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HOWARD KREMER, M.D.
M.D.
Surgery Physician
NPI: 1801858386IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
R1F67(MO)
CMS Specialties
PrimaryGENERAL SURGERY
Education
UNIVERSITY OF MISSOURI, KANSAS CITY, SCHOOL OF MEDICINE
Class of 1984
Research & Publications (20)
CSF studies facilitate DNA diagnosis in familial Alzheimer's disease due to a presenilin-1 mutation.
PMID 19494431·J Alzheimers Dis·2009
5-case
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.
PMID 19628817·Science·2009
8-other
Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1.
PMID 19548389·Ann Otol Rhinol Laryngol·2009
8-other
HIV or HIV-therapy? Causal attributions of symptoms and their impact on treatment decisions among women and men with HIV.
PMID 19380286·Eur J Med Res·2009
4-observational
The fork in the road: HIV as a potential positive turning point and the role of spirituality.
PMID 19280412·AIDS Care·2009
8-other
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3.
PMID 19372648·Audiol Neurootol·2009
8-other
Postural instability in cerebellar ataxia: correlations of knee, arm and trunk movements to center of mass velocity.
PMID 19136042·Neuroscience·2009
8-other
Spiritual and mind-body beliefs as barriers and motivators to HIV-treatment decision-making and medication adherence? A qualitative study.
PMID 19133751·AIDS Patient Care STDS·2009
8-other
Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.
PMID 19462854·Ann Otol Rhinol Laryngol·2009
8-other
GRM7 variants confer susceptibility to age-related hearing impairment.
PMID 19047183·Hum Mol Genet·2009
7-preclinical
Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear.
PMID 19005249·Audiol Neurootol·2009
8-other
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.
PMID 18826961·Hum Mol Genet·2009
7-preclinical
[Diagnostic and treatment of HIV-affected couples who wish to have children].
PMID 19172553·Dtsch Med Wochenschr·2009
6-review
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Density, refractive index, interfacial tension, and viscosity of ionic liquids [EMIM][EtSO4], [EMIM][NTf2], [EMIM][N(CN)2], and [OMA][NTf2] in dependence on temperature at atmospheric pressure.
PMID 18767789·J Phys Chem B·2008
8-other
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.
PMID 18760390·Am J Hum Genet·2008
8-other
Diagnostics and treatment of HIV-affected couples who wish to have children.
PMID 19073393·Eur J Med Res·2008
8-other
Prevention of exercise-induced asthma by a fixed combination of disodium cromoglycate plus reproterol compared with montelukast in young patients.
PMID 18677973·Arzneimittelforschung·2008
2-rct
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2301 HOLMES ST
KANSAS CITY, MO 64108 - Phone
- (816) 404-0099
Quick Facts
- NPI
- 1801858386
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 42
- Publications
- 20
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