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Very early electrodiagnostic findings in Guillain-Barré syndrome

Journal of the peripheral nervous system, 2011-06, Vol.16 (2), p.136-142

2011

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Phenotypic spectrum of MFN2 mutations in the Spanish population

Journal of medical genetics, 2010-04, Vol.47 (4), p.249-256

2010

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18F-FDG PET/CT in the evaluation of POEMS syndrome

European journal of radiology, 2010-11, Vol.76 (2), p.180-182

2010

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Multifocal acquired demyelinating sensory and motor neuropathy presenting as idiopathic hypertrophic brachial neuropathy

Journal of neurology, neurosurgery and psychiatry, 2009-06, Vol.80 (6), p.674-675

2009

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Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

Neuromuscular disorders : NMD, 2008-12, Vol.18 (12), p.929-933

2008

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Antibodies against disialosyl and terminal NeuNAc(α2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy

Journal of neurology, 2008-05, Vol.255 (5), p.764-766

2008

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Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population

Clinical genetics, 2006-12, Vol.70 (6), p.516-523

2006

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Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

Neuropathology and applied neurobiology, 1997-12, Vol.23 (6), p.475-482

1997

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Insulin regulation of leptin synthesis and secretion in humans: the model of myotonic dystrophy

Clinical endocrinology (Oxford), 1999-05, Vol.50 (5), p.569-575

1999

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Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

Neuropathology and applied neurobiology, 1997-12, Vol.23 (6), p.475-482

1997

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Two Spanish families with Charcot–Marie–Tooth type 2A: Clinical, electrophysiological and molecular findings

Neuromuscular disorders : NMD, 2008-12, Vol.18 (12), p.974-978

2008

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Diagnosis of Charcot-Marie-Tooth disease

BioMed research international, 2009-01, Vol.2009, p.985415-10

2009

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Survival in amyotrophic lateral sclerosis with home mechanical ventilation : The impact of systematic respiratory assessment and bulbar involvement

Chest, 2005-06, Vol.127 (6), p.2132-2138

2005

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Musk-antibody positive myasthenia gravis presenting with isolated neck extensor weakness

Neuromuscular disorders : NMD, 2007-07, Vol.17 (7), p.544-546

2007

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Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

Human molecular genetics, 2001-04, Vol.10 (9), p.947-952

2001

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Apoptosis is not the mechanism of cell death of muscle fibers in human muscular dystrophies and inflammatory myopathies

Muscle & nerve, 1997-10, Vol.20 (10), p.1328-1330

1997

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Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance

Journal of neuroimmunology, 2001-11, Vol.120 (1), p.78-83

2001

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The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathy

Neurology, 2002-10, Vol.59 (7), p.1112-1113

2002

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Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance

Journal of the peripheral nervous system, 2002-06, Vol.7 (2), p.137-137

2002

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GH secretion status in myotonic dystrophy

Psychoneuroendocrinology, 1993, Vol.18 (3), p.183-190

1993

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Guillain-Barré Syndrome in Spain, 1985–1997: Epidemiological and Public Health Views

European neurology, 2001-01, Vol.46 (2), p.83-91

2001

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Pure sensory Guillain-Barré syndrome

Journal of neurology, neurosurgery and psychiatry, 1992-05, Vol.55 (5), p.411-412

1992

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Syringomyelia extending to the corona radiata

Journal of neurology, 2006-06, Vol.253 (6), p.817-818

2006

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Study on growth hormone and insulin secretion in myotonic dystrophy

The Clinical Investigator, 1994-07, Vol.72 (7), p.508-511

1994

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Peripheral neuropathy associated with angioimmunoblastic lymphadenopathy

Clinical neurology and neurosurgery, 1988, Vol.90 (2), p.159-162

1988

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Very early electrodiagnostic findings in Guillain-Barré syndrome

Phenotypic spectrum of MFN2 mutations in the Spanish population

18F-FDG PET/CT in the evaluation of POEMS syndrome

Multifocal acquired demyelinating sensory and motor neuropathy presenting as idiopathic hypertrophic brachial neuropathy

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

Antibodies against disialosyl and terminal NeuNAc(α2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy

Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population

Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

Insulin regulation of leptin synthesis and secretion in humans: the model of myotonic dystrophy

Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

Two Spanish families with Charcot–Marie–Tooth type 2A: Clinical, electrophysiological and molecular findings

Diagnosis of Charcot-Marie-Tooth disease

Survival in amyotrophic lateral sclerosis with home mechanical ventilation : The impact of systematic respiratory assessment and bulbar involvement

Musk-antibody positive myasthenia gravis presenting with isolated neck extensor weakness

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

Apoptosis is not the mechanism of cell death of muscle fibers in human muscular dystrophies and inflammatory myopathies

Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance

The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathy

Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance

GH secretion status in myotonic dystrophy

Guillain-Barré Syndrome in Spain, 1985–1997: Epidemiological and Public Health Views

Pure sensory Guillain-Barré syndrome

Syringomyelia extending to the corona radiata

Study on growth hormone and insulin secretion in myotonic dystrophy

Peripheral neuropathy associated with angioimmunoblastic lymphadenopathy

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