Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier.
Front Genet. 2023 Aug 31;14:1251675. doi: 10.3389/fgene.2023.1251675. eCollection 2023.
Front Genet. 2023.
PMID: 37719708
Free PMC article.
IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC).
De Kinderen P, Rabaut L, Perik MHAM, Peeters S, Ponsaerts P, Loeys B, Mortier G, Meester JAN, Verstraeten A.
De Kinderen P, et al. Among authors: perik mham.
Stem Cell Res. 2023 Jun;69:103080. doi: 10.1016/j.scr.2023.103080. Epub 2023 Mar 21.
Stem Cell Res. 2023.
PMID: 36966641
Free PMC article.
Item in Clipboard
A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.
Van Gucht I, Meester JAN, Bento JR, Bastiaansen M, Bastianen J, Luyckx I, Van Den Heuvel L, Neutel CHG, Guns PJ, Vermont M, Fransen E, Perik MHAM, Velchev JD, Alaerts M, Schepers D, Peeters S, Pintelon I, Almesned A, Ferla MP, Taylor JC, Dallosso AR, Williams M, Evans J; Genomics England Research Consortium; Rosenfeld JA, Sluysmans T, Rodrigues D, Chikermane A, Bharmappanavara G, Vijayakumar K, Mottaghi Moghaddam Shahri H, Hashemi N, Torbati PN, Toosi MB, Al-Hassnan ZN, Vogt J, Revencu N, Maystadt I, Miller EM, Weaver KN, Begtrup A, Houlden H, Murphy D, Maroofian R, Pagnamenta AT, Van Laer L, Loeys BL, Verstraeten A.
Van Gucht I, et al. Among authors: perik mham.
Am J Hum Genet. 2021 Jun 3;108(6):1115-1125. doi: 10.1016/j.ajhg.2021.04.019. Epub 2021 May 18.
Am J Hum Genet. 2021.
PMID: 34010605
Free PMC article.
Item in Clipboard
Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia.
Persu A, Dobrowolski P, Gornik HL, Olin JW, Adlam D, Azizi M, Boutouyrie P, Bruno RM, Boulanger M, Demoulin JB, Ganesh SK, J Guzik T, Januszewicz M, Kovacic JC, Kruk M, de Leeuw P, Loeys BL, Pappaccogli M, Perik MHAM, Touzé E, Van der Niepen P, Van Twist DJL, Warchoł-Celińska E, Prejbisz A, Januszewicz A.
Persu A, et al. Among authors: perik mham.
Cardiovasc Res. 2022 Jan 7;118(1):65-83. doi: 10.1093/cvr/cvab086.
Cardiovasc Res. 2022.
PMID: 33739371
Free PMC article.
Review.
Item in Clipboard
Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
Verstraeten A, Perik MHAM, Baranowska AA, Meester JAN, Van Den Heuvel L, Bastianen J, Kempers M, Krapels IPC, Maas A, Rideout A, Vandersteen A, Sobey G, Johnson D, Fransen E, Ghali N, Webb T, Al-Hussaini A, de Leeuw P, Delmotte P, Lopez-Sublet M, Pappaccogli M, Sprynger M, Toubiana L; European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI); Van Laer L, Van Dijk FS, Vikkula M, Samani NJ, Persu A, Adlam D, Loeys B; Collaborators of the European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI).
Verstraeten A, et al. Among authors: perik mham.
Circulation. 2020 Sep 8;142(10):1021-1024. doi: 10.1161/CIRCULATIONAHA.120.045946. Epub 2020 Sep 8.
Circulation. 2020.
PMID: 32897753
Free article.
No abstract available.
Item in Clipboard
Cite
Cite