Výsledky vyhledávání - "Santana-Artiles A"

Estudios de inmovilización de Saccharomyces cerevisiae sobre distintos soportes para segunda fermentación del cava

Publikováno v: RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
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[ES] En la producción de vino espumoso tienen lugar dos fermentaciones sucesivas llevadas a cabo por la levadura Saccharomyces cerevisiae. En la actualidad, se estudian nuevas metodologías para mejorar el rendimiento de esta segunda fermentación,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::06ddcf3c213dca333788e38df9c869a7
https://hdl.handle.net/10251/171355

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Akademický článek

Numerical investigation of the effect of bone cement porosity on osteoporotic femoral augmentation.

Autor: Santana Artiles, María E.¹, Venetsanos, Demetrios T.² ac6109@coventry.ac.uk

Publikováno v: International Journal for Numerical Methods in Biomedical Engineering. Aug2018, Vol. 34 Issue 8, p1-1. 14p.

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A new evolutionary optimization method for osteoporotic bone augmentation

Autor: Demetrios T. Venetsanos, María E. Santana Artiles

Publikováno v: Computer Methods in Biomechanics and Biomedical Engineering. 20:691-700

Bone augmentation is a preventative osteoporosis intervention, comprising the injection of bone cement into an osteoporotic bone. As injection of excessive amounts of bone cement may result into thermal necrosis of bone tissue or even embolism, the m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81f86d4e46d4d042d5b6654ecce5cdb
https://doi.org/10.1080/10255842.2017.1291805

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Molecular characterization of congenital myasthenic syndromes in Spain

Publikováno v: NEUROMUSCULAR DISORDERS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
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r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Neuromuscular disorders : NMD
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe

Congenital myasthenic syndromes (CMS) are a heterogeneous group of genetic disorders, all of which impair neuromuscular transmission. Epidemiological data and frequencies of gene mutations are scarce in the literature. Here we describe the molecular

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b967c96669f268f9a18032854a15ab37
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13108

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Notes on the biology of the deep-sea crab Paramola cuvieri (Risso, 1816) (Decapoda, Homolidae) in the Canary Islands (central-east Atlantic)

Autor: Y. Pérez-González, V. Hernández-García, J. A. Martí-Trujillo, José J. Castro, A. T. Santana-Ortega, G. Santana-Artiles

Publikováno v: Crustaceana. 87:1-18

The box crab (Paramola cuvieri) was relatively frequent in trap catches from 288 to 906 m depth off the Canary Islands (central-east Atlantic), the greatest abundance being recorded between 400 and 700 m. From winter to the beginning of summer, a dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::14421d1bca58720c2f03b09067597682
https://doi.org/10.1163/15685403-00003271

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[Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report]

Autor: Florido-Rodriguez A, Eiris-Punal J, Barros-Angueira F, Toledo-Bravo de Laguna L, Santana-Artiles A, Sebastian-Garcia I, Santana-Rodriguez A, Jc, Cabrera-Lopez

Publikováno v: Europe PubMed Central

Aicardi-Goutieres syndrome is a rare progressive subacute encephalopathy of early onset - generally in the first year of life - characterised by psychomotor retardation, microcephaly, alterations in the white matter of the brain, intracranial calcifi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8043b35b872e0cf09fe3fc30b74d0f6f
https://pubmed.ncbi.nlm.nih.gov/27658362

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[X-linked hereditary spastic paraplegia due to mutation in the L1CAM gene: three cases reports of CRASH syndrome]

Autor: Abián, Muñoz, José C, Cabrera-López, Alfredo, Santana-Rodríguez, Laura, Toledo-Bravo de Laguna, Alexandre, Santana-Artiles, Irma, Sebastián-García

Publikováno v: Revista de neurologia. 62(5)

Hereditary spastic paraplegia (HSP) is a set of neurodegenerative clinical features characterised by a progressive loss of strength in the lower limbs together with spasticity. It is the result of an axonal lesion in the corticospinal tracts. Type 1,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::88b05be14ea532e050a13adf167999e6
https://pubmed.ncbi.nlm.nih.gov/26916325

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