Compounds > tryptophan

tryptophan and Deafness

tryptophan has been researched along with Deafness in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lucia, A; Pastore, V; Pirozzi, C; Volpe, AD1
Baek, JI; Cho, HJ; Choi, SJ; Jeong, SW; Kim, LS; Kim, UK; Sagong, BR; Zhao, C1
Belknap, B; Ikebe, M; Ikebe, R; Inoue, A; Sato, O; White, HD1
Bellet, H; Cheminal, R; Duran, M; Echenne, B1
Curran, SP; Koehler, CM; Roesch, K; Tranebjaerg, L1
Bennett, M; Brown, R; Hansotia, P; Peters, H1

Other Studies

6 other study(ies) available for tryptophan and Deafness

ArticleYear
Comparative Study between the use of Melatonin and A Solution with Melatonin, Tryptophan, and Vitamin B6 as an Inducer of Spontaneous Sleep in Children During an Auditory Response Test: An Alternative to Commonly Used Sedative Drugs.
    The journal of international advanced otology, 2017, Volume: 13, Issue:1

    Topics: Audiometry, Evoked Response; Child; Child, Preschool; Deafness; Drug Combinations; Early Diagnosis; Electroencephalography; Evoked Potentials, Auditory, Brain Stem; Female; Hearing Loss; Hearing Tests; Humans; Hypnotics and Sedatives; Male; Melatonin; Tryptophan; Vitamin B 6

2017
The Trp117Arg mutation of the COCH gene causes deafness in Koreans.
    Clinical genetics, 2010, Volume: 77, Issue:4

    Topics: Amino Acid Substitution; Arginine; Asian People; Base Sequence; Deafness; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Family; Female; Haplotypes; Humans; Lod Score; Male; Microsatellite Repeats; Molecular Sequence Data; Mutation; Pedigree; Proteins; Republic of Korea; Tryptophan

2010
Human deafness mutation of myosin VI (C442Y) accelerates the ADP dissociation rate.
    The Journal of biological chemistry, 2004, Jul-09, Volume: 279, Issue:28

    Topics: Actins; Adenosine Diphosphate; Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Calcium; Deafness; Humans; Mice; Molecular Motor Proteins; Mutation, Missense; Myosin Heavy Chains; Protein Binding; Tryptophan

2004
Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria.
    Journal of inherited metabolic disease, 1996, Volume: 19, Issue:1

    Topics: Algeria; Brain Diseases; Child; Child, Preschool; Coma; Deafness; Female; Humans; Infant; Intellectual Disability; Kynurenine; Male; Pedigree; Renal Aminoacidurias; Tryptophan

1996
Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex.
    Human molecular genetics, 2002, Mar-01, Volume: 11, Issue:5

    Topics: Amino Acid Substitution; Carrier Proteins; Cells, Cultured; Deafness; DNA-Binding Proteins; Dystonia; Fibroblasts; Humans; Intracellular Membranes; Membrane Transport Proteins; Mitochondria; Mitochondrial Precursor Protein Import Complex Proteins; Molecular Weight; Mutation, Missense; Point Mutation; Syndrome; Tryptophan

2002
Chelation therapy in Wegener's granulomatosis. Treatment with EDTA.
    The Annals of otology, rhinology, and laryngology, 1969, Volume: 78, Issue:2

    Topics: Adult; Anti-Bacterial Agents; Cellulitis; Copper; Deafness; Edetic Acid; Eye Diseases; Female; Granulomatosis with Polyangiitis; Humans; Neurologic Manifestations; Nose Deformities, Acquired; Ophthalmoplegia; Otitis Media; Porphyrins; Prednisolone; Skin Manifestations; Tryptophan; Zinc

1969