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Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy

Neurology, 2015-03, Vol.84 (13), p.1346-1354

2015

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Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body Myositis

Neurology, 2022-11, Vol.99 (20), p.e2212

2022

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Neuropathology of neurometabolic diseases in children with epilepsy

Brain & development (Tokyo. 1979), 2011-10, Vol.33 (9), p.726-733

Goebel, Hans H

2011

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Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson’s disease

Acta neuropathologica, 2012-03, Vol.123 (3), p.419-432

2012

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Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

Neuromuscular disorders : NMD, 2002-02, Vol.12 (2), p.151-158

2002

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McLeod myopathy revisited: more neurogenic and less benign

Brain (London, England : 1878), 2007-12, Vol.130 (12), p.3285-3296

2007

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Extracerebral biopsies in neurodegenerative diseases of childhood

Brain & development (Tokyo. 1979), 1999-10, Vol.21 (7), p.435-443

Goebel, Hans H

1999

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Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expression

Muscle & nerve, 2014-01, Vol.49 (1), p.144-145

2014

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Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two

Neuromuscular disorders : NMD, 2009-03, Vol.19 (3), p.223-228

2009

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Camptocormia associated with focal myositis in multiple-system atrophy

Movement disorders, 2006-03, Vol.21 (3), p.390-394

2006

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Actin-Related Myopathy Without Any Missense Mutation in the ACTA1 Gene

Journal of child neurology, 2004-02, Vol.19 (2), p.149-153

2004

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Infantile Intranuclear Rod Myopathy

Journal of child neurology, 1997-01, Vol.12 (1), p.22-30

1997

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Polyneuropathy Due to Acute Arsenic Intoxication: Biopsy Studies

Journal of neuropathology and experimental neurology, 1990-03, Vol.49 (2), p.137-149

1990

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Focal myositis of the temporal muscle

Muscle & nerve, 1993-12, Vol.16 (12), p.1374-1376

1993

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Hamartoma of the triceps surae muscle

Acta neuropathologica, 1997-07, Vol.94 (1), p.91-94

1997

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Congenital Cytoplasmic Body Myopathy: Case Report

Journal of child neurology, 1997-02, Vol.12 (2), p.149-152

1997

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Ultrastructural Pathology of Eccrine Sweat Gland Epithelial Cells in Globoid Cell Leukodystrophy

Journal of child neurology, 1993-04, Vol.8 (2), p.171-174

1993

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Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach

Brain & development (Tokyo. 1979), 1995-03, Vol.17 (2), p.83-88

1995

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Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome

Archives of neurology (Chicago), 1998-10, Vol.55 (10), p.1329

1998

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Neonatal Form of Nemaline Myopathy, Muscle Immaturity, and a Microvascular Injury

Journal of child neurology, 1990-04, Vol.5 (2), p.122-126

1990

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Infantile neuroaxonal dystrophy: Diagnosis by skin biopsy

Brain & development (Tokyo. 1979), 1991-07, Vol.13 (4), p.256-259

1991

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Congenital myopathy with excess of thin myofilaments

Neuromuscular disorders : NMD, 1997-05, Vol.7 (3), p.160-168

1997

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Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism

Brain (London, England : 1878), 1990-04, Vol.113 (2), p.433-445

1990

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Congenital myopathy with cytoplasmic bodies

Neuropediatrics, 1981-05, Vol.12 (2), p.166-180

1981

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Congenital muscular dystrophy (CMD) — A collagen formative disease?

Journal of the neurological sciences, 1982-07, Vol.55 (1), p.79-90

1982

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Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy

Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body Myositis

Neuropathology of neurometabolic diseases in children with epilepsy

Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson’s disease

Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

McLeod myopathy revisited: more neurogenic and less benign

Extracerebral biopsies in neurodegenerative diseases of childhood

Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expression

Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two

Camptocormia associated with focal myositis in multiple-system atrophy

Actin-Related Myopathy Without Any Missense Mutation in the ACTA1 Gene

Infantile Intranuclear Rod Myopathy

Polyneuropathy Due to Acute Arsenic Intoxication: Biopsy Studies

Focal myositis of the temporal muscle

Hamartoma of the triceps surae muscle

Congenital Cytoplasmic Body Myopathy: Case Report

Ultrastructural Pathology of Eccrine Sweat Gland Epithelial Cells in Globoid Cell Leukodystrophy

Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach

Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome

Neonatal Form of Nemaline Myopathy, Muscle Immaturity, and a Microvascular Injury

Infantile neuroaxonal dystrophy: Diagnosis by skin biopsy

Congenital myopathy with excess of thin myofilaments

Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism

Congenital myopathy with cytoplasmic bodies

Congenital muscular dystrophy (CMD) — A collagen formative disease?

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