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Update citations for papers by Abe, S (Satoko)


Title New Now Web Updated Status
Parotid Gland Metastasis of Breast Cancer: Case Report and Review of the Literature.
 0 0 0000-00-00
Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study.
 0 0 0000-00-00
Early Results of an Endoscopic Nipple-Sparing Mastectomy for Breast Cancer.
 1 3 2011-10-18
False-negative ultrasound-guided vacuum-assisted biopsy of the breast: difference with US-detected and MRI-detected lesions.
 2 3 2011-10-11
Preoperative MRI marking technique for the planning of breast-conserving surgery.
 1 1 2010-12-15
MR-guided vacuum-assisted breast biopsy: is it an essential technique?
 1 4 2010-10-19
Monitoring of early response to neoadjuvant chemotherapy in breast cancer with (1)H MR spectroscopy: Comparison to sequential 2-[18F]-fluorodeoxyglucose positron emission tomography.
 7 17 2011-07-21
The responsible genes in Japanese deafness patients and clinical application using Invader assay.
 8 15 2011-10-29
Bilateral breast MR imaging: is it superior to conventional methods for the detection of contralateral breast cancer?
 4 8 2011-11-20
New preoperative MRI marking technique for a patient with ductal carcinoma in situ.
 1 2 2010-09-28
Categorization of non-mass-like breast lesions detected by MRI.
 4 4 2010-05-15
Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay.
 9 14 2011-11-03
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations.
 5 12 2011-06-16
Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
 10 12 2011-06-06
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.
 3 7 2010-10-02
Type IX collagen knock-out mouse shows progressive hearing loss.
 7 15 2009-10-29
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.
 13 0 2010-01-06
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.
 0 0 2011-08-12
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss.
 9 11 2011-03-16
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
 22 1 2012-01-24
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.
 37 71 2011-10-10
Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification.
 5 8 2011-09-07
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
 47 80 2010-12-06
Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.
 36 59 2011-11-12
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
 6 16 2010-12-10
Molecular diagnosis of deafness: impact of gene identification.
 6 1 2012-02-19
[A case of enlarged vestibular aqueduct syndrome with PDS gene mutations]
 0 0 2012-01-16
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