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KATHERINE MARIE BINKOWSKI HOLDEN DO
DO
Obstetrics & Gynecology Physician
NPI: 1770144198IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
5151013929(MI)
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
5101027628(MI)
Education
PHILADELPHIA COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2019
Research & Publications (20)
Synthesis of chiral pilocarpine analogues via a C-8 ketone intermediate.
PMID 12182622·J Org Chem·2002
8-other
Adherence and complementary and alternative medicine use among Honduran people with epilepsy.
PMID 19435580·Epilepsy Behav·2009
8-other
A questionnaire study of the approach to the anorexia-cachexia syndrome in patients with cancer by staff in a district general hospital.
PMID 18663481·Support Care Cancer·2009
8-other
Serum leptin level and cognition in the elderly: Findings from the Health ABC Study.
PMID 18358569·Neurobiol Aging·2009
8-other
Finding new etiologies of mental retardation and hypotonia: X marks the spot.
PMID 18190539·Dev Med Child Neurol·2008
6-review
The modified Atkins diet: a potential treatment for developing countries.
PMID 18782218·Epilepsia·2008
5-case
FIRST: a practical approach to the causes and management of febrile seizures.
PMID 19073858·J Child Neurol·2008
6-review
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
PMID 18660473·J Child Neurol·2008
5-case
Persistence of Borrelia burgdorferi following antibiotic treatment in mice.
PMID 18316520·Antimicrob Agents Chemother·2008
7-preclinical
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
PMID 18674751·Am J Hum Genet·2008
7-preclinical
Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
PMID 18184946·J Child Neurol·2008
5-case
A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
PMID 19073849·J Child Neurol·2008
8-other
Humour experience in schizophrenia: relationship with executive dysfunction and psychosocial impairment.
PMID 18177530·Psychol Med·2008
8-other
Audit of symptoms and prescribing in patients with the anorexia-cachexia syndrome.
PMID 18246443·Pharm World Sci·2008
8-other
Early onset alpha-mannosidosis with slow progression in three Hispanic males.
PMID 17979865·Dev Med Child Neurol·2007
5-case
Developing a neurology training program in Honduras: a joint project of neurologists in Honduras and the World Federation of Neurology.
PMID 17188302·J Neurol Sci·2007
8-other
Expansion of the deletion 13q syndrome phenotype: a case report.
PMID 17890413·J Child Neurol·2007
5-case
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: exploration of the 1-position.
PMID 17904842·Bioorg Med Chem Lett·2007
8-other
Are there predictors of outcome in depressed elderly nursing home residents during treatment with mirtazapine orally disintegrating tablets?
PMID 17447229·Int J Geriatr Psychiatry·2007
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 601 JOHN ST STE N1200
KALAMAZOO, MI 49007 - Phone
- (269) 341-7979
Quick Facts
- NPI
- 1770144198
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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