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Amyotrophic lateral sclerosis causes small fiber pathology

European journal of neurology, 2016-02, Vol.23 (2), p.416-420

2016

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Observation of phonon-polaritons in thin flakes of hexagonal boron nitride on gold

Applied physics letters, 2018-04, Vol.112 (15)

2018

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Design and simulation of losses in Ge/SiGe terahertz quantum cascade laser waveguides

Optics express, 2020-02, Vol.28 (4), p.4786-4800

2020

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Electron-phonon coupling in n -type Ge two-dimensional systems

Physical review. B, 2020-11, Vol.102 (20), p.205302, Article 205302

2020

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Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series

European journal of neurology, 2013-01, Vol.20 (1), p.138-146

2013

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Monomelic amyotrophy in cervical myelopathy associated with anterior dural sac displacement induced by neck flexion

Journal of neurology, 2016-04, Vol.263 (4), p.823-825

2016

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Journal (22 août 1937 - 10 juin 1940). Premier volume

2015

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Dynasore enhances the formation of mitochondrial antiviral signalling aggregates and endocytosis‐independent NF‐κB activation

British journal of pharmacology, 2015-08, Vol.172 (15), p.3748-3763

2015

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Osmotic stress and the cytoskeleton: the R(h)ole of Rho GTPases

Acta Physiologica, 2006-05, Vol.187 (1-2), p.257-272

2006

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Giant SEPs and SEP-recovery function in Unverricht–Lundborg disease

Clinical neurophysiology, 2013-05, Vol.124 (5), p.1013-1018

2013

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Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease

Neurology, 2004-12, Vol.63 (12), p.2309

2004

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Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG–EMG relationship estimated using autoregressive models

Clinical neurophysiology, 2003-06, Vol.114 (6), p.1041-1052

2003

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Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht–Lundborg disease

NeuroImage (Orlando, Fla.), 2006-10, Vol.33 (1), p.161-168

2006

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POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantation

Neuromuscular disorders : NMD, 2007-12, Vol.17 (11), p.980-982

2007

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Dynasore enhances the formation of mitochondrial antiviral signalling aggregates and endocytosis-independent NF-[kappa]B activation

British journal of pharmacology, 2015-08, Vol.172 (15), p.3748

2015

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Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

Neurology, 2000-04, Vol.54 (8), p.1696

2000

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P23-14 Action myoclonus in sialidosis: a comparative study with Unverricht-Lundborg disease

Clinical neurophysiology, 2010, Vol.121, p.S242-S242

2010

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P14-7 Somatosensory evoked potentials recovery function in patients with cortical myoclonus

Clinical neurophysiology, 2010, Vol.121, p.S186-S186

2010

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Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancer

Journal of neurology, neurosurgery and psychiatry, 2006-03, Vol.77 (3), p.422-424

2006

Volltextzugriff (PDF)

Childhood-onset multifocal motor neuropathy with conduction blocks

Neurology, 2006-03, Vol.66 (6), p.922

2006

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Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotonia

Neurology, 2005-04, Vol.64 (7), p.1290

2005

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Polymyography in the diagnosis of childhood onset movement disorders

European journal of paediatric neurology, 2008-11, Vol.12 (6), p.480-483

2008

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Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Neurology, 1996-04, Vol.46 (4), p.1133

1996

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Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial

Lancet neurology, 2011-04, Vol.10 (4), p.320-328

2011

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Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

Neurology, 1999-04, Vol.52 (7), p.1472

1999

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Amyotrophic lateral sclerosis causes small fiber pathology

Observation of phonon-polaritons in thin flakes of hexagonal boron nitride on gold

Design and simulation of losses in Ge/SiGe terahertz quantum cascade laser waveguides

Electron-phonon coupling in n -type Ge two-dimensional systems

Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series

Monomelic amyotrophy in cervical myelopathy associated with anterior dural sac displacement induced by neck flexion

Journal (22 août 1937 - 10 juin 1940). Premier volume

Dynasore enhances the formation of mitochondrial antiviral signalling aggregates and endocytosis‐independent NF‐κB activation

Osmotic stress and the cytoskeleton: the R(h)ole of Rho GTPases

Giant SEPs and SEP-recovery function in Unverricht–Lundborg disease

Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease

Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG–EMG relationship estimated using autoregressive models

Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht–Lundborg disease

POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantation

Dynasore enhances the formation of mitochondrial antiviral signalling aggregates and endocytosis-independent NF-[kappa]B activation

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

P23-14 Action myoclonus in sialidosis: a comparative study with Unverricht-Lundborg disease

P14-7 Somatosensory evoked potentials recovery function in patients with cortical myoclonus

Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancer

Childhood-onset multifocal motor neuropathy with conduction blocks

Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotonia

Polymyography in the diagnosis of childhood onset movement disorders

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

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