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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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2024 update: European consensus statement on gene therapy for spinal muscular atrophy

European journal of paediatric neurology, 2024-07, Vol.51, p.73-78

2024

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On the cutting edge: anterior transpetrosal approach – the middle fossa approach. Clinical application, surgical anatomy, and results

Sechenovskiĭ vestnik, 2021-11, Vol.12 (4), p.19-28

2021

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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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311P Development and pilot validation of the DuMAND checklist to screen for Duchenne muscular dystrophy-associated neurobehavioral difficulties (DuMAND)

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.506

2024

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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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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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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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Use of Peek Cervical Prosthesis

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

2012

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312P Genotype and corticosteroid treatment are associated with distinctive variations in gray matter characteristics among patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.507

2024

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

2024 update: European consensus statement on gene therapy for spinal muscular atrophy

On the cutting edge: anterior transpetrosal approach – the middle fossa approach. Clinical application, surgical anatomy, and results

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

311P Development and pilot validation of the DuMAND checklist to screen for Duchenne muscular dystrophy-associated neurobehavioral difficulties (DuMAND)

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

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

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

Use of Peek Cervical Prosthesis

312P Genotype and corticosteroid treatment are associated with distinctive variations in gray matter characteristics among patients with Duchenne muscular dystrophy

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

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