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The Treatment of Drooling by Ultrasound-Guided Intraglandular Injections of Botulinum Toxin Type A Into the Salivary Glands

The Laryngoscope, 2003-01, Vol.113 (1), p.107-111

2003

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MR Imaging and Proton MR Spectroscopic Studies in Sjogren-Larsson Syndrome: Characterization of the Leukoencephalopathy

American journal of neuroradiology : AJNR, 2004-04, Vol.25 (4), p.649-657

2004

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Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome

Brain (London, England : 1878), 2001-07, Vol.124 (Pt 7), p.1426-1437

2001

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Muscle Reflexes and Synergies Triggered by an Unexpected Support Surface Height During Walking

Journal of neurophysiology, 2007-05, Vol.97 (5), p.3639-3650

2007

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Validity and reproducibility of hand-held dynamometry in children aged 4-11 years

Journal of rehabilitation medicine, 2006-01, Vol.38 (1), p.57-64

2006

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Validity and reproducibility of the Jamar dynamometer in children aged 4 - 11 years

Disability and rehabilitation, 2006-01, Vol.28 (21), p.1303-1309

2006

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The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients

Pediatrics (Evanston), 1997-04, Vol.99 (4), p.567-574

1997

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Biochemical hallmarks of tyrosine hydroxylase deficiency

Clinical chemistry (Baltimore, Md.), 1998-09, Vol.44 (9), p.1897-1904

1998

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Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis

Brain (London, England : 1878), 2000-05, Vol.123 (5), p.908-919

2000

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Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings

Radiology, 2000-12, Vol.217 (3), p.869-876

2000

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Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With Vanishing White Matter

Journal of child neurology, 1999-11, Vol.14 (11), p.728-731

1999

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A new motor performance test in a prospective study on children with suspected myopathy

Developmental medicine and child neurology, 2006-09, Vol.48 (9), p.739-743

2006

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Comparison of 3 instruments to measure muscle strength in children: A prospective study

European journal of paediatric neurology, 2011-11, Vol.15 (6), p.512-518

2011

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Botulinum toxin A : a new option for treatment of drooling in children with cerebral palsy. Presentation of a case series

European journal of pediatrics, 2001-08, Vol.160 (8), p.509-512

2001

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Spina Bifida and Parental Occupation

Epidemiology (Cambridge, Mass.), 1996-03, Vol.7 (2), p.188-193

1996

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A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome

Annals of neurology, 1993-09, Vol.34 (3), p.410-412

1993

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Building centres of expertise according to the Dutch model?

Orphanet journal of rare diseases, 2010-10, Vol.5 (S1), p.O6-O6, Article O6

2010

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Nonmuscular involvement in merosin-negative congenital muscular dystrophy

Pediatric neurology, 2002, Vol.26 (1), p.30-36

2002

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Diagnosis and Differential Diagnosis of Muscle Cramps: A Clinical Approach

Journal of clinical neuromuscular disease, 2002-12, Vol.4 (2), p.89-94

2002

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Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy

Developmental medicine and child neurology, 2006-01, Vol.48 (1), p.20-27

2006

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A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome

European journal of human genetics : EJHG, 2000-06, Vol.8 (6), p.464-467

2000

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Molecular genetic analysis of human folate receptors in neural tube defects

European journal of human genetics : EJHG, 1999-04, Vol.7 (3), p.393-396

1999

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Peripheral Nerve Elongation by Laser Doppler Flowmetry-Monitored Expansion: An Experimental Basis for Future Application in the Management of Peripheral Nerve Defects

Plastic and reconstructive surgery (1963), 1996-03, Vol.97 (3), p.568-576

1996

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Intramedullary spinal cord abscess : a case report

Spine (Philadelphia, Pa. 1976), 1995-05, Vol.20 (10), p.1199-1204

1995

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Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease

Journal of neurology, neurosurgery and psychiatry, 2000-06, Vol.68 (6), p.797-798

2000

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The Treatment of Drooling by Ultrasound-Guided Intraglandular Injections of Botulinum Toxin Type A Into the Salivary Glands

MR Imaging and Proton MR Spectroscopic Studies in Sjogren-Larsson Syndrome: Characterization of the Leukoencephalopathy

Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome

Muscle Reflexes and Synergies Triggered by an Unexpected Support Surface Height During Walking

Validity and reproducibility of hand-held dynamometry in children aged 4-11 years

Validity and reproducibility of the Jamar dynamometer in children aged 4 - 11 years

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients

Biochemical hallmarks of tyrosine hydroxylase deficiency

Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis

Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings

Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With Vanishing White Matter

A new motor performance test in a prospective study on children with suspected myopathy

Comparison of 3 instruments to measure muscle strength in children: A prospective study

Botulinum toxin A : a new option for treatment of drooling in children with cerebral palsy. Presentation of a case series

Spina Bifida and Parental Occupation

A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome

Building centres of expertise according to the Dutch model?

Nonmuscular involvement in merosin-negative congenital muscular dystrophy

Diagnosis and Differential Diagnosis of Muscle Cramps: A Clinical Approach

Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy

A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome

Molecular genetic analysis of human folate receptors in neural tube defects

Peripheral Nerve Elongation by Laser Doppler Flowmetry-Monitored Expansion: An Experimental Basis for Future Application in the Management of Peripheral Nerve Defects

Intramedullary spinal cord abscess : a case report

Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease

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