E-LIB Suche - Ergebnisse für: Calleja Pérez, Beatriz

1

Atomoxetine for Attention Deficit Hyperactivity Disorder in..:

Fernández-Jaén, Alberto ; Fernández-Mayoralas, Daniel Martín ; Calleja Pérez, Beatriz..
Pediatric Neurology. 43 (2010) 5 - p. 341-347 , 2010

Link: https://doi.org/10.1016/..

2

Fetal Alcohol Syndrome, Tourette Syndrome, and Hyperactivit..:

Fernández-Mayoralas, Daniel Martín ; Fernández-Jaén, Alberto ; Muñoz-Jareño, Nuria..
Pediatric Neurology. 43 (2010) 2 - p. 110-116 , 2010

Link: https://doi.org/10.1016/..

3

Meralgia Paresthetica in the Pediatric Population: A Propos..:

Fernández-Mayoralas, Daniel Martín ; Fernández-Jaén, Alberto ; Jareño, Nuria Muñoz...
Journal of Child Neurology. 25 (2009) 1 - p. 110-113 , 2009

Link: https://doi.org/10.1177/..

4

Mutations in the COL18A1 gen associated with knobloch syndr..:

Irene Díez García-Prieto, I ; Lopez-Martín, Sara ; Albert, Jacobo...
Neurocase. 28 (2022) 1 - p. 11-18 , 2022

Link: https://doi.org/10.1080/..

5

A Novel Loss-of-Function SEMA3E Mutation in a Patient with ..:

Paganoni, Alyssa J. J. ; Amoruso, Federica ; Porta Pelayo, Javier...
International Journal of Molecular Sciences. 23 (2022) 10 - p. 5632 , 2022

Link: https://doi.org/10.3390/..

6

Biallelic ELMO3 mutations and loss of function for DOCK-med..:

Tran, Viviane ; Goyette, Marie-Anne ; Martínez García, Mónica...
https://doi.org/10.1080/21541248.2021.1888557. , 2022

Link: http://hdl.handle.net/11..

7

A mild clinical and neuropsychological phenotype of Renpenn..:

Lopez-Martín, Sara ; Albert, Jacobo ; Peña Vila-Belda, Mᵃ del Mar...
Applied Neuropsychology: Child. 11 (2021) 4 - p. 921-927 , 2021

Link: https://doi.org/10.1080/..

8

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Gia..:

Young, Natalie ; Asif, Maria ; Jackson, Matthew...
Genes. 12 (2021) 9 - p. 1294 , 2021

Link: https://doi.org/10.3390/..

9

BiallelicELMO3mutations and loss of function for DOCK-media..:

Tran, Viviane ; Goyette, Marie-Anne ; Martínez-García, Mónica...
Small GTPases. 13 (2021) 1 - p. 48-55 , 2021

Link: https://doi.org/10.1080/..

10

Abnormal frontal gyrification pattern and uncinate developm..:

Jiménez de la Peña, Mar ; Fernández-Mayoralas, Daniel Martín ; López-Martín, Sara...
European Journal of Paediatric Neurology. 35 (2021) - p. 8-15 , 2021

Link: https://doi.org/10.1016/..

11

Bi-Allelic c.1746G>T; p.Leu582= Variants in TUBGCP4 in a Bo..:

Fernández Mayoralas, Daniel Martín ; Albert, Jacobo ; López Martín, Sara...
https://doi.org/10.1159/000519365. , 2021

Link: http://hdl.handle.net/11..

12

Bi-Allelic c.1746G>T; p.Leu582= Variants in TUBGCP4 in a Bo..:

Fernández Mayoralas, Daniel Martín ; Albert, Jacobo ; López Martín, Sara...
https://doi.org/10.1159/000519365. , 2021

Link: http://hdl.handle.net/11..

13

ANO3 and early-onset dyskinetic encephalopathy:

Jiménez de Domingo, Ana ; Lopez-Martín, Sara ; Albert, Jacobo...
European Journal of Medical Genetics. 63 (2020) 12 - p. 104085 , 2020

Link: https://doi.org/10.1016/..

14

Trastorno por déficit de atención/hiperactividad. Hábitos d..:

Calleja Pérez, Beatriz ; Párraga, Juan Luis ; Albert, Jacobo...
https://www.medicinabuenosaires.com/indices-de-2010-a-2019/volumen-79-ano-2019-suplemento-1/trastorno-por-deficit-de-atencion-hiperactividad-habitos-de-estudio/. , 2019

Link: http://hdl.handle.net/11..

15

Mutations in BRAT1 cause autosomal recessive progressive en..:

Fernández-Jaén, Alberto ; Álvarez, Sara ; Young So, Eui...
European Journal of Paediatric Neurology. 20 (2016) 3 - p. 421-425 , 2016

Link: https://doi.org/10.1016/..