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JAMES KLEPPER, M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1043303233IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
162875(NY)
Education
NEW YORK UNIVERSITY SCHOOL OF MEDICINE
Class of 1983
Research & Publications (20)
Expect the unexpected: favourable outcome in Munchausen by proxy syndrome.
PMID 17987314·Eur J Pediatr·2008
5-case
Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
PMID 19049586·Epilepsia·2008
6-review
GLUT1 deficiency with delayed myelination responding to ketogenic diet.
PMID 17675029·Pediatr Neurol·2007
5-case
Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.
PMID 16217704·Neuropediatrics·2005
3-trial
Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1.
PMID 16171377·Biochemistry·2005
8-other
Impaired glucose transport into the brain: the expanding spectrum of glucose transporter type 1 deficiency syndrome.
PMID 15021248·Curr Opin Neurol·2004
6-review
Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome.
PMID 14769490·Prostaglandins Leukot Essent Fatty Acids·2004
8-other
Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?
PMID 14643395·Pediatr Neurol·2003
8-other
Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.
PMID 12548383·Eur J Pediatr·2003
8-other
Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review.
PMID 12029447·Eur J Pediatr·2002
6-review
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
PMID 11389907·FEBS Lett·2001
7-preclinical
An electro-encephalogram beta gap after induction with diazepam: a localization method in epileptogenic lesions.
PMID 19464946·Clin Neurophysiol·2009
4-observational
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?
PMID 19259135·Eur J Hum Genet·2009
8-other
Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group.
PMID 18823325·Epilepsia·2009
8-other
The ketogenic diet in children with Glut1 deficiency syndrome and epilepsy.
PMID 18940357·J Pediatr·2008
8-other
Pyridoxal phosphate-dependent neonatal epileptic encephalopathy.
PMID 18296573·Arch Dis Child Fetal Neonatal Ed·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 175 E MAIN ST, SUITE 200
HUNTINGTON, NY 11743 - Phone
- (631) 549-5700
Quick Facts
- NPI
- 1043303233
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 43
- Publications
- 20
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