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JULIUS GOROSPE, M.D.
M.D.
Family Medicine Physician
NPI: 1215999842IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
ME77263(FL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1992
Research & Publications (15)
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant.
PMID 19444543·J Neurol·2009
5-case
Host and habitat preferences of polypore fungi in Micronesian tropical flooded forests.
PMID 18495449·Mycol Res·2008
4-observational
Genetic and clinical heterogeneity in eIF2B-related disorder.
PMID 18263758·J Child Neurol·2008
8-other
Randomized trial to improve fracture prevention in nursing home residents.
PMID 17904460·Am J Med·2007
4-observational
Prevalence and predictors of osteoporosis treatment in nursing home residents with known osteoporosis or recent fracture.
PMID 17120179·Osteoporos Int·2007
8-other
Decreased platelet expression of myosin regulatory light chain polypeptide (MYL9) and other genes with platelet dysfunction and CBFA2/RUNX1 mutation: insights from platelet expression profiling.
PMID 17059412·J Thromb Haemost·2007
4-observational
Translating evidence-based falls prevention into clinical practice in nursing facilities: Results and lessons from a quality improvement collaborative.
PMID 16970651·J Am Geriatr Soc·2006
8-other
Alexander disease and megalencephalic leukoencephalopathy with subcortical cysts: leukodystrophies arising from astrocyte dysfunction.
PMID 16807904·Ment Retard Dev Disabil Res Rev·2006
6-review
Propensity for paternal inheritance of de novo mutations in Alexander disease.
PMID 16365765·Hum Genet·2006
8-other
DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.
PMID 15952989·Clin Genet·2005
8-other
Definition of the unique human extraocular muscle allotype by expression profiling.
PMID 15855387·Physiol Genomics·2005
8-other
Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation.
PMID 15037685·Neurology·2004
8-other
Megalencephalic leukoencephalopathy with subcortical cysts.
PMID 14572144·J Child Neurol·2003
6-review
Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.
PMID 12034785·Neurology·2002
8-other
Expression profiling reveals metabolic and structural components of extraocular muscles.
PMID 12006673·Physiol Genomics·2002
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7751 BAYMEADOWS RD E STE H
JACKSONVILLE, FL 32256 - Phone
- (904) 425-6963
Quick Facts
- NPI
- 1215999842
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 34
- Publications
- 15
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