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Page last updated: 2024-09-05

biotin and Optic Atrophy

biotin has been researched along with Optic Atrophy in 8 studies

Research

Studies (8)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (12.50)	18.7374
1990's	3 (37.50)	18.2507
2000's	1 (12.50)	29.6817
2010's	1 (12.50)	24.3611
2020's	2 (25.00)	2.80

Authors

Authors	Studies
Kellom, ER; Rice, GM; Stepien, KE; Wolf, B	1
Khan, AO	1
De Zaeytijd, J; Dermaut, B; Hemelsoet, D; Laureys, G; Sindic, CJM; Sprengers, M; Van Iseghem, V; Willekens, B	1
Baumgartner, ER; Scholl, S; Weber, P	1
Brab, M; Heimann, G; Ramaekers, VT; Rau, G	1
Dalton, RN; Pike, MG; Rahman, S; Standing, S	1
Baumgartner, ER; Brab, M; Heimann, G; Ramaekers, VT; Reim, M	1
Campana, G; Giovannucci-Uzielli, ML; Legnaioli, MI; Pavari, E; Valentini, G	1

Other Studies

8 other study(ies) available for biotin and Optic Atrophy

Article	Year
Reversal of Vision Loss in a 49-Year-Old Man With Progressive Optic Atrophy Due to Profound Biotinidase Deficiency. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society, 2021, 03-01, Volume: 41, Issue:1 Topics: Biotin; Biotinidase; Biotinidase Deficiency; Exome Sequencing; Humans; Male; Middle Aged; Mutation; Optic Atrophy; Vision Disorders; Visual Acuity; Visual Fields; Vitamin B Complex	2021
Juvenile progressive optic atrophy as the presenting feature of biotinidase deficiency, a treatable metabolic disorder. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 2021, Volume: 25, Issue:4 Topics: Adolescent; Biotin; Biotinidase; Biotinidase Deficiency; Child; Female; Humans; Optic Atrophy; Vision Disorders	2021
Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults Multiple sclerosis and related disorders, 2019, Volume: 32 Topics: Biotin; Biotinidase Deficiency; Humans; Male; Optic Atrophy; Spinal Cord Diseases; Young Adult	2019
Outcome in patients with profound biotinidase deficiency: relevance of newborn screening. Developmental medicine and child neurology, 2004, Volume: 46, Issue:7 Topics: Adaptation, Psychological; Adolescent; Adult; Biotin; Biotinidase Deficiency; Child; Child, Preschool; Female; Follow-Up Studies; Hearing Disorders; Humans; Infant; Infant, Newborn; Male; Motor Skills Disorders; Neonatal Screening; Optic Atrophy; Outcome Assessment, Health Care; Severity of Illness Index; Social Adjustment; Speech Disorders	2004
Recovery from neurological deficits following biotin treatment in a biotinidase Km variant. Neuropediatrics, 1993, Volume: 24, Issue:2 Topics: Administration, Oral; Adolescent; Amidohydrolases; Biotin; Biotinidase; Blood Chemical Analysis; Cognition; Colorimetry; Evoked Potentials, Visual; Follow-Up Studies; Humans; Male; Multiple Carboxylase Deficiency; Muscle Spasticity; Optic Atrophy; Paralysis; Vision Disorders; Visual Acuity	1993
Late presentation of biotinidase deficiency with acute visual loss and gait disturbance. Developmental medicine and child neurology, 1997, Volume: 39, Issue:12 Topics: Amidohydrolases; Biotin; Biotinidase; Child, Preschool; Female; Gait; Humans; Metabolism, Inborn Errors; Optic Atrophy; Treatment Outcome; Vision Disorders	1997
[Juvenile optic neuropathy caused by Km variants of biotinidase]. Klinische Monatsblatter fur Augenheilkunde, 1992, Volume: 200, Issue:3 Topics: Adolescent; Amidohydrolases; Biopsy; Biotin; Biotinidase; Fluorescein Angiography; Humans; Immunoglobulin Allotypes; Male; Nerve Fibers, Myelinated; Optic Atrophy; Optic Neuritis; Synaptic Transmission; Syndrome; Visual Field Tests	1992
Ocular aspects in biotinidase deficiency. Clinical and genetic original studies. Ophthalmic paediatrics and genetics, 1987, Volume: 8, Issue:2 Topics: Alopecia; Amidohydrolases; Biotin; Biotinidase; Child, Preschool; Genes, Recessive; Humans; Keratoconjunctivitis; Male; Multiple Carboxylase Deficiency; Optic Atrophy	1987