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ROBERT TAWIL, M.D.
M.D.
Specialist
NPI: 1669568143Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
59-2748330(FL)
Research & Publications (20)
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy.
PMID 19359275·Hum Mol Genet·2009
7-preclinical
Relation between extent of myostatin depletion and muscle growth in mature mice.
PMID 19654287·Am J Physiol Endocrinol Metab·2009
7-preclinical
Skeletal muscle gene expression after myostatin knockout in mature mice.
PMID 19509079·Physiol Genomics·2009
7-preclinical
Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers.
PMID 18281700·Nucleic Acids Res·2008
8-other
Sex-related differences in gene expression in human skeletal muscle.
PMID 18167544·PLoS One·2008
8-other
A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy.
PMID 18335515·Ann Neurol·2008
3-trial
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
PMID 17151338·Neurology·2007
8-other
An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients.
PMID 17658255·Neuromuscul Disord·2007
8-other
Management and treatment of Andersen-Tawil syndrome (ATS).
PMID 17395133·Neurotherapeutics·2007
6-review
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
PMID 17229919·Neurology·2007
8-other
Muscle growth after postdevelopmental myostatin gene knockout.
PMID 17148752·Am J Physiol Endocrinol Metab·2007
7-preclinical
The primary periodic paralyses: diagnosis, pathogenesis and treatment.
PMID 16195244·Brain·2006
6-review
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophy.
PMID 17130433·Neurology·2006
8-other
Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.
PMID 15835264·J Neuropathol Exp Neurol·2005
8-other
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.
PMID 15911703·Circulation·2005
8-other
Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis.
PMID 15852401·Ann Neurol·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3741 NEPTUNE STREET
TAMPA, FL 33629 - Phone
- (813) 254-4262
Quick Facts
- NPI
- 1669568143
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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