Výsledky vyhledávání - "Marta Cerezo-García"

Predicting conversion to multiple sclerosis by assessing cognitive impairment in radiologically isolated syndrome

Autor: Juan Antonio Hernández-Tamames, M Luisa Martínez-Ginés, Yolanda Higueras-Hernández, Andrés Labiano-Fontcuberta, Lucía Ayuso-Peralta, Marta Cerezo-García, Verónica Puertas-Martín, Virginia Mato-Abad, Julián Benito-León, Juan Álvarez-Linera, Yolanda Aladro-Benito, Ángela Domingo-Santos

Publikováno v: Multiple sclerosis and related disorders. 49

Up to a third of patients with radiologically isolated syndrome (RIS) exhibit lower-than-expected cognitive performances in neuropsychological evaluations, but the relationship between cognitive impairment (CI) and quantitative magnetic resonance (MR

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b386d8896ef153bd1967b889b68e4a
https://pubmed.ncbi.nlm.nih.gov/33486398

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Central Hypothyroidism and Novel Clinical Phenotypes in Hemizygous Truncation of TBL1X

Autor: Juan Martínez-San Millán, Isabel González-Casado, Ana C Barreda-Bonis, Elena Vallespín, Arancha Ortiz, Paula Jiménez, José Moreno, Angela del Pozo, Ignacio Rabanal, Marta Cerezo García

Publikováno v: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Journal of the Endocrine Society

Transducin β-like 1 X-linked (TBL1X) gene encodes a subunit of the nuclear corepressor-silencing mediator for retinoid and thyroid hormone receptor complex (NCoR-SMRT) involved in repression of thyroid hormone action in the pituitary and hypothalamu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fad1e6d63a8ffb2b122cdb43654db0f7
https://doi.org/10.1210/js.2018-00144

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Relationship between episodic memory and volume of the brain regions of two functional cortical memory systems in multiple sclerosis

Autor: Juan Antonio Hernández-Tamames, Laudino López-Alvarez, Jorge Mario Sánchez-Reyes, Helena Melero, Marta Cerezo-García, Israel Thuissard, Sandra Rubio-Fernández, Yolanda Aladro

Publikováno v: Journal of Neurology, 265(10), 2182-2189. D. Steinkopff-Verlag

Background/objective: Two functional networks are proposed as neuronal support for the complex processes of memory: the anterior temporal and the medial posterior systems. We examined the atrophy of hippocampus (HC) and of those areas constituting th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374d114020ea96392bac78b47f261008
https://doi.org/10.1007/s00415-018-8965-x

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Central Hypothyroidism Due to a TRHR Mutation Causing Impaired Ligand Affinity and Transactivation of Gq

Autor: Leonardo Pardo, Jesús González de Buitrago, José Moreno, Patricia M. Hinkle, Mireia Jiménez-Rosés, Marta Cerezo García

Publikováno v: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid

Context:Central congenital hypothyroidism (CCH) is an underdiagnosed disorder characterized by deficient production and bioactivity of thyroid-stimulating hormone (TSH) leading to low thyroid hormone synthesis. Thyrotropin-releasing hormone (TRH) rec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdadc8b022faeb2e5c84045ca2fc84ec
https://europepmc.org/articles/PMC5505191/

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The syndrome of central hypothyroidism and macroorchidism: IGSF1 controls TRHR and FSHB expression by differential modulation of pituitary TGFβ and Activin pathways

Publikováno v: Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Scientific Reports
Scientific Reports, 7. Nature Publishing Group

IGSF1 (Immunoglobulin Superfamily 1) gene defects cause central hypothyroidism and macroorchidism. However, the pathogenic mechanisms of the disease remain unclear. Based on a patient with a full deletion of IGSF1 clinically followed from neonate to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b16c19fb1e502a0d9ed25df18d2008a

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Alteration profile of executive functions in multiple sclerosis

Autor: Yolanda Aladro Benito, Pilar Martín Plasencia, Marta Cerezo García

Publikováno v: Acta neurologica Scandinavica. 131(5)

Objective Executive functions (EF) in multiple sclerosis (MS) have been only partially studied, mainly trough the evaluation of subfunctions. The main objective was to analyse the EF alteration profile in a patients with MS sample. Participants and m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5ddfca2d0b5d011e9b54fb7042bce4
https://pubmed.ncbi.nlm.nih.gov/25659411

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Neuropsychological syndromes in multiple sclerosis

Autor: Ma José, Gil Moreno, Marta, Cerezo García, Raluca, Marasescu, Ana, Pinel González, Laudino, López Álvarez, Yolanda, Aladro Benito

Publikováno v: Psicothema. 25(4)

Cognitive impairment in multiple sclerosis (MS) is common (45-65%).Deficits occur in speed of information processing (SIP), memory, attention, executive functions (EF) and visuoconstruction.Involvement of cognitive functions like language and gnosis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f4fe82a8ba886d58206aa3edad04945f
https://pubmed.ncbi.nlm.nih.gov/24124777

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Executive function and memory in patients with relapsing-remitting multiple sclerosis

Autor: Marta, Cerezo García, Pilar, Martín Plasencia, Yolanda, Aladro Benito, José Jesús, Balseiro Gómez, Almudena, Rueda Marcos

Publikováno v: Psicothema. 21(3)

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system very heterogeneous in its characteristics. In contrast to the well known sensitive/motor deficits, the cognitive dysfunction has only been analyzed in the last fe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::71b99bf9c1656ee03ea10bdb0235133f
https://pubmed.ncbi.nlm.nih.gov/19622322

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Craniofacial dyssynostosis: description of the first four Spanish cases and review

Autor: Alicia Delicado, Pablo Lapunzina, Enrique Galán, Isidora López-Pajares, Eva Bermejo, María-Dolores Márquez, Angel Pantoja, Virginia Soler, Alicia Ureta, María Luisa Martínez-Frías, Emiliano Mora, L. Cuevas, Marta Cerezo García, Valentín Félix

Publikováno v: American journal of medical genetics. Part A. (1)

Craniofacial dyssynostosis (CD) is characterized by premature fusion of the lambdoid and posterior part of the sagittal sutures, and short stature. Thus, the skull shape becomes dolichocephalic with protuberant forehead and either bulging or flat occ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7d5a63a44af446cdd9f91f44024d00
https://pubmed.ncbi.nlm.nih.gov/15551327

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