M. Arias

发表

Status epilepticus secondary to luetic encephalitis: evolution of neuroimaging findings

I. Pereiró, Á. Sesar, M. Arias, 2008, Journal of Neurology.

Rasmussen Encephalitis in the Sixth Decade: Magnetic Resonance Image Evolution and Immunoglobulin Response

Á. Sesar, M. Arias, S. Arias-Rivas, 2006, European Neurology.

“Santiaguiño” sign in multisystem atrophy

I. Pereiró, M. Arias, I. Requena, 2010 .

Devic disease to the ‘ neuromyelitis optica spectrum ’ : an unfinished tale bridging three centuries

M. Arias, 2017 .

Neurology of ecstatic religious and similar experiences: ecstatic, orgasmic, and musicogenic seizures. Stendhal syndrome and autoscopic phenomena

M. Arias, 2019, Neurología (English Edition).

Neurology of ecstatic religious and similar experiences: Ecstatic, orgasmic, and musicogenic seizures. Stendhal syndrome and autoscopic phenomena.

M. Arias, 2019, Neurologia.

Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo.

L. Petrucelli, D. Dickson, M. Disney, 2020, Cell reports.

Cavernomas of the central nervous system: clinical and neuroimaging manifestations in 47 patients.

Santiago de Compostela, I. Pereiró, M. Arias, 1991, Journal of neurology, neurosurgery, and psychiatry.

47 patients . clinical and neuroimaging manifestations in Cavernomas of the central nervous system :

I. Pereiró, E. Mont, M. Arias, 2022 .

[Coma associated with migraine].

C. Lema, M. Arias, I. Requena, 1999, Revista de neurologia.

Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: first families detected in Spain.

P. Mir, M. Sobrido, J. Arpa, 2021, Neurologia.

[Headache and fainting as initial symptoms of syringomyelia associated to Arnold-Chiari and facial angiomatous nevus].

Á. Sesar-Ignacio, M. Arias, S. Arias-Rivas, 2004, Revista de neurologia.

Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation

Á. Carracedo, M. Sobrido, L. Goldfarb, 2006, Neuromuscular Disorders.

Recurrent leukoencephalopathy with microhemorrhages: gradient-echo MRI study diagnostic value in CNS primary angiitis

M. Arias, S. Arias-Rivas, D. Dapena, 2008, Multiple sclerosis.

[CT vs MRI in the diagnosis of acute stroke].

M. E. Amigo, I. Pereiró, M. Arias, 1992, Archivos de neurobiologia.

[Brachial plexitis and myelitis and herpes-zoster lumbar plexus disorder in patient treated with infliximab].

M. Arias, S. Arias-Rivas, D. Dapena, 2005, Neurologia.

‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization

Á. Carracedo, M. Sobrido, F. Rodríguez-Trelles, 2012, Brain : a journal of neurology.

Keys to overcoming the challenge of diagnosing autosomal recessive spinocerebellar ataxia

M. Arias, 2019, Neurología (English Edition).

A long acting local anaesthetic, with less cardiac and neurotoxicity

M. Arias, 2007 .

[Malignant prolactinoma with intra- and extracranial metastasis: clinico-radiologic study].

I. Pereiró, C. Lema, M. Arias, 2000, Anales de medicina interna.

[Syndromes of continuous muscular activity: report of a central case (stiff-man) and a peripheral case (neuromyotonia) associated with neuroborreliosis].

J. Pardo, M. Arias, I. Requena, 1995, Revista de neurologia.

[Rapidly progressing dementia as the presenting symptom of Waldenstrom's macroglobulinemia: findings from magnetic resonance imaging of the brain in Bing Neel syndrome].

M. Arias, I. Requena Caballero, S. Arias Rivas, 2004, Revista de neurologia.

[Past hepatitis B virus infection and demyelinating multiphasic disease: casual or causal relationship?].

D. Santos-García, M. Arias, S. Arias-Rivas, 2007, Neurologia.

Anti-TNF-alpha inhibitors therapy and non infectious neurologic adverse effects

M. Arias, I. Requena, S. Arias-Rivas, 2013, Journal of Neurological Sciences.

Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic survey

A. Jiménez-Escrig, M. Sobrido, J. Pardo, 2011, European journal of neurology.

Acute Spinal Epidural Hematoma and Systemic Mastocytosis

I. Pereiró, Á. Sesar, M. Arias, 2004, Spine.

PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36

Á. Ruibal, M. Sobrido, M. Fernández-Prieto, 2017, Movement disorders : official journal of the Movement Disorder Society.

Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)

Á. Carracedo, R. Cruz, M. Sobrido, 2020, The Cerebellum.

A case of deaf–mutism as an expression of pure word deafness: neuroimaging and electrophysiological data

I. Pereiró, M. Arias, I. Requena, 1995, European journal of neurology.

Late onset multiple sclerosis.

J. Prieto, M. Arias, E. Corredera, 2011, Neurologia.

[Neurology of laughter and humour: pathological laughing and crying].

M. Arias, 2011, Revista de neurologia.

[Is fibromyalgia a neurological disease?].

M. Arias, 2008, Neurología.

The autoscopic phenomena in neurological clinic: A study of two cases

Á. Sesar, M. Arias, S. Arias-Rivas, 2007, Journal of the Neurological Sciences.

Acute respiratory failure as the first sign of Arnold-Chiari malformation associated with syringomyelia.

I. Pereiró, L. Valdés, M. Arias, 1995, The European respiratory journal.

[From writer's cramp to butcher's spasms: a case of interprofessional dystonia].

C. Lema, M. Arias, I. Requena, 1998, Revista de neurologia.

Targeted NGS meets expert clinical characterization: Efficient diagnosis of spastic paraplegia type 11

Á. Carracedo, J. Amigo, M. Sobrido, 2015, Applied & translational genomics.

Numb ears in resurrection: Great auricular nerve injury in hanging attempt

M. Arias, S. Arias-Rivas, M. R. Alende-Sixto, 2005, Neurology.

Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: First families detected in Spain.

P. Mir, M. Sobrido, J. Arpa, 2019, Neurologia.

Spinocerebellar ataxia type 36

M. Sobrido, M. Arias, B. Quintáns, 2014, Definitions.

Primary malignant meningeal melanomatosis: a clinical, radiological and pathologic case study.

M. Alberte-Woodward, M. Arias, J. Suárez-Peñaranda, 2011, Acta neurologica Belgica.

Keys to overcoming the challenge of diagnosing autosomal recessive spinocerebellar ataxia.

M. Arias, 2016, Neurología.

Multiple sclerosis and hypertrophic demyelinating neuropathy.

I. Pereiró, M. Arias, I. Requena, 1992, Journal of neurology, neurosurgery, and psychiatry.