ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB) (Q2041423): Difference between revisions
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(Created claim: summary (P836): 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, Adding English s...) |
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Property / summary | |||
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) | |||
Property / summary: 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) / rank | |||
Normal rank |
Revision as of 09:38, 23 March 2020
Project in Italy financed by DG Regio
Language | Label | Description | Also known as |
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English | ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB) |
Project in Italy financed by DG Regio |
Statements
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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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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Identifiers
E76D17000080009
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