Associate Professor, Pediatrics, Tufts Medical Center
Pediatrics
Dr. Mark S. Korson, MD
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Mark Korson works in the field of Pediatrics. Mark Korson is also published. He has 39 publications published. The lastest publication: "Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.' He accepts Medicare payments and is listed with Medicare.gov.
Publications
- Methylmalonic acidemia: A megamitochondrial disorder affecting the kidney.
- Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots.
- Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer.
- The importance of gut motility in the metabolic control of propionic acidemia.
- Neuropsychiatric illness in a patient with cobalamin G disease, an inherited disorder of vitamin B12 metabolism.
- Four cases with hypoplastic thumbs and encephaloceles.
- Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes.
- N-carbamylglutamate markedly enhances ureagenesis in N-acetylglutamate deficiency and propionic acidemia as measured by isotopic incorporation and blood biomarkers.
- Maple syrup urine disease in Cypriot families: identification of three novel mutations and biochemical characterization of the p.Thr211Met mutation in the E1alpha subu...
- Newborn screening compared to clinical identification of biochemical genetic disorders.
- Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food.
- Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
- Severe folate deficiency and pancytopenia in a nutritionally deprived infant and homocystinuria caused by cystathionine beta-synthase deficiency.
- Pitfalls in diagnosing galactosemia: false negative newborn screening following red blood cell transfusion.
- Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management.
- A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotype.
- Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneys.
- The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three families.
- Bilateral infantile cataractogenesis in a patient with deficiency of complex I, a mitochondrial electron transport chain enzyme.
- Oxidative phosphorylation defect associated with primary adrenal insufficiency.
- Metabolic etiologies of cyclic or recurrent vomiting.
- Infantile onset of hereditary ascending spastic paralysis with bulbar involvement.
- Cardiac mitochondrial dysfunction in Leigh syndrome.
- Clinical approach to genetic cardiomyopathy in children.
- Central apnea in a child with congenital autonomic dysfunction and universal pain loss.
- Perioperative white matter degeneration and death in a patient with a defect in mitochondrial oxidative phosphorylation.
- Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic diet.
- Inadequate laboratory technique for amino acid analysis resulting in missed diagnoses of homocystinuria.
- Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
- Protein status of infants with phenylketonuria undergoing nutrition management.
- Quantification of glutaric acid by isotope dilution mass spectrometry for patients with glutaric acidemia type I: selected ion monitoring vs. selected ion storage.
- A GC/MS/MS screening method for multiple organic acidemias from urine specimens.
- Quality of life assessment in adults with type 1 Gaucher disease.
- Advances in newborn screening for metabolic disorders: what the pediatrician needs to know.
- Urinary lactate excretion to monitor the efficacy of treatment of type I glycogen storage disease.
- New England Consortium: a model for medical evaluation of expanded newborn screening with tandem mass spectrometry.
- Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids.
- Rod photoreceptor function in children with mitochondrial disorders.
Schools
University of Toronto Faculty of Medicine
St Josephs Health Center
Hospital Sick Chldn
Children39s Hospital Boston
Doctors Specialties
- Clinical Biochemical Genetics
- Clinical Genetics
- Pediatrics
Accepted Insurances
- Aetna
- Blue Card PPO
- CHAMPVA
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- Community Health Network
- Emblem Health
- First Health (Coventry Health Care) PPO
- GEHA
- Harvard Pilgrim Health Care PPO
- Medicare Advantage PFFS
- Medica
- Medicaid
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Network Health
- PHP-Physicians Health Plan
- Tufts Health Plans
- United Healthcare
Education
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University of Toronto Faculty of Medicine
Hospital
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Tufts Medical Center
Drug Facts
| NPI NUMBER | 1245347616 | |
| NPPES Provider LastName | KORSON | |
| NPPES Provider FirstName | MARK | |
| NPPES Provider ZIPCode | 021111526 | |
| NPPES Provider State | MA | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 110.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1245347616 |
| Last Name Of The Provider | KORSON |
| First Name Of The Provider | MARK |
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