Found: 40
Select item for more details and to access through your institution.
Nutritional quality and patterns of lunch menus at child care centers in South Korea and Japan.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Comparison of the nutrient-based standards for school lunches among South Korea, Japan, and Taiwan.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Clinical features of patients withGJB2(connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 2, p. 76, doi. 10.1007/s10038-004-0223-7
- By:
- Publication type:
- Article
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.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 564, doi. 10.1007/s10038-003-0079-2
- By:
- Publication type:
- Article
Rapid mass screening method and counseling for the 1555A⇾G mitochondrial mutation.
- Published in:
- Journal of Human Genetics, 1999, v. 44, n. 5, p. 304, doi. 10.1007/s100380050165
- By:
- Publication type:
- Article
EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family.
- Published in:
- Journal of Human Genetics, 1999, v. 44, n. 4, p. 261, doi. 10.1007/s100380050156
- By:
- Publication type:
- Article
Early Results of an Endoscopic Nipple-Sparing Mastectomy for Breast Cancer.
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2009, v. 16, n. 12, p. 3406, doi. 10.1245/s10434-009-0661-8
- By:
- Publication type:
- Article
Molecular diagnosis of deafness: impact of gene identification.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Relationship Between Performance Improvement in Activities of Daily Living and Energy Intake in Older Patients With Hip Fracture Undergoing Rehabilitation.
- Published in:
- Annals of Rehabilitation Medicine, 2019, v. 43, n. 5, p. 562, doi. 10.5535/arm.2019.43.5.562
- By:
- Publication type:
- Article
Comprehensive Genetic Screening of <i>KCNQ4</i> in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063231
- By:
- Publication type:
- Article
Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031276
- By:
- Publication type:
- Article
Monitoring of early response to neoadjuvant chemotherapy in breast cancer with <sup>1</sup>H MR spectroscopy: Comparison to sequential 2-[18F]-fluorodeoxyglucose positron emission tomography.
- Published in:
- Journal of Magnetic Resonance Imaging, 2008, v. 28, n. 2, p. 420, doi. 10.1002/jmri.21454
- By:
- Publication type:
- Article
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
- Published in:
- Human Genetics, 2003, v. 112, n. 4, p. 329, doi. 10.1007/s00439-002-0889-x
- By:
- Publication type:
- Article
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.
- Published in:
- 2004
- By:
- Publication type:
- Correction Notice
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.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 12, p. 916, doi. 10.1038/sj.ejhg.5201073
- By:
- Publication type:
- Article
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 744, doi. 10.1038/sj.ejhg.5201043
- By:
- Publication type:
- Article
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
- Published in:
- European Journal of Human Genetics, 1998, v. 6, n. 6, p. 563, doi. 10.1038/sj.ejhg.5200239
- By:
- Publication type:
- Article
Quantification of HPV16 E7 Oncoproteins in Urine Specimens from Women with Cervical Intraepithelial Neoplasia.
- Published in:
- Microorganisms, 2024, v. 12, n. 6, p. 1205, doi. 10.3390/microorganisms12061205
- By:
- Publication type:
- Article
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63690-5
- By:
- Publication type:
- Article
Prevalence and clinical features of hearing loss caused by EYA4 variants.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60259-0
- By:
- Publication type:
- Article
Detection of human papillomavirus infection in oral squamous cell carcinoma: a cohort study of Japanese patients.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Parotid Gland Metastasis of Breast Cancer: Case Report and Review of the Literature.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Diagnostic pitfalls for GJB2‐related hearing loss: A novel deletion detected by Array‐CGH analysis in a Japanese patient with congenital profound hearing loss.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A-->G mitochondrial mutation.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Isepamicin sulfate-induced sensorineural hearing loss in patients with the 1555 A-->G mitochondrial mutation.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Comparison of the nutrient-based standards for school lunches among South Korea, Japan, and Taiwan.
- Published in:
- Asia Pacific Journal of Clinical Nutrition, 2017, v. 26, n. 1, p. 160, doi. 10.6133/apjcn.102015.16
- By:
- Publication type:
- Article
Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-onset Progressive Hearing Loss.
- Published in:
- Genes, 2020, v. 11, n. 3, p. 273, doi. 10.3390/genes11030273
- By:
- Publication type:
- Article
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss.
- Published in:
- Genes, 2019, v. 10, n. 10, p. 744, doi. 10.3390/genes10100744
- By:
- Publication type:
- Article
Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort.
- Published in:
- Genes, 2019, v. 10, n. 10, p. 735, doi. 10.3390/genes10100735
- By:
- Publication type:
- Article
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss.
- Published in:
- Genes, 2019, v. 10, n. 9, p. 715, doi. 10.3390/genes10090715
- By:
- Publication type:
- Article
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients.
- Published in:
- PLoS ONE, 2019, v. 14, n. 5, p. 1, doi. 10.1371/journal.pone.0215932
- By:
- Publication type:
- Article
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
- Published in:
- Human Mutation, 2002, v. 20, n. 1, p. 15, doi. 10.1002/humu.10096
- By:
- Publication type:
- Article
False-negative ultrasound-guided vacuum-assisted biopsy of the breast: difference with US-detected and MRI-detected lesions.
- Published in:
- Breast Cancer (13406868), 2010, v. 17, n. 2, p. 110, doi. 10.1007/s12282-009-0112-1
- By:
- Publication type:
- Article
Preoperative MRI marking technique for the planning of breast-conserving surgery.
- Published in:
- Breast Cancer (13406868), 2009, v. 16, n. 3, p. 223, doi. 10.1007/s12282-008-0088-2
- By:
- Publication type:
- Article
MR-guided vacuum-assisted breast biopsy: is it an essential technique?
- Published in:
- Breast Cancer (13406868), 2009, v. 16, n. 2, p. 121, doi. 10.1007/s12282-008-0074-8
- By:
- Publication type:
- Article
New preoperative MRI marking technique for a patient with ductal carcinoma in situ.
- Published in:
- Breast Cancer (13406868), 2008, v. 15, n. 4, p. 309, doi. 10.1007/s12282-008-0039-y
- By:
- Publication type:
- Article
Categorization of non-mass-like breast lesions detected by MRI.
- Published in:
- Breast Cancer (13406868), 2008, v. 15, n. 3, p. 241, doi. 10.1007/s12282-007-0028-6
- By:
- Publication type:
- Article
Bilateral breast MR imaging: is it superior to conventional methods for the detection of contralateral breast cancer?
- Published in:
- Breast Cancer (13406868), 2008, v. 15, n. 2, p. 169, doi. 10.1007/s12282-007-0025-9
- By:
- Publication type:
- Article
Genetic and Clinical Features of Sensorineural Hearing Loss Associated With the 1555 Mitochondrial Mutation.
- Published in:
- Laryngoscope, 1997, v. 107, n. 4, p. 483, doi. 10.1097/00005537-199704000-00011
- By:
- Publication type:
- Article
OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-95
- By:
- Publication type:
- Article