Zobrazeno 1 - 10
of 36
pro vyhledávání: '"F J Ramos"'
Autor:
D López-Pedrajas, M Jiménez-Vázquez, A M Borreguero, F J Ramos, I Garrido, J F Rodríguez, M Carmona
Publikováno v:
Journal of Physics: Conference Series. 2116:012104
Gypsums with improved thermal properties have been obtained using a thermoregulatory nanocapsulated slurry (NPCS) as additive. In order to determine the effects of the slurries in the gypsum, physical, mechanical and thermal properties of the differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5aa29d285d8bcd333c6c9a68a1cc47
https://doi.org/10.1088/1742-6596/2116/1/012104
https://doi.org/10.1088/1742-6596/2116/1/012104
Publikováno v:
Journal of infrared, millimeter, and terahertz waves
39 (2018): 273–287. doi:10.1007/s10762-017-0451-5
info:cnr-pdr/source/autori:Martinez-Fernandez, J.; Simonetto, A.; Cappa, A.; Rincon, M. E.; Cabrera, S.; Ramos, F. J./titolo:Performance Analysis of the ITER Plasma Position Reflectometry (PPR) Ex-vessel Transmission Lines/doi:10.1007%2Fs10762-017-0451-5/rivista:Journal of infrared, millimeter, and terahertz waves (Print)/anno:2018/pagina_da:273/pagina_a:287/intervallo_pagine:273–287/volume:39
39 (2018): 273–287. doi:10.1007/s10762-017-0451-5
info:cnr-pdr/source/autori:Martinez-Fernandez, J.; Simonetto, A.; Cappa, A.; Rincon, M. E.; Cabrera, S.; Ramos, F. J./titolo:Performance Analysis of the ITER Plasma Position Reflectometry (PPR) Ex-vessel Transmission Lines/doi:10.1007%2Fs10762-017-0451-5/rivista:Journal of infrared, millimeter, and terahertz waves (Print)/anno:2018/pagina_da:273/pagina_a:287/intervallo_pagine:273–287/volume:39
As the design of the ITER Plasma Position Reflectometry (PPR) diagnostic progresses, some segments of the transmission line have become fully specified and estimations of their performance can already be obtained. This work presents the calculations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb90dd4f1e9e734c2d8281dfe98a72e
https://doi.org/10.1007/s10762-017-0451-5
https://doi.org/10.1007/s10762-017-0451-5
Autor:
A. Vera-Hernandez, Carlos Alvarado-Serrano, D. Mirabent-Amor, F. J. Ramos-Becerril, J. G. Franco-Sanchez, G. Vega-Martinez, L. Leija-Salas
Publikováno v:
2018 Global Medical Engineering Physics Exchanges/Pan American Health Care Exchanges (GMEPE/PAHCE).
Physical inactivity has a negative impact on people's health condition. Several international organisms have proposed guidelines for general populations to maintain a minimum physical activity. Overweight and obesity are triggers of physical inactivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c2be612795f06c1322e715f615dade4
https://doi.org/10.1109/gmepe-pahce.2018.8400756
https://doi.org/10.1109/gmepe-pahce.2018.8400756
Autor:
I, Parenti, C, Gervasini, J, Pozojevic, K S, Wendt, E, Watrin, J, Azzollini, D, Braunholz, K, Buiting, A, Cereda, H, Engels, L, Garavelli, R, Glazar, B, Graffmann, L, Larizza, H J, Lüdecke, M, Mariani, M, Masciadri, J, Pié, F J, Ramos, S, Russo, A, Selicorni, M, Stefanova, T M, Strom, R, Werner, J, Wierzba, G, Zampino, G, Gillessen-Kaesbach, D, Wieczorek, F J, Kaiser
Publikováno v:
Clinical Genetics, 89(5), 564-573. Wiley-Blackwell Publishing Ltd
Clinical Genetics
Clinical Genetics, Wiley, 2016, 89 (5), pp.564-573. ⟨10.1111/cge.12717⟩
Clinical Genetics, 2016, 89 (5), pp.564-573. ⟨10.1111/cge.12717⟩
Clinical Genetics
Clinical Genetics, Wiley, 2016, 89 (5), pp.564-573. ⟨10.1111/cge.12717⟩
Clinical Genetics, 2016, 89 (5), pp.564-573. ⟨10.1111/cge.12717⟩
International audience; Cornelia de Lange syndrome (CdLS) is a clinically heterogeneous disorder characterized by typical facial dysmorphism, cognitive impairment and multiple congenital anomalies. Approximately 75% of patients carry a variant in one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e59bb9753566cf4c587bcbcc9e5a3167
http://hdl.handle.net/10807/115198
http://hdl.handle.net/10807/115198
Autor:
Rossella Parini, Konstantinos Tsiakas, A. Broomfield, Persephone Augoustides-Savvopoulou, Markus A. Landolt, Pavel Ješina, P Jardine, L. De Meirleir, E Blair, Viktor Kožich, Johannes Koch, M. Zerjav Tansek, Brian Fowler, Katarina Brennerova, Andrea Schlune, Amelie S. Lotz-Havla, Terttu Suormala, Heidi Peters, Stefan Lorenzl, Barbara Plecko, Matthias R. Baumgartner, J Noss, Gülden Gökçay, Martina Huemer, Céline Bürer, Julia B. Hennermann, F J Ramos
Publikováno v:
JOURNAL OF INHERITED METABOLIC DISEASE
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Europe PubMed Central
Journal of Inherited Metabolic Disease
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Europe PubMed Central
Journal of Inherited Metabolic Disease
Background: The cobalamin E (cblE) (MTRR, methionine synthase reductase) and cobalamin G (cblG) (MTR, methionine synthase) defects are rare inborn errors of cobalamin metabolism leading to impairment of the remethylation of homocysteine to methionine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99d90fa6c54f30ce43ec9a10286d1a2
https://biblio.vub.ac.be/vubir/clinical-onset-and-course-response-to-treatment-and-outcome-in-24-patients-with-the-cble-or-cblg-remethylation-defect-complemented-by-genetic-and-in-vitro-enzyme-study-data(798936b4-79c6-4cdc-b513-bb7826bcb877).html
https://biblio.vub.ac.be/vubir/clinical-onset-and-course-response-to-treatment-and-outcome-in-24-patients-with-the-cble-or-cblg-remethylation-defect-complemented-by-genetic-and-in-vitro-enzyme-study-data(798936b4-79c6-4cdc-b513-bb7826bcb877).html
Publikováno v:
2014 Pan American Health Care Exchanges (PAHCE).
The present article is a summary of noninvasive imaging techniques, which aim is to assess feet and legs' ulcer formation and development. The objective is to early detect if an ulcer is about to develop to apply prompt treatment and reverse the proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5488f1d7b6ae4791d727e254c8f7a1f
https://doi.org/10.1109/pahce.2014.6849618
https://doi.org/10.1109/pahce.2014.6849618
Autor:
C, Baquero-Montoya, M C, Gil-Rodríguez, M E, Teresa-Rodrigo, M, Hernández-Marcos, G, Bueno-Lozano, I, Bueno-Martínez, S, Remeseiro, R, Fernández-Hernández, M, Bassecourt-Serra, M, Rodríguez de Alba, E, Queralt, A, Losada, B, Puisac, F J, Ramos, J, Pié
Publikováno v:
Clinical genetics. 85(5)
The disorders caused by mutations in genes encoding subunits and accessory proteins of cohesin complex are collectively termed as cohesinopathies. The best known cohesinopathy is Cornelia de Lange Syndrome (CdLS), which is a multisystem developmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c46c721d11f3ba8ffff190742495a22f
https://pubmed.ncbi.nlm.nih.gov/23683030
https://pubmed.ncbi.nlm.nih.gov/23683030
Autor:
P, Lapunzina Badía, M, del Campo Casanelles, A, Delicado Navarro, J, Fernández-Toral, A, García-Alix, L, García-Guereta, L A, Pérez Jurado, F J, Ramos Fuentes, A, Sánchez Díaz, M, Urioste Azcorra
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 64(3)
Beckwith-Wiedemann syndrome (BWS) is characterized by congenital overgrowth, macroglossia and omphalocele or umbilical hernia. Children with BWS may also have all or some of the following features: asymmetry (hemihypertrophy) of the limbs, torso or f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f7d22e91cc9f2f002c44f22e4d0a877
https://pubmed.ncbi.nlm.nih.gov/16527093
https://pubmed.ncbi.nlm.nih.gov/16527093
Autor:
F J, Ramos-Fuentes
Publikováno v:
Revista de neurologia. 42
Mental retardation (MR) affects approximately 2-3% of the general population and around 75% of the known causes of MR are thought to have a genetic origin. The aim of this work is to describe a standardised model of diagnostic approach to patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::befb4b23ac3e176fb23ca4fc12a1cce3
https://pubmed.ncbi.nlm.nih.gov/16506140
https://pubmed.ncbi.nlm.nih.gov/16506140
Autor:
Joaquín Olivares, M. Varea, F. J. Ramos, Antonio Clavel, A. C. Arnal, Javier Castillo, Joaquín Quílez, J. Fleta
Publikováno v:
European Journal of Clinical Microbiology & Infectious Diseases. 15:77-79
The seasonal distribution of cryptosporidiosis in children in Aragón, a region in northeastern Spain, was determined. Over a period of six years (October 1988 to September 1994), 10,034 stool samples from 4,508 children with gastrointestinal symptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b29741e78ed3273395d796061c80243a
https://doi.org/10.1007/bf01586190
https://doi.org/10.1007/bf01586190