thymine has been researched along with Decreased Muscle Tone in 2 studies
Excerpt | Relevance | Reference |
---|---|---|
"The first Hungarian report of a case of myotubular myopathy is presented here, which is a recessive congenital disorder linked to X chromosome." | 2.44 | [Myotubular myopathy. Case report and review of the literature]. ( Bereg, E; Bódi, I; Endreffy, E; Hortobágyi, T; Katona, M; Korcsik, J; Kovács, SK; Szabó, H; Sztriha, L; Túri, S, 2007) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brussel, W | 1 |
van Kuilenburg, AB | 1 |
Janssens, PM | 1 |
Kovács, SK | 1 |
Korcsik, J | 1 |
Szabó, H | 1 |
Bódi, I | 1 |
Katona, M | 1 |
Bereg, E | 1 |
Endreffy, E | 1 |
Túri, S | 1 |
Hortobágyi, T | 1 |
Sztriha, L | 1 |
1 review available for thymine and Decreased Muscle Tone
Article | Year |
---|---|
[Myotubular myopathy. Case report and review of the literature].
Topics: Biopsy; DNA Mutational Analysis; Frameshift Mutation; Genetic Diseases, X-Linked; Humans; Infant; In | 2007 |
1 other study available for thymine and Decreased Muscle Tone
Article | Year |
---|---|
A neonate with recurrent vomiting and generalized hypotonia diagnosed with a deficiency of dihydropyrimidine dehydrogenase.
Topics: Developmental Disabilities; Dihydrouracil Dehydrogenase (NADP); Female; Homozygote; Humans; Infant; | 2006 |