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FRANK GOODMAN, DO

DO

Family Medicine Physician

NPI: 1336641828IndividualAccepts Medicare

Specialties, Licenses & Credentials

Neuromusculoskeletal Medicine & OMM Physician

Neuromusculoskeletal Medicine & OMM

Code: 204D00000X

T8824(TX)
Family Medicine PhysicianPrimary

Family Medicine

Code: 207Q00000X

T8824(TX)

CMS Specialties

PrimaryFAMILY PRACTICE

Education

WILLIAM CAREY UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE

Class of 2018

Research & Publications (20)

Gabapentin in the treatment of mental illness: the echo chamber of the case series.
PMID 19034206·J Psychiatr Pract·2008
1-meta
Effectiveness of antiepileptic drugs for the treatment of bipolar disorder: findings from a systematic review.
PMID 19034205·J Psychiatr Pract·2008
1-meta
Best practices: comparing medication treatments in mental health: drug class reviews and policy challenges.
PMID 17535934·Psychiatr Serv·2007
8-other
Implementation of buprenorphine in the Veterans Health Administration: results of the first 3 years.
PMID 17493771·Drug Alcohol Depend·2007
8-other
Mild case of Curry-Jones syndrome.
PMID 16531740·Clin Dysmorphol·2006
5-case
Evaluating potentially aberrant outpatient prescriptions for extended-release oxycodone.
PMID 16333058·Am J Health Syst Pharm·2005
8-other
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus.
PMID 15662696·Prenat Diagn·2005
5-case
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second family.
PMID 15521984·Clin Genet·2004
5-case
Congenital abnormalities of body patterning: embryology revisited.
PMID 12944067·Lancet·2003
6-review
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome.
PMID 12919145·Clin Genet·2003
4-observational
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.
PMID 12807964·J Med Genet·2003
4-observational
An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function.
PMID 12620993·Development·2003
7-preclinical
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families.
PMID 12567410·Am J Med Genet A·2003
8-other
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.
PMID 12414828·J Med Genet·2002
5-case
The mutational spectrum of brachydactyly type C.
PMID 12357473·Am J Med Genet·2002
7-preclinical
Limb malformations and the human HOX genes.
PMID 12357469·Am J Med Genet·2002
6-review
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.
PMID 11968094·Hum Mutat·2002
8-other
A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.
PMID 11778160·Am J Hum Genet·2002
8-other
Efficacy of an amitraz-impregnated collar in preventing transmission of Borrelia burgdorferi by adult Ixodes scapularis to dogs.
PMID 11469572·J Am Vet Med Assoc·2001
7-preclinical
A novel acropectoral syndrome maps to chromosome 7q36.
PMID 11333865·J Med Genet·2001
5-case

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

Contact & Hours

Via practice · 3 locations total

Address
415 N AVENUE F
DENVER CITY, TX 79323

Locations (3)

Practice Location

415 N AVENUE F, DENVER CITY, TX
(806) 592-9501

Practice Location

412 MUSTANG AVENUE, DENVER CITY, TX
(806) 592-2121

Practice Location

100 S BLISS AVE, TAHLEQUAH, OK
(918) 458-3100

Quick Facts

NPI
1336641828
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
2
Locations
3
Years in Practice
8
Publications
20

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