Search Results - "Roche, Jose C."
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A proposed staging system for amyotrophic lateral sclerosis
Published in Brain (London, England : 1878) (01-03-2012)“…Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive loss of upper and lower motor neurons, with a median survival of 2-3…”
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Increased serum interleukin-17 levels in patients with myasthenia gravis
Published in Muscle & nerve (01-08-2011)“…It has been suggested that interleukin‐17 (IL‐17) plays a crucial role in the development of several autoimmune diseases. However, there are no data about the…”
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A proposed staging system for amyotrophic lateral sclerosis
Published in Brain (London, England : 1878) (01-03-2012)Get full text
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Reply: Idiopathic hypertrophic pachymeningitis mimicking neurosarcoidosis
Published in Clinical neurology and neurosurgery (01-07-2012)“…The authors reported an interesting case with multiple cranial neuropathies who underwent extensive evaluation consistent with neurosarcoidosis, but whose…”
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Increased glycolipid storage produced by the inheritance of a complex intronic haplotype in the α-galactosidase A (GLA) gene
Published in BMC genetics (03-09-2015)“…Accumulation of galactosphingolipids is a general characteristic of Fabry disease, a lysosomal storage disorder caused by the deficient activity of…”
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Cranial multineuritis and transverse myelitis as complications of pneumococcal meningitis
Published in Revista de neurologiá (01-07-2022)“…Pneumococcal meningitis is a condition associated with a high rate of morbidity and mortality. We report the clinical case of a 41-year-old man who, following…”
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Relationship between homocysteinaemia and sympathetic skin response in Parkinson's disease
Published in Revista de neurologiá (16-10-2017)“…High levels of homocysteine linked to treatment with levodopa have been observed in patients with Parkinsons disease (PD). Our aim was to assess the influence…”
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Increased glycolipid storage produced by the inheritance of a complex intronic haplotype in the [alpha]-galactosidase A gene
Published in BMC genetics (03-09-2015)“…Accumulation of galactosphingolipids is a general characteristic of Fabry disease, a lysosomal storage disorder caused by the deficient activity of…”
Get full text
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Multineuritis craneal y mielitis transversa como complicaciones de una meningitis neumocócica
Published in Revista de neurologiá (01-07-2022)Get full text
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Relación entre homocisteinemia y respuesta simpaticocutánea en la enfermedad de Parkinson
Published in Revista de neurologiá (16-10-2017)Get full text
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Parálisis aislada de la mano debido a un infarto isquémico
Published in Revista de neurologiá (2019)Get full text
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