Back to Search
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)
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
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
Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.
PMID 17982369·Ear Hear·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
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
PMID 11850618·Nat Genet·2002
7-preclinical
Deafness due to degeneration of cochlear neurons in caspase-3-deficient mice.
PMID 11374883·Biochem Biophys Res Commun·2001
7-preclinical
A subunit of the mammalian oligosaccharyltransferase, DAD1, interacts with Mcl-1, one of the bcl-2 protein family.
PMID 10965038·J Biochem·2000
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
- 700 UNIVERSITY BLVD
GALVESTON, TX 77550 - Phone
- (409) 747-5800
Quick Facts
- NPI
- 1518980911
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 34
- Publications
- 13
Are you this provider?
Claim Your Profile