Page last updated: 2024-08-17

histidine and Optic Atrophy

histidine has been researched along with Optic Atrophy in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (66.67)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Annesi, G; Bruno, E; Cavalcanti, F; Dibilio, V; Gagliardi, M; Gambardella, A; Mostile, G; Nicoletti, A; Quattrone, A; Tarantino, P; Zappia, M	1
Harper, PS	1
Frey, HJ; Frey, ML; Riekkinen, PJ; Tuomola, HO	1

Reviews

1 review(s) available for histidine and Optic Atrophy

Article	Year
Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen. Journal of medical genetics, 1977, Volume: 14, Issue:6 Topics: Alzheimer Disease; Animals; Chromosome Aberrations; Chromosome Disorders; Creutzfeldt-Jakob Syndrome; Erythroblastosis, Fetal; Female; Genes, Dominant; Genetic Diseases, Inborn; Haplorhini; Hepatitis B; Hepatitis B Surface Antigens; Histidine; Humans; Huntington Disease; Infant, Newborn; Kuru; Liver Diseases; Male; Maternal-Fetal Exchange; Mice; Myotonia Congenita; Nephritis, Hereditary; Optic Atrophy; Phenylketonurias; Pregnancy; Scrapie; Sheep; Slow Virus Diseases	1977

Article

Year

Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.

Journal of medical genetics, 1977, Volume: 14, Issue:6

Topics: Alzheimer Disease; Animals; Chromosome Aberrations; Chromosome Disorders; Creutzfeldt-Jakob Syndrome; Erythroblastosis, Fetal; Female; Genes, Dominant; Genetic Diseases, Inborn; Haplorhini; Hepatitis B; Hepatitis B Surface Antigens; Histidine; Humans; Huntington Disease; Infant, Newborn; Kuru; Liver Diseases; Male; Maternal-Fetal Exchange; Mice; Myotonia Congenita; Nephritis, Hereditary; Optic Atrophy; Phenylketonurias; Pregnancy; Scrapie; Sheep; Slow Virus Diseases

1977

Other Studies

2 other study(ies) available for histidine and Optic Atrophy

Article	Year
Sacsin-related spastic ataxia caused by a novel missense mutation p.Arg272His in a patient from Sicily, southern Italy. Cerebellum (London, England), 2013, Volume: 12, Issue:4 Topics: Adult; Arginine; Female; Heat-Shock Proteins; Histidine; Humans; Intellectual Disability; Italy; Muscle Spasticity; Mutation, Missense; Optic Atrophy; Sicily; Spinocerebellar Ataxias	2013
A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings. Annals of clinical research, 1973, Volume: 5, Issue:3 Topics: Action Potentials; Adult; Aged; Ataxia; Beta-Globulins; Cerebellar Ataxia; Electromyography; Female; Foot Deformities, Congenital; Histidine; Humans; Lysine; Male; Methods; Middle Aged; Neural Conduction; Nystagmus, Pathologic; Optic Atrophy; Pedigree	1973

Article

Year

Cerebellum (London, England), 2013, Volume: 12, Issue:4

Topics: Adult; Arginine; Female; Heat-Shock Proteins; Histidine; Humans; Intellectual Disability; Italy; Muscle Spasticity; Mutation, Missense; Optic Atrophy; Sicily; Spinocerebellar Ataxias

2013

A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings.

Annals of clinical research, 1973, Volume: 5, Issue:3

Topics: Action Potentials; Adult; Aged; Ataxia; Beta-Globulins; Cerebellar Ataxia; Electromyography; Female; Foot Deformities, Congenital; Histidine; Humans; Lysine; Male; Methods; Middle Aged; Neural Conduction; Nystagmus, Pathologic; Optic Atrophy; Pedigree

1973