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The role of SLC26A4 in bony labyrinth development and otoconial mineralization in mouse models.
- Published in:
- Frontiers in Molecular Neuroscience, 2024, p. 01, doi. 10.3389/fnmol.2024.1384764
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- Publication type:
- Article
Rapid screening of copy number variations in STRC by droplet digital PCR in patients with mild-to-moderate hearing loss.
- Published in:
- Human Genome Variation, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41439-019-0075-5
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- Publication type:
- Article
Relationship between cardiac calcification and left ventricular hypertrophy in patients with chronic kidney disease at hemodialysis initiation.
- Published in:
- Heart & Vessels, 2017, v. 32, n. 9, p. 1109, doi. 10.1007/s00380-017-0969-4
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- Publication type:
- Article
Otological complications associated with hyperbaric oxygen therapy.
- Published in:
- European Archives of Oto-Rhino-Laryngology, 2016, v. 273, n. 9, p. 2487, doi. 10.1007/s00405-015-3845-9
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- Publication type:
- Article
Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2045, doi. 10.1093/hmg/ddw078
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- Publication type:
- Article
A suspected case of plasma cell-rich acute renal transplant rejection associated with de novo donor-specific antibody.
- Published in:
- Nephrology, 2015, v. 20, p. 66, doi. 10.1111/nep.12471
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- Publication type:
- Article
Pleomorphic adenoma presenting with conductive hearing loss in the ear canal: a case report and review of the literature.
- Published in:
- 2014
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- Publication type:
- Case Study
A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 83, doi. 10.1111/ahg.12053
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- Publication type:
- Article
Pleomorphic adenoma presenting with conductive hearing loss in the ear canal: a case report and review of the literature.
- Published in:
- 2014
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- Publication type:
- journal article
Association between AST-120 and abdominal aortic calcification in predialysis patients with chronic kidney disease.
- Published in:
- Clinical & Experimental Nephrology, 2013, v. 17, n. 3, p. 365, doi. 10.1007/s10157-012-0717-0
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- Publication type:
- Article
Estimation of Tsunami-Inundated Areas in Asahi City, Chiba Prefecture, after the 2011 Tohoku-Oki Earthquake.
- Published in:
- Earthquake Spectra, 2013, v. 29, p. 201, doi. 10.1193/1.4000123
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- Publication type:
- Article
Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 772, doi. 10.1038/jhg.2012.109
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- Publication type:
- Article
Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 3, p. 147, doi. 10.1038/jhg.2009.143
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- Publication type:
- Article
Additional heterozygous 2507A>C mutation of WFS1 in progressive hearing loss at lower frequencies.
- Published in:
- Laryngoscope, 2010, v. 120, n. 1, p. 166, doi. 10.1002/lary.20691
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- Publication type:
- Article
Vestibular evoked myogenic potentials in patients with the mitochondrial A1555G mutation.
- Published in:
- Laryngoscope, 2009, v. 119, n. 9, p. 1874, doi. 10.1002/lary.20584
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- Publication type:
- Article
A case of acute rejection with adenovirus infection after ABO-incompatible kidney transplantation.
- Published in:
- Clinical Transplantation, 2009, v. 23, p. 27, doi. 10.1111/j.1399-0012.2009.01005.x
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- Publication type:
- Article
Partial stripping of Ag atoms from silver bilayer on a Au(111) surface accompanied with the reductive desorption of hexanethiol SAM.
- Published in:
- Journal of Solid State Electrochemistry, 2009, v. 13, n. 7, p. 1141, doi. 10.1007/s10008-008-0764-3
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- Publication type:
- Article
Insidious transmission of membranous nephropathy from kidney donor with no clinical manifestations before and after transplantation.
- Published in:
- Clinical Transplantation, 2008, v. 22, p. 76, doi. 10.1111/j.1399-0012.2008.00855.x
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- Publication type:
- Article
A familial case of mitochondrial disease resembling Alport syndrome.
- Published in:
- Clinical & Experimental Nephrology, 2008, v. 12, n. 2, p. 159, doi. 10.1007/s10157-007-0022-5
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- Publication type:
- Article
Vlgr1 is required for proper stereocilia maturation of cochlear hair cells.
- Published in:
- Genes to Cells, 2007, v. 12, n. 2, p. 235, doi. 10.1111/j.1365-2443.2007.01046.x
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- Publication type:
- Article
R037: Survey of Acute Low-Tone Sensorineural Hearing Loss in Japan
- Published in:
- 2006
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- Publication type:
- Abstract
R037: Survey of Acute Low‐Tone Sensorineural Hearing Loss in Japan.
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Multiple Quantitative Trait Loci Modify Cochlear Hair Cell Degeneration in the Beethoven (Tmc1<sup>Bth</sup>) Mouse Model of Progressive Hearing Loss DFNAS6.
- Published in:
- Genetics, 2006, v. 173, n. 4, p. 2111, doi. 10.1534/genetics.106.057372
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- Publication type:
- Article
SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Butyrate blocks interferon-γ-inducible protein-10 release in human intestinal subepithelial myofibroblasts.
- Published in:
- Journal of Gastroenterology, 2005, v. 40, n. 5, p. 483, doi. 10.1007/s00535-005-1573-4
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- Publication type:
- Article
Suppression of interleukin-1ß- and tumor necrosis factor-·-induced inflammatory responses by leukocytapheresis therapy in patients with ulcerative colitis.
- Published in:
- Journal of Gastroenterology, 2004, v. 39, n. 12, p. 1150, doi. 10.1007/s00535-004-1464-0
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- Publication type:
- Article
A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 5, p. 256, doi. 10.1007/s10038-004-0142-7
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- Publication type:
- Article
COMPARISON OF ACUTE LOW-TONE SENSORINEURAL HEARING LOSS VERSUS MENIERE'S DISEASE BY ELECTROCOCHLEOGRAPHY.
- Published in:
- Annals of Otology, Rhinology & Laryngology, 2004, v. 113, n. 3, p. 194, doi. 10.1177/000348940411300304
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- Publication type:
- Article
Audiovestibular Findings in Patients with Mitochondrial A1555G Mutation.
- Published in:
- Laryngoscope, 2004, v. 114, n. 2, p. 344
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- Publication type:
- Article
Late laryngo-tracheal cartilage necrosis with external fistula 44 years after radiotherapy.
- Published in:
- Journal of Laryngology & Otology, 2003, v. 117, n. 8, p. 658
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- Publication type:
- Article
Temporal Bone Histopathological and Quantitative Analysis of Mitochondrial DNA in MELAS.
- Published in:
- Laryngoscope, 2003, v. 113, n. 8, p. 1362
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- Publication type:
- Article
Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 5, p. 453, doi. 10.1093/hmg/ddg042
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- Publication type:
- Article
Phenotype of DFNA11: A Nonsyndromic Hearing Loss Caused by a Myosin VIIA Mutation.
- Published in:
- Laryngoscope, 2002, v. 112, n. 2, p. 292, doi. 10.1097/00005537-200202000-00017
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- Publication type:
- Article
γ-Rays enhance rAAV-mediated transgene expression and cytocidal effect of AAV-HSVtk/ganciclovir on cancer cells.
- Published in:
- Cancer Gene Therapy, 2001, v. 8, n. 2, p. 99, doi. 10.1038/sj.cgt.7700282
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- Publication type:
- Article
Effects of peptidase inhibitors on anti-nociceptive action of dynorphin-(1–8) in rats.
- Published in:
- Naunyn-Schmiedeberg's Archives of Pharmacology, 2000, v. 361, n. 3, p. 273, doi. 10.1007/s002109900182
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- Publication type:
- Article
Hereditary sensorineural hearing loss of unknown cause involving mitochondrial DNA 1555 mutation.
- Published in:
- 2000
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- Publication type:
- journal article
A new mutation in the POU3F4 gene in a japanese family with x-linked mixed deafness (DFN3).
- Published in:
- Laryngoscope, 1998, v. 108, n. 10, p. 1544, doi. 10.1097/00005537-199810000-00022
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- Publication type:
- Article
Localization of plasminogen activators and their inhibitor in squamous cell carcinomas of the head and neck.
- Published in:
- Head & Neck, 1997, v. 19, n. 7, p. 611, doi. 10.1002/(SICI)1097-0347(199710)19:7<611::AID-HED8>3.0.CO;2-A
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- Publication type:
- Article
A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness (DFNA11) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 6, p. 849, doi. 10.1093/hmg/5.6.849
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- Publication type:
- Article
Spontaneous nystagmus in normal subjects.
- Published in:
- 1996
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- Publication type:
- journal article
Congenital Cholesteatoma of the Petrous Pyramid.
- Published in:
- ORL, 1993, v. 55, n. 4, p. 236, doi. 10.1159/000276430
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- Publication type:
- Article
Mucinous carcinoma of the external auditory canal: Case report.
- Published in:
- Head & Neck, 1990, v. 12, n. 5, p. 417, doi. 10.1002/hed.2880120508
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- Publication type:
- Article
Fluctuating hearing loss in lipoma of the cerebellopontine angle.
- Published in:
- 1990
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- Publication type:
- journal article
Clinical and experimental results with focused ultrasound.
- Published in:
- 1983
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- Publication type:
- journal article