Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Rebeca Losada Del Pozo"'
Autor:
Víctor Soto Insuga, Beatriz Moreno Vinués, Rebeca Losada del Pozo, María Rodrigo Moreno, Marta Martínez González, Raquel Cutillas Ruiz, Carmen Mateos Carmen
Publikováno v:
Anales de Pediatría, Vol 88, Iss 4, Pp 191-195 (2018)
Resumen: Introducción: La marcha de puntillas idiopática (MPI) se describe como el patrón de marcha sin apoyo del talón en niños mayores de 3 años. El diagnóstico es clínico y obliga a descartar otras enfermedades neurológicas y traumatológ
Externí odkaz:
https://doaj.org/article/a93aad51350b4513a80061577efd624f
Autor:
Víctor Soto Insuga, Beatriz Moreno Vinués, Rebeca Losada del Pozo, María Rodrigo Moreno, Marta Martínez González, Raquel Cutillas Ruiz, Carmen Mateos Carmen
Publikováno v:
Anales de Pediatría (English Edition), Vol 88, Iss 4, Pp 191-195 (2018)
Introduction: Idiopathic toe-walking (ITW) is described as a gait pattern with no contact between the heels and the ground in children older than 3 years. The diagnosis is clinical, making it necessary to rule out other neurological and orthopaedic c
Externí odkaz:
https://doaj.org/article/fb63733c99b64526bc3da0c447772fa9
Autor:
Eulàlia Turón-Viñas, Mercè Pineda, Victòria Cusí, Eduardo López-Laso, Rebeca Losada del Pozo, Luis González Gutiérrez-Solana, David Conejo Moreno, Concha Sierra-Córcoles, Naiara Olabarrieta-Hoyos, Marcos Madruga-Garrido, Javier Aguirre-Rodríguez, Verónica González-Álvarez, Mar O’Callaghan, Jordi Muchart, Judith Armstrong-Moron
Publikováno v:
Journal of Central Nervous System Disease, Vol 2014, Iss 6, Pp 59-68 (2014)
Externí odkaz:
https://doaj.org/article/7d82afabc4a44215a8fb849d52ef7c8b
Autor:
Elena Martinez-Cayuelas, Teresa Gavela-Pérez, María Rodrigo-Moreno, Rebeca Losada-Del Pozo, Beatriz Moreno-Vinues, Carmen Garces, Leandro Soriano-Guillén
Publikováno v:
Journal of Autism and Developmental Disorders.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f84db710117b865a4c9a285aed366bfa
https://doi.org/10.1007/s10803-023-05934-7
https://doi.org/10.1007/s10803-023-05934-7
[Oral desensitization with Ketocal® in an infant with ketogenic diet and cow's milk protein allergy]
Autor:
Cristina Benítez Provedo, María Angeles Martínez Ibeas, Rebeca Losada del Pozo, Ana María Montes Arjona, Miriam Blanco Rodríguez, Genoveva del Río Camacho
Publikováno v:
Nutricion hospitalaria. 39(6)
Introduction: ketogenic diet is a treatment with proven efficacy in drug-refractory childhood epilepsy. Cow's milk protein allergy may be a limitation for treating infants with ketogenic diet, as they need a product that contains cow's milk protein (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9fb1ba9fe0d2fb59f3d814ded568026
https://pubmed.ncbi.nlm.nih.gov/36250770
https://pubmed.ncbi.nlm.nih.gov/36250770
Autor:
Elena Martinez-Cayuelas, Milagros Merino-Andreu, Rebeca Losada-Del Pozo, Teresa Gavela-Pérez, Carmen Garcés, Leandro Soriano-Guillén
Publikováno v:
Journal of Child Neurology. :088307382311736
Melatonin is one of the most used pharmacologic treatments for sleep problems in autism spectrum disorder, though its relationship with circadian and sleep parameters is still not well stablished. A naturalistic study was conducted in children with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c29cb22bcd8051cd4a2f12a32144f54
https://doi.org/10.1177/08830738231173606
https://doi.org/10.1177/08830738231173606
Autor:
Elena Martinez-Cayuelas, Fiona Blanco-Kelly, Fermina Lopez-Grondona, Saoud Tahsin Swafiri, Rosario Lopez-Rodriguez, Rebeca Losada-Del Pozo, Ignacio Mahillo-Fernandez, Beatriz Moreno, Maria Rodrigo-Moreno, Didac Casas-Alba, Aitor Lopez-Gonzalez, Sixto García-Miñaúr, Maria Ángeles Mori, Marta Pacio-Minguez, Emi Rikeros-Orozco, Fernando Santos-Simarro, Jaime Cruz-Rojo, Juan Francisco Quesada-Espinosa, Maria Teresa Sanchez-Calvin, Jaime Sanchez-del Pozo, Raquel Bernado Fonz, Maria Isidoro-Garcia, Irene Ruiz-Ayucar, Maria Isabel Alvarez-Mora, Raquel Blanco-Lago, Begoña De Azua, Jesus Eiris, Juan Jose Garcia-Peñas, Belen Gil-Fournier, Carmen Gomez-Lado, Nadia Irazabal, Vanessa Lopez-Gonzalez, Irene Madrigal, Ignacio Malaga, Beatriz Martinez-Menendez, Soraya Ramiro-Leon, Maria Garcia-Hoyos, Pablo Prieto-Matos, Javier Lopez-Pison, Sergio Aguilera-Albesa, Sara Alvarez, Alberto Fernández-Jaén, Isabel Llano-Rivas, Blanca Gener-Querol, Carmen Ayuso, Ana Arteche-Lopez, Maria Palomares-Bralo, Anna Cueto-González, Irene Valenzuela, Antonio Martinez-Monseny, Isabel Lorda-Sanchez, Berta Almoguera
SUMMARYBackgroundKBG syndrome is a highly variable neurodevelopmental disorder and clinical diagnostic criteria have changed as new patients have been published. Both loss-of-function sequence variants and large deletions (CNVs) involving ANKRD11 hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::772e2630b0edef5f7aa24d37fceea547
https://doi.org/10.1101/2022.04.11.22271283
https://doi.org/10.1101/2022.04.11.22271283
Autor:
Marta Rodriguez de Alba, María Rodrigo-Moreno, Rosa Riveiro-Alvarez, Berta Almoguera, Carolina Sanchez-Jimeno, Carmen Ayuso, María Fenollar-Cortés, Fiona Blanco-Kelly, Beatriz Moreno, Elena Martinez-Cayuelas, Isabel Lorda-Sanchez, Fermina López-Grondona, Rebeca Losada-Del Pozo
Publikováno v:
Genes
Volume 12
Issue 9
Genes, Vol 12, Iss 1360, p 1360 (2021)
Volume 12
Issue 9
Genes, Vol 12, Iss 1360, p 1360 (2021)
Haploinsufficiency of AUTS2 has been associated with a syndromic form of neurodevelopmental delay characterized by intellectual disability, autistic features, and microcephaly, also known as AUTS2 syndrome. While the phenotype associated with large d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359c4edcced05df6790ed37ed2127744
http://europepmc.org/articles/PMC8471078
http://europepmc.org/articles/PMC8471078
Autor:
María Rodrigo Moreno, Víctor Soto Insuga, Rebeca Losada del Pozo, Marta Martínez González, Carmen Mateos Carmen, Beatriz Moreno Vinués, Raquel Cutillas Ruiz
Publikováno v:
Anales de Pediatría (English Edition), Vol 88, Iss 4, Pp 191-195 (2018)
Introduction: Idiopathic toe-walking (ITW) is described as a gait pattern with no contact between the heels and the ground in children older than 3 years. The diagnosis is clinical, making it necessary to rule out other neurological and orthopaedic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a477f5493b137ba7ac2eadf6673c6951
http://www.sciencedirect.com/science/article/pii/S2341287918300450
http://www.sciencedirect.com/science/article/pii/S2341287918300450
Autor:
Ester Díaz-Gómez, Elena Martínez Cayuelas, Rebeca Losada-Del Pozo, Rosa Guerrero López, Víctor Soto-Insuga, Gema Sánchez-Martín, Laura Olivié García, Grupo Español de Genética de las Epilepsias de la Infancia, Beatriz G. Giráldez, María Rodrigo-Moreno, José M. Serratosa
Publikováno v:
Epilepsy research. 154
Glucose transporter type 1 deficiency syndrome (GLUT1-DS) is a rare genetic disorder caused by pathogenic variants in SLC2A1, resulting in impaired glucose uptake through the blood-brain barrier. Our objective is to analyze the frequency of GLUT1-DS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a03b4e8c4adcf16c497813408b672026
https://pubmed.ncbi.nlm.nih.gov/31035243
https://pubmed.ncbi.nlm.nih.gov/31035243