arginine has been researched along with Cochlear Hearing Loss in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (9.09) | 18.2507 |
| 2000's | 10 (90.91) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdelmaksoud, S; Abdelwhab, S; Lotfy, G | 1 |
| Ishinaga, H; Majima, Y; Shimizu, T; Tsukamoto, K; Usami, S; Yuta, A | 1 |
| Huh, K; Joo, IS; Joo, SY; Ki, CS; Kim, JW | 1 |
| Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U | 1 |
| Ge, J; Katz, BJ; Kosmorsky, G; Li, C; Traboulsi, EI; Zhang, K | 1 |
| Büsse-Ratzka, M; Collmann, H; Hoppe, F; Krauss, J; Kress, W; Kunz, J; Lieb, G; Pahnke, J; Petersen, B; Reinhart, E; Schäfer, WD; Schropp, C; Sold, J; Sörensen, N; Trusen, A | 1 |
| Branham, K; Cantrell, AD; Iannaccone, A; Jennings, BJ; Othman, MI; Swaroop, A | 1 |
| Adato, A; Bonné-Tamir, B; Kalinsky, H; Korostishevsky, M; Kwitek-Black, AE; Nystuen, A; Seroussi, E; Sheffield, VC | 1 |
| Cucci, RA; Green, GE; Prasad, S; Smith, RJ | 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 |
1 review(s) available for arginine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome | 2004 |
10 other study(ies) available for arginine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Relation between asymmetric dimethylarginine (ADMA) and hearing loss in patients with renal impairment.
Topics: Adult; Arginine; C-Reactive Protein; Case-Control Studies; Creatinine; Female; Hearing Loss, Sensorineural; Humans; Lipids; Male; Middle Aged; Renal Insufficiency, Chronic; Risk Factors | 2008 |
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 |
A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.
Topics: Adult; Arginine; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Exons; Family Health; Female; Hearing Loss, Sensorineural; Humans; Male; Myelin Proteins; Pedigree; Phenotype; Point Mutation; Threonine | 2004 |
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 |
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
Topics: Acrocephalosyndactylia; Adolescent; Amino Acid Substitution; Arginine; Child, Preschool; Ear; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Intracranial Pressure; Mutation; Nuclear Proteins; Pedigree; Proline; Receptor, Fibroblast Growth Factor, Type 3; Repetitive Sequences, Nucleic Acid; Syndrome; Synostosis; Twist-Related Protein 1 | 2006 |
Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
Topics: Arginine; DNA Mutational Analysis; Electroretinography; Eye Proteins; Female; Genetic Diseases, X-Linked; Hearing Loss, Sensorineural; Heterozygote; Humans; Male; Mutation, Missense; Otitis Media; Pedigree; Phenotype; Respiratory Tract Infections; Retina; Retinitis Pigmentosa; Usher Syndromes | 2008 |
Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.
Topics: Arginine; Base Sequence; Chromosomes, Human, Pair 11; Consanguinity; DNA; Female; Genes, Recessive; Genetic Linkage; Genetics, Population; Haplotypes; Hearing Loss, Sensorineural; Humans; Male; Middle East; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Syndrome; Tryptophan; Vestibular Diseases; Vision Disorders | 1997 |
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Topics: Alleles; Amino Acid Substitution; Arginine; Connexin 26; Connexins; Cysteine; Deafness; Genetic Testing; Genetic Variation; Hearing Loss, Sensorineural; Humans; Mutation; Sequence Deletion | 2000 |
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 |