• A case of familial X-linked thrombocytopenia with a novel WAS gene mutation
• A comprehensive narrative review of epilepsy with eyelid myoclonia
• A live-attenuated RhCMV/SIV vaccine shows long-term efficacy against heterologous SIV challenge
• Acute coronary syndrome is an independent risk factor for late incomplete stent apposition after sirolimus-eluting stent implantation
• Acute myocardial infarction: clinical characteristics and plaque morphology between expansive remodeling and constrictive remodeling by intravascular ultrasound
• Age-related effects of smoking on coronary artery disease assessed by gray scale and virtual histology intravascular ultrasound
• American Association for the Surgery of Trauma-World Society of Emergency Surgery guidelines on diagnosis and management of peripheral vascular injuries
• Apelin: a potential marker of coronary artery stenosis and atherosclerotic plaque stability in ACS patients
• Assessment of left atrial functions in cardiac syndrome X
• Assessment of left ventricular diastolic function and Tei index by tissue Doppler imaging in patients with Cushing's Syndrome
• Association between late incomplete stent apposition after sirolimus eluting stent implantation and clinical outcomes in patients with acute coronary syndrome
• Association between metabolic syndrome and fragmented QRS complexes: Speckle tracking echocardiography study
• Association between sleep-disordered breathing, aminoterminal pro-brain natriuretic peptide (NT-proBNP) levels and insulin resistance in morbidly obese young women
• Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)
• Association of ectodermal dysplasia, ectrodactyly, and macular dystrophy: the EEM syndrome
• Association of insulin resistance and coronary artery remodeling: an intravascular ultrasound study
• CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations
• Cell-permeable succinate prodrugs bypass mitochondrial complex I deficiency
• Clinical and angiographic characteristics of patients likely to have vulnerable plaques: analysis from the PROSPECT study
• Clinical presentation and evaluation of epilepsy with eyelid myoclonia: Results of an international expert consensus panel
• Comparison Between Q-Adjusted LASIK and Small-Incision Lenticule Extraction for Correction of Myopia and Myopic Astigmatism
• Coronary artery size in North Indian population - Intravascular ultrasound-based study
• Correlation of Left Ventricular Diastolic Function and Left Ventricular Geometry in Patients with Obstructive Sleep Apnoea Syndrome
• Correlations between exploratory eye movement, hallucination, and cortical gray matter volume in people with schizophrenia
• Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
• Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings
• Ectrodactyly, ectodermal dysplasia, macular degeneration syndrome: a further contribution
• EEM syndrome: report of a family and results of a ten-year follow-up
• Elevated levels of systemic pentraxin 3 are associated with thin-cap fibroatheroma in coronary culprit lesions: assessment by optical coherence tomography and intravascular ultrasound
• EMPACT syndrome
• Eosinophilic Endomyocarditis: A Rare Case of Neonatal Mortality
• Epidemiology of erythema exsudativum multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis in Germany (1990-1992): structure and results of a population-based registry
• Erythema exsudativum multiforme (EEM) syndrome, Stevens-Johnson syndrome (SJS)
• Erythema exsudativum multiforme after a Leishmania skin test
• Evaluation of left ventricular functions in patients with pseudoexfoliation syndrome using tissue Doppler echocardiography and its association with plasma BNP levels
• Evaluation of syndromic management guidelines for treatment of sexually transmitted infections in South African women
• Extent and direction of arterial remodeling in stable versus unstable coronary syndromes : an intravascular ultrasound study
• Extent of coronary atherosclerosis and arterial remodelling in women: the NHLBI-sponsored Women's Ischemia Syndrome Evaluation
• Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <em>GPR98</em> Locus on 5q14.3
• Heterogeneity of atherosclerotic plaque characteristics in human coronary artery disease: a three-dimensional intravascular ultrasound study
• Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
• Immuno-Thrombotic Complications of COVID-19: Implications for Timing of Surgery and Anticoagulation
• Impact of arterial remodelling and plaque rupture on target and non-target lesion revascularisation after stent implantation in patients with acute coronary syndrome: an intravascular ultrasound study
• Impact of culprit plaque volume and composition on myocardial microcirculation following primary angioplasty in patients with ST-segment elevation myocardial infarction: virtual histology intravascular ultrasound analysis
• Impact of positive and negative lesion site remodeling on clinical outcomes: insights from PROSPECT
• Impact of vascular remodeling on the coronary plaque compositions: an investigation with in vivo tissue characterization using integrated backscatter-intravascular ultrasound
• Intrathoracic transmural esophageal perforation (Boerhaave syndrome): Challenges in management of the delayed presentation
• Intrathoracic transmural esophageal perforation (Boerhaave's syndrome): Challenges in management of the delayed presentation
• Intravascular ultrasound study of coronary remodeling and determination of matrix metalloproteinase and hypersensitive C-reactive protein
• Is diastolic dysfunction associated with atrial electrocardiographic parameters in Behçet's disease?
• Is there a role for tissue plasminogen activator as a novel treatment for refractory COVID-19 associated acute respiratory distress syndrome?
• Klf5 defines alveolar epithelial type 1 cell lineage commitment during lung development and regeneration
• Left ventricular diastolic dysfunction in newly diagnosed untreated hypertensive patients
• Left Ventricular Structural and Functional Changes in Children With β-Thalassemia and Sickle Cell Disease: Relationship to Sleep-disordered Breathing
• Lipid-core burden response to stent implantation assessed with near-infrared spectroscopy and intravascular ultrasound evaluation in patients with myocardial infarction
• Macular dystrophy and hypotrichosis: the EEM-Albrectsen syndrome
• Management of epilepsy with eyelid myoclonia: Results of an international expert consensus panel
• Markers of inflammation and fibrosis are related to cardiovascular damage in hypertensive patients with metabolic syndrome
• Metabolic syndrome impacts the right ventricle: true or false?
• Mild progressive multifocal leukoencephalopathy after switching from natalizumab to ocrelizumab
• Modified Atkins diet in children with epilepsy with eyelid myoclonia (Jeavons syndrome)
• Multimodality Intravascular Imaging Assessment of Plaque Erosion versus Plaque Rupture in Patients with Acute Coronary Syndrome
• Neuropsychiatric comorbidities and cognition in epilepsy with eyelid myoclonia: A retrospective pediatric case series
• New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
• Non-fibroatheroma lesion phenotype and long-term clinical outcomes: a substudy analysis from the PROSPECT study
• Ophthalmological findings in ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome: a case report
• Outcomes in patients with atypical hemolytic uremic syndrome treated with eculizumab in a long-term observational study
• P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle
• Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report
• Predictive factors for new-onset atrial fibrillation in acute coronary syndrome patients undergoing percutaneous coronary intervention
• Present status of the erythema exsudativum multiforme-problem, with special consideration of its relationship to erythema nodosum and to Baader's dermatostomatitis
• Prognostic value of echocardiographic and Doppler parameters in horses admitted for colic complicated by systemic inflammatory response syndrome
• Relation between baseline plaque features and subsequent coronary artery remodeling determined by optical coherence tomography and intravascular ultrasound
• Relationship among soluble CD105, hypersensitive C-reactive protein and coronary plaque morphology: an intravascular ultrasound study
• Relationship between atheroma regression and change in lumen size after infusion of apolipoprotein A-I Milano
• Relationship between coronary arterial remodeling and clinical presentation
• Relationship between hs-CRP, proMMP-1, TIMP-1 and coronary plaque morphology: intravascular ultrasound study
• Rescue therapy for severe COVID-19-associated acute respiratory distress syndrome with tissue plasminogen activator: A case series
• Safety of minimizing preoperative starvation in critically ill and intubated trauma patients
• Serum Uric Acid is Independently Associated with Diastolic Dysfunction in Apparently Healthy Subjects with Essential Hypertension
• Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia
• Splice site mutations in the P-cadherin gene underlie hypotrichosis with juvenile macular dystrophy
• Subclinical cardiac structural and electrical abnormalities in fibromyalgia syndrome
• Subclinical left ventricular dysfunction in women with polycystic ovary syndrome: an observational study
• The first reported case of <em>CDH3</em>-related hypotrichosis with juvenile macular dystrophy from Jordan: a case report
• The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
• The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study
• Therapeutic Modulation of RNA Splicing in Malignant and Non-Malignant Disease
• Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC)