B. Calleja-Pérez

Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings

T. Pihlajaniemi, S. López-Martín, J. Albert, 2022, Neurocase.

Cingulate Cortical Thickness and Dopamine Transporter (DAT1) Genotype in Children and Adolescents With ADHD

S. López-Martín, J. Albert, D. Fernández-Mayoralas, 2018, Journal of attention disorders.

Migraine Symptoms Related to the Percutaneous Closure of An Ostium Secundum Atrial Septal Defect: Report of Four Paediatric Cases and Review of the Literature

B. Calleja-Pérez, A. Fernández-Jaén, F. Gutiérrez‐Larraya, 2007, Cephalalgia : an international journal of headache.

Cortical thickness at the time of the initial attack in two patients with paediatric relapsing-remitting multiple sclerosis.

J. Albert, D. Fernández-Mayoralas, M. Jiménez de la Peña, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotype

S. López-Martín, J. Albert, M. R. Rodríguez, 2015, Psychiatry Research: Neuroimaging.

Cortical thickness in fetal alcohol syndrome and attention deficit disorder.

J. García-Segura, D. Fernández-Mayoralas, B. Calleja-Pérez, 2011, Pediatric neurology.

A Novel Loss-of-Function SEMA3E Mutation in a Patient with Severe Intellectual Disability and Cognitive Regression

P. Duminuco, A. Cariboni, V. Vezzoli, 2022, International journal of molecular sciences.

Mutations in BRAT1 cause autosomal recessive progressive encephalopathy: Report of a Spanish patient.

T. Ouchi, E. So, J. Albert, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: The critical role of LBX

Karl R. Wotton, J. Cigudosa, J. Suela, 2014, American journal of medical genetics. Part A.

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism

A. Noegel, P. Nürnberg, M. Jackson, 2021, Genes.