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FLOYD GOODMAN, M.D.
M.D.
Obstetrics & Gynecology Physician
NPI: 1487626552Individual
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
23887(OK)
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
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
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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 CHOCTAW WAY
TALIHINA, OK 74571 - Phone
- (918) 567-7000
Quick Facts
- NPI
- 1487626552
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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