Các bài viết có thể truy cập công khai - Miikka VikkulaTìm hiểu thêm
Tổng thểFNRSNIHEuropean CommissionSNSFFWOLeducq Foundation, USAAcademy of FinlandINSERMBHFWellcomeBELSPONIHRDFGHHMICancer Research UKANRGovernment of SpainFAPESPNHMRCKnut and Alice Wallenberg FoundationSwedish Research CouncilMRCZonMwDHFChildren's Tumor Foundation, USANSFAHAFWFHelmholtzBanking Foundation "la Caixa"EPSRCMotor Neurone Disease Association, UKNCNTuberous Sclerosis Alliance, USAMedical Research Future Fund, Australia
Không có ở bất kỳ nơi nào: 13
Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes
M Basha, B Demeer, N Revencu, R Helaers, S Theys, SB Saba, O Boute, ...
Journal of medical genetics 55 (7), 449-458, 2018
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium, Belgian Science Policy Office
Recessive primary congenital lymphoedema caused by a VEGFR3 mutation
A Ghalamkarpour, W Holnthoner, P Saharinen, LM Boon, JB Mulliken, ...
Journal of medical genetics 46 (6), 399-404, 2009
Các cơ quan ủy nhiệm: Austrian Science Fund
Primary lymphoedema
P Brouillard, MH Witte, RP Erickson, RJ Damstra, C Becker, I Quéré, ...
Nature reviews Disease primers 7 (1), 77, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, National Fund for Scientific Research, Belgium
Genetics of vascular malformations
HL Nguyen, LM Boon, M Vikkula
Seminars in pediatric surgery 23 (4), 221-226, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, National Fund for Scientific Research, Belgium
Inheritance patterns of infantile hemangioma
E Castrén, P Salminen, M Vikkula, A Pitkäranta, T Klockars
Pediatrics 138 (5), 2016
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium
RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation
N Revencu, E Fastre, M Ravoet, R Helaers, P Brouillard, ...
Journal of medical genetics 57 (1), 48-52, 2020
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium
Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema.
E Fastré, L Lanteigne, R Helaers, G Giacalone, N Revencu, D Dionyssiou, ...
Clinical genetics 94 (1), 2018
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium, Belgian Science Policy Office
Congenital plaque‐type glomuvenous malformations associated with fetal pleural effusion and ascites
E Goujon, KM Cordoro, M Barat, T Rousseau, P Brouillard, M Vikkula, ...
Pediatric dermatology 28 (5), 528-531, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
Antenatal presentation of hereditary lymphedema type I
E Boudon, Y Levy, T Abossolo, F Cartault, P Brouillard, M Vikkula, ...
European Journal of Medical Genetics 58 (6-7), 329-331, 2015
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium
Reconstructive surgery in the management of a patient with CLOVES syndrome
F Ballieux, A Modarressi, F Hammer, P Clapuyt, PL Docquier, C Godfraind, ...
Journal of Plastic, Reconstructive & Aesthetic Surgery 66 (12), 1813-1815, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute, Wellcome …
Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery.
MH Witte, RP Erickson, L Luy, P Brouillard, M Vikkula
Lymphology 54 (4), 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, National Fund for Scientific Research, Belgium
Molecular genetics of lymphatic and complex vascular malformations
MJ Schlögel, P Brouillard, LM Boon, M Vikkula
Lymphedema: a concise compendium of theory and practice, 753-763, 2018
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium, Belgian Science Policy Office
Capillary malformation/arteriovenous malformation
N Revencu, LM Boon, M Vikkula
Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics …, 2020
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium
Có tại một số nơi: 125
Chromosome instability is common in human cleavage-stage embryos
E Vanneste, T Voet, C Le Caignec, M Ampe, P Konings, C Melotte, ...
Nature medicine 15 (5), 577, 2009
Các cơ quan ủy nhiệm: Research Foundation (Flanders)
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
TC Pansuriya, R van Eijk, P d'Adamo, MAJH van Ruler, ML Kuijjer, ...
Nature genetics 43 (12), 1256-1261, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
B Lorenz-Depiereux, M Bastepe, A Benet-Pagès, M Amyere, ...
Nature genetics 38 (11), 1248-1250, 2006
Các cơ quan ủy nhiệm: German Research Foundation
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations
N Limaye, V Wouters, M Uebelhoer, M Tuominen, R Wirkkala, JB Mulliken, ...
Nature genetics 41 (1), 118-124, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma
M Jinnin, D Medici, L Park, N Limaye, Y Liu, E Boscolo, J Bischoff, ...
Nature medicine 14 (11), 1236-1246, 2008
Các cơ quan ủy nhiệm: US National Institutes of Health
Genetics of lymphatic anomalies
P Brouillard, L Boon, M Vikkula
The Journal of clinical investigation 124 (3), 898-904, 2014
Các cơ quan ủy nhiệm: National Fund for Scientific Research, Belgium
Venous malformation: update on aetiopathogenesis, diagnosis and management
A Dompmartin, M Vikkula, LM Boon
Phlebology 25 (5), 224-235, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
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