Research Explorer

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Researcher

Laura Muiño Mosquera

Awards & Distinctions

95 Results

2025

Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease : results from the Montalcino Aortic Consortium

Michelle Su-Anne LimDong-Chuan GuoWalter Velasco TorrezAndrew LaiJonathan SchweberNikita GargJulie FleischerCatherine BoileauJulie De BackerArtur Evangelista et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Beyond the usual suspects : autosomal recessive forms of childhood-onset thoracic aortic disease

Simon D'hulstLaura Muiño Mosquera

U Journal Article in INTERNATIONAL JOURNAL OF CARDIOLOGY

2024

Assessment of myocardial fibrosis in Marfan syndrome using cardiac magnetic resonance imaging

Anthony DemolderDaniel DevosJulie De BackerLaura Muiño Mosquera

A1 Journal Article in MOLECULAR GENETICS & GENOMIC MEDICINE

Association of lifelong exercise characteristics with aortic pathology in patients with Marfan syndrome

Bibi SchreursSimon D'hulstHajar RotbiMaria HopmanDaan BosshardtMaarten GroeninkLaura Muiño MosqueraJulie De BackerThijs EijsvogelsRoland Van Kimmenade

Bicuspid aortic valve disease with early-onset complications : characteristics and aortic outcomes

Maximilian A. SelbstColin R. WardMegan L. SvetgoffHector I. MichelenaAnna Sabate-RotesJulie De BackerLaura Muiño MosqueraAnji T. YetmanMalenka M. BissellMaria Grazia Andreassi et al.

A2 Journal Article in HEARTS (BASEL)

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy

Sophie HespeAmber WaddellBabken AsatryanEmma OwensCourtney ThaxtonMhy-lanie AdduruKailyn AndersonEmily BrownLily Hoffman-AndrewsElizabeth Jordan et al.

Editorial : rising stars in pediatric cardiology 2023

Liqun SunLaura Muiño Mosquera

Editorial material

Evaluation of a nurse-led multi-component transition program for adolescents with congenital heart disease

Michèle de HossonKatya De GrooteAnn Van HeckeDaniël De WolfKristof VandekerckhoveLaura Muiño MosqueraJoseph PanzerKaren LoggheSaskia MelsLaurent Demulier et al.

A1 Journal Article in PATIENT EDUCATION AND COUNSELING

Genetics of aortic disease

Julie De BackerLaura Muiño MosqueraJohn A. Elefteriades

Bookchapter in Biomechanics of the aorta : modeling for patient care

Management of aortic disease in children with FBN1-related Marfan syndrome

Laura Muiño MosqueraElena CerviKatya De GrooteWendy DewalsZina FejzicKalliopi KazamiaSujeev MathurOlivier MilleronThomas S MirDorte G Nielsen et al.

A1 Journal Article in EUROPEAN HEART JOURNAL

Mitral annular disjunction in heritable thoracic aortic disease : insights from the Montalcino Aortic Consortium

Kishan L AsokanJennifer R LandesWannes RendersLaura Muiño MosqueraJulie De BackerDavid W JantzenAnji T YetmanGisela Teixido-TuraArturo EvangelistaRichmond Jeremy et al.

A1 Journal Article in JOURNAL OF THE AMERICAN HEART ASSOCIATION

Mitral valve phenotypes in SMAD3-related thoracic aortic disease : insights from the Montalcino Aortic Consortium

S K PrakashK L AsokanWannes RendersLaura Muiño MosqueraJulie De BackerD JantzenA T YetmanG Teixido-TuraR JeremyE G Jones et al.

New insights into the structural role of EMILINs within the human skin microenvironment

Alvise SchiavinatoFady MarcousAlexandra V. ZukDouglas R. KeeneSara F. TufaLaura Muiño MosqueraPaola ZigrinoCornelia MauchBeate EckesKatrien Francois et al.

A1 Journal Article in SCIENTIFIC REPORTS

Physical fitness in children with Marfan and Loeys-Dietz syndrome : associations between cardiovascular parameters, systemic manifestations, fatigue, and pain

Jessica Warnink-KavelaarsLisanne E. de KoningAnnelies E. van der HulstAnnemieke I. BuizerNicole PoissonnierLaura E. WijningaLeonie A. MenkeLaura Muiño MosqueraLies RombautRaoul H. H. Engelbert

A1 Journal Article in EUROPEAN JOURNAL OF PEDIATRICS

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

Steven G. CarlisleHasan AlbashaHector I. MichelenaAnna Sabate-RotesLisa BiancoJulie De BackerLaura Muiño MosqueraAnji T. YetmanMalenka M. BissellMaria Grazia Andreassi et al.

A1 Journal Article in PLOS ONE

Spontaneous resolution of an intrapericardial thrombus as a complication of pericardiocentesis in a neonate

Joy CrombezWendy DewalsLaura Muiño MosqueraThomas MartensKarlijn Van DammeLuc Bruyndonckx

A1 Journal Article in CARDIOLOGY IN THE YOUNG

Success rate of primary percutaneous balloon angioplasty in children with pulmonary stenosis and Noonan syndrome

Lukas RubbensLaura Muiño MosqueraJoseph PanzerDaniël De WolfHans De WildeKatya De GrooteIlse MeerschautWendy De WalsLuc BruyndonckxKristof Vandekerckhove et al.

A2 Journal Article in BELGIAN JOURNAL OF PAEDIATRICS

Unraveling Marfan hearts : ultrastructural evidence for myocardial remodeling and cardiomyopathy

Violette DeleeuwSimon D'hulstAnthony DemolderFelke SteijnsMarjolijn RenardRiet De RyckeJo Van DorpeLaura Muiño MosqueraKatrien FrancoisKálmán Benke et al.

Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications

Sara MansoorshahiAnji T YetmanMalenka M BissellYuli Y KimHector I MichelenaJulie De BackerLaura Muiño MosqueraDawn S HuiAnthony CaffarelliMaria G Andreassi et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

2023

A growing piece in the diagnostic puzzle

Simon D'hulstLaura ChometteLaura Muiño MosqueraAntoine Bondue

A4 Journal Article in TIJDSCHRIFT VOOR CARDIOLOGIE

Editorial : women in pediatric cardiology 2021

Laura Muiño MosqueraSarah Nordmeyer

Editorial material

Evaluation of late cardiac effects after multisystem inflammatory syndrome in children

Rik De WolfMahmoud ZaqoutKaoru TanakaLaura Muiño MosqueraGerlant van BerlaerKristof VandekerckhoveWENDY DEWALSDaniël De Wolf

A1 Journal Article in FRONTIERS IN PEDIATRICS

Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing

Jeffrey AaldersLaurens LégerAnthony DemolderLaura Muiño MosqueraPaul CouckeBjörn MentenJulie De BackerJolanda van Hengel

A1 Journal Article in STEM CELL RESEARCH

Genetic testing in patients with congenital heart disease : you do no harm when using the right tools!

Julie De BackerLaura Muiño Mosquera

Editorial material

HTAD patient pathway : strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) : a statement from the HTAD working group of VASCERN

Maryanne CaruanaMarieke J. BaarsEvy BashiardesKalman BenkeErik BjörckAndrei CodreanuElena de Moya RubioJulia DumfarthArturo EvangelistaMaarten Groenink et al.

A1 Journal Article in EUROPEAN JOURNAL OF MEDICAL GENETICS

Physical activity and physical fitness in children with heritable connective tissue disorders

Lisanne de KoningJessica Warnink-KavelaarsMarion van RossumSelina LimmenRuth Van der LoovenLaura Muiño MosqueraAnnelies van der HulstJaap OosterlaanLies RombautRaoul Engelbert

A1 Journal Article in FRONTIERS IN PEDIATRICS

Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage

Michèle de HossonKatya De GrooteHerlinde WynendaeleLaura Muiño MosqueraEva GoossensJulie De Backer

A1 Journal Article in EUROPEAN JOURNAL OF PEDIATRICS

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

Steven G. CarlisleHasan AlbashaHector MichelenaAnna Sabate-RotesLisa BiancoJulie De BackerLaura Muiño MosqueraAnji T. YetmanMalenka M BissellMaria Grazia Andreassi et al.

Shedding light on type B aortic dissection in Marfan syndrome : implications for patient counselling and research priorities

Julie De BackerIsabelle Van HerzeeleLaura Muiño Mosquera

Editorial material

TGFB3-related heritable thoracic aortic disease : results from the montalcino aortic consortium

Michelle LimAndrew LaiJonathan SchweberNikita GargJulie FleischerJulie De BackerLaura Muiño MosqueraAnji YetmanAnthony David CaffarelliGuillaume Jondeau et al.

Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse models

Violette DeleeuwEric CarlsonMarjolijn RenardKeith D. ZientekPhillip A. WilmarthAshok P. ReddyElise C. ManaloSara F. TufaDouglas R. KeeneMargie Olbinado et al.

A1 Journal Article in MATRIX BIOLOGY

2022

Arrhythmia and impaired myocardial function in heritable thoracic aortic disease : an international retrospective cohort study

Anthony DemolderLisa BiancoMaryanne CaruanaElena CerviArturo EvangelistaGuillaume JondeauLisa Lauren ButtigiegÁngela López-SainzElena Montañés DelmásAlessandro Pini et al.

A1 Journal Article in EUROPEAN JOURNAL OF MEDICAL GENETICS

Cardiac isomerism : a 20 year retrospective cohort at a single institution

Gilles MetsThierry BovéHans De WildeKatrien FrancoisThomas MartensLaura Muiño MosqueraJoseph PanzerEllen RoetsNoortje Van OostrumKristof Vandekerckhove et al.

Clinical and genetic correlates of mitral valve pathology in patients with heritable thoracic aortic disease: results from the montalcino aortic consortium

J De BackerWannes RendersA BravermanR JeremyG JondeauS PrakashG Teixido TuraS ShalhubA YetmanD Milewicz et al.

U Journal Article in European Heart Journal

Defects in the first hybrid domain of fibrillin-1 affect vascular wall homeostasis in the thoracic aorta

Violette DeleeuwMatthias Van ImpeGerlinde LoggheMarine VanhomwegenMargie OlbinadoMarco StampanoniPatrick SegersLaura Muiño MosqueraLynn SakaiPatrick Sips et al.

Defects in the first hybrid domain of fibrillin-1 affect vascular wall homeostasis in the thoracic aorta

Violette DeleeuwMatthias Van ImpeGerlinde LoggheMarine VanhomwegenMargie OlbinadoMarco StampanoniPatrick SegersLaura Muiño MosqueraLynn SakaiPatrick Sips et al.

Exploring the mutational landscape of isolated congenital heart defects : an exome sequencing study using cardiac DNA

Ilse MeerschautWouter SteyaertThierry BovéKatrien FrancoisThomas MartensKatya De GrooteHans De WildeLaura Muiño MosqueraJoseph PanzerKristof Vandekerckhove et al.

A1 Journal Article in GENES

How to measure the aorta in the setting of genetic aortic disease

Julie De BackerLaura Muiño MosqueraLaurence Campens

Bookchapter in Diseases of the aorta

In vitro modelling of Marfan-related cardiomyopathy points to abnormalities in mechanobiology of the heart muscle cells

Jeffrey AaldersLaurens LégerLouis Van der MeerenPatrick SipsLaura Muiño MosqueraAndre SkirtachSanjay SinhaJulie De BackerJolanda van Hengel

In vitro modelling of Marfan-related cardiomyopathy points to abnormalities in mechanobiology of the heart muscle cells

Jeffrey AaldersLaurens LégerLouis Van der MeerenPatrick SipsLaura Muiño MosqueraAndre SkirtachSanjay SinhaJulie De BackerJolanda van Hengel

Local TGF-beta sequestration by fibrillin-1 regulates vascular wall homeostasis in the thoracic aorta

Violette DeleeuwMatthias Van ImpeGerlinde LoggheMarine VanhomwegenMargie OlbinadoMarco StampanoniPatrick SegersLaura Muiño MosqueraLynn SakaiPatrick Sips et al.

Local TGF-beta sequestration by fibrillin-1 regulates vascular wall homeostasis in the thoracic aorta

Julie De BackerViolette DeleeuwMatthias Van ImpeMarine VanhomwegenGerlinde LoggheMargie OblinadoMarco StampanoniPatrick SegersLaura Muiño MosqueraLynn Sakai et al.

Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage

Michèle de HossonE GoossensKatya De GrooteLaura Muiño MosqueraHerlinde WynendaeleJulie De Backer

2021

A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations

BM WengerN PatelM LuiA MoscatiR DoDR StewartM TartagliaLaura Muiño MosqueraJulie De BackerAR Kontorovich et al.

A1 Journal Article in GENETICS IN MEDICINE

A reassessment of copy number variations in congenital heart defects : picturing the whole genome

Ilse MeerschautSarah VergultAnnelies DheedeneBjörn MentenKatya De GrooteHans De WildeLaura Muiño MosqueraJoseph PanzerKristof VandekerckhovePaul Coucke et al.

A1 Journal Article in GENES

Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO

Andrea de la Fuente-AlonsoMarta ToralAlvaro AlfayateMaría Jesús Ruiz-RodríguezElena Bonzón-KulichenkoGisela Teixido-TuraSara Martínez-MartínezMaría José Méndez-OlivaresDolores López-MaderueloIleana González-Valdés et al.

A1 Journal Article in NATURE COMMUNICATIONS

Arrhythmia and cardiomyopathy in heritable thoracic aortic disease : an international retrospective cohort study

Anthony DemolderLaura Muiño MosqueraA PiniA EvangelistaA Lopez-SainzG Teixido-TuraG JondeauK SzocsY Von KodolitschM Caruana et al.

Association of mitral annular disjunction with cardiovascular outcomes among patients with Marfan syndrome

Anthony DemolderFrank TimmermansMattias DuytschaeverLaura Muiño MosqueraJulie De Backer

A1 Journal Article in JAMA CARDIOLOGY

Cardiomyopathy in genetic aortic diseases

Laura Muiño MosqueraJulie De Backer

A1 Journal Article in FRONTIERS IN PEDIATRICS

More than meets the eye : expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome

Tibbe DhoogeTim Van DammeDelfien SyxLaura Muiño MosqueraSheela NampoothiriAnil RadhakrishnanPelin O. Simsek-KiperGulen E. UtineMaryse BonduelleIsabelle Migeotte et al.

A1 Journal Article in HUMAN MUTATION

Oxygen uptake kinetics and local muscle oxygenation during submaximal exercise in children after the Fontan procedure compared to healthy peers

Yrik BagdasarianIlse CoomansDaniël De WolfKatya De GrooteJoseph PanzerLaura Muiño MosqueraHans De WildeThierry BovéKatrien FrancoisJan Boone et al.

Recovery kinetics of gas exchange parameters and heart rate after maximal exercise in children with repaired Tetralogy of Fallot compared to controls

Ilse CoomansSara De KinderHannah Van BelleghemDaniël De WolfKatya De GrooteJoseph PanzerLaura Muiño MosqueraHans De WildeThierry BovéKatrien Francois et al.

2020

Analysis of the recovery phase after maximal exercise in children with repaired tetralogy of Fallot and the relationship with ventricular function

Ilse CoomansSara De KinderHannah Van BelleghemKatya De GrooteJoseph PanzerHans De WildeLaura Muiño MosqueraKatrien FrançoisThierry BovéThomas Martens et al.

A1 Journal Article in PLOS ONE

Genetics in congenital heart disease : are we ready for it?

Julie De BackerBert CallewaertLaura Muiño Mosquera

A2 Journal Article in REVISTA ESPAÑOLA DE CARDIOLOGÍA (ENGLISH ED.)

Genética en la cardiopatía congénita : ¿estamos preparados?

Julie De BackerBert CallewaertLaura Muiño Mosquera

A1 Journal Article in REVISTA ESPANOLA DE CARDIOLOGIA

Myocardial disease and ventricular arrhythmia in Marfan syndrome : a prospective study

Laura Muiño MosqueraHans De WildeDaniel DevosDanilo BabinLuc JordaensAnthony DemolderKatya De GrooteDaniël De WolfJulie De Backer

A1 Journal Article in ORPHANET JOURNAL OF RARE DISEASES

Myocardial function, heart failure and arrhythmia in Marfan syndrome : a systematic literature review

Anthony DemolderYskert von KodolitschLaura Muiño MosqueraJulie De Backer

A1 Journal Article in DIAGNOSTICS

2019

Angiotensin-II receptor blockade in Marfan syndrome

Laura Muiño MosqueraJulie De Backer

Editorial material

Case-matched comparison of cardiovascular outcome in Loeys-Dietz syndrome versus Marfan syndrome

Kristina MühlstädtJulie De BackerYskert von KodolitschKerstin KutscheLaura Muiño MosqueraJens BrickwedelEvaldas GirdauskasThomas S MirAdrian MahlmannNikolaos Tsilimparis et al.

A1 Journal Article in JOURNAL OF CLINICAL MEDICINE

Features of Marfan syndrome not listed in the Ghent nosology : the dark side of the disease

Yskert von KodolitschAnthony DemolderEvaldas GirdauskasHarald KaemmererKatharina KornhuberLaura Muiño MosqueraShaine MorrisEnid NeptuneReed PyeritzSvend Rand-Hendriksen et al.

A2 Journal Article in EXPERT REVIEW OF CARDIOVASCULAR THERAPY

Marfan syndrome

Laura Muiño MosqueraLaurence Campens

Bookchapter in Reference Module in Biomedical Sciences

SMAD3 pathogenic variants : risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium

Ellen M HostetlerEllen S RegaladoDong-Chuan GuoNadine HannaPauline ArnaudLaura Muiño MosqueraBert CallewaertKwanghyuk LeeSuzanne M LealStephanie E Wallace et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome

Laura Muiño MosqueraFre BautersKarlien DhondtHans De WildeLuc JordaensKatya De GrooteDaniël De WolfKatrien HertegonneJulie De Backer

A1 Journal Article in MOLECULAR GENETICS & GENOMIC MEDICINE

The cardiovascular spectrum of Marfan syndrome : a study of clinical and genetic modifiers

Laura Muiño MosqueraJulie De BackerDaniël De Wolf

2018

Arterial tortuosity syndrome : 40 new families and literature review

Aude BeyensJuliette AlbuissonAnnekatrien BoelMazen Al-EssaWaheed Al-ManeaDamien BonnetOzlem BostanOdile BouteTiffany BusaNathalie Canham et al.

A1 Journal Article in GENETICS IN MEDICINE

Frequency of ventricular arrhythmias and other rhythm abnormalities in children and young adults with the Marfan syndrome

Douglas Y MahLynn A SleeperJane E CrossonRichard J CzosekBarry A LoveBrian W McCridleLaura Muiño MosqueraAaron K OlsonThomas A PilcherElif Seda Selamet Tierney et al.

A1 Journal Article in AMERICAN JOURNAL OF CARDIOLOGY

Looking for the missing links : challenges in the search for genotype-phenotype correlation in Marfan syndrome

Julie De BackerLaurence CampensLaura Muiño Mosquera

Editorial material

Myocardial disease and arrhythmia in Marfan syndrome

Laura Muiño MosqueraHans De WildeDaniël De WolfJulie De Backer

Prevalence of obstructive sleep apnea and its relation to cardiovascular disease in Marfan syndrome

Laura Muiño MosqueraFre BautersKarlien DhondtHans De WildeDaniël De WolfKatrien HertegonneJulie De Backer

Sex, pregnancy and aortic disease in Marfan syndrome

Marjolijn RenardLaura Muiño MosqueraElise ManaloSara TufaEric CarlsonDouglas KeeneJulie De BackerLynn Sakai

Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline

Laura Muiño MosqueraFelke SteijnsTjorven AudenaertIlse MeerschautAnne De PaepeWouter SteyaertSofie SymoensPaul CouckeBert CallewaertMarjolijn Renard et al.

A1 Journal Article in CIRCULATION-GENOMIC AND PRECISION MEDICINE

2017

Aortic root growth in children with Marfan syndrome : evidence for gender differences

Laura Muiño MosqueraKatya De GrooteKristof VandekerckhoveJoseph PanzerHans De WildeDaniël De WolfJulie De Backer

Julie De BackerLaura Muiño MosqueraLAURENT DEMULIER

Bookchapter in Pregnancy and congenital heart disease

Arterial tortuosity syndrome : 37 new families and literature review

Aude BeyensJuliette AlbuissonT BusaN CanhamJM ChopinM DasoukiK DevriendtH DietzBjörn Fischer-ZirnsakAlper Gezdirici et al.

Arterial tortuosity syndrome : 40 new families and literature review

Aude BeyensJuliette AlbuissonAnnekatrien BoelMazen Al-EssaDamien BonnetO BostanOdile BouteT BusaN CanhamErgun Cil et al.

Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome : a randomized, double-blind clinical trial

Laura Muiño MosqueraSylvia De NobeleDaniel DevosLaurence CampensAnne De PaepeJulie De Backer

A1 Journal Article in ACTA CARDIOLOGICA

Pregnancy in women with SMAD3 mutation

Iris M van HagenDenise van der LindeIngrid MBH van de LaarLaura Muiño MosqueraJulie De BackerJolien W Roos-Hesselink

A1 Journal Article in JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Sex, pregnancy and aortic disease in Marfan syndrome

Marjolijn RenardLaura Muiño MosqueraElise C ManaloSara TufaEric J CarlsonDouglas R KeeneJulie De BackerLynn Y Sakai

A1 Journal Article in PLOS ONE

Tailoring the ACMG and AMP recommendations for the interpretation of genetic variants in the FBN1 gene : a gene-specific guideline

Laura Muiño MosqueraFelke SteijnsMarjolijn RenardJulie De Backer

2016

Arterial tortuosity syndrome : 29 novel families

Aude BeyensJuliette AlbuissonT BusaN CanhamJM CM. DasoukiK DevriendtH DietzBjörn Fischer-ZirnsakAlper Gezdirici et al.

Can aortic root replacement with a graft affect cardiac function in patients with Marfan syndrome?

Laura Muiño MosqueraKatrien FrancoisThierry BovéJulie De Backer

International registry of patients carrying TGFBR1 or TGFBR2 mutations results of the MAC (Montalcino Aortic Consortium)

Guillaume JondeauJacques RopersEllen RegaladoAlan BravermanArturo EvangelistaGuisela TeixedoJulie De BackerLaura Muiño MosqueraSophie NaudionCecile Zordan et al.

A1 Journal Article in CIRCULATION-CARDIOVASCULAR GENETICS

Is pregnancy a risk factor for aortic complications in Marfan syndrome?

Laura Muiño MosqueraLAURENT DEMULIERDaniël De WolfJulie De Backer

Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses

Arnaud VanlanderLaura Muiño MosqueraJoseph PanzerTine DeconinckJoél SmetSara SenecaJo Van DorpeLiesbeth FerdinandeChantal Ceuterick-de GrootePeter De Jonghe et al.

A1 Journal Article in MITOCHONDRION

Mitral valve prolapse syndrome and MASS phenotype : stability of aortic dilatation but progression of mitral valve prolapse

Moritz RippeJulie De BackerKerstin KutscheLaura Muiño MosqueraHelke SchülerMeike RybczynskiAlexander M BernhardtBritta KeyserMathias HillebrandThomas S Mir et al.

A2 Journal Article in IJC HEART & VASCULATURE

PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure

Renate ZeevaertEmmanuel ScalaisLaura Muiño MosqueraLinda De MeirleirCarine De BeaufortMichael WitschJaak JaekenJean De Schepper

A1 Journal Article in ACTA CLINICA BELGICA

Zorg voor de volwassenen met een congenitale hart afwijking : verslag van de thematische sessie georganiseerd door de BWGACHD naar aanleiding van het jaarlijkse congres van de Belgische Vereniging voor Cardiologie

Michèle de HossonLaura Muiño MosqueraAntoine BondueJulie De Backer

Editorial material

2015

Gene panel sequencing in heritable thoracic aortic disorders and related entities: results of comprehensive testing in a cohort of 264 patients

Laurence CampensBert CallewaertLaura Muiño MosqueraMarjolijn RenardSofie SymoensAnne De PaepePaul CouckeJulie De Backer

A1 Journal Article in ORPHANET JOURNAL OF RARE DISEASES

Intrinsic cardiomyopathy in Marfan syndrome: results from in- and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans

Laurence CampensMarjolijn RenardBram TrachetPatrick SegersLaura Muiño MosqueraJohan De SutterLynn SakaiAnne De PaepeJulie De Backer

A1 Journal Article in PEDIATRIC RESEARCH

Managing aortic aneurysms and dissections during pregnancy

Laura Muiño MosqueraJulie De Backer

A2 Journal Article in EXPERT REVIEW OF CARDIOVASCULAR THERAPY

Marfan syndrome and related heritable thoracic aortic aneurysms and dissections

Julie De BackerMarjolijn RenardLaurence CampensLaura Muiño MosqueraAnne De PaepePaul CouckeBert CallewaertYskert von Kodolitsch

A1 Journal Article in CURRENT PHARMACEUTICAL DESIGN

Thoracaal aorta-aneurysma: verslag van de thematische sessie georganiseerd door de BWGACHD

Laura Muiño MosqueraJulie De Backer

Editorial material

2014

Een expeditie stroomafwaarts uit het linkerventrikel: verslag van het Lentesymposium georganiseerd door het Hartcentrum UZ Gent en de Dienst Cardiologie UZ Antwerpen op 21 maart 2013, Gent

Laurence CampensWendy DewalsLaura Muiño Mosquera

Mutation detection rate and - characteristics in thoracic aortic aneurysm (TAA) related disorders: results from next generation sequencing (NGS) panel testing

Laurence CampensLaura Muiño MosqueraBert CallewaertMarjolijn RenardMachteld BaetensAnne De PaepePaul CouckeJulie De Backer

2012

Closure of a lateral baffle leak in a Fontan patient with an Amplatzer PDA II AS plug

Laura Muiño MosqueraBert SuysDaniël De Wolf

A1 Journal Article in ACTA CARDIOLOGICA