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BRYAN ZOLL, MD, MBA

MD, MBA

Gastroenterology Physician

NPI: 1437619350IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine Physician

Internal Medicine

Code: 207R00000X

292423(MA)
Gastroenterology PhysicianPrimary

Internal Medicine — Gastroenterology

Code: 207RG0100X

1015406(MA)

CMS Specialties

PrimaryGASTROENTEROLOGY

Education

TEMPLE UNIVERSITY SCHOOL OF MEDICINE

Class of 2019

Research & Publications (20)

Fetal alcohol syndrome in association with Rett syndrome.
PMID 15287421·Genet Couns·2004
5-case
First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter --> q22.1::q22.1 --> pter) is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q- syndrome.
PMID 15103719·Am J Med Genet A·2004
5-case
Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.
PMID 12497637·Hum Mutat·2003
8-other
Modulation of cell surface markers on NK-like T lymphocytes by using IL-2, IL-7 or IL-12 in vitro stimulation.
PMID 10975999·Cytokine·2000
8-other
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.
PMID 19284615·Mol Cytogenet·2009
8-other
Impairment of gastric acid secretion and increase of embryonic lethality in Foxq1-deficient mice.
PMID 18544931·Cytogenet Genome Res·2008
7-preclinical
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay.
PMID 17431920·Am J Med Genet A·2007
8-other
Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.
PMID 16506277·Prenat Diagn·2006
5-case
Manifestations of hereditary hemorrhagic telangiectasia in children and adolescents.
PMID 15976991·Eur Arch Otorhinolaryngol·2006
8-other
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
PMID 16007665·Am J Med Genet A·2005
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

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Contact & Hours

Via practice · 2 locations total

Address
330 BROOKLINE AVE
BOSTON, MA 02215

Locations (2)

Practice Location

330 BROOKLINE AVE, BOSTON, MA
(610) 999-2757

Practice Location

3400 Spruce St, Philadelphia, PA
(610) 999-2757

Quick Facts

NPI
1437619350
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
2
Locations
2
Years in Practice
7
Publications
20

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