Zobrazeno 1 - 10
of 18
pro vyhledávání: '"J. M. Fernández Rodríguez"'
Publikováno v:
Materiales de Construccion, Vol 54, Iss 275, Pp 39-52 (2004)
This paper describes the analysis of Roman mortars in two rooms of a villa at El Ruedo, Almedinilla, Cordoba. The techniques or procedures used included grain size distribution analysis and X ray diffraction. The decorative materials used in the vari
Externí odkaz:
https://doaj.org/article/254fa325b6174db1895308ff337ca914
Autor:
J. P. Miramontes González, J. M. Fernández Rodríguez, E. Puerto Pérez, J. M. Sánchez Tocino, N. Cubino Bóveda, S. Carrero García
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 101, Iss 6, Pp 424-426 (2009)
Externí odkaz:
https://doaj.org/article/1ef7cdd4c0f34849ad9480cb44410fb2
Autor:
J, Carretero Gómez, J C, Arévalo Lorido, R, Gómez Huelgas, M T, Sánchez Vidal, M, Suárez Tembra, J M, Varela Aguilar, I, Munielo Voces, E, Fernández Pérez, J M, Fernández Rodríguez, J, Ena Muñoz
Publikováno v:
Revista clinica espanola. 217(2)
To estimate the prevalence of obesity in patients treated by departments of Internal Medicine and to classify the patients according to the Edmonton Obesity Staging System (EOSS).An observational, descriptive cross-sectional study included outpatient
Publikováno v:
Materiales de Construcción. 54:39-52
This paper describes the analysis of Roman mortars in two rooms of a villa at El Ruedo, Almedinilla, Cordoba. The techniques or procedures used included grain size distribution analysis and X ray diffraction. The decorative materials used in the vari
Publikováno v:
Scandinavian journal of medicinescience in sports. 24(1)
To analyze the effects of an intervention focused on increasing the time and intensity of Physical Education (PE), on adolescents' cognitive performance and academic achievement. A 4-month group-randomized controlled trial was conducted in 67 adolesc
Autor:
S. Carrero García, J. M. Fernández Rodríguez, J.P. Miramontes González, J. M. Sánchez Tocino, E. Puerto Pérez, N. Cubino Bóveda
Publikováno v:
Revista Española de Enfermedades Digestivas v.101 n.6 2009
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
We report the case of a 22-year-old male patient who was admitted at the ER because of abdominal pain for 9 days. His personal record did not reveal any significant findings, operations, toxic habits, or regular medications. The patient reported abdo
[Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification]
Autor:
S, Teijeira-Bautista, D, García-García, A, Teijeiro-Ferreira, R, Fernández-Hojas, J M, Fernández-Rodríguez, C, Navarro-Fernández-Balbuena
Publikováno v:
Revista de neurologia. 26(154)
To review the up-dated classification of limb girdle muscular dystrophies (LGMDs) in relation to the defective protein and the genetic abnormality. To explain how these proteins are related to dystrophin and to the proteins of the extracellular matri
Autor:
D, García-García, S, Teijeira-Bautista, J M, Fernández-Rodríguez, J, Flores-Calvete, P, Sánchez-Espíldora, D, Fernández-Couto, I, Cimas-Hernando, A, Teijeiro-Ferreira, R, Fernández-Hojas, J, Brasa-Fernández Fierros, A, Martínez de Alegría, J L, Escribano-Arias, M, Núñez-Delgado, C, Navarro-Fernández Balbuena
Publikováno v:
Revista de neurologia. 26(154)
Limb Girdle Muscular Dystrophy type 2C (LGMD2C) is an autosomal recessive dystrophy due to the deficit of gamma-sarcoglycan, one of the proteins of the dystrophin-associated proteins complex (DAP). A new mutation in the gamma-sarcoglycan gene, 13q12,
Autor:
Fernández-Hojas R, D García-García, A Teijeiro-Ferreira, S Teijeira-Bautista, C Navarro-Fernández-Balbuena, J M Fernández-Rodríguez
Publikováno v:
Revista de Neurología. 26:1021
Objectives To review the up-dated classification of limb girdle muscular dystrophies (LGMDs) in relation to the defective protein and the genetic abnormality. To explain how these proteins are related to dystrophin and to the proteins of the extracel
Autor:
Sánchez-Espíldora P, Flores-Calvete J, Fernández-Hojas R, Martínez de Alegría A, Núñez-Delgado M, A Teijeiro-Ferreira, D García-García, Cimas-Hernando I, Navarro-Fernández Balbuena C, J M Fernández-Rodríguez, Fernández-Couto D, Escribano-Arias Jl, S Teijeira-Bautista, Brasa-Fernández Fierros J
Publikováno v:
Revista de Neurología. 26:905
INTRODUCTION Limb Girdle Muscular Dystrophy type 2C (LGMD2C) is an autosomal recessive dystrophy due to the deficit of gamma-sarcoglycan, one of the proteins of the dystrophin-associated proteins complex (DAP). A new mutation in the gamma-sarcoglycan