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Content Provider : Academic Search Premier Subject : genetic testing Subject : mitochondrial dna
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Academic Journal

Cerebellar vermis hypoplasia and bilateral basal ganglia calcification in maternally inherited diabetes and deafness.

Subjects: *BASAL ganglia; *DEAFNESS; *CALCIFICATION

  • Source: Neurological Sciences. Apr2023, Vol. 44 Issue 4, p1469-1470. 2p. 1 Color Photograph.

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Academic Journal

The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review.

Subjects: *LITERATURE reviews; *DEAFNESS; *MITOCHONDRIAL DNA

  • Source: Clinical Case Reports. Feb2024, Vol. 12 Issue 2, p1-9. 9p.

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Academic Journal

Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications.

Subjects: *MITOCHONDRIAL DNA; *DEAFNESS; *MITOCHONDRIA

  • Source: Journal of International Advanced Otology. Sep2023, Vol. 19 Issue 5, p414-419. 6p.

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Academic Journal

Mitochondrial DNA mutations and the risk for aminoglycoside-induced deafness.

Subjects: *MITOCHONDRIAL DNA; *DEAFNESS; *LEBER'S hereditary optic atrophy

  • Source: Macedonian Pharmaceutical Bulletin / Makedonsko Farmacevtski Bilten. 2022 Supplement, Vol. 68, p411-412. 2p.

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Academic Journal

Computational analysis based on audioprofiles: A new possibility for patient stratification in office-based otology.

Subjects: *DEAFNESS; *COMPUTATIONAL biology; *BONE conductionUNITED States

  • Source: Audiology Research. 2019, Vol. 9 Issue 2, p27-32. 6p.

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Academic Journal

Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.

Subjects: *HEARING disorders; *DEAFNESS; *RUSSIANSRUSSIA

  • Source: International Journal of Molecular Sciences. Dec2022, Vol. 23 Issue 24, p15748. 12p.

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Academic Journal

The responsible genes in Japanese deafness patients and clinical application using Invader assay.

Subjects: *GENETICS of deafness; *DEAFNESS; *DEAF people

  • Source: Acta Oto-Laryngologica. Apr2008, Vol. 128 Issue 4, p446-454. 9p. 3 Diagrams, 1 Chart.

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Academic Journal

Detection of deafness-causing mutations in the Greek mitochondrial genome.

Subjects: *DEAFNESS; *GENETIC mutation; *MITOCHONDRIAL DNA

  • Source: Disease Markers. 2011, Vol. 30 Issue 6, p283-289. 7p. 3 Charts.

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Academic Journal

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

Subjects: *DEAFNESS; *ETIOLOGY of diseases; *GENETIC mutation

  • Source: Journal of Human Genetics. May2010, Vol. 55 Issue 5, p265-269. 5p. 1 Chart.

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Academic Journal

Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: A report from Nigeria.

Subjects: *DEAFNESS; *GENETIC mutation; *MITOCHONDRIAL DNANIGERIA; SUB-Saharan Africa

  • Source: International Journal of Pediatric Otorhinolaryngology. Nov2014, Vol. 78 Issue 11, p1870-1873. 4p.

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  • 1-10 of  717 results for ""Deafness""