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Cerebral cavernous malformation: new molecular and clinical insights

Journal of Medical Genetics, 2006-09, Vol.43 (9), p.716-721

2006

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Pathogénie et génétique des anomalies vasculaires

Annales de chirurgie plastique et esthétique, 2006-08, Vol.51 (4), p.282-286

Vikkula, M.

2006

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Venous malformation: update on aetiopathogenesis, diagnosis and management

Phlebology, 2010-10, Vol.25 (5), p.224-235

2010

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Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel data

Critical reviews in oncology/hematology, 2018-12, Vol.132, p.138-144

2018

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Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations

Molecular syndromology, 2013-04, Vol.4 (4), p.179-183

2013

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Traitement d’un hémangiome infantile résistant au propranolol par une courte cure de sirolimus

Annales de Dermatologie et de Vénéréologie - FMC, 2023-12, Vol.3 (8), p.A320-A321

2023

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Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

Thrombosis research, 2015-06, Vol.135 (6), p.1057-1063

2015

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Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

Molecular syndromology, 2013-09, Vol.4 (6), p.257-266

2013

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Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema

Clinical genetics, 2018-07, Vol.94 (1), p.179-181

2018

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Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

Lymphology, 2021, Vol.54 (4), p.167

2021

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Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene

Clinical genetics, 2015-04, Vol.87 (4), p.378-382

2015

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[OP.6B.03] KIF1B AND NF1 ARE THE MOST FREQUENTLY MUTATED GENES IN PARAGANGLIOMAS AND PHEOCHROMOCYTOMAS TUMOURS FROM A BELGIAN MULTICENTRIC COHORT

Journal of hypertension, 2017-09, Vol.35 Suppl 2 - ESH 2017 Abstract Book (Supplement 2), p.e58-e58

2017

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Les malformations veineuses : aspects cliniques et diagnostic différentiel

Annales de chirurgie plastique et esthétique, 2006-08, Vol.51 (4), p.373-387

2006

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Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene

Thrombosis research, 2016-01, Vol.137, p.224-227

2016

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A Novel Association between RASA1 Mutations and Spinal Arteriovenous Anomalies

American journal of neuroradiology : AJNR, 2010-04, Vol.31 (4), p.775-779

2010

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Recessive primary congenital lymphoedema caused by a VEGFR3 mutation

Journal of medical genetics, 2009-06, Vol.46 (6), p.399-404

2009

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6C.05: STK39 AND WNK1 ARE POTENTIAL HYPERTENSION SUSCEPTIBILITY GENES IN THE BELHYPGEN COHORT

Journal of hypertension, 2015-06, Vol.33 Suppl 1 - ESH 2015 Abstract Book (Supplement 1), p.e80-e80

2015

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Vascular malformations: localized defects in vascular morphogenesis

Clinical genetics, 2003-05, Vol.63 (5), p.340-351

2003

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Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree

Journal of bone and mineral research, 2013-02, Vol.28 (2), p.341-350

2013

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Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep

Neurology, 2008-07, Vol.71 (1), p.64

2008

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Genetic causes of vascular malformations

Human molecular genetics, 2007-10, Vol.16 (R2), p.R140-R149

2007

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Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.516-522

2015

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3

Human molecular genetics, 2017-11, Vol.26 (21), p.4095-4104

2017

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Trametinib as a promising therapeutic option in alleviating vascular defects in an endothelial KRAS-induced mouse model

Human molecular genetics, 2023-01, Vol.32 (2), p.276-289

2023

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Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect

Journal of medical genetics, 2005-02, Vol.42 (2), p.e13-e13

2005

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Cerebral cavernous malformation: new molecular and clinical insights

Pathogénie et génétique des anomalies vasculaires

Venous malformation: update on aetiopathogenesis, diagnosis and management

Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel data

Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations

Traitement d’un hémangiome infantile résistant au propranolol par une courte cure de sirolimus

Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema

Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene

[OP.6B.03] KIF1B AND NF1 ARE THE MOST FREQUENTLY MUTATED GENES IN PARAGANGLIOMAS AND PHEOCHROMOCYTOMAS TUMOURS FROM A BELGIAN MULTICENTRIC COHORT

Les malformations veineuses : aspects cliniques et diagnostic différentiel

Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene

A Novel Association between RASA1 Mutations and Spinal Arteriovenous Anomalies

Recessive primary congenital lymphoedema caused by a VEGFR3 mutation

6C.05: STK39 AND WNK1 ARE POTENTIAL HYPERTENSION SUSCEPTIBILITY GENES IN THE BELHYPGEN COHORT

Vascular malformations: localized defects in vascular morphogenesis

Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree

Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep

Genetic causes of vascular malformations

Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A

Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3

Trametinib as a promising therapeutic option in alleviating vascular defects in an endothelial KRAS-induced mouse model

Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect

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