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TOFEY LEON, MD
MD
Internal Medicine Physician
NPI: 1104480425IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD.41867(AL)
Education
UNIVERSITY OF ALABAMA SCHOOL OF MEDICINE
Class of 2019
Research & Publications (18)
The effects of pregabalin on sleep disturbance symptoms among individuals with fibromyalgia syndrome.
PMID 19410509·Sleep Med·2009
2-rct
Add-on treatment with pregabalin for partial seizures with or without generalisation: pooled data analysis of four randomised placebo-controlled trials.
PMID 18951818·Seizure·2009
8-other
Association of subjective anxiety, depression, and sleep disturbance with quality-of-life ratings in adults with epilepsy.
PMID 19170734·Epilepsia·2009
8-other
A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma.
PMID 19176457·J Natl Cancer Inst·2009
5-case
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
PMID 19196962·Proc Natl Acad Sci U S A·2009
8-other
Pregabalin add-on therapy using a flexible, optimized dose schedule in refractory partial epilepsies: a double-blind, randomized, placebo-controlled, multicenter trial.
PMID 19222545·Epilepsia·2009
4-observational
Perturbation of hoxb5 signaling in vagal neural crests down-regulates ret leading to intestinal hypoganglionosis in mice.
PMID 18395091·Gastroenterology·2008
4-observational
SARRAH: provision of allied health services to regional and remote Aboriginal and Torres Strait Islander communities.
PMID 18808495·Aust J Rural Health·2008
8-other
Pregabalin for the treatment of generalized anxiety disorder: a novel pharmacologic intervention.
PMID 17610384·Expert Rev Neurother·2007
6-review
Evaluation of the thyroid transcription factor-1 gene (TITF1) as a Hirschsprung's disease locus.
PMID 17640327·Ann Hum Genet·2007
7-preclinical
Correlation between genetic variations in Hox clusters and Hirschsprung's disease.
PMID 17274802·Ann Hum Genet·2007
8-other
Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population.
PMID 17440194·Gut·2007
8-other
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
PMID 16254195·Clin Chem·2006
8-other
A characteristic pharmacological action of 'Yang-invigorating' Chinese tonifying herbs: enhancement of myocardial ATP-generation capacity.
PMID 16647252·Phytomedicine·2006
7-preclinical
Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease.
PMID 16040858·Clin Chem·2005
8-other
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease.
PMID 15548547·Hum Mol Genet·2005
8-other
Evaluation of individually tailored interventions on exercise adherence.
PMID 14528615·West J Nurs Res·2003
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1521 11TH AVE S
BIRMINGHAM, AL 35205 - Phone
- (205) 996-0741
Quick Facts
- NPI
- 1104480425
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 18
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