ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB) (Q2041423)

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Revision as of 09:22, 16 December 2021 by DG Regio (talk | contribs) (‎Changed label, description and/or aliases in fr, and other parts: Adding French translations)
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Project Q2041423 in Italy
Language Label Description Also known as
English
ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB)
Project Q2041423 in Italy

    Statements

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    1,618,074.93 Euro
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    3,236,149.85 Euro
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    50.0 percent
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    29 September 2016
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    1 November 2019
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    ITALFARMACO S.P.A.
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    FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO
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    OPIS S.R.L.
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    45°33'21.82"N, 9°12'50.44"E
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    LA DISTROFIA MUSCOLARE DI BECKER (DMB) UNA PATOLOGIA NEUROMUSCOLARE APPARTENENTE AL GRUPPO DELLE DISTROFINOPATIE, DI CUI LA DISTROFIA MUSCOLARE DI DUCHENNE (DMD) RAPPRESENTA LA FORMA PI GRAVE. LE DISTROFINOPATIE SONO CAUSATE DA MUTAZIONI A CARICO DEL GENE DELLA DISTROFINA, UNA PROTEINA FONDAMENTALE PER LA STABILIZZAZIONE DEL CITOSCHELETRO NELLE FIBRE MUSCOLARI SCHELETRICHE E CARDIACHE. LA DMB UNA MALATTIA RARA, DIAGNOSTICATA TRA I 10 E 30 ANNI DI ET, CHE COLPISCE I MASCHI, CON INCIDENZA D (Italian)
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    THE MUSCULAR DYSTROPHY OF THE BECKER (DMB) MUSCULAR DYSTROPHY BELONGING TO THE DISTROFINOPATIE GROUP, OF WHICH DUCHENNE MUSCULAR DYSTROPHY (DMD) IS IN THE FORM OF A SERIOUS IP. DISTROFINOPATIE IS CAUSED BY DISTRACTED MUTATIONS OF THE DYSTROPHIN GENE, A KEY PROTEIN FOR THE STABILISATION OF MUSCULO-SKELETAL FIBRES INTO SKELETAL FIBRES. DMB IS A RARE DISEASE, DIAGNOSED IN 10 TO 30 YEARS OF ET, WHICH AFFECTS MALES, WITH INCIDENCE D (English)
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    LA DYSTROPHIE MUSCULAIRE DE BECKER (DMB) EST UNE PATHOLOGIE NEUROMUSCULAIRE APPARTENANT AU GROUPE DISTROFINOPATIE, DONT LA DYSTROPHIE MUSCULAIRE DE DUCHENNE (DMD) EST LA FORME SÉVÈRE DE PI. LES DISTROFINOPATIES SONT CAUSÉES PAR DES MUTATIONS DANS LE GÈNE DYSTROPHINE, UNE PROTÉINE FONDAMENTALE POUR LA STABILISATION DU CYTOSQUELETTE DANS LES FIBRES MUSCULAIRES SQUELETTIQUES ET CARDIAQUES. DMB EST UNE MALADIE RARE, DIAGNOSTIQUÉE ENTRE 10 ET 30 ANS ET, AFFECTANT LES HOMMES, AVEC INCIDENCE DE: (French)
    16 December 2021
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    Identifiers

    E76D17000080009
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