Back to Search

JOSE BAL, M.D.

M.D.

Family Medicine Physician

NPI: 1407833288Individual

Specialties, Licenses & Credentials

Family Medicine PhysicianPrimary

Family Medicine

Code: 207Q00000X

210281(NY)

Research & Publications (20)

Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease.
PMID 19628420·Parkinsonism Relat Disord·2010
8-other
A family with paroxysmal nonkinesigenic dyskinesia: genetic and treatment issues.
PMID 19589464·Pediatr Neurol·2009
5-case
[The role of selected molecular pathways in the pathogenesis of ovarian teratomas].
PMID 19502685·Postepy Hig Med Dosw (Online)·2009
6-review
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.
PMID 18985073·Eur J Hum Genet·2009
8-other
Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) family.
PMID 19012350·Am J Med Genet A·2008
5-case
A circularly permuted beta-lactamase as a novel reporter for evaluation of protein cyclization efficiency.
PMID 18758738·J Microbiol·2008
8-other
[Search for the etiopathogenesis of polycystic ovary syndrome (PCOS)].
PMID 18050612·Ginekol Pol·2007
6-review
Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystonia.
PMID 17539945·Eur J Neurol·2007
8-other
Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation.
PMID 17082467·Neurology·2006
8-other
Analysis of CFTR, SPINK1, PRSS1 and AAT mutations in children with acute or chronic pancreatitis.
PMID 16954950·J Pediatr Gastroenterol Nutr·2006
8-other
Passive transfer of maternal antibodies and their existence in eggs, larvae and fry of Indian major carp, Labeo rohita (Ham.).
PMID 16157486·Fish Shellfish Immunol·2006
4-observational
Molecular analysis of defects in the CFTR gene and AZF locus of the Y chromosome in male infertility.
PMID 16572913·J Reprod Med·2006
8-other
The ARX mutations: a frequent cause of X-linked mental retardation.
PMID 16523516·Am J Med Genet A·2006
8-other
GJB2 mutations and degree of hearing loss: a multicenter study.
PMID 16380907·Am J Hum Genet·2005
4-observational
[Genetic polymorphism and outcome in acute lymphoblastic leukaemia of childhood].
PMID 16786762·Przegl Lek·2005
6-review
Standardized protocol improves asthma management in emergency department.
PMID 15046374·J Asthma·2004
8-other
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign.
PMID 14685937·Am J Hum Genet·2004
8-other
Prolongation of QTc interval: relationship with etiology and severity of liver disease, mortality and liver transplantation.
PMID 12895263·Liver Int·2003
8-other
TIPS for management of refractory ascites: response and survival are both unpredictable.
PMID 12757168·Dig Dis Sci·2003
4-observational
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
PMID 11857751·Hum Mutat·2002
8-other

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

Contact & Hours

Address
STEPHENSON AVE, BUILDING 1075
FORT MONMOUTH, NJ 07703

Location

Practice Location

STEPHENSON AVE, FORT MONMOUTH, NJ
(732) 532-1244

Quick Facts

NPI
1407833288
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

Are you this provider?

Claim Your Profile