Dr. Jonathan Chad Levy M.D.
Doctor
5597 N Dixie Hwy Fort Lauderdale FL, 33334About
Dr. Jonathan Chad Levy M.D. is a top Doctor in Tampa, FL. With a passion for the field and an unwavering commitment to their specialty, Dr. Jonathan Chad Levy M.D. is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Dr. Jonathan Chad Levy M.D. is a prime example of a true leader in health care. As a leader and expert in their field, Dr. Jonathan Chad Levy M.D. is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In Tampa, FL, Dr. Jonathan Chad Levy M.D. is a true asset to their field and dedicated to the profession of medicine.
Education and Training
Northwestern University The Feinberg School of Medicine 2000
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes.
- The gene INPPL1, encoding the lipid phosphatase SHIP2, is a candidate for type 2 diabetes in rat and man.
- Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.
- Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility.
- Young-onset type 2 diabetes families are the major contributors to genetic loci in the Diabetes UK Warren 2 genome scan and identify putative novel loci on chromosomes 8q21, 21q22, and 22q11.
- Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility.
- Evidence from a large U.K. family collection that genes influencing age of onset of type 2 diabetes map to chromosome 12p and to the MODY3/NIDDM2 locus on 12q24.
- Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome.
- Association studies of insulin receptor substrate 1 gene (IRS1) variants in type 2 diabetes samples enriched for family history and early age of onset.
- Islet amyloid polypeptide gene promoter polymorphisms are not associated with Type 2 diabetes or with the severity of islet amyloidosis.
- Significant linkage of BMI to chromosome 10p in the U.K. population and evaluation of GAD2 as a positional candidate.
- The variable number of tandem repeats upstream of the insulin gene is a susceptibility locus for latent autoimmune diabetes in adults.
- The reverse shoulder prosthesis for glenohumeral arthritis associated with severe rotator cuff deficiency. a minimum two-year follow-up study of sixty patients surgical technique.
- Asymptomatic chronic radial head dislocation after traumatic dislocation.
- Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes.
Treatments
- Arthritis
- Osteoarthritis
- Frozen Shoulder
- Rotator Cuff Syndrome
- Pain
- Rotator Cuff Tear
- Tennis Elbow
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