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- BELGIEN
- OOST-VLAANDEREN
- GENT
- Molecular genetic characterisation of defects in extracellular matrix microfibrils and their correlation with morphological and functional defects of the cardiovascular system.
- Ghent University Hospital - UZGent
- Center for Medical Genetics Ghent
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- DEUTSCHLAND
- Niedersachsen
- HANNOVER
- Klinische und kernspintomographische Kiefergelenkbefunde bei Patienten mit Marfan-Syndrom
- Fachpraxis PD Dr. Dr. Oskar Bauss
- Fachpraxis Bauss -Kieferorthopädie
- Mehr Details
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- DEUTSCHLAND
- Niedersachsen
- HANNOVER
- Einfluss einer kieferorthopädischen Therapie auf Zähne von Marfan Patienten
- Fachpraxis PD Dr. Dr. Oskar Bauss
- Fachpraxis Bauss -Kieferorthopädie
- Mehr Details
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- DEUTSCHLAND
- Niedersachsen
- HANNOVER
- Entwicklung eines diagnostischen Chips für das Marfan-Syndrom und TAAD
- Medizinische Hochschule Hannover
- Institut für Humangenetik
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- FRANKREICH
- BOURGOGNE
- DIJON
- Phenotype-genotype correlation study in type I fibrillinopathies
- CHU de Dijon - Complexe du Bocage
- Centre de génétique
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- FRANKREICH
- ILE-DE-FRANCE
- MONTROUGE
- Metalloproteinases expression in aortic and pulmonary artery walls and skin in conjonctivodysplasias
- Faculté de chirurgie dentaire
- Laboratoire de physiopathologie des tissus non minéralisés
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- Clinical and economical impact of multidisciplinary outpatient clinic dedicated to Marfan disease and generalisation to orphan diseases
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- Ascending aorta aneurysm in the Marfan syndrome: clinical, genetic and phenotypic diversity
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- Genetic diversity and phenotypic monotonicity of non-atheromatous arterial aneurysms
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- VARIARFAN: study of the correlation between fibrilline gene expression variability and clinical affect in patients affecting by Marfan syndrome
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- FAD: vascular remodelling in aneurysmal disease
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- Influence of losartan in the growth of children affected by Marfan syndrome
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- GDPM-2 : phenotypical monotony and genetic diversity of non-atherosclerotic arterial disease
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Mehr Details
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- FRANKREICH
- ILE-DE-FRANCE
- PARIS
- Non-invasive characterization of the arterial phenotype in Marfan syndrome
- CHU Paris Ouest - Hôpital Européen Georges Pompidou
- Département de pharmacologie - Toxicologie
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- FRANKREICH
- PAYS DE LA LOIRE
- NANTES
- MITRAL: genetics of myxoid mitral valve's dystrophies
- CHU de Nantes - Hôpital Nord Guillaume et René Laënnec
- Clinique cardiologique et maladies vasculaires
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- Genotype-phenotype correlation in Marfan syndrome : from clinical silent phenotpyes to aortic dissection and valvular cardiomyopathies
- Fondazione IRCCS Policlinico San Matteo
- Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
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- New genetic syndromes with aortic tortuosity and dissection
- Fondazione IRCCS Policlinico San Matteo
- Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
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- Effects of angiotensin II receptor blocker (Losartan) vs selective ß1 receptor blocker (Nebivolol) vs the association of both on the quantitative gene expression of the TGFb pathway and TGFb levels in 300 fbn1-genotyped patients with Marfan Syndrome
- Fondazione IRCCS Policlinico San Matteo
- Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
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- Regulation of tgf-beta signaling by emilins and other proteins of elastic fiber. role in mouse models of monogenic forms of hypertension, marfan syndrome and supra-valvular aortic stenosis
- Università degli Studi di Padova
- Dipartimento di Istologia, Microbiologia e Tecnologie Mediche
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- KANADA
- Colombie-Britannique
- VANCOUVER
- FORGE - Finding of Rare Disease Genes in Canada
- University of British Columbia
- Faculty of Medicine
- Mehr Details
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- KANADA
- Ontario
- OTTAWA, ONTARIO
- FORGE - Finding of Rare Disease Genes in Canada
- University of Ottawa
- Faculty of Medicine -
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- FORGE - Finding of Rare Disease Genes in Canada
- Centre hospitalier universitaire Sainte-Justine
- Pédiatrie
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- Molecular consequences of Marfan mutations in fibrillin-1
- McGill University - Dentistry Building
- Department of Anatomy and Cell Biology
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- SCHWEIZ
- Suisse Alémanique
- SCHLIEREN
- Molecular basis of Marfan syndrome and related disorders: Whole-exome sequencing and targeted therapy
- Center for Cardiovascular Genetics and Gene Diagnostics
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- SPANIEN
- Cataluña
- BARCELONA
- Chronic activation of the TGF-beta signaling pathway en Marfan syndrome: alterations in membrane trafficking and the extracellular matrix
- Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
- Grupo de investigación en biología celular de procesos patológicos
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- SPANIEN
- Cataluña
- BARCELONA
- Membrane Trafficking of TGF-b receptors in Marfan cell lines: a new strategy to handle the TGF-b-induced signaling
- Universitat de Barcelona. Facultat de Medicina
- Departamento de Biología Celular, Inmunología y Neurociencias
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