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STEPHEN ROBB, M.D.
M.D.
Family Medicine Physician
NPI: 1245269661Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
185365(NY)
Research & Publications (20)
A review of music-based intervention reporting in pediatrics.
PMID 19383649·J Health Psychol·2009
6-review
Perinatal dyskinesia as a presenting feature in Prader Willi syndrome.
PMID 18722147·Eur J Paediatr Neurol·2009
8-other
A reader responds to "Passive dissemination of printed educational materials in medicine has no or negligible effect on patient outcomes".
PMID 19295928·Medscape J Med·2009
8-other
Management of cardiac health in trastuzumab-treated patients with breast cancer: updated United Kingdom National Cancer Research Institute recommendations for monitoring.
PMID 19259090·Br J Cancer·2009
6-review
Michael-type addition reactions in NIPAAm-cysteamine copolymers follow second order rate laws with steric hindrance.
PMID 19669882·Ann Biomed Eng·2009
8-other
The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy.
PMID 19272779·Neuromuscul Disord·2009
8-other
A non-randomized [corrected] controlled trial of the active music engagement (AME) intervention on children with cancer.
PMID 18033724·Psychooncology·2008
4-observational
Spinal stability is improved by inducing a lumbar lordosis in boys with Duchenne Muscular Dystrophy: a pilot study.
PMID 18096390·Gait Posture·2008
8-other
Brain involvement in muscular dystrophies with defective dystroglycan glycosylation.
PMID 19067344·Ann Neurol·2008
8-other
Congenital myasthenic syndromes in childhood: diagnostic and management challenges.
PMID 18707767·J Neuroimmunol·2008
8-other
MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes.
PMID 18025269·Genome Res·2008
7-preclinical
SmedGD: the Schmidtea mediterranea genome database.
PMID 17881371·Nucleic Acids Res·2008
7-preclinical
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.
PMID 17376685·Neuromuscul Disord·2007
5-case
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.
PMID 17483490·Brain·2007
8-other
Simultaneously physically and chemically gelling polymer system utilizing a poly(NIPAAm-co-cysteamine)-based copolymer.
PMID 17567067·Biomacromolecules·2007
8-other
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan.
PMID 17878207·Brain·2007
4-observational
Muscular dystrophies due to defective glycosylation of dystroglycan.
PMID 18646561·Acta Myol·2007
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 630 BAY RD
WEBSTER, NY 14580 - Phone
- (585) 671-1110
Quick Facts
- NPI
- 1245269661
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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