Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Noelia García González"'
Publikováno v:
INFAD, Vol 2, Iss 1, Pp 155-162 (2014)
Este trabajo pretende dar a conocer el programa preventivo ADHISO diseñado para la mejora de las habilidades atencionales y cognitivas, así como las conductas hiperactivas e impulsivas de los alumnos de educación infantil que presentan sintomatolo
Externí odkaz:
https://doaj.org/article/5c647150bb554709b537103682490048
Autor:
Igor Vazquez-Osorio, Noelia García-González, Mónica Viejo-Díaz, Pablo Gonzalvo-Rodríguez, Eloy Rodríguez-Díaz
Publikováno v:
Indian Journal of Dermatology, Vol 66, Iss 1, Pp 93-95 (2021)
Externí odkaz:
https://doaj.org/article/44476ddf174c4279bd614cf708466cd7
Autor:
Rubén Cabanillas, Marta Diñeiro, Guadalupe A. Cifuentes, David Castillo, Patricia C. Pruneda, Rebeca Álvarez, Noelia Sánchez-Durán, Raquel Capín, Ana Plasencia, Mónica Viejo-Díaz, Noelia García-González, Inés Hernando, José L. Llorente, Alfredo Repáraz-Andrade, Cristina Torreira-Banzas, Jordi Rosell, Nancy Govea, Justo Ramón Gómez-Martínez, Faustino Núñez-Batalla, José A. Garrote, Ángel Mazón-Gutiérrez, María Costales, María Isidoro-García, Belén García-Berrocal, Gonzalo R. Ordóñez, Juan Cadiñanos
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-17 (2018)
Abstract Background Sensorineural hearing loss (SNHL) is the most common sensory impairment. Comprehensive next-generation sequencing (NGS) has become the standard for the etiological diagnosis of early-onset SNHL. However, accurate selection of targ
Externí odkaz:
https://doaj.org/article/349bbb0f700a431083cd99f349786e3a
Autor:
Elisa García-García, Mercedes Rodríguez-Pérez, David Pérez-Solís, Carlos Pérez-Méndez, Cristina Molinos-Norniella, Ángeles Cobo-Ruisánchez, Eva María Fernández Fernández, Noelia García González, Laura Calle-Miguel
Publikováno v:
World Journal of Pediatrics. 18:835-844
Updated seroprevalence estimates are important to describe the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) landscape and to guide public health decisions. The aims are to describe longitudinal changes in seroprevalence in children in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::693edd0eabcf79120cc6019c9c3e83ca
https://doi.org/10.1007/s12519-022-00617-2
https://doi.org/10.1007/s12519-022-00617-2
Autor:
Alicia M Lois Bermejo, Juan C Rial, Sonsoles Suárez Saavedra, Noelia García González, Marta Costa-Romero, Helena Fernández-Rodríguez, Andrea Álvarez-Álvarez
Publikováno v:
Archivos Argentinos de Pediatria. 119
Hydrocephalus is a clinical condition that consists of an accumulation of cerebrospinal fluid around the brain; Dandy- Walker syndrome is a rare cause of it. We present the case of a newborn with prenatal diagnose of hydrocephalus due to a Dandy-Walk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3688f33df31497b24da96ce66abfc31
https://doi.org/10.5546/aap.2021.e526
https://doi.org/10.5546/aap.2021.e526
Autor:
Ann Sophie Kaiser, Fowzan S. Alkuraya, Trevor Cole, Paul A. Mulder, Pablo Lapunzina, Inge B. Mathijssen, Jan Liebelt, Claire G. Salter, Pierre Sarda, Jill A. Fahrner, Manuela Priolo, Dorothee Neubauer, Nursel Elcioglu, Denny Schanze, Katrin Tatton-Brown, Sarah F. Smithson, Jair Tenorio, Thomas E. Neumann, Charles Shaw-Smith, Letizia Pintomalli, Shane McKee, Emilia K. Bijlsma, Sally J. Davies, Sue Price, Rajesh V. Thakker, Noelia García González, Rita Valdez, Sally Ann Lynch, Nataliya Di Donato, Arie van Haeringen, Astrid S. Plomp, Inés Hernández Acero, Ilka Huber, Marcela Zollino, Laura Bernardini, Raoul C.M. Hennekam, Martin Zenker, Mohnish Suri, Mabel Segovia, Johanna M. van Hagen, Ghayda Mirzaa, Leonie A. Menke, Kreepa Kooblall, Arveen Kamath, Christine Coubes, I. Dapia, Corrado Mammì, Alison Foster, Tara Montgomery, Pedro Arias, Fernando Santos-Simarro, Maria Iascone, Maria Antonietta Pisanti, Saskia M. Maas
Publikováno v:
Human Mutation
Human mutation, 39(9), 1226-1237. Wiley-Liss Inc.
Human Mutation, 39(9), 1226-1237
Priolo, M, Schanze, D, Tatton-Brown, K, Mulder, P A, Tenorio, J, Kooblall, K, Acero, I H, Alkuraya, F S, Arias, P, Bernardini, L, Bijlsma, E K, Cole, T, Coubes, C, Dapia, I, Davies, S, Di Donato, N, Elcioglu, N H, Fahrner, J A, Foster, A, González, N G, Huber, I, Iascone, M, Kaiser, A S, Kamath, A, Liebelt, J, Lynch, S A, Maas, S M, Mammì, C, Mathijssen, I B, McKee, S, Menke, L A, Mirzaa, G M, Montgomery, T, Neubauer, D, Neumann, T E, Pintomalli, L, Pisanti, M A, Plomp, A S, Price, S, Salter, C, Santos-Simarro, F, Sarda, P, Segovia, M, Shaw-Smith, C, Smithson, S, Suri, M, Valdez, R M, Van Haeringen, A, Van Hagen, J M, Zollino, M, Lapunzina, P, Thakker, R V, Zenker, M & Hennekam, R C 2018, ' Further delineation of Malan syndrome ', Human Mutation, vol. 39, no. 9, pp. 1226-1237 . https://doi.org/10.1002/humu.23563
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Priolo, M, Schanze, D, Tatton-Brown, K, Mulder, P A, Tenorio, J, Kooblall, K, Acero, I H, Alkuraya, F S, Arias, P, Bernardini, L, Bijlsma, E K, Cole, T, Coubes, C, Dapia, I, Davies, S, di Donato, N, Elcioglu, N H, Fahrner, J A, Foster, A, González, N G, Huber, I, Iascone, M, Kaiser, A-S, Kamath, A, Liebelt, J, Lynch, S A, Maas, S M, Mammì, C, Mathijssen, I B, McKee, S, Menke, L A, Mirzaa, G M, Montgomery, T, Neubauer, D, Neumann, T E, Pintomalli, L, Pisanti, M A, Plomp, A S, Price, S, Salter, C, Santos-Simarro, F, Sarda, P, Segovia, M, Shaw-Smith, C, Smithson, S, Suri, M, Valdez, R M, van Haeringen, A, van Hagen, J M, Zollino, M, Lapunzina, P, Thakker, R V, Zenker, M & Hennekam, R C 2018, ' Further delineation of Malan syndrome ', Human Mutation, vol. 39, no. 9, pp. 1226-1237 . https://doi.org/10.1002/humu.23563
Human Mutation, 39(9), 1226-1237. Wiley-Liss Inc.
Human mutation, 39(9), 1226-1237. Wiley-Liss Inc.
Human Mutation, 39(9), 1226-1237
Priolo, M, Schanze, D, Tatton-Brown, K, Mulder, P A, Tenorio, J, Kooblall, K, Acero, I H, Alkuraya, F S, Arias, P, Bernardini, L, Bijlsma, E K, Cole, T, Coubes, C, Dapia, I, Davies, S, Di Donato, N, Elcioglu, N H, Fahrner, J A, Foster, A, González, N G, Huber, I, Iascone, M, Kaiser, A S, Kamath, A, Liebelt, J, Lynch, S A, Maas, S M, Mammì, C, Mathijssen, I B, McKee, S, Menke, L A, Mirzaa, G M, Montgomery, T, Neubauer, D, Neumann, T E, Pintomalli, L, Pisanti, M A, Plomp, A S, Price, S, Salter, C, Santos-Simarro, F, Sarda, P, Segovia, M, Shaw-Smith, C, Smithson, S, Suri, M, Valdez, R M, Van Haeringen, A, Van Hagen, J M, Zollino, M, Lapunzina, P, Thakker, R V, Zenker, M & Hennekam, R C 2018, ' Further delineation of Malan syndrome ', Human Mutation, vol. 39, no. 9, pp. 1226-1237 . https://doi.org/10.1002/humu.23563
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Priolo, M, Schanze, D, Tatton-Brown, K, Mulder, P A, Tenorio, J, Kooblall, K, Acero, I H, Alkuraya, F S, Arias, P, Bernardini, L, Bijlsma, E K, Cole, T, Coubes, C, Dapia, I, Davies, S, di Donato, N, Elcioglu, N H, Fahrner, J A, Foster, A, González, N G, Huber, I, Iascone, M, Kaiser, A-S, Kamath, A, Liebelt, J, Lynch, S A, Maas, S M, Mammì, C, Mathijssen, I B, McKee, S, Menke, L A, Mirzaa, G M, Montgomery, T, Neubauer, D, Neumann, T E, Pintomalli, L, Pisanti, M A, Plomp, A S, Price, S, Salter, C, Santos-Simarro, F, Sarda, P, Segovia, M, Shaw-Smith, C, Smithson, S, Suri, M, Valdez, R M, van Haeringen, A, van Hagen, J M, Zollino, M, Lapunzina, P, Thakker, R V, Zenker, M & Hennekam, R C 2018, ' Further delineation of Malan syndrome ', Human Mutation, vol. 39, no. 9, pp. 1226-1237 . https://doi.org/10.1002/humu.23563
Human Mutation, 39(9), 1226-1237. Wiley-Liss Inc.
Malan syndrome is an overgrowth disorder described in a limited number of individuals. We aim to delineate the entity by studying a large group of affected individuals. We gathered data on 45 affected individuals with a molecularly confirmed diagnosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e8c7db7dc828e88348f7ed242503f89
http://europepmc.org/articles/PMC6175110
http://europepmc.org/articles/PMC6175110
Autor:
Manuel Cañas Encinas, Noelia García Martín, Ruth Pinedo González, Noelia García González, Eoep Alcobendas
Producción Científica
La capacidad metacognitiva es una competencia docente clave para instaurar el Aprendizaje Basado en el Pensamiento en las aulas. El objetivo de este estudio es desvelar las concepciones que los docentes tienen sobre el pe
La capacidad metacognitiva es una competencia docente clave para instaurar el Aprendizaje Basado en el Pensamiento en las aulas. El objetivo de este estudio es desvelar las concepciones que los docentes tienen sobre el pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e66b8e4dca4dffd440e77d80536129
https://doi.org/10.23923/rpye2019.01.173
https://doi.org/10.23923/rpye2019.01.173
Autor:
Eloy Rodríguez-Díaz, Pablo Gonzalvo-Rodríguez, Mónica Viejo-Díaz, Igor Vázquez-Osorio, Noelia García-González
Publikováno v:
Indian Journal of Dermatology, Vol 66, Iss 1, Pp 93-95 (2021)
Indian Journal of Dermatology
Indian Journal of Dermatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a036e53a49d4ffd10e0ea50c69dc8e8
https://doi.org/10.4103/ijd.ijd_594_19
https://doi.org/10.4103/ijd.ijd_594_19
Autor:
Alfredo Repáraz-Andrade, María Isidoro-García, Noelia García-González, Mónica Viejo-Díaz, Ana Plasencia, Cristina Torreira-Banzas, Faustino Núñez-Batalla, Nancy Govea, Rebeca Álvarez, María Costales, Gonzalo R. Ordóñez, Noelia Sánchez-Durán, Marta Diñeiro, Raquel Capín, David Castillo, Justo R. Gómez-Martínez, Patricia C. Pruneda, Juan Cadiñanos, Jordi Rosell, Ángel Mazón-Gutiérrez, Belén García-Berrocal, José Luis Llorente, Inés Hernando, José Antonio Garrote, Rubén Cabanillas, Guadalupe A. Cifuentes
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-17 (2018)
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-17 (2018)
Background: Sensorineural hearing loss (SNHL) is the most common sensory impairment. Comprehensive next-generation sequencing (NGS) has become the standard for the etiological diagnosis of early-onset SNHL. However, accurate selection of target genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00944c691e692906bdbc488fb1deab92
https://hdl.handle.net/20.500.13003/9217
https://hdl.handle.net/20.500.13003/9217
Publikováno v:
INFAD, Vol 2, Iss 1, Pp 155-162 (2014)
This paper intends to present the preventive program called ADHISO, designed for the improvement in the attention and cognitive skills as well as the reduction of hyperactive and impulsive behaviour in the students of pre-school education with ADHD s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad83b8a4fb269156c78641b198800d2d
https://doi.org/10.17060/ijodaep.2014.n1.v2.428
https://doi.org/10.17060/ijodaep.2014.n1.v2.428