B. Pérez Dueñas

Human Metapneumovirus in the Cerebrospinal Fluid of a Patient With Acute Encephalitis.

I. Sánchez Fernández, C. Muñoz-Almagro, Laura Monfort Carretero, 2012, Archives of neurology.

Encephalopathies with intracranial calcification in children: clinical and genetic characterization

A. Pichiecchio, N. Nardocci, L. Chiapparini, 2018, Orphanet Journal of Rare Diseases.

The European Reference Network for Rare Neurological Diseases

E. Bertini, R. Vandenberghe, L. Schöls, 2021, Frontiers in Neurology.

[Usefulness of analysis of cerebrospinal fluid for the diagnosis of neurotransmitters and pterin defects and glucose and folate transport deficiencies across blood brain barrier].

B. Cormand, M. Ribasés, A. Ormazabal, 2006, Medicina clinica.

A Population‐Based Study on Congenital Disorders of Protein N‐ and Combined with O‐Glycosylation Experience in Clinical and Genetic Diagnosis

C. Pérez-Cerdá, R. Artuch, P. Briones, 2017, The Journal of pediatrics.

Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study

M. Stamelou, P. Martínez-Martín, N. Nardocci, 2017, Movement disorders : official journal of the Movement Disorder Society.

Dystonia Management: What to Expect From the Future? The Perspectives of Patients and Clinicians Within DystoniaNet Europe

R. Reilly, M. Edwards, A. Albanese, 2021, Frontiers in Neurology.

A framework for paediatric neuromodulation - Recognising the challenges and a platform for data sharing.

Shekeeb S Mohammad, Belen Perez Duenas, S. Mohammad, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.