E. Fernández‐Álvarez

发表

Palatal tremor in childhood: clinical and therapeutic considerations.

E. Fernández-Álvarez, J. Campistol-Plana, A. Majumdar, 2006, Developmental medicine and child neurology.

Autosomal dominant Emery–Dreifuss muscular dystrophy: a new family with late diagnosis

S. Manilal, K. Schwartz, E. Fernández-Álvarez, 2002, Neuromuscular Disorders.

E. Fernández-Álvarez, E. Fernández‐Álvarez, 2014 .

Transient benign paroxysmal movement disorders in infancy.

E. Fernández-Álvarez, E. Fernández‐Álvarez, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly

A. Ballabio, D. Pilz, A. Fogli, 1999, Annals of neurology.

Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency

J. Obeso, C. Depienne, R. Artuch, 2012, Movement disorders : official journal of the Movement Disorder Society.

Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

M. Orozco, J. Gelpí, A. Ribes, 2000, Pediatric Research.

HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins

A. Ormazabal, R. Artuch, E. Fernández-Álvarez, 2005, Journal of Neuroscience Methods.

Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency.

S. Duarte, C. Ortez, A. Ormazabal, 2015, Molecular genetics and metabolism.

Characterization of tremor in phenylketonuric patients

J. Valls-Solé, R. Artuch, B. Pérez-Dueñas, 2005, Journal of Neurology.

A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS‐ES Task Force

A. Albanese, J. Krauss, I. Rektor, 2006, European journal of neurology.

[Ataxia telangiectasia: review of 13 new cases].

E. Fernández-Álvarez, J. Campistol, E. Geán, 1996, Revista de neurologia.

Inborn errors of metabolism and motor disturbances in children

S. Dimauro, M. Pineda, À. García‐Cazorla, 2009, Journal of Inherited Metabolic Disease.

GAMT deficiency

M. Durán, R. Surtees, A. Adami, 2006, Neurology.

Dystonia. The paediatric perspective

E. Fernández-Álvarez, E. Fernández‐Álvarez, 2010, European journal of neurology.

Movement disorders in children: Recent advances in management

E. Fernández-Álvarez, E. Fernández‐Álvarez, 2009, Indian journal of pediatrics.

Paroxysmal movement disorders and episodic ataxias.

B. Pérez-Dueñas, E. Fernández-Álvarez, E. Fernández‐Álvarez, 2013, Handbook of clinical neurology.

Secondary abnormalities of neurotransmitters in infants with neurological disorders

A. Ormazabal, R. Artuch, M. Pineda, 2007, Developmental medicine and child neurology.

Benign nocturnal alternating hemiplegia of childhood: A clinical and nomenclatural reappraisal.

E. Kamsteeg, M. Willemsen, J. Nicolai, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Determination of 5-methyltetrahydrofolate in cerebrospinal fluid of paediatric patients: reference values for a paediatric population.

A. Ormazabal, R. Artuch, M. Pineda, 2006, Clinica chimica acta; international journal of clinical chemistry.

Childhood chorea with cerebral hypotrophy: a treatable GLUT1 energy failure syndrome.

R. Artuch, X. Setoain, B. Pérez-Dueñas, 2009, Archives of neurology.

Syndrome of fixed dystonia in adolescents--short term outcome in 4 cases.

L. Lingappa, E. Fernández-Álvarez, J. Colomer, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Primary degeneration of the granular layer of the cerebellum (Norman type)

I. Ferrer, E. Galofré, J. Manresa, 1987, Acta Neuropathologica.

Movement Disorders in Children

Jean Aicardi, J. Aicardi, E. Fernández-Álvarez, 2001 .

Treatment for dystonia in childhood

E. Roze, E. Fernández-Álvarez, A. Roubertie, 2012, European journal of neurology.

Hand tremor and orofacial dyskinesia: Clinical manifestations of glutaric aciduria type I in a young girl

A. Ribes, Á. García-Cazorla, E. Fernández-Álvarez, 2003 .

Hypokinetic-rigid syndrome in children and inborn errors of metabolism.

C. Ortez, M. Pineda, À. García‐Cazorla, 2011, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Fine structure based on the golgi method of the abnormal cortex and heterotopic nodules in pachygyria

E. Fernández-Álvarez, I. Ferrer, Isidre Fábregues, 1984, Brain and Development.

Association between male gender and pediatric essential tremor

B. Ford, E. Louis, S. Frucht, 2005, Movement disorders : official journal of the Movement Disorder Society.

Update on pediatric dystonias: etiology, epidemiology, and management.

N. Nardocci, E. Fernández-Álvarez, E. Fernández‐Álvarez, 2012, Degenerative neurological and neuromuscular disease.

Degenerative Neurological and Neuromuscular Disease Update on pediatric dystonias : etiology , epidemiology , and management

N. Nardocci, E. Fernández‐Álvarez, 2012 .

Transient movement disorders in children

E. Fernández-Álvarez, E. Fernández‐Álvarez, 1997, Journal of Neurology.

Dystonia as a presenting sign of subacute necrotising encephalomyelopathy in infancy

E. Fernández-Álvarez, V. Cusí, J. Campistol, 1986, European Journal of Pediatrics.

Polymorphic, Benign, Nonepileptic, Paroxysmal, Infantile Movements (Fejerman Condition)

E. Fernández-Álvarez, E. Fernández‐Álvarez, 2015, Journal of Pediatric Neurology.