Back to Search
JOSHUA HERSH, M.D.
M.D.
Neurology Physician
NPI: 1457679987IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
251252-1(NY)25MA08822400(NJ)
CMS Specialties
PrimaryNEUROLOGY
Education
STATE UNIVERSITY OF NEW YORK DOWNSTATE MEDICAL CENTER
Class of 2005
Research & Publications (20)
Aggressive osteoblastoma: a case report involving a unique chromosomal aberration.
PMID 18611933·Int J Surg Pathol·2010
5-case
Improving colorectal cancer screening and care in the Veterans Affairs Healthcare system.
PMID 19203893·Clin Colorectal Cancer·2009
6-review
Fetal alcohol spectrum disorders (FASD): what medical professionals need to know.
PMID 19548521·J Ky Med Assoc·2009
5-case
Neurokinin 1 receptor antagonism as a possible therapy for alcoholism.
PMID 18276852·Science·2008
2-rct
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
PMID 18811697·Clin Genet·2008
5-case
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
PMID 18471269·Mol Cytogenet·2008
8-other
Pre-stem cell transplantation enzyme replacement therapy in Hurler syndrome does not lead to significant antibody formation or delayed recovery of the endogenous enzyme post-transplant: a case report.
PMID 17631030·Pediatr Transplant·2007
5-case
Intellectual abilities and adaptive behavior of children and adolescents with Kabuki syndrome: a preliminary study.
PMID 15523605·Am J Med Genet A·2005
8-other
Chromosome 20q deletion and progression to monosomy 7 in a patient with Shwachman-Diamond syndrome without MDS/AML.
PMID 12794535·J Pediatr Hematol Oncol·2003
5-case
Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
PMID 12522795·Am J Med Genet A·2003
5-case
Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
PMID 12210328·Am J Med Genet·2002
5-case
Developmental field defects: coming together of associations and sequences during blastogenesis.
PMID 12116204·Am J Med Genet·2002
5-case
Craniosynostosis, telecanthus, scalp hair abnormalities, and sensorineural deafness in two sibs.
PMID 11992488·Am J Med Genet·2002
8-other
Toriello-Carey syndrome: an additional case and summary of previously reported cases.
PMID 11310996·Clin Dysmorphol·2001
5-case
Fetal valproate syndrome and autism: additional evidence of an association.
PMID 11263692·Dev Med Child Neurol·2001
8-other
Case of partial duplication 2q3 with characteristic phenotype: rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion.
PMID 10748411·Am J Med Genet·2000
5-case
Mathematical analysis of the relative contributions of decreased production and increased peripheral destruction in idiopathic thrombocytopenic purpura and implications in splenectomy.
PMID 10704299·J Theor Biol·2000
4-observational
Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review.
PMID 10607952·Am J Med Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 51 VERONICA AVE
SOMERSET, NJ 08873 - Phone
- (732) 246-1311
Quick Facts
- NPI
- 1457679987
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 21
- Publications
- 20
Are you this provider?
Claim Your Profile