• 1-Year Clinical Outcomes of All Comers Treated With 2 Bioresorbable Polymer-Coated Sirolimus-Eluting Stents: Propensity Score-Matched Comparison of the COMBO and Ultrathin-Strut Orsiro Stents
• 4D flow MRI of type B dissection with later retrograde progression to type A dissection in Marfan: a case report
• A Case of Fulminant Listeria Rhombencephalitis with Brainstem Abscesses in a 37-Year-Old Immunocompetent Patient: From Vestibular Neuritis to Ondine's Curse
• A cross-sectional study on fatigue, anxiety, and symptoms of depression and their relation with medical status in adult patients with Marfan syndrome. Psychological consequences in Marfan syndrome
• A Kinome-Wide Small Interfering RNA Screen Identifies Proviral and Antiviral Host Factors in Severe Acute Respiratory Syndrome Coronavirus Replication, Including Double-Stranded RNA-Activated Protein Kinase and Early Secretory Pathway Proteins
• A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes
• A specific plasma lipid signature associated with high triglycerides and low HDL cholesterol identifies residual CAD risk in patients with chronic coronary syndrome
• Abnormal aortic hemodynamics are associated with risk factors for aortic complications in patients with marfan syndrome
• Acute Coronary Syndrome Subphenotypes Based on Repeated Biomarker Measurements in Relation to Long-Term Mortality Risk
• Age-related and regional changes of aortic stiffness in the Marfan syndrome: assessment with velocity-encoded MRI
• Alterations in Blood Chemistry Levels Associated With Nipah Virus Disease in the Syrian Hamster Model
• An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection
• Aortic disease in patients with Marfan syndrome: aortic volume assessment for surveillance
• Aortic distensibility in Marfan syndrome: a potential predictor of aortic events?
• Arthroscopy of the ankle joint
• Ascending aorta curvature and flow displacement are associated with accelerated aortic growth at long-term follow-up: A MRI study in Marfan and thoracic aortic aneurysm patients
• Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
• Association of Circulating Neutrophils with Relative Volume of Lipid-Rich Necrotic Core of Coronary Plaques in Stable Patients: A Substudy of SMARTool European Project
• Association of MMP9 with adverse features of plaque progression and residual inflammatory risk in patients with chronic coronary syndrome (CCS)
• Association of PCSK9 plasma levels with metabolic patterns and coronary atherosclerosis in patients with stable angina
• Autistic disorder symptoms in Rett syndrome
• Azithromycin in chronic fatigue syndrome (CFS), an analysis of clinical data
• Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan Syndrome
• Biventricular performance in patients with marfan syndrome without significant valvular disease: comparison to normal subjects and longitudinal follow-up
• Blood Monocyte Phenotype Fingerprint of Stable Coronary Artery Disease: A Cross-Sectional Substudy of SMARTool Clinical Trial
• Brief report: The use of WAIS-III in adults with HFA and Asperger syndrome
• Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome
• Chronic fatigue syndrome and sexual dysfunction
• Circulating transforming growth factor-beta as a prognostic biomarker in Marfan syndrome
• Circulating transforming growth factor-β as a prognostic biomarker in Marfan syndrome
• Clinical features differ substantially between Caucasian and Asian populations of Marfan syndrome
• Cognitive behaviour therapy for chronic fatigue syndrome
• Coherent versus component motion perception in autism spectrum disorder
• Comparison of 3 biodegradable polymer and durable polymer-based drug-eluting stents in all-comers (BIO-RESORT): rationale and study design of the randomized TWENTE III multicenter trial
• Comparison of high-sensitive cardiac troponin T and I in patients with chronic coronary syndrome
• Complementation of the genetic defect in Gunn rat hepatocytes in vitro by highly efficient gene transfer with cationic liposomes
• Craniomandibular disorders. A retrospective study of patients referred to the department of Special Dental Care Utrecht
• Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome
• Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
• Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia
• Determinants of physical health parameters in individuals with intellectual disability who use long-term antipsychotics
• Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis B
• Epidemiology and transmission of Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans among children and their family members. A report of 4 surveys
• Evaluation of sampling density on the accuracy of aortic pulse wave velocity from velocity-encoded MRI in patients with Marfan syndrome
• Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
• Exploratory open label, randomized study of acetyl- and propionylcarnitine in chronic fatigue syndrome
• Exploring inactivation of SARS-CoV-2, MERS-CoV, Ebola, Lassa, and Nipah viruses on N95 and KN95 respirator material using photoactivated methylene blue to enable reuse
• First-in-man evaluation of the novel balloon delivery system STENTYS Xposition S for the self-apposing coronary artery stent: impact on longitudinal geographic miss during stenting
• Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment
• Gated myocardial SPECT imaging; true additional value in AMI?
• Genome-wide methylation patterns in Marfan syndrome
• Genotype impacts survival in Marfan syndrome
• Griffithsin Inhibits Nipah Virus Entry and Fusion and Can Protect Syrian Golden Hamsters From Lethal Nipah Virus Challenge
• Impact of COVID-19 Pandemic on Cardiovascular Testing in Asia: The IAEA INCAPS-COVID Study
• Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study
• Increased aortic tortuosity indicates a more severe aortic phenotype in adults with Marfan syndrome
• Inflammation aggravates disease severity in Marfan syndrome patients
• Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial beta-oxidation defects
• Intrinsic biventricular dysfunction in Marfan syndrome
• Local information processing in adults with high functioning autism and asperger syndrome: the usefulness of neuropsychological tests and self-reports
• Long-term clinical outcomes of losartan in patients with Marfan syndrome: follow-up of the multicentre randomized controlled COMPARE trial
• Losartan reduces aortic dilatation rate in adults with Marfan syndrome: a randomized controlled trial
• Losartan therapy in adults with Marfan syndrome: study protocol of the multi-center randomized controlled COMPARE trial
• Maternal parenting stress in families with a child with Angelman syndrome or Prader-Willi syndrome
• Mental retardation, premature balding, small genitalia, small acra and small patellae in brothers: confirmation of an entity
• Mitochondrial encephalomyopathy, lactic acidosis and stroke in adults: two cases
• Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type
• Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction
• MRI-assessed regional pulse wave velocity for predicting absence of regional aorta luminal growth in marfan syndrome
• Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography
• Outcomes and regional differences in practice in a worldwide coronary stent registry
• Parenting Stress in CHARGE Syndrome and the Relationship with Child Characteristics
• Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity
• Pearson syndrome and the role of deletion dimers and duplications in the mtDNA
• Prevention of neurological involvement as a sequela of an atlanto-axial dislocation in persons with Down syndrome
• Prevention of neurological involvement as sequela of an atlanto-axial dislocation in persons with Down syndrome
• Prognostic value of coronary computed tomography angiography in diabetic patients without chest pain syndrome
• Rapid aortic aneurysm formation in Marfan patient with dissection of the entire aorta
• Rupture of silicone gel breast implants and symptoms of pain and fatigue
• Simultaneous analysis of the behavioural phenotype, physical factors, and parenting stress in people with Cornelia de Lange syndrome
• Social and emotional detachment: a cross-cultural comparison of the non-disruptive behavioural psychopathic traits in children
• Stable Occupancy of the Crimean-Congo Hemorrhagic Fever Virus-Encoded Deubiquitinase Blocks Viral Infection
• Successful treatment of UGT1A1 deficiency in a rat model of Crigler-Najjar disease by intravenous administration of a liver-specific lentiviral vector
• The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive family
• The development of a rating scale to screen social and emotional detachment in children and adolescents
• The development of adaptive skills in young people with Down syndrome
• The effect of losartan therapy on ventricular function in Marfan patients with haploinsufficient or dominant negative FBN1 mutations
• The risk for type B aortic dissection in Marfan syndrome
• The syndrome of Capgras: converging models
• Theory of mind in adults with HFA and Asperger syndrome
• Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation
• Triglycerides and low HDL cholesterol predict coronary heart disease risk in patients with stable angina
• Two sisters with mental retardation, cataract, ataxia, progressive hearing loss, and polyneuropathy
• Unknown syndrome: mental retardation with dysmorphic features, early balding, patella luxations, acromicria, and hypogonadism
• Use of cardiac imaging in chronic coronary syndromes: the EURECA Imaging registry
• Value of Coronary Computed Tomography Angiography in Tailoring Aspirin Therapy for Primary Prevention of Atherosclerotic Events in Patients at High Risk With Diabetes Mellitus
• Verbal fluency in adults with high functioning autism or Asperger syndrome
• Very thin strut biodegradable polymer everolimus-eluting and sirolimus-eluting stents versus durable polymer zotarolimus-eluting stents in allcomers with coronary artery disease (BIO-RESORT): a three-arm, randomised, non-inferiority trial
• Withdrawal symptoms and previous attempts to quit smoking: associations with self-efficacy
• X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts