Concepedia

Author

Mark Korson

Boston Children's Hospital

Also Known As

M S Korson, M. Korson, M. S. Korson, M.S. Korson, Mark Korson, Mark S Korson, Mark S. Korson, Mark S. Korson

57

Publications

2.1K

Citations

25

H-Index

65

Concepts

All Affiliations

Boston Children's HospitalTufts Medical CenterUniversity of Colorado DenverStanford UniversityMedical College of Wisconsin
MK

About

Mark Korson is an author at Boston Children's Hospital specializing in medicine, metabolism, and physiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

17

20

874

2

Biochemistry

4

4

297

3

Health Sciences

1

1

27

4

Nursing

1

1

48

5

Public Health

1

1

56

Mark Korson

×

30

Publications

1.3K

Citations

22

H-Index

YearCitations

Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots

Pierre Allard, A Grenier, Mark Korson,

Clinical Biochemistry

2004

98

Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate

George A. Díaz, Lauren Krivitzky, Masoud Mokhtarani,

Hepatology

2012

93

N-carbamylglutamate Markedly Enhances Ureagenesis in N-acetylglutamate Deficiency and Propionic Acidemia as Measured by Isotopic Incorporation and Blood Biomarkers

Mendel Tuchman, Ljubica Caldovic, Yevgeny Daikhin,

Pediatric Research

2008

88

Quality of life assessment in adults with type 1 Gaucher disease

Bruce J. Masek, Katherine B. Sims, Catherine Bove,

Quality of Life Research

1999

71

Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency

Gerald F. Cox, Masayoshi Souri, Toshifumi Aoyama,

The Journal of Pediatrics

1998

70

Neonatal-onset propionic acidemia: Neurologic and developmental profiles, and implications for management

Kathryn N. North, Mark Korson, Yasodha R. Gopal,

The Journal of Pediatrics

1995

65

The 8993 mtDNA Mutation:Heteroplasmy and ClinicalPresentation in Three Families

Y. Tatuch, Roberta A Pagon, B Vlcek,

European Journal of Human Genetics

1994

65

A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotype.

Vivian E. Shih, J.M. Fringer, Roseann Mandell,

PubMed

1995

63

Methylmalonic acidemia: A megamitochondrial disorder affecting the kidney

Zsuzsanna K. Zsengellér, Nika Aljinovic, Lisa A. Teot,

Pediatric Nephrology

2014

61

Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food

Steven Yannicelli, Phyllis B. Acosta, Antonio Velázquez,

Molecular Genetics and Metabolism

2003

56

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