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TOMOKO MAKISHIMA, MD

MD

Otology & Neurotology Physician

NPI: 1518980911IndividualAccepts Medicare

Specialties, Licenses & Credentials

Otolaryngology Physician

Otolaryngology

Code: 207Y00000X

N1752(TX)
Otology & Neurotology PhysicianPrimary

Otolaryngology — Otology & Neurotology

Code: 207YX0901X

N1752(TX)

CMS Specialties

PrimaryOTOLARYNGOLOGY

Education

OTHER

Class of 1992

Research & Publications (13)

Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss.
PMID 18412859·Int J Dermatol·2008
5-case
Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.
PMID 17982369·Ear Hear·2007
8-other
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.
PMID 17877751·Clin Genet·2007
8-other
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
PMID 17567890·Am J Med Genet A·2007
8-other
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.
PMID 17250663·Clin Genet·2007
8-other
Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.
PMID 16648588·Genetics·2006
7-preclinical
Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.
PMID 16078052·Hum Genet·2005
7-preclinical
Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.
PMID 15354000·Otol Neurotol·2004
8-other
Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype.
PMID 15141750·Acta Otolaryngol·2004
7-preclinical
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
PMID 12107438·Hum Genet·2002
4-observational

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

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Contact & Hours

Address
700 UNIVERSITY BLVD
GALVESTON, TX 77550

Quick Facts

NPI
1518980911
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
2
Locations
1
Years in Practice
34
Publications
13

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