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Efficacy and safety of adeno‐associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapy

Journal of thrombosis and haemostasis, 2007-01, Vol.5 (1), p.16-24

2007

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Myotonic dystrophy type 1: Long term natural history data

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S195-S196

2016

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Toward an appropriate neuropsychological assessment protocol for children with myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S196-S196

2016

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The missing link

Acta gastro-enterologica belgica, 2018-10, Vol.81 (4), p.531

2018

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Evaluation of three serum i-ELISAs using monoclonal antibodies and protein G as peroxidase conjugate for the diagnosis of bovine brucellosis

Veterinary microbiology, 2004-05, Vol.100 (1), p.91-105

2004

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P39 – 2771: Variable phenotype in epilepsy caused by KCNQ2 mutations

European journal of paediatric neurology, 2015-05, Vol.19, p.S105-S105

2015

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La neurochirurgie fonctionnelle des nerfs crâniens

Neuro-chirurgie, 2009, Vol.55 (2), p.282-290

2009

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Baseline data from a European prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy – NatHis-SMA

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S103-S103

2016

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P76 Bethlem myopathy presenting as a limb girdle muscular dystrophy

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S28-S28

2012

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PP08.8 – 2833: Multiple sclerosis in Belgian children: A multicentric retrospective study

European journal of paediatric neurology, 2015-05, Vol.19, p.S62-S62

2015

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G.P.173

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.857-858

2014

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G.P.172

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.857-857

2014

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P248 DuMAND checklist: a screening tool for behavioural difficulties in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S176-S177

2023

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PP15.1 – 2964: Long-term renal outcome of a large cohort of patients with tuberous sclerosis complex

European journal of paediatric neurology, 2015-05, Vol.19, p.S89-S90

2015

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P100 The International Dysferlinopathy Registry and an international clinical outcome study for dysferlinopathy

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S35-S35

2012

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PP15.3 – 2545: Everolimus for patients with subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis complex (TSC): Results from an expanded access study

European journal of paediatric neurology, 2015-05, Vol.19, p.S90-S90

2015

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51Cr-EDTA plasma clearance in children: One, two, or multiple samples?

Medicine (Baltimore), 2022-01, Vol.101 (3), p.e28608

2022

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Use of Peek Cervical Prosthesis

World neurosurgery, 2012, Vol.77 (1), p.215-215

2012

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P77 Autosomal recessive desminopathy with desmin-null mutations presenting in childhood

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S28-S28

2012

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Incorporation of Navigated Transcranial Magnetic Stimulation Data in Preoperative Navigation Planning

World neurosurgery, 2012, Vol.77 (1), p.205-206

2012

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P.16 Parental illness intrusiveness, parental well-being and youth well-being in families confronted with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S50

2022

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Diagnosis of bovine brucellosis by skin test: conditions for the test and evaluation of its performance

Veterinary record, 1999-08, Vol.145 (8), p.214-218

1999

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Musculoskeletal simulations capture the experimentally observed response to ankle-foot-orthosis use in a healthy subject

Gait & posture, 2022-09, Vol.97, p.S34-S35

2022

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OUTCOME MEASURES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S149

2021

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OUTCOME MEASURES: EP.327 The relationship between illness perceptions and quality of life outcomes in adolescents with neuromuscular disorders

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S149-S149

2021

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Efficacy and safety of adeno‐associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapy

Myotonic dystrophy type 1: Long term natural history data

Toward an appropriate neuropsychological assessment protocol for children with myotonic dystrophy type 1

The missing link

Evaluation of three serum i-ELISAs using monoclonal antibodies and protein G as peroxidase conjugate for the diagnosis of bovine brucellosis

P39 – 2771: Variable phenotype in epilepsy caused by KCNQ2 mutations

La neurochirurgie fonctionnelle des nerfs crâniens

Baseline data from a European prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy – NatHis-SMA

P76 Bethlem myopathy presenting as a limb girdle muscular dystrophy

PP08.8 – 2833: Multiple sclerosis in Belgian children: A multicentric retrospective study

G.P.173

G.P.172

P248 DuMAND checklist: a screening tool for behavioural difficulties in Duchenne muscular dystrophy

PP15.1 – 2964: Long-term renal outcome of a large cohort of patients with tuberous sclerosis complex

P100 The International Dysferlinopathy Registry and an international clinical outcome study for dysferlinopathy

PP15.3 – 2545: Everolimus for patients with subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis complex (TSC): Results from an expanded access study

51Cr-EDTA plasma clearance in children: One, two, or multiple samples?

Use of Peek Cervical Prosthesis

P77 Autosomal recessive desminopathy with desmin-null mutations presenting in childhood

Incorporation of Navigated Transcranial Magnetic Stimulation Data in Preoperative Navigation Planning

P.16 Parental illness intrusiveness, parental well-being and youth well-being in families confronted with Duchenne muscular dystrophy

Diagnosis of bovine brucellosis by skin test: conditions for the test and evaluation of its performance

Musculoskeletal simulations capture the experimentally observed response to ankle-foot-orthosis use in a healthy subject

OUTCOME MEASURES

OUTCOME MEASURES: EP.327 The relationship between illness perceptions and quality of life outcomes in adolescents with neuromuscular disorders

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