histidine has been researched along with Cochlear Hearing Loss in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (83.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ando, F; Hibi, T; Kato, K; Nakashima, T; Nishio, N; Otake, H; Shimokata, H; Sone, M; Sugiura, S; Tagaya, M; Teranishi, M; Uchida, Y; Yoshida, T | 1 |
| Ishinaga, H; Majima, Y; Shimizu, T; Tsukamoto, K; Usami, S; Yuta, A | 1 |
| Bax, R; Freisinger, P; Horn, N; Horváth, R; Jaksch, M; Mayr, JA; Merl, T; Moller, LB; Müller-Höcker, J; Pongratz, D; Rubio, R | 1 |
| Ge, J; Katz, BJ; Kosmorsky, G; Li, C; Traboulsi, EI; Zhang, K | 1 |
| Abe, S; Hoshino, T; Isoda, H; Iwasaki, S; Usami , S; Watanabe, T | 1 |
| Furuhashi, A; Miura, Y; Mori, N; Murakami, H; Naganawa, S; Nakashima, T; Nakayama, A; Sato, E; Tadokoro, M | 1 |
6 other study(ies) available for histidine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Complement Factor H; Diabetes Complications; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Hearing Loss, Sudden; Histidine; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Tyrosine; Young Adult | 2012 |
Pendred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutation.
Topics: Aged; Arginine; Biological Transport; Carrier Proteins; DNA Mutational Analysis; Female; Goiter; Hearing Loss, Sensorineural; Histidine; Humans; Membrane Transport Proteins; Mutation, Missense; Pedigree; Sulfate Transporters | 2002 |
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism.
Topics: Adenosine Triphosphatases; Blotting, Southern; Brain; Cataract; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Cytochrome-c Oxidase Deficiency; Developmental Disabilities; DNA Mutational Analysis; Electrophysiology; Exons; Fibroblasts; Hearing Loss, Sensorineural; Histidine; Humans; Immunoblotting; Immunohistochemistry; Infant; Magnetic Resonance Imaging; Male; Mitochondria; Muscle Hypotonia; Muscle, Skeletal; Muscles; Mutation; Myoblasts; Recombinant Fusion Proteins; Superoxide Dismutase | 2005 |
Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation.
Topics: Adult; Amino Acid Substitution; Arginine; Child; Female; Genetic Linkage; GTP Phosphohydrolases; Haplotypes; Hearing Loss, Sensorineural; Hearing Tests; Histidine; Humans; Male; Middle Aged; Mutation; Optic Atrophy, Autosomal Dominant | 2005 |
Long-term audiological feature in Pendred syndrome caused by PDS mutation.
Topics: Adult; Arginine; Biological Transport; Carrier Proteins; Chromosomes, Human, Pair 7; Disease Progression; DNA Mutational Analysis; Evoked Potentials, Auditory, Brain Stem; Female; Goiter; Hearing Loss, Sensorineural; Histidine; Humans; Magnetic Resonance Imaging; Membrane Transport Proteins; Mutation, Missense; Sulfate Transporters; Syndrome; Time Factors; Vestibular Aqueduct | 2001 |
Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene.
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Carrier Proteins; Child; Endolymphatic Duct; Endolymphatic Sac; Female; Goiter; Hearing Loss, Sensorineural; Heterozygote; Histidine; Homozygote; Humans; Iodides; Iodine; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Mutation, Missense; Phenotype; RNA Splicing; Sequence Analysis, DNA; Sulfate Transporters; Syndrome; Thyroglobulin; Vestibular Aqueduct | 2001 |