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biotin and Hearing Loss

biotin has been researched along with Hearing Loss in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Al-Dirbashi, OY; Chakraborty, P; DiRaimo, J; Gannavarapu, S; Geraghty, MT; Goobie, S; Karaceper, M; Li, L; MacKenzie, J; Munoz, T; Napier, M; Potter, M; Prasad, C; Rupar, CA; Schulze, A1
Wolf, B1
Campistol, J; Castiñeiras, D; Couce, ML; Fraga, JM; García Cazorla, A; García Silva, MT; Martín-Hernández, E; Navarrete, R; Pérez, B; Pérez-Cerdá, C; Pineda, M; Ugarte, M1
Bressman, S; Brin, M; Eisenberg, M; Fahn, S; Maltese, W1

Reviews

1 review(s) available for biotin and Hearing Loss

ArticleYear
Clinical issues and frequent questions about biotinidase deficiency.
    Molecular genetics and metabolism, 2010, Volume: 100, Issue:1

    Topics: Animals; Biotin; Biotinidase Deficiency; Evidence-Based Medicine; False Positive Reactions; Hearing Loss; Humans; Infant, Newborn; Infant, Premature; Lysine; Neonatal Screening; Protein Binding; Specimen Handling

2010

Other Studies

3 other study(ies) available for biotin and Hearing Loss

ArticleYear
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014).
    Molecular genetics and metabolism, 2015, Volume: 116, Issue:3

    Topics: Alleles; Amidohydrolases; Biotin; Biotinidase; Biotinidase Deficiency; Child; Child, Preschool; Disease Management; Female; Genetic Association Studies; Hearing Loss; Heterozygote; Homozygote; Humans; Infant; Infant, Newborn; Male; Mutation; Neonatal Screening; Ontario; Pilot Projects

2015
[Clinical and genetic findings in patients with biotinidase deficiency detected through newborn screening or selective screening for hearing loss or inherited metabolic disease].
    Medicina clinica, 2011, Oct-22, Volume: 137, Issue:11

    Topics: Adolescent; Biotin; Biotinidase; Biotinidase Deficiency; Child, Preschool; Hearing Loss; Humans; Infant; Infant, Newborn; Metabolic Diseases; Mutation; Neonatal Screening; Vitamin B Complex

2011
Biotin-responsive encephalopathy with myoclonus, ataxia, and seizures.
    Advances in neurology, 1986, Volume: 43

    Topics: Adult; Amidohydrolases; Ataxia; Biotin; Biotinidase; Brain Diseases, Metabolic; Electroencephalography; Electromyography; Female; Hearing Loss; Humans; Myoclonus; Pyruvate Carboxylase; Seizures

1986