Page last updated: 2024-10-20

thiamine and Genetic Diseases

thiamine has been researched along with Genetic Diseases in 1 studies

thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.

Research Excerpts

ExcerptRelevanceReference
"Despite advances in device closure for atrial septal defect, post-closure heart failure remains a clinical problem in adult patients but is seen only rarely in children."5.39Heart failure after transvenous closure of atrial septal defect associated with atrial standstill and thiamine-responsive megaloblastic anemia. ( Ceylan, O; Doğan, V; Orün, UA; Senocak, F, 2013)
"Despite advances in device closure for atrial septal defect, post-closure heart failure remains a clinical problem in adult patients but is seen only rarely in children."1.39Heart failure after transvenous closure of atrial septal defect associated with atrial standstill and thiamine-responsive megaloblastic anemia. ( Ceylan, O; Doğan, V; Orün, UA; Senocak, F, 2013)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Doğan, V1
Senocak, F1
Orün, UA1
Ceylan, O1

Other Studies

1 other study available for thiamine and Genetic Diseases

ArticleYear
Heart failure after transvenous closure of atrial septal defect associated with atrial standstill and thiamine-responsive megaloblastic anemia.
    Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, 2013, Volume: 41, Issue:7

    Topics: Anemia, Megaloblastic; Cardiomyopathies; Child; Genetic Diseases, Inborn; Heart Atria; Heart Block;

2013