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Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry

European journal of neurology, 2015-07, Vol.22 (7), p.1056-1061

2015

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Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome

Genes, brain and behavior, 2013-11, Vol.12 (8), p.812-820

2013

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AB0642 Are Anti-Srp Autoantibodies Specific for Myositis?

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.1017-1018

2014

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Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.2847-2858

2015

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Assay of Succinate Dehydrogenase Activity by a Colorimetric-Continuous Method Using Iodonitrotetrazolium Chloride as Electron Acceptor

Analytical biochemistry, 1993-08, Vol.212 (2), p.506-509

1993

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Survey on the current situation of the young neurologists in Spain: analysis of their current working stability and degree of social protection

Neurología (Barcelona, Spain), 2006-03, Vol.21 (2), p.68-79

2006

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Chloroquine-induced myopathy and neuropathy: progressive tetraparesis with areflexia that simulates a polyradiculoneuropathy. Two case reports

Revista de neurologiá, 2003-03, Vol.36 (6), p.523

2003

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Brain pyruvate oxidation in experimental thiamin-deficiency encephalopathy

Clinica chimica acta, 1996-11, Vol.255 (1), p.13-25

1996

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Left hemiasomatognosia probably induced by imipenem

Medicina clínica, 2000-09, Vol.115 (9), p.358

2000

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Central nervous system disease in Sjögren's syndrome

Annales de médecine interne, 1995, Vol.146 (4), p.239

1995

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Guillain-Barre syndrome and IVIg: does early initiation of treatment influence the mean hospital stay?

Neurología (Barcelona, Spain), 2009-05, Vol.24 (4), p.217-219

2009

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Are anti-ganglioside antibodies detectable in serum from patients with critical illness myopathy and polyneuropathy?

Revista Médica de Trujillo, 2020-03, Vol.15 (1), p.26-34

2020

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Identification and biochemical characterization of the novel mutation m. 8839G >C in the mitochondrial ATP6 gene associated with NARP syndrome

Genes, brain and behavior, 2013-11, Vol.12 (8), p.812-820

2013

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Primer Congreso Virtual Iberoamericano de Neurología. Un análisis crítico

Revista de neurologiá, 1999-07, Vol.29 (1), p.71

1999

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Neuropathy due to necrotizing vasculitis: a study of the clinical anatomy, neurophysiological characteristics, and clinical course of the disorder in 27 patients

Revista de neurologiá, 2001-12, Vol.33 (11), p.1033-1036

2001

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Churg-Strauss syndrome and antineutrophil cytoplasmic antibodies

Medicina clínica, 1997-05, Vol.108 (20), p.797

1997

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Diagnostic strategy for mitochondrial diseases

Revista de neurologiá, 1999-07, Vol.29 (1), p.52-58

1999

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First Virtual Ibero-American Congress in Neurology. A critical analysis

Revista de neurologiá, 1999-07, Vol.29 (1), p.71-72

1999

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Encefalomiopatía mitocondrial, acidosis láctica y accidentes cerebrovasculares (MELAS) en edad pediátrica con la mutación A3243G en el gen del ARNtLeu(UUR) del ADN mitocondrial

Revista de neurologiá, 2000, Vol.31 (9), p.804

2000

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Estrategia diagnóstica de las enfermedades mitocondriales

Revista de neurologiá, 1999-07, Vol.29 (1), p.52

1999

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Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA

Revista de neurologiá, 2000-11, Vol.31 (9), p.804-811

2000

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Pituitary apoplexy. Case contribution and review of the literature

Archivos de neurobiologia, 1983-09, Vol.46 (5), p.311

1983

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Glycogenosis type V of adults: muscle phosphorylase deficiency

Medicina clínica, 1986-03, Vol.86 (8), p.335-338

1986

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The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1

Genes, 2020-07, Vol.11 (7), p.757

2020

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Les auto-anticorps anti-SRP ne sont pas spécifiques des myosites : 8 cas

Revue du rhumatisme (Ed. française : 1993), 2017-10, Vol.84 (5), p.463-465

2017

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Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry

Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome

AB0642 Are Anti-Srp Autoantibodies Specific for Myositis?

Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Assay of Succinate Dehydrogenase Activity by a Colorimetric-Continuous Method Using Iodonitrotetrazolium Chloride as Electron Acceptor

Survey on the current situation of the young neurologists in Spain: analysis of their current working stability and degree of social protection

Chloroquine-induced myopathy and neuropathy: progressive tetraparesis with areflexia that simulates a polyradiculoneuropathy. Two case reports

Brain pyruvate oxidation in experimental thiamin-deficiency encephalopathy

Left hemiasomatognosia probably induced by imipenem

Central nervous system disease in Sjögren's syndrome

Guillain-Barre syndrome and IVIg: does early initiation of treatment influence the mean hospital stay?

Are anti-ganglioside antibodies detectable in serum from patients with critical illness myopathy and polyneuropathy?

Identification and biochemical characterization of the novel mutation m. 8839G >C in the mitochondrial ATP6 gene associated with NARP syndrome

Primer Congreso Virtual Iberoamericano de Neurología. Un análisis crítico

Neuropathy due to necrotizing vasculitis: a study of the clinical anatomy, neurophysiological characteristics, and clinical course of the disorder in 27 patients

Churg-Strauss syndrome and antineutrophil cytoplasmic antibodies

Diagnostic strategy for mitochondrial diseases

First Virtual Ibero-American Congress in Neurology. A critical analysis

Encefalomiopatía mitocondrial, acidosis láctica y accidentes cerebrovasculares (MELAS) en edad pediátrica con la mutación A3243G en el gen del ARNtLeu(UUR) del ADN mitocondrial

Estrategia diagnóstica de las enfermedades mitocondriales

Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA

Pituitary apoplexy. Case contribution and review of the literature

Glycogenosis type V of adults: muscle phosphorylase deficiency

The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1

Les auto-anticorps anti-SRP ne sont pas spécifiques des myosites : 8 cas

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