arginine and Dysphagia

arginine has been researched along with Dysphagia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Casaubón-Garcín, PR; Ferreiro-Marin, A; González-Cruz, MÁ; Parra, PR1
Cintoni, M; Mele, MC; Pizzoferrato, M; Rinninella, E; Servidei, S1
Finnilä, S; Hassinen, I; Hinttala, R; Kärppä, M; Komulainen, T; Majamaa, K; Pajunen, L; Rantala, H; Tuominen, H; Uusimaa, J1

Other Studies

3 other study(ies) available for arginine and Dysphagia

ArticleYear
L-arginine-induced esophagitis, report of six cases.
    Boletin medico del Hospital Infantil de Mexico, 2020, Volume: 77, Issue:1

    Topics: Adolescent; Arginine; Chest Pain; Child; Deglutition Disorders; Esophageal Mucosa; Esophagitis; Female; Humans; Male; Omeprazole; Sucralfate; Ulcer

2020
Nutritional support in mitochondrial diseases: the state of the art.
    European review for medical and pharmacological sciences, 2018, Volume: 22, Issue:13

    Topics: Arginine; Deglutition Disorders; Diet, High-Fat; Energy Metabolism; Humans; Mitochondria; Mitochondrial Diseases; Nutritional Support; Thioctic Acid; Ubiquinone

2018
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
    BMC neurology, 2010, May-03, Volume: 10

    Topics: Aged, 80 and over; Arginine; Brain; Deglutition Disorders; Diabetes Mellitus, Type 2; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Histidine; Humans; Male; Mitochondrial Diseases; Mutation; Ophthalmoplegia; Phenotype

2010