Navegar por autor "Pardo Fernández, Julio"

A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis

2013- Sánchez Ares, María; García Vidal, Marina; Espinosa Estévez, Antucho; Pardo Fernández, Julio; Vazquez Martul, Eduardo; [et al.]

A profile of chronic demyelinating dysimmune neuropathies at a university hospital

2015- Corredera García, Enrique; Arias Gómez, Manuel; Pardo Fernández, Julio; Costa Arpín, Eva; Prieto González, José María; [et al.]

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing

2014- Sobrido Gómez, María Jesús; Quintans Castro, Beatriz; Pardo Fernández, Julio; Ordoñez Ugalde, Andrés

Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

2013- Pardo Fernández, Julio

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

2015- Pardo Fernández, Julio

Antibodies against neurofascin-155 (NF155) in CIDP associate with disabling tremor, distal weakness and poor response to IVIg

2014- Pardo Fernández, Julio

Antibodies against neurofascin-155 (NF155) in CIDP associated with disabling tremor, distal weakness and poor response to IVIg

2014- Pardo Fernández, Julio

Can we predict the response in the treatment of epilepsy with vagus nerve stimulation?

2014- Prieto González, Angel; Pardo Fernández, Julio; Rodríguez Osorio, Xiana; Gelabert González, Miguel

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

2011- Sobrido Gómez, María Jesús; Arias Gómez, Manuel; Pardo Fernández, Julio

Clinical and neuroimaging features of familial C9FTD/ALS: A case report

2013- Cebrián Pérez, Ernesto Manuel; Sobrido Gómez, María Jesús; Quintans Castro, Beatriz; Pardo Fernández, Julio; Pardo Parrado, María; [et al.]

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; García Murias, María; Quintans Castro, Beatriz; [et al.]

Description of four cases of simple-partial status epilepticus presenting as epilepticaphasia

2011- Corredera García, Enrique; Pardo Fernández, Julio; Rodríguez Osorio, Xiana; Fernandez Ferro, Jose Carlos; Moreno Morales, Eros Yamel; [et al.]

Diagnosis of Charcot Marie Tooth disease in patients with chronic inflammatory demyelinating polyneuropathy: Report of two cases

2012- Sobrido Gómez, María Jesús; Blanco Arias, Patricia; Pardo Fernández, Julio; Costa Arpín, Eva; García Sobrino, Tania; [et al.]

Distal myasthenia simulating radial nerve palsy: A case report

2013- Pardo Fernández, Julio; Pardo Parrado, María; García Sobrino, Tania; Santamaría Cadavid, María; Fernández Pajarín, Gustavo; [et al.]

Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome

2022- Cortés-Vicente, E.; Álvarez-Velasco, R.; Pla-Junca, F.; Rojas-Garcia, R.; Paradas, C.; [et al.]

Efficacy of intravenous levetiracetam as an add-on treatment in status epilepticus: A multicentric observational study.

2011- Aiguabella, Maria; Falip, Mercè; Villanueva, Vicente; de la Peña, Pilar; Molins, Albert; [et al.]

Epileptc aphasia: A description of 10 new cases

2012- Rodríguez Yáñez, Manuel; Corredera García, Enrique; Arias Gómez, Manuel; Pardo Fernández, Julio; Rodríguez Osorio, Xiana; [et al.]

Epileptic aphasia: An unusual presentation of epilepsy in 10 patients

2013- Corredera García, Enrique; Pardo Fernández, Julio; Rodríguez Osorio, Xiana; Costa Arpín, Eva; López Ferreiro, Ana; [et al.]

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; Cacheiro Martínez, Pilar; García Murias, María; [et al.]

Gastrointestinal symptoms in late-onset Pompe disease: Early response to enzyme replacement therapy

2015- Pardo Fernández, Julio; López Ferreiro, Ana; García Sobrino, Tania

Repositorio digital RUNA

Navegar por autor "Pardo Fernández, Julio"

A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis ﻿

A profile of chronic demyelinating dysimmune neuropathies at a university hospital ﻿

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing ﻿

Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide ﻿

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain ﻿

Antibodies against neurofascin-155 (NF155) in CIDP associate with disabling tremor, distal weakness and poor response to IVIg ﻿

Antibodies against neurofascin-155 (NF155) in CIDP associated with disabling tremor, distal weakness and poor response to IVIg ﻿

Can we predict the response in the treatment of epilepsy with vagus nerve stimulation? ﻿

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

Clinical and neuroimaging features of familial C9FTD/ALS: A case report ﻿

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization ﻿

Description of four cases of simple-partial status epilepticus presenting as epilepticaphasia ﻿

Diagnosis of Charcot Marie Tooth disease in patients with chronic inflammatory demyelinating polyneuropathy: Report of two cases ﻿

Distal myasthenia simulating radial nerve palsy: A case report ﻿

Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome ﻿

Efficacy of intravenous levetiracetam as an add-on treatment in status epilepticus: A multicentric observational study. ﻿

Epileptc aphasia: A description of 10 new cases ﻿

Epileptic aphasia: An unusual presentation of epilepsy in 10 patients ﻿

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families ﻿

Gastrointestinal symptoms in late-onset Pompe disease: Early response to enzyme replacement therapy ﻿

A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis

A profile of chronic demyelinating dysimmune neuropathies at a university hospital

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing

Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Antibodies against neurofascin-155 (NF155) in CIDP associate with disabling tremor, distal weakness and poor response to IVIg

Antibodies against neurofascin-155 (NF155) in CIDP associated with disabling tremor, distal weakness and poor response to IVIg

Can we predict the response in the treatment of epilepsy with vagus nerve stimulation?

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

Clinical and neuroimaging features of familial C9FTD/ALS: A case report

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

Description of four cases of simple-partial status epilepticus presenting as epilepticaphasia

Diagnosis of Charcot Marie Tooth disease in patients with chronic inflammatory demyelinating polyneuropathy: Report of two cases

Distal myasthenia simulating radial nerve palsy: A case report

Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome

Efficacy of intravenous levetiracetam as an add-on treatment in status epilepticus: A multicentric observational study.

Epileptc aphasia: A description of 10 new cases

Epileptic aphasia: An unusual presentation of epilepsy in 10 patients

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families

Gastrointestinal symptoms in late-onset Pompe disease: Early response to enzyme replacement therapy