Revision history of "Optical glioma in neurofibromatosis type1: genetic studies and exosomes analysis for the identification of susceptibility and prognostic biomarkers." (Q3141618)

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8 October 2024

  • curprev 10:2210:22, 8 October 2024DG Regio talk contribs 71,360 bytes +5 Changed label, description and/or aliases in pt
  • curprev 10:2210:22, 8 October 2024DG Regio talk contribs 71,355 bytes +45 Set a claim value: summary (P836): A neurofibromatose tipo 1 (NF1) é uma das doenças hereditárias mais comuns que predispõem ao desenvolvimento de certos tumores benignos e malignos no sistema nervoso e na pele. O tumor mais prevalente em doentes pediátricos é o glioma óptico de grau I ou astrocitoma pilocítico que se desenvolve nos nervos ópticos ou quiasma, produzindo morbidade importante. A NF1 é causada por mutações no gene NF1, mas não há correlação entre genótipo e fenótipo em...

7 March 2024

20 December 2023

12 June 2023

10 June 2023

17 August 2022

  • curprev 20:1520:15, 17 August 2022DG Regio talk contribs 70,038 bytes +47,573 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 12:3212:32, 2 December 2021DG Regio talk contribs 15,004 bytes +2,424 Created claim: summary (P836): La neurofibromatose de type 1 (NF1) est l’une des maladies héréditaires les plus courantes qui prédispose au développement de certaines tumeurs bénignes et malignes dans le système nerveux et la peau. La tumeur la plus répandue chez les patients pédiatriques est le gliome optique de grade I ou l’astrocytome pilocytique qui se développe dans les nerfs optiques ou le chiasme, provoquant une morbidité importante. La NF1 est causée par des mutations...
  • curprev 12:3212:32, 2 December 2021DG Regio talk contribs 12,580 bytes +231 Changed label, description and/or aliases in fr: translated_label

12 October 2021

  • curprev 13:1713:17, 12 October 2021DG Regio talk contribs 12,349 bytes +208 Changed label, description and/or aliases in en: translated_label
  • curprev 13:1713:17, 12 October 2021DG Regio talk contribs 12,141 bytes +2,143 Created claim: summary (P836): Neurofibromatosis type 1 (NF1) is one of the most common hereditary diseases that predispose to the development of certain benign and malignant tumors in the nervous system and skin. The most prevalent tumor in paediatric patients is grade I optic glioma or pilocytic astrocytoma that develops in the optic nerves or chiasma, producing important morbidity. NF1 is caused by mutations in the NF1 gene, but there is no correlation between genotype and...

10 October 2021

9 October 2021

7 October 2021