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LEEOR PELEG, D.O.
D.O.
Emergency Medicine Physician
NPI: 1508954744IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
L2545(TX)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
DES MOINES UNIVERSITY OF OSTEOPATHIC MEDICINE AND HEALTH SCIENCES
Class of 1995
Research & Publications (20)
Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
PMID 18425478·Methods Mol Biol·2008
8-other
Carrier screening for Gaucher disease: lessons for low-penetrance, treatable diseases.
PMID 17878420·JAMA·2007
8-other
Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.
PMID 17705235·Prenat Diagn·2007
8-other
Signs of bruxism and temporomandibular disorders among psychiatric patients.
PMID 17178495·Oral Surg Oral Med Oral Pathol Oral Radiol Endod·2007
4-observational
844ins68 in the cystathionine beta-synthase gene in Israel and review of its distribution in the world.
PMID 15228193·Anthropol Anz·2004
3-trial
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis.
PMID 14727180·Hum Genet·2004
8-other
Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestor.
PMID 14648242·Neurogenetics·2004
8-other
Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis.
PMID 12811781·Muscle Nerve·2003
8-other
Chemotoxicity and survival of tumor-bearing mice under exposure to randomized photoperiodic regimen.
PMID 12427483·Life Sci·2002
7-preclinical
Keratin-9 gene mutation in a family with epidermolytic palmoplantar keratoderma.
PMID 12046815·J Eur Acad Dermatol Venereol·2002
8-other
Circadian variation of nitric oxide synthase activity in mouse tissue.
PMID 12025932·Chronobiol Int·2002
7-preclinical
Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in Israel.
PMID 11876000·Isr Med Assoc J·2002
8-other
A HEXA polymorphism (V436I) common to African-Americans and Ethiopian Jews.
PMID 11180612·Hum Mutat·2001
8-other
Screening for fragile X syndrome in women of reproductive age.
PMID 10951469·Prenat Diagn·2000
8-other
A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin.
PMID 10852376·Clin Genet·2000
4-observational
Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques.
PMID 10759956·Int J Dermatol·2000
8-other
Differences in rhythms of enzymatic activity of maternal and fetal blood.
PMID 10757466·Chronobiol Int·2000
3-trial
Clinical manifestations of psychiatric patients who are carriers of tay-sachs disease. Possible role of psychotropic drugs.
PMID 10754426·Neuropsychobiology·2000
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 18220 STATE HIGHWAY 249
HOUSTON, TX 77070 - Phone
- (281) 363-3156
Quick Facts
- NPI
- 1508954744
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 31
- Publications
- 20
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