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Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene

Neurology, 2006-03, Vol.66 (5), p.745-747

2006

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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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Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report

European journal of neurology, 2003-09, Vol.10 (5), p.547-549

2003

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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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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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A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin

Neuromuscular disorders : NMD, 2004-03, Vol.14 (3), p.229-232

2004

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Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene

Acta myologica, 2007-10, Vol.26 (2), p.108-111

2007

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Charcot-Marie-Tooth type 1C disease coexisting with progressive multiple sclerosis: a study of an overlapping syndrome

Folia neuropathologica, 2012, Vol.50 (4), p.369-374

2012

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N.P.3 04 A novel Pro105Thr mutation in the MPZ gene causes late onset CMT2 disease with hearing impairment

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.665-665

2006

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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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Coexistence of various vascular malformations within the brain

Folia neuropathologica, 1995, Vol.33 (4), p.247

1995

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On the specificity of focal thickenings of myelin in peripheral nerves

Neuropatologia polska, 1989, Vol.27 (2), p.151

Drac, H

1989

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Phenomenon of Schwann cell apoptosis in a case of congenital hypomyelinating neuropathy with basal lamina onion bulb formation

Brain & development (Tokyo. 1979), 2002-10, Vol.24 (7), p.727-731

2002

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An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

Journal of the peripheral nervous system, 2004-03, Vol.9 (1), p.1-2

2004

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Familial inclusion body myopathy with desmin storage

Acta neuropathologica, 1999-05, Vol.97 (5), p.509-514

1999

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Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy

Neuropatologia polska, 1977-01, Vol.15 (1), p.1

Drac, H

1977

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Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene

European journal of paediatric neurology, 2004-01, Vol.8 (4), p.221-224

2004

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Axonal form of Guillain-Barre syndrome?

Neurologia i neurochirurgia polska, 1997-03, Vol.31 (2), p.343

1997

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Electrophysiological abnormalities in acute and chronic inflammatory demyelinating polyneuropathies

Neurologia i neurochirurgia polska, 1999-01, Vol.33 (1), p.31

1999

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Chronic progressive axonal polyneuropathy simulating Guillain-Barré syndrome

Neuropatologia polska, 1992, Vol.30 (1), p.81

1992

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Morphological and biochemical changes in peripheral nerves with aging

Neuropatologia polska, 1991, Vol.29 (1-2), p.49

1991

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Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord

Neuropatologia polska, 1993, Vol.31 (1-2), p.55

1993

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Inclusion body myositis (IBM). Morphological study

Neuropatologia polska, 1992, Vol.30 (3-4), p.199

1992

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Paraneoplastic syndrome in the course of lung adenocarcinoma: morphological picture and immunohistochemical analysis of the inflammatory infiltrates and PECAM-1 expression

Folia neuropathologica, 2000, Vol.38 (1), p.29

2000

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Neuroacanthocytosis. Review of literature and case report

Folia neuropathologica, 1996, Vol.34 (4), p.178

1996

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Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene

A novel MPZ gene mutation in congenital neuropathy with hypomyelination

Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report

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

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

A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin

Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene

Charcot-Marie-Tooth type 1C disease coexisting with progressive multiple sclerosis: a study of an overlapping syndrome

N.P.3 04 A novel Pro105Thr mutation in the MPZ gene causes late onset CMT2 disease with hearing impairment

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

Coexistence of various vascular malformations within the brain

On the specificity of focal thickenings of myelin in peripheral nerves

Phenomenon of Schwann cell apoptosis in a case of congenital hypomyelinating neuropathy with basal lamina onion bulb formation

An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

Familial inclusion body myopathy with desmin storage

Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy

Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene

Axonal form of Guillain-Barre syndrome?

Electrophysiological abnormalities in acute and chronic inflammatory demyelinating polyneuropathies

Chronic progressive axonal polyneuropathy simulating Guillain-Barré syndrome

Morphological and biochemical changes in peripheral nerves with aging

Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord

Inclusion body myositis (IBM). Morphological study

Paraneoplastic syndrome in the course of lung adenocarcinoma: morphological picture and immunohistochemical analysis of the inflammatory infiltrates and PECAM-1 expression

Neuroacanthocytosis. Review of literature and case report

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