M. Tomás-Vila

Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center

C. Espinós, J. Vázquez-Costa, T. Sevilla, 2021, Annals of clinical and translational neurology.

A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism

M. Roselló, C. Orellana, F. Martínez, 2018, International journal of endocrinology and metabolism.

[Epidemiological surveillance of vertically-transmitted Chagas disease at three maternity hospitals in the Valencian Community].

R. Igual-Adell, M. Tomás-Vila, B. Beseler-Soto, 2008, Enfermedades Infecciosas y Microbiologia Clinica.

Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene

I. Azorín, F. Martínez-Castellano, J. J. Vilchez Padilla, 2021, Clinical genetics.

Apparent Radiological Improvement in an Infant With Labrune Syndrome Treated With Bevacizumab.

Y. Crow, L. Pedrola, F. Martínez-Castellano, 2020, Pediatric neurology.

The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease

J. Millán, T. Jaijo, G. García-García, 2017, Clinical chemistry and laboratory medicine.

Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

A. Vanderver, X. Montalban, M. Tintoré, 2020, The Lancet Neurology.

A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy

C. Marco-Marín, Miguel Ángel Martín, I. Azorín, 2022, Neuropathology and applied neurobiology.

[Schizencephaly associated with porencephaly in a girl with congenital cytomegalovirus infection].

M. Tomás-Vila, P. García-Tamarit, A. García-Colino, 2000, Revista de neurología (Ed. impresa).