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Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology

Acta neuropathologica, 2004-03, Vol.107 (3), p.197-203

2004

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Altered topography of systemic veins following lung tissue resection: the effect on de novo cardiac implantable electronic device implantation

Folia morphologica, 2017-01, Vol.76 (2), p.322-325

2017

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Lambert–Eaton myasthenic syndrome in childhood

European journal of paediatric neurology, 2009-03, Vol.13 (2), p.194-196

2009

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A novel MPZ gene mutation in congenital neuropathy with hypomyelination

Neurology, 2004-06, Vol.62 (11), p.2122-2123

2004

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Identification of Gal(β1-3)GalNAc bearing glycoproteins in cerebrospinal fluid of amyotrophic lateral sclerosis (ALS) patients

European journal of neurology, 2000-12, Vol.7 (6), p.679-683

2000

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Atypical motor unit potentials in Emery–Dreifuss muscular dystrophy (EDMD)

Clinical neurophysiology, 2005-11, Vol.116 (11), p.2520-2527

2005

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Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene

Acta myologica, 2006-06, Vol.25 (1), p.34

2006

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The auditory system involvement in Parkinson disease: electrophysiological and neuropsychological correlations

Journal of clinical neurophysiology, 2009-12, Vol.26 (6), p.430-437

2009

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Motor unit hyperexcitability in amyotrophic lateral sclerosis vs amino acids acting as neurotransmitters

Acta neurologica Scandinavica, 2002-07, Vol.106 (1), p.34-38

2002

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Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene

Neuropediatrics, 2005-06, Vol.36 (3), p.206-209

2005

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Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci

Neurology, 2005-02, Vol.64 (3), p.533-535

2005

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Diagnostic value of satellite potentials in clinical EMG

Electromyography and clinical neurophysiology, 1997-11, Vol.37 (8), p.483

1997

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Clinical, electrophysiological and immunological remissions after thymectomy in myasthenia gravis

Clinical neurophysiology, 2002-04, Vol.113 (4), p.615-619

2002

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Shape irregularity of motor unit potentials in some neuromuscular disorders

Muscle & nerve, 1998-09, Vol.21 (9), p.1181-1187

1998

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Macroemg in manifesting carriers of Duchenne muscular dystrophy

Electromyography and clinical neurophysiology, 1999-03, Vol.39 (2), p.87

1999

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Single-fibre electromyography (SFEMG) at different firing rates in myasthenia with and without thymoma

Acta neurobiologiae experimentalis, 1993, Vol.53 (1), p.305-311

1993

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Fibre density in demyelinating and axonal polyneuropathies

Electromyography and clinical neurophysiology, 1987-04, Vol.27 (3), p.177

1987

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A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot–Marie–Tooth type 4 disease

Journal of the neurological sciences, 2006-02, Vol.241 (1), p.7-11

2006

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Pseudoselectivity of the neuromuscular block in ocular myasthenia: a SFEMG study

Electromyography and clinical neurophysiology, 1990-01, Vol.30 (1), p.53

1990

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Carpal tunnel syndrome or congenital hand anomaly: a clinical and electromyographic study

Journal of the peripheral nervous system, 2005-09, Vol.10 (3), p.338-339

2005

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Fiber density in congenital muscle fiber type disproportion. I. Congenital myopathies

Electromyography and clinical neurophysiology, 1990-12, Vol.30 (8), p.475

1990

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True remissions in myasthenia gravis? Doubts revisited

Neuromuscular disorders : NMD, 1994-09, Vol.4 (5), p.S9-S9

1994

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Chronic acquired demyelinating motor neuropathy

Acta neurologica Scandinavica, 1991-07, Vol.84 (1), p.40-45

1991

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Electrophysiological criteria separate childhood CIDP from HNPP

European journal of paediatric neurology, 2008, Vol.12, p.S51-S52

2008

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Carpal tunnel syndrome in children – we need to find out what caused it

European journal of paediatric neurology, 2008, Vol.12, p.S52-S52

2008

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Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology

Altered topography of systemic veins following lung tissue resection: the effect on de novo cardiac implantable electronic device implantation

Lambert–Eaton myasthenic syndrome in childhood

A novel MPZ gene mutation in congenital neuropathy with hypomyelination

Identification of Gal(β1-3)GalNAc bearing glycoproteins in cerebrospinal fluid of amyotrophic lateral sclerosis (ALS) patients

Atypical motor unit potentials in Emery–Dreifuss muscular dystrophy (EDMD)

Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene

The auditory system involvement in Parkinson disease: electrophysiological and neuropsychological correlations

Motor unit hyperexcitability in amyotrophic lateral sclerosis vs amino acids acting as neurotransmitters

Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene

Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci

Diagnostic value of satellite potentials in clinical EMG

Clinical, electrophysiological and immunological remissions after thymectomy in myasthenia gravis

Shape irregularity of motor unit potentials in some neuromuscular disorders

Macroemg in manifesting carriers of Duchenne muscular dystrophy

Single-fibre electromyography (SFEMG) at different firing rates in myasthenia with and without thymoma

Fibre density in demyelinating and axonal polyneuropathies

A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot–Marie–Tooth type 4 disease

Pseudoselectivity of the neuromuscular block in ocular myasthenia: a SFEMG study

Carpal tunnel syndrome or congenital hand anomaly: a clinical and electromyographic study

Fiber density in congenital muscle fiber type disproportion. I. Congenital myopathies

True remissions in myasthenia gravis? Doubts revisited

Chronic acquired demyelinating motor neuropathy

Electrophysiological criteria separate childhood CIDP from HNPP

Carpal tunnel syndrome in children – we need to find out what caused it

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