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ANTHONY BALSAMO, MD

MD

Orthopaedic Surgery Physician

NPI: 1104812239IndividualAccepts Medicare

Specialties, Licenses & Credentials

Orthopaedic Surgery PhysicianPrimary

Orthopaedic Surgery

Code: 207X00000X

MD036494L(PA)

CMS Specialties

PrimaryORTHOPEDIC SURGERY

Education

MEDICAL COLLEGE OF PENNSYLVANIA

Class of 1974

Research & Publications (20)

New emerging prospects in the pharmacotherapy of hypertension.
PMID 18220718·Cardiovasc Hematol Agents Med Chem·2008
6-review
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1.
PMID 17287415·Eur J Endocrinol·2007
8-other
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes.
PMID 16520942·Eur J Pediatr·2006
8-other
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
PMID 15884018·Am J Med Genet A·2005
5-case
Synthesis of heteroaromatic analogues of (2-aryl-1-cyclopentenyl-1-alkylidene)-(arylmethyloxy)amine COX-2 inhibitors: effects on the inhibitory activity of the replacement of the cyclopentene central core with pyrazole, thiophene or isoxazole ring.
PMID 12620660·Eur J Med Chem·2003
7-preclinical
Synthesis and prostaglandin synthase inhibitory activity of new aromatic O-alkyloxime ethers substituted with methylsulfonamido or methylsulfonyl groups on their aliphatic portion.
PMID 13679164·Farmaco·2003
4-observational
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency.
PMID 14671153·J Clin Endocrinol Metab·2003
8-other
(E)-[2-(4-Methylsulphonylphenyl)-1-cyclopentenyl-1-methyliden](arylmethyloxy)amines. Methyleneaminoxymethyl (MAOM) analogues of diarylcyclopentenyl cyclooxygenase-2 inhibitors: synthesis and biological properties.
PMID 12008053·Eur J Med Chem·2002
7-preclinical
Aryl-substituted methyleneaminoxymethyl (MAOM) analogues of diarylcyclopentenyl cyclooxygenase-2 inhibitors: effects of some structural modifications on their biological properties.
PMID 12126777·Eur J Med Chem·2002
7-preclinical
Conformationally restrained analogues of sympathomimetic catecholamines. Synthesis and adrenergic activity of 5,6- and 6,7-dihydroxy-3,4-dihydrospiro[naphthalen-1(2H)-2',5'-morpholines].
PMID 11841871·Eur J Med Chem·2002
7-preclinical

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

Contact & Hours

Address
1175 E MOUNTAIN BLVD
WILKES BARRE, PA 18702

Quick Facts

NPI
1104812239
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
52
Publications
20

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