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Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy

Annals of the rheumatic diseases, 2006-12, Vol.65 (12), p.1635-1638

2006

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Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders

Journal of applied physiology (1985), 2006-06, Vol.100 (6), p.1837-1841

2006

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Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies

Journal of neurology, neurosurgery and psychiatry, 2004-01, Vol.75 (1), p.136-139

2004

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Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Neurology, 2008-05, Vol.70 (20), p.1876-1882

2008

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Complex regional pain syndrome type I (RSD): pathology of skeletal muscle and peripheral nerve

Neurology, 1998-07, Vol.51 (1), p.20-25

1998

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Posttraumatic Stress Disorder in Adopted Children From Romania

American journal of orthopsychiatry, 2003-07, Vol.73 (3), p.255-265

2003

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Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

Journal of neurology, neurosurgery and psychiatry, 2004-10, Vol.75 (10), p.1499-1501

2004

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Primary respiratory failure in inclusion body myositis

Neurology, 2004-12, Vol.63 (11), p.2191-2192

2004

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A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

Brain (London, England : 1878), 2003-07, Vol.126 (7), p.1545-1551

2003

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The Draw-A-Person Test: An Indicator of Children's Cognitive and Socioemotional Adaptation?

The Journal of genetic psychology, 2005-03, Vol.166 (1), p.77-93

2005

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Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation system

Neuropediatrics, 2006-06, Vol.37 (3), p.142-147

2006

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Histology of hereditary neuralgic amyotrophy

Journal of neurology, neurosurgery and psychiatry, 2005-03, Vol.76 (3), p.445-447

2005

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Early diagnosis of ALS: The search for signs of denervation in clinically normal muscles

Journal of the neurological sciences, 2007-12, Vol.263 (1), p.154-157

2007

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Impaired Oxygen Utilization in Skeletal Muscle of CRPS I Patients

The Journal of surgical research, 2012-03, Vol.173 (1), p.145-152

2012

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Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

Journal of neurology, 2007-11, Vol.254 (11), p.1614-1615

2007

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The Oxidative Response in the Chronic Constriction Injury Model of Neuropathic Pain

The Journal of surgical research, 2009-03, Vol.152 (1), p.84-88

2009

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A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Annals of neurology, 1999-01, Vol.45 (1), p.130-133

1999

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Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease

Neurobiology of aging, 1990, Vol.11 (1), p.3-13

1990

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Genetic characteristics of myoadenylate deaminase deficiency

Annals of neurology, 1998-07, Vol.44 (1), p.140-143

1998

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Developmental Tasks: Towards a Cultural Analysis of Human Development

1, 1994

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Hypovitaminosis D-related myopathy in immigrant teenagers

Neuropediatrics, 2004-10, Vol.35 (5), p.290

2004

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Deficiency of the voltage-dependent anion channel : A novel cause of mitochondriopathy

Pediatric research, 1996-05, Vol.39 (5), p.760-765

1996

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Muscle-fiber conduction velocity and electromyography as diagnostic tools in patients with suspected inflammatory myopathy: A prospective study

Muscle & nerve, 2004-01, Vol.29 (1), p.46-50

2004

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Fatigue in type I fiber predominance: A muscle force and surface EMG study on the relative role of type I and type II muscle fibers

Muscle & nerve, 1991-09, Vol.14 (9), p.829-837

1991

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Are psychosocial factors, risk factors for symptoms and signs of the shoulder, elbow, or hand/wrist?: A review of the epidemiological literature

American journal of industrial medicine, 2002-05, Vol.41 (5), p.315-342

2002

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Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy

Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders

Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies

Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Complex regional pain syndrome type I (RSD): pathology of skeletal muscle and peripheral nerve

Posttraumatic Stress Disorder in Adopted Children From Romania

Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

Primary respiratory failure in inclusion body myositis

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

The Draw-A-Person Test: An Indicator of Children's Cognitive and Socioemotional Adaptation?

Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation system

Histology of hereditary neuralgic amyotrophy

Early diagnosis of ALS: The search for signs of denervation in clinically normal muscles

Impaired Oxygen Utilization in Skeletal Muscle of CRPS I Patients

Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

The Oxidative Response in the Chronic Constriction Injury Model of Neuropathic Pain

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease

Genetic characteristics of myoadenylate deaminase deficiency

Developmental Tasks: Towards a Cultural Analysis of Human Development

Hypovitaminosis D-related myopathy in immigrant teenagers

Deficiency of the voltage-dependent anion channel : A novel cause of mitochondriopathy

Muscle-fiber conduction velocity and electromyography as diagnostic tools in patients with suspected inflammatory myopathy: A prospective study

Fatigue in type I fiber predominance: A muscle force and surface EMG study on the relative role of type I and type II muscle fibers

Are psychosocial factors, risk factors for symptoms and signs of the shoulder, elbow, or hand/wrist?: A review of the epidemiological literature

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