arginine and Deaf Mutism

arginine has been researched along with Deaf Mutism in 9 studies

Research

Studies (9)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (11.11)	18.2507
2000's	5 (55.56)	29.6817
2010's	3 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Fukuda, M; Nagao, Y	1
Briand, G; Cheillan, D; Feillet, F; Montaut-Verient, B; Schmitt, E; Sorlin, A; Wiedemann, A	1
Amin, HJ; Sauve, RS; Soraisham, AS	1
Baek, JI; Cho, HJ; Choi, SJ; Jeong, SW; Kim, LS; Kim, UK; Sagong, BR; Zhao, C	1
Baserer, N; Baykal, C; Emiroglu, M; Eris, H; Ghanbari, A; Hafiz, G; Tukel, T; Uyguner, O; Wollnik, B; Yuksel-Apak, M	1
Altenberg, GA; Chen, Y; Deng, Y; Reuss, L	1
Blanché, H; Byrne, MM; Clément, K; Fiet, J; Froguel, P; Passa, P; Polonsky, KS; Pueyo, ME; Robert, JJ; Sturis, J; Velho, G; Vionnet, N	1
Cucci, RA; Green, GE; Prasad, S; Smith, RJ	1
Brändle, M; Lehmann, R; Maly, FE; Schmid, C; Spinas, GA	1

Trials

1 trial(s) available for arginine and Deaf Mutism

Article	Year
Neurodevelopmental outcomes of premature infants treated with l-arginine for prevention of necrotising enterocolitis. Journal of paediatrics and child health, 2009, Volume: 45, Issue:4 Topics: Alberta; Arginine; Blindness; Cerebral Palsy; Child, Preschool; Cognition Disorders; Deafness; Developmental Disabilities; Enterocolitis, Necrotizing; Female; Follow-Up Studies; Humans; Infant, Newborn; Male; Premature Birth; Treatment Outcome	2009

Article

Year

Neurodevelopmental outcomes of premature infants treated with l-arginine for prevention of necrotising enterocolitis.

Journal of paediatrics and child health, 2009, Volume: 45, Issue:4

Topics: Alberta; Arginine; Blindness; Cerebral Palsy; Child, Preschool; Cognition Disorders; Deafness; Developmental Disabilities; Enterocolitis, Necrotizing; Female; Follow-Up Studies; Humans; Infant, Newborn; Male; Premature Birth; Treatment Outcome

2009

Other Studies

8 other study(ies) available for arginine and Deaf Mutism

Article	Year
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report. Journal of medical case reports, 2019, Oct-21, Volume: 13, Issue:1 Topics: Arginine; Aspartic Acid; Biomarkers; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Growth Differentiation Factor 15; Humans; Male; MELAS Syndrome; Middle Aged; Mitochondrial Diseases; Mutation	2019
Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency. Neuropediatrics, 2016, Volume: 47, Issue:3 Topics: Alanine Transaminase; Arginine; Aspartate Aminotransferases; Child; Child, Preschool; Deafness; Developmental Disabilities; Fatty Acids; Female; Humans; Infant; Membrane Proteins; Muscle Hypotonia; Peroxisomal Disorders; Phytanic Acid; Pipecolic Acids; Sialorrhea	2016
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
The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family. Clinical genetics, 2002, Volume: 62, Issue:4 Topics: Amino Acid Substitution; Arginine; Connexin 26; Connexins; Deafness; Female; Genes, Dominant; Glutamic Acid; Heterozygote; Humans; Keratoderma, Palmoplantar; Male; Pedigree; Point Mutation; Turkey	2002
Mutations of connexin 26 at position 75 and dominant deafness: essential role of arginine for the generation of functional gap-junctional channels. Hearing research, 2006, Volume: 220, Issue:1-2 Topics: Amino Acids, Aromatic; Analysis of Variance; Animals; Arginine; Connexins; Deafness; Gap Junctions; Ion Channel Gating; Mutagenesis, Site-Directed; Mutation; Oocytes; Xenopus laevis	2006
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation. Diabetes, 1996, Volume: 45, Issue:4 Topics: Adenine; Adolescent; Adult; Aged; Arginine; Blood Glucose; Body Mass Index; C-Peptide; Child; Child, Preschool; Deafness; Diabetes Mellitus, Type 2; Female; Genomic Imprinting; Glucose Tolerance Test; Glycated Hemoglobin; Guanine; Humans; Insulin; Insulin Secretion; Male; Middle Aged; Pedigree; Periodicity; Phenotype; Point Mutation; Reference Values; RNA, Transfer, Leu; Sex Characteristics	1996
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). Human mutation, 2000, Volume: 16, Issue:6 Topics: Alleles; Amino Acid Substitution; Arginine; Connexin 26; Connexins; Cysteine; Deafness; Genetic Testing; Genetic Variation; Hearing Loss, Sensorineural; Humans; Mutation; Sequence Deletion	2000
Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation. Diabetes care, 2001, Volume: 24, Issue:7 Topics: Adult; Arginine; Blood Glucose; C-Peptide; Deafness; Diabetes Complications; Diabetes Mellitus; DNA, Mitochondrial; Female; Genomic Imprinting; Glucagon; Glucose Tolerance Test; Humans; Insulin; Insulin Secretion; Islets of Langerhans; Kinetics; Male; Nuclear Family; Pedigree; Point Mutation; Reference Values; RNA; RNA, Mitochondrial; RNA, Transfer, Leu; Time Factors	2001