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adenosine and Abnormalities, Multiple

adenosine has been researched along with Abnormalities, Multiple in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ali, S; Gouin, S1
Arnout, J; Eyssen, M; Freson, K; Hoylaerts, MF; Jaeken, J; Van Geet, C; Vermylen, J1
Bradshaw, C; Francke, U; Kernahan, C1

Other Studies

3 other study(ies) available for adenosine and Abnormalities, Multiple

ArticleYear
A patient with chaotic atrial tachycardia.
    Pediatric emergency care, 2003, Volume: 19, Issue:2

    Topics: Abnormalities, Multiple; Adenosine; Anti-Asthmatic Agents; Asthma; Bronchiolitis; Combined Modality Therapy; Diagnosis, Differential; Dyspnea; Electroencephalography; Emergencies; Female; Fluid Therapy; Furosemide; Heart Failure; Heart Septal Defects, Atrial; Humans; Infant; Procainamide; Recurrence; Tachycardia; Tachycardia, Ectopic Atrial

2003
Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding.
    Thrombosis and haemostasis, 2001, Volume: 86, Issue:3

    Topics: Abnormalities, Multiple; Adenosine; Adenylyl Cyclases; Adolescent; Alprostadil; Alternative Splicing; Amino Acid Sequence; Amino Acid Substitution; Bleeding Time; Blood Platelets; Child; Chromogranins; Cyclic AMP; Female; Fingers; Gene Frequency; Genomic Imprinting; GTP-Binding Protein alpha Subunits, Gs; Hemorrhagic Disorders; Heterotrimeric GTP-Binding Proteins; Humans; Hyperkinesis; Hypoparathyroidism; Iloprost; Intellectual Disability; Male; Molecular Sequence Data; Muscle Hypotonia; Mutagenesis, Insertional; Nerve Tissue Proteins; Phenotype; Platelet Aggregation; Platelet Function Tests; Polymorphism, Genetic; Protein Subunits; Repetitive Sequences, Amino Acid; Risk Factors; Second Messenger Systems; Structure-Activity Relationship; Wounds and Injuries

2001
Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.
    Humangenetik, 1975, Volume: 26, Issue:4

    Topics: Abnormalities, Multiple; Adenosine; Alanine Transaminase; Aminohydrolases; Blood Group Antigens; Blood Proteins; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Cytogenetics; Dermatoglyphics; Erythrocytes; Esterases; Female; Growth Disorders; Head; Heterozygote; Humans; Intellectual Disability; Karyotyping; Polymorphism, Genetic; Syndrome

1975