Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anabel Rico"'
Autor:
Anabel Rico, Andrea Valls, Garazi Guembelzu, Margarita Azpitarte, Ana Aiastui, Mónica Zufiria, Oihane Jaka, Adolfo López de Munain, Amets Sáenz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-16 (2023)
Abstract Background Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy due to mutations in the CAPN3 gene. While the pathophysiology of this disease has not been clearly established yet, Wnt and
Externí odkaz:
https://doaj.org/article/c98a543474c243b18fb6ae233988a467
Autor:
Leire Casas-Fraile, Frederique M. Cornelis, Domiziana Costamagna, Anabel Rico, Robin Duelen, Maurilio M. Sampaolesi, Adolfo López de Munain, Rik J. Lories, Amets Sáenz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-18 (2020)
Abstract Background Limb-girdle muscular dystrophy recessive 1 calpain3-related (LGMDR1), previously known as LGMD2A, is a disease caused by mutations in the CAPN3 gene. It is characterized by progressive weakness and muscle degeneration. Frizzled re
Externí odkaz:
https://doaj.org/article/5f3946e625b847ba8cc43717179513b4
Autor:
Anabel Rico, Garazi Guembelzu, Valle Palomo, Ana Martínez, Ana Aiastui, Leire Casas-Fraile, Andrea Valls, Adolfo López de Munain, Amets Sáenz
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 14, p 7367 (2021)
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while the pathophysiological mec
Externí odkaz:
https://doaj.org/article/f620c792fcf24c9dbeb406f528e23112
Autor:
Leire Casas-Fraile, Valle Palomo, Garazi Guembelzu, Anabel Rico, Ana Aiastui, Amets Sáenz, Adolfo López de Munain, Andrea Valls, Ana Martínez
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7367, p 7367 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7367, p 7367 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
18 p.-8 fig.-1 tab.
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while t
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while t
Autor:
Rik Lories, Anabel Rico, Robin Duelen, Amets Sáenz, Maurilio Sampaolesi, Leire Casas-Fraile, F.M. Cornelis, Adolfo López de Munain, Domiziana Costamagna
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-18 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-18 (2020)
Background Limb-girdle muscular dystrophy recessive 1 calpain3-related (LGMDR1), previously known as LGMD2A, is a disease caused by mutations in the CAPN3 gene. It is characterized by progressive weakness and muscle degeneration. Frizzled related pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a92d1e1bf7f42ef73d15ae91d9ff318
https://lirias.kuleuven.be/handle/123456789/655917
https://lirias.kuleuven.be/handle/123456789/655917
Autor:
Domiziana Costamagna, A. López de Munain, F.M. Cornelis, Amets Sáenz, L. Casas-Fraile, Rik Lories, Anabel Rico, Maurilio Sampaolesi
Publikováno v:
Osteoarthritis and Cartilage. 26:S401
Publikováno v:
Molecules in Time and Space ISBN: 0306485788
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::578fca011803c3b520205d887d0598f6
https://doi.org/10.1007/0-306-48579-6_9
https://doi.org/10.1007/0-306-48579-6_9