Revision history of "Application of more sensitive genetic diagnostic techniques, study of phenotypic modulators and prognosis in patients with myotonic dystrophy" (Q3141561)

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9 October 2024

  • curprev 22:4522:45, 9 October 2024DG Regio talk contribs 75,870 bytes −2 Changed label, description and/or aliases in pt
  • curprev 22:4522:45, 9 October 2024DG Regio talk contribs 75,872 bytes +12 Set a claim value: summary (P836): As distrofias miotónicas são miopatias progressivas com herança autossómica dominante, miotonia e envolvimento multiorgânico. Eles são divididos em distrofia miotónica tipo I (DM1) e distrofia miotónica tipo II (DM2). Ambos são causados por expansões de nucleótidos em genes específicos, que exercem um efeito de «ARN tóxico» através da abdução de proteínas que alteram o funcionamento celular adequado. Caracterizam-se por uma ampla variabilidade fenot...

23 March 2024

20 December 2023

12 June 2023

10 June 2023

17 August 2022

  • curprev 20:1420:14, 17 August 2022DG Regio talk contribs 74,587 bytes +51,193 Changed label, description and/or aliases in el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl, nl, fr, de, it, es, and other parts: Adding translations: el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl,

16 January 2022

17 December 2021

9 December 2021

2 December 2021

  • curprev 12:1812:18, 2 December 2021DG Regio talk contribs 15,484 bytes +2,584 Created claim: summary (P836): Les dystrophies myotoniques sont des myopathies progressives avec un héritage autosomal dominant, une myotonie et une implication multiorganique. Ils sont divisés en dystrophie myotonique de type I (DM1) et en dystrophie myotonique de type II (DM2). Les deux sont causées par l’expansion des nucléotides dans des gènes spécifiques, qui exercent un effet d’ARN toxique par l’enlèvement de protéines qui altèrent le bon fonctionnement cellulaire. Ils...
  • curprev 12:1812:18, 2 December 2021DG Regio talk contribs 12,900 bytes +229 Changed label, description and/or aliases in fr: translated_label

12 October 2021

  • curprev 13:1613:16, 12 October 2021DG Regio talk contribs 12,671 bytes +201 Changed label, description and/or aliases in en: translated_label
  • curprev 13:1613:16, 12 October 2021DG Regio talk contribs 12,470 bytes +2,305 Created claim: summary (P836): Myotonic dystrophys are progressive myopathies with autosomal dominant inheritance, myotonia and multiorganic involvement. They are divided into myotonic type I dystrophy (DM1) and myotonic dystrophy type II (DM2). Both are caused by nucleotide expansions in specific genes, which exert a ‘toxic RNA’ effect by abducting proteins that alter proper cellular functioning. They are characterised by broad phenotypic variability. In DM1, the greater the...

10 October 2021

9 October 2021

7 October 2021