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Enfermedad de Charcot-Marie-Tooth: revisión con énfasis en la fisiopatología del pie cavo

Revista española de cirugía ortopédica y traumatología, 2011-03, Vol.55 (2), p.140-150

2011

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Genetic risk score predicting accelerated progression from mild cognitive impairment to Alzheimer’s disease

Journal of Neural Transmission, 2013-05, Vol.120 (5), p.807-812

2013

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Low serum VEGF levels are associated with Alzheimer's disease

Acta neurologica Scandinavica, 2007-07, Vol.116 (1), p.56-58

2007

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Serum heme oxygenase-1 levels are increased in Parkinson's disease but not in Alzheimer's disease

Acta neurologica Scandinavica, 2010-02, Vol.121 (2), p.136-138

2010

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Reduced serum progranulin level might be associated with Parkinson's disease risk

European journal of neurology, 2013-12, Vol.20 (12), p.1571-1573

2013

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Charcot–Marie–Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study

Journal of neurology, neurosurgery and psychiatry, 2006-10, Vol.77 (10), p.1169-1176

2006

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Synergistic effect of two oxidative stress-related genes (heme oxygenase-1 and GSK3β) on the risk of Parkinson's disease

European journal of neurology, 2010-05, Vol.17 (5), p.760-762

2010

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Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation

Journal of neurology, 2008-07, Vol.255 (7), p.986-992

2008

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Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype

Journal of neurology, neurosurgery and psychiatry, 2008-02, Vol.79 (2), p.205-208

2008

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Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis

Acta neurologica Scandinavica, 2005-06, Vol.111 (6), p.391-399

2005

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Inflammation-related genes and the risk of Parkinson's disease: a multilocus approach

European journal of neurology, 2008-04, Vol.15 (4), p.431-433

2008

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Epistasis between tau phosphorylation regulating genes (CDK5R1 and GSK-3β) and Alzheimer's disease risk

Acta neurologica Scandinavica, 2009-08, Vol.120 (2), p.130-133

2009

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Gene-gene interaction between 14-3-3 zeta and butyrylcholinesterase modulates Alzheimer's disease risk

European journal of neurology, 2008-03, Vol.15 (3), p.219-222

2008

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Serum levels and genetic variation of TGF- beta 1 are not associated with Alzheimer's disease

Acta neurologica Scandinavica, 2007-12, Vol.116 (6), p.409-412

2007

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Aromatase and interleukin-10 genetic variants interactively modulate Alzheimer’s disease risk

Journal of Neural Transmission, 2008-06, Vol.115 (6), p.863-867

2008

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Serum levels and genetic variation of TGF-β1 are not associated with Alzheimer's disease

Acta neurologica Scandinavica, 2007-12, Vol.116 (6), p.409-412

2007

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Isolated unilateral hypoglossal nerve palsy : nine cases

Journal of neurology, 1998-02, Vol.245 (2), p.98-100

1998

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GAA expansion size and age at onset of Friedreich's ataxia

Neurology, 2003-07, Vol.61 (2), p.274-275

2003

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Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease

Neurology, 2013-02, Vol.80 (7), p.621-626

2013

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Meta-analysis of genetic variability in the β-amyloid production, aggregation and degradation metabolic pathways and the risk of Alzheimer's disease

Acta neurologica Scandinavica, 2008-01, Vol.117 (1), p.1-14

2008

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Expanded GAA repeats and clinical variation in Friedreich's ataxia

Acta neurologica Scandinavica, 2004-01, Vol.109 (1), p.75-78

2004

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Candidate gene association studies in sporadic Alzheimer's disease

Dementia and geriatric cognitive disorders, 2002-01, Vol.14 (1), p.41-54

2002

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Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

Journal of medical genetics, 2004-03, Vol.41 (3), p.193-197

2004

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Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

Muscle & nerve, 2001-09, Vol.24 (9), p.1149-1155

2001

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Consistency in gene-Alzheimer’s disease association studies

Journal of epidemiology and community health (1979), 2005-01, Vol.59 (1), p.83-85

2005

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Enfermedad de Charcot-Marie-Tooth: revisión con énfasis en la fisiopatología del pie cavo

Genetic risk score predicting accelerated progression from mild cognitive impairment to Alzheimer’s disease

Low serum VEGF levels are associated with Alzheimer's disease

Serum heme oxygenase-1 levels are increased in Parkinson's disease but not in Alzheimer's disease

Reduced serum progranulin level might be associated with Parkinson's disease risk

Charcot–Marie–Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study

Synergistic effect of two oxidative stress-related genes (heme oxygenase-1 and GSK3β) on the risk of Parkinson's disease

Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation

Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis

Inflammation-related genes and the risk of Parkinson's disease: a multilocus approach

Epistasis between tau phosphorylation regulating genes (CDK5R1 and GSK-3β) and Alzheimer's disease risk

Gene-gene interaction between 14-3-3 zeta and butyrylcholinesterase modulates Alzheimer's disease risk

Serum levels and genetic variation of TGF- beta 1 are not associated with Alzheimer's disease

Aromatase and interleukin-10 genetic variants interactively modulate Alzheimer’s disease risk

Serum levels and genetic variation of TGF-β1 are not associated with Alzheimer's disease

Isolated unilateral hypoglossal nerve palsy : nine cases

GAA expansion size and age at onset of Friedreich's ataxia

Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease

Meta-analysis of genetic variability in the β-amyloid production, aggregation and degradation metabolic pathways and the risk of Alzheimer's disease

Expanded GAA repeats and clinical variation in Friedreich's ataxia

Candidate gene association studies in sporadic Alzheimer's disease

Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

Consistency in gene-Alzheimer’s disease association studies

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