Revision history of "Therapeutic approaches to Celia Encephalopathy (PELD) in murine models “knock in” BSCL2Celia/Celia" (Q3148579)

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9 October 2024

  • curprev 10:0510:05, 9 October 2024DG Regio talk contribs 77,142 bytes +1 Changed label, description and/or aliases in pt
  • curprev 10:0510:05, 9 October 2024DG Regio talk contribs 77,141 bytes 0 Set a claim value: summary (P836): A encefalopatia celíaca é uma doença neurodegenerativa infantil de prognóstico infausto antes de 9 anos devido à mutação c.985C>T no gene BSCL2/seipin. Até à data, foram comunicados apenas 7 casos, dos quais apenas um continua vivo (8,8 anos). Recentemente, o nosso grupo identificou uma variante deste distúrbio devido à mutação c.974dup no mesmo gene em uma menina espanhola e uma menina americana. Estudos anteriores do nosso grupo descobriram, duran...

20 March 2024

20 December 2023

12 June 2023

10 June 2023

17 August 2022

  • curprev 21:5721:57, 17 August 2022DG Regio talk contribs 75,869 bytes +52,118 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 16:2316:23, 2 December 2021DG Regio talk contribs 15,731 bytes +2,663 Created claim: summary (P836): L’encéphalopathie de Celia est une maladie neurodégénérative infantile du pronostic infaust avant 9 ans due à la mutation c.985C>T dans le gène BSCL2/seipin. À ce jour, seuls 7 cas ont été signalés, dont un seul reste en vie (8,8 ans). Récemment, notre groupe a identifié une variante de ce trouble en raison de la mutation c.974dup dans le même gène chez une fille espagnole et une fille américaine. Des études antérieures de notre groupe ont révé...
  • curprev 16:2316:23, 2 December 2021DG Regio talk contribs 13,068 bytes +177 Changed label, description and/or aliases in fr: translated_label

12 October 2021

  • curprev 15:0715:07, 12 October 2021DG Regio talk contribs 12,891 bytes +2,419 Created claim: summary (P836): Celia encephalopathy is a childhood neurodegenerative disease of infaust prognosis before 9 years due to c.985C>T mutation in the BSCL2/seipin gene. To date, only 7 cases have been reported, of which only one remains alive (8.8 years). Recently, our group has identified a variant of this disorder due to the c.974dup mutation in the same gene in a Spanish girl and an American girl. Previous studies of our group have found, for 5.5 years, that tr...
  • curprev 15:0715:07, 12 October 2021DG Regio talk contribs 10,472 bytes −2,419 Removed claim: summary (P836): Celia encephalopathy is a childhood neurodegenerative disease of infaust prognosis before 9 years due to c.985C>T mutation in the BSCL2/seipin gene. To date, only 7 cases have been reported, of which only one remains alive (8.8 years). Recently, our group has identified a variant of this disorder due to the c.974dup mutation in the same gene in a Spanish girl and an American girl. Previous studies of our group have found, for 5.5 years, that...
  • curprev 14:4714:47, 12 October 2021DG Regio talk contribs 12,891 bytes +162 Changed label, description and/or aliases in en: translated_label
  • curprev 14:4714:47, 12 October 2021DG Regio talk contribs 12,729 bytes +2,419 Created claim: summary (P836): Celia encephalopathy is a childhood neurodegenerative disease of infaust prognosis before 9 years due to c.985C>T mutation in the BSCL2/seipin gene. To date, only 7 cases have been reported, of which only one remains alive (8.8 years). Recently, our group has identified a variant of this disorder due to the c.974dup mutation in the same gene in a Spanish girl and an American girl. Previous studies of our group have found, for 5.5 years, that tr...

10 October 2021

9 October 2021

8 October 2021