Compounds > deoxyuridine
Page last updated: 2024-08-21

deoxyuridine and Cholera Infantum

deoxyuridine has been researched along with Cholera Infantum in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (85.71)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chinnery, PF; Coulter, LL; Parkes, M; Patel, R; Rimmer, J; Swift, O1
Bain, MD; Bax, BE; Moran, NF; Muqit, MM1
Copeland, WC; Hirano, M; Martí, R; Nishigaki, Y1
Hirano, M; Martí, R; Nishigaki, Y; Nishino, I; Spinazzola, A; Tadesse, S1
Andreu, AL; Anikster, Y; Hirano, M; Illa, I; Lara, MC; Madoz, P; Martí, R; Massuet, L; Valentino, ML; Weiss, B1
Christensen, E; Christensen, M; Elmaci, M; Ozel, A; Schwartz, M; Vissing, J; Yavuz, H1
Carelli, V; Hahn, A; Hirano, M; López, LC; Lyzak, J; Manes, JL; Martí, R; Tadesse, S; Valentino, ML1

Other Studies

7 other study(ies) available for deoxyuridine and Cholera Infantum

ArticleYear
Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease.
    BMC gastroenterology, 2019, Jan-15, Volume: 19, Issue:1

    Topics: Adult; Age of Onset; Azathioprine; Crohn Disease; Deoxyuridine; Diagnosis, Differential; Female; Gastrointestinal Diseases; Humans; Mitochondrial Encephalomyopathies; Phenotype; Point Mutation; Retrospective Studies; Thymidine; Thymidine Phosphorylase; White Matter

2019
Carrier erythrocyte entrapped thymidine phosphorylase therapy for MNGIE.
    Neurology, 2008, Aug-26, Volume: 71, Issue:9

    Topics: Adult; Deoxyuridine; Drug Delivery Systems; Erythrocyte Transfusion; Erythrocytes; Fatal Outcome; Female; Gastrointestinal Diseases; Genetic Predisposition to Disease; Humans; Liver Diseases; Mitochondrial Diseases; Mutation; Peripheral Nervous System Diseases; Pneumonia; Syndrome; Thymidine; Thymidine Phosphorylase; Treatment Failure

2008
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency.
    The Journal of clinical investigation, 2003, Volume: 111, Issue:12

    Topics: Base Sequence; Cells, Cultured; Deoxyuridine; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex IV; Gastrointestinal Diseases; Humans; Mitochondrial Encephalomyopathies; Models, Genetic; Point Mutation; Polymorphism, Restriction Fragment Length; Sequence Deletion; Thymidine Phosphorylase

2003
Definitive diagnosis of mitochondrial neurogastrointestinal encephalomyopathy by biochemical assays.
    Clinical chemistry, 2004, Volume: 50, Issue:1

    Topics: Chromatography, High Pressure Liquid; Deoxyuridine; Gastrointestinal Diseases; Humans; Mitochondrial Encephalomyopathies; Mutation; Thymidine; Thymidine Phosphorylase

2004
Infusion of platelets transiently reduces nucleoside overload in MNGIE.
    Neurology, 2006, Oct-24, Volume: 67, Issue:8

    Topics: Adolescent; Adult; Deoxyuridine; Female; Gastrointestinal Diseases; Humans; Male; Mitochondrial Encephalomyopathies; Nervous System Diseases; Platelet Transfusion; Thymidine; Thymidine Phosphorylase

2006
Treatment of mitochondrial neurogastrointestinal encephalomyopathy with dialysis.
    Archives of neurology, 2007, Volume: 64, Issue:3

    Topics: Adolescent; Deoxyuridine; Female; Gastrointestinal Diseases; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Mitochondrial Encephalomyopathies; Peritoneal Dialysis; Thymidine

2007
Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    FEBS letters, 2007, Jul-24, Volume: 581, Issue:18

    Topics: Adolescent; Adult; Autopsy; Biopsy; Deoxyuridine; Female; Gastrointestinal Diseases; Humans; Infant; Male; Mitochondrial Encephalomyopathies; Oxygen; Thymidine; Thymidine Phosphorylase

2007