Zobrazeno 1 - 10
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pro vyhledávání: '"Valls, Andrea"'
Autor:
García, Juan Fernando, Reguera, David, Valls, Andrea, Aviñó, Anna, Dominguez, Arnau, Eritja, Ramon, Gargallo, Raimundo
Publikováno v:
In Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 5 September 2023 297
Autor:
Rico, Anabel1,2 (AUTHOR), Valls, Andrea1,2 (AUTHOR), Guembelzu, Garazi1,2 (AUTHOR), Azpitarte, Margarita3 (AUTHOR), Aiastui, Ana4 (AUTHOR), Zufiria, Mónica1,2 (AUTHOR), Jaka, Oihane1,2 (AUTHOR), López de Munain, Adolfo1,2,4,5,6 (AUTHOR), Sáenz, Amets1,2 (AUTHOR) amets.saenzpena@osakidetza.eus
Publikováno v:
Orphanet Journal of Rare Diseases. 10/10/2023, Vol. 18 Issue 1, p1-16. 16p.
Akademický článek
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Rotating-coil magnetometers, which rely on induction-coil arrays, are commonly used for magnetic measurements of particle accelerator magnets. In order to characterize magnetic fields with high accuracy using the induced voltages, it is essential to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3484::27cac59af328b3a17e60aae20def43c9
https://hdl.handle.net/2117/375131
https://hdl.handle.net/2117/375131
Akademický článek
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Autor:
Rodríguez Valls, Andrea
Publikováno v:
RIULL. Repositorio Institucional de la Universidad de La Laguna
Universidad de La Laguna (ULL)
Universidad de La Laguna (ULL)
The written documents referring to the Bat emblem do not provide enough details to properly identify its features. In the study of this sacred element, it is convenient to undertake an iconographic analysis of its depictions in order to determine its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::36d6d39547b886d9dab88c7087fd345e
http://riull.ull.es/xmlui/handle/915/22127
http://riull.ull.es/xmlui/handle/915/22127
Autor:
Rico, Anabel, Guembelzu, Garazi, Palomo, Valle, Martínez, Ana, Aiastui, Ana, Casas-Fraile, Leire, Valls, Andrea, López de Munain, Adolfo, Sáenz, Amets
Publikováno v:
International Journal of Molecular Sciences; Jul2021, Vol. 22 Issue 14, p7367-7367, 1p
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
instname
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
3D Hall probes designed and produced by ALBA Synchrotron are currently being used at ALBA magnetic measurements laboratory to carry out accurate magnetic characterization of magnets and insertion devices. In order to characterize the magnetic fields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::848e2a347bfac69baf709082886a58d9
http://hdl.handle.net/2117/168009
http://hdl.handle.net/2117/168009
Autor:
Coll Martínez, Sandra, Pons Benaiges, Oriol, Torres Valls, Andrea, Vives Bordoy, Antònia Maria
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat. Dipósit de la Recerca de Catalunya
instname
Aquest treball pretén analitzar l’ús dels procediments heurístics i els seus biaixos. Per això, hemrealitzat un estudi entre dues poblacions: 4rt d’Humanitats i 4rt d’ECO/ADE. Per dur a termeaquesta comparació hem realitzat una enquesta qu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9a3d2cee1c43e21355e8c7729dfd5c3d
http://hdl.handle.net/10230/16229
http://hdl.handle.net/10230/16229
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