Page last updated: 2024-08-17

histidine and Deafness

histidine has been researched along with Deafness 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	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Coucke, PJ; Cremers, CW; Ensink, RJ; Huygen, P; Van Camp, G; Van Hauwe, P	1
Baumann, H; Berlin, A; Lubs, H; Peters, WH; Rose, HJ	1
Corner, BD; Holton, JB; Norman, RM; Williams, PM	1

Trials

1 trial(s) available for histidine and Deafness

Article	Year
[Histidine tolerance in low skin histidase activity]. Acta biologica et medica Germanica, 1975, Volume: 34?710 Topics: Adolescent; Adult; Ammonia-Lyases; Child; Chromatography, Thin Layer; Clinical Trials as Topic; Deafness; Female; Histidine; Histidine Ammonia-Lyase; Humans; Imidazoles; Male; Phenylalanine; Skin	1975

Other Studies

2 other study(ies) available for histidine and Deafness

Article	Year
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region. American journal of medical genetics, 2000, Jul-31, Volume: 93, Issue:3 Topics: Amino Acid Sequence; Base Sequence; Chromosomes, Human, Pair 1; Connexins; Deafness; DNA Mutational Analysis; Exons; Genes, Dominant; Genetic Linkage; Histidine; Humans; KCNQ Potassium Channels; Leucine; Models, Biological; Molecular Sequence Data; Mutation; Mutation, Missense; Potassium Channels; Potassium Channels, Voltage-Gated; Sequence Homology, Amino Acid	2000
A case of histidinemia controlled with a low histidine diet. Pediatrics, 1968, Volume: 41, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Blindness; Brain; Brain Damage, Chronic; Brain Diseases; Chromatography, Ion Exchange; Deafness; Diet Therapy; Dietary Proteins; Electrophoresis; Growth; Histidine; Humans; Infant; Intellectual Disability; Male; Serotonin	1968

Article

Year

Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.

American journal of medical genetics, 2000, Jul-31, Volume: 93, Issue:3

Topics: Amino Acid Sequence; Base Sequence; Chromosomes, Human, Pair 1; Connexins; Deafness; DNA Mutational Analysis; Exons; Genes, Dominant; Genetic Linkage; Histidine; Humans; KCNQ Potassium Channels; Leucine; Models, Biological; Molecular Sequence Data; Mutation; Mutation, Missense; Potassium Channels; Potassium Channels, Voltage-Gated; Sequence Homology, Amino Acid

2000

A case of histidinemia controlled with a low histidine diet.

Pediatrics, 1968, Volume: 41, Issue:6

Topics: Amino Acid Metabolism, Inborn Errors; Blindness; Brain; Brain Damage, Chronic; Brain Diseases; Chromatography, Ion Exchange; Deafness; Diet Therapy; Dietary Proteins; Electrophoresis; Growth; Histidine; Humans; Infant; Intellectual Disability; Male; Serotonin

1968