette Feigenbaum
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
November 23, 2006
A child with an underrecognized form of developmental delay: a congenital disorder of glycosylation
Sanjay Mahant, Annette Feigenbaum
Neuroimaging Clinics of North America
|
June 9, 2004
A neuroimaging approach to inborn errors of metabolism
Susan Blaser, Annette Feigenbaum
Molecular Genetics and Metabolism Reports
|
January 9, 2023
Considerations for prenatal and postpartum management of a female patient with ornithine transcarbamylase deficiency
Annette Feigenbaum, Leah Lamale-Smith, Lawrence Weinstein
Pediatric Neurology
|
October 23, 2008
Stepwise developmental regression associated with novel CACNA1A mutation
Andrea A Guerin, Annette Feigenbaum, Elizabeth J Donner, et al.
Molecular Genetics and Metabolism Reports
|
October 17, 2022
Characterization of a novel exonic deletion in the <i>GALNS</i> gene causing Morquio A syndrome
Kathryn DeLong, Annette Feigenbaum, Laura Pollard, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2007
Late-onset cobalamin-C disorder: a challenging diagnosis
Tawfeg I Ben-Omran, Hubert Wong, Susan Blaser, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
October 14, 2008
Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type
Christina Gerth, Chantal F Morel, Annette Feigenbaum, et al.
Journal of Radiology Case Reports
|
June 8, 2018
Brain Magnetic Resonance Imaging Findings in Poorly Controlled Homocystinuria
Charles Q Li, Bruce A Barshop, Annette Feigenbaum, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Pediatric Research
|
August 24, 2002
Answers to missing mtDNA found at last
Annette Feigenbaum
Molecular Genetics and Metabolism Reports
|
January 9, 2023
Challenges of managing ornithine transcarbamylase deficiency in female heterozygotes
Annette Feigenbaum
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
November 23, 2006
A child with an underrecognized form of developmental delay: a congenital disorder of glycosylation
Sanjay Mahant, Annette Feigenbaum
Neuroimaging Clinics of North America
|
June 9, 2004
A neuroimaging approach to inborn errors of metabolism
Susan Blaser, Annette Feigenbaum
Molecular Genetics and Metabolism Reports
|
January 9, 2023
Considerations for prenatal and postpartum management of a female patient with ornithine transcarbamylase deficiency
Annette Feigenbaum, Leah Lamale-Smith, Lawrence Weinstein
Pediatric Neurology
|
October 23, 2008
Stepwise developmental regression associated with novel CACNA1A mutation
Andrea A Guerin, Annette Feigenbaum, Elizabeth J Donner, et al.
Molecular Genetics and Metabolism Reports
|
October 17, 2022
Characterization of a novel exonic deletion in the <i>GALNS</i> gene causing Morquio A syndrome
Kathryn DeLong, Annette Feigenbaum, Laura Pollard, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2007
Late-onset cobalamin-C disorder: a challenging diagnosis
Tawfeg I Ben-Omran, Hubert Wong, Susan Blaser, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
October 14, 2008
Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type
Christina Gerth, Chantal F Morel, Annette Feigenbaum, et al.
Journal of Radiology Case Reports
|
June 8, 2018
Brain Magnetic Resonance Imaging Findings in Poorly Controlled Homocystinuria
Charles Q Li, Bruce A Barshop, Annette Feigenbaum, et al.
Page
of 7