Back to Search
DR. PHILIP ANDREW ROTHBERG MD, MPH&TM
MD, MPH&TM
Surgery Physician
NPI: 1093077307IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
0101254601(VA)ME148056(FL)
Education
TULANE UNIVERSITY SCHOOL OF MEDICINE
Class of 2012
Research & Publications (20)
Laboratory practice guidelines for detecting and reporting BCR-ABL drug resistance mutations in chronic myelogenous leukemia and acute lymphoblastic leukemia: a report of the Association for Molecular Pathology.
PMID 19095773·J Mol Diagn·2009
6-review
Phase II study of a TLR-9 agonist (1018 ISS) with rituximab in patients with relapsed or refractory follicular lymphoma.
PMID 19519691·Br J Haematol·2009
3-trial
Rapid method for detection of mutations in the nucleophosmin gene in acute myeloid leukemia.
PMID 18556765·J Mol Diagn·2008
8-other
Detection of clonality in lymphoproliferations using PCR of the antigen receptor genes: does size matter?
PMID 17588658·Leuk Res·2008
5-case
Mixed chimerism in SCT: conflict or peaceful coexistence?
PMID 18660844·Bone Marrow Transplant·2008
6-review
A 46 XY phenotypic female adolescent with bilateral gonadal tumors consisting of five different components.
PMID 18580319·Int J Gynecol Pathol·2008
5-case
A case of JAK2 positive essential thrombocythemia 16.5 years after autologous marrow transplantation for AML.
PMID 17401398·Bone Marrow Transplant·2007
5-case
Is there an association between ocular adnexal lymphoma and infection with Chlamydia psittaci? The University of Rochester experience.
PMID 16246419·Leuk Res·2006
8-other
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosis.
PMID 16542512·Dev Med Child Neurol·2006
8-other
Homogeneous PCR nucleobase quenching assays to detect four mutations that cause neuronal ceroid lipofuscinosis: T75P and R151X in CLN1, and IVS5-1G>C and R208X in CLN2.
PMID 16720047·J Neurosci Methods·2006
4-observational
A clinical rating scale for Batten disease: reliable and relevant for clinical trials.
PMID 16043799·Neurology·2005
8-other
Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.
PMID 15728308·Neurology·2005
4-observational
Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
PMID 15818814·Hum Genet·2005
8-other
Homogeneous amplification nucleobase quenching assay to detect the E474Q LCHAD deficiency mutation.
PMID 15857179·Genet Test·2005
8-other
Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
PMID 15991331·Hum Genet·2005
8-other
Re: Prognostic significance of a short sequence insertion in the MCL-1 promoter in chronic lymphocytic leukemia.
PMID 16030309·J Natl Cancer Inst·2005
8-other
Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotype.
PMID 16087292·Neurosci Lett·2005
8-other
Sequence diversity in the glycoprotein B gene complicates real-time PCR assays for detection and quantification of cytomegalovirus.
PMID 16207949·J Clin Microbiol·2005
8-other
Liver transplantation for type 1 primary hyperoxaluria as a cure for combined thrombophilia.
PMID 15543348·Thromb Haemost·2004
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 2 SHIRCLIFF WAY STE 500
JACKSONVILLE, FL 32204 - Phone
- (904) 389-8861
Quick Facts
- NPI
- 1093077307
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 14
- Publications
- 20
Are you this provider?
Claim Your Profile