Hypertrophic Cardiomyopathy With Evolution to a Mixed Hypertrophic Noncompaction Phenotype. [PDF]
Abadi NE, Abadi CA.
europepmc +1 more source
ABSTRACT Background Osteosarcoma (OS) and Ewing sarcoma (EWS) are the most common primary bone cancers in children, but acute thrombosis is poorly characterized in this population. Our study evaluated the rates of venous thromboembolism (VTE) and associated risk factors in pediatric patients with bone sarcomas treated over a 10‐year period encompassing
Sarah Kappa +8 more
wiley +1 more source
Secondary stroke evaluation in patients admitted for CRAO in a large national inpatient sample. [PDF]
Doshi S +5 more
europepmc +1 more source
The Role of Hematopoietic Cell Transplantation in Ataxia‐Telangiectasia
ABSTRACT Background Ataxia‐telangiectasia (A‐T) is a DNA repair disorder characterized by neurodegeneration, immunodeficiency, and cancer predisposition. Hematopoietic cell transplantation (HCT) is an established therapy in related disorders such as Fanconi anemia (FA) and Nijmegen breakage syndrome (NBS), but its role in A‐T is unclear.
Laila Alkhouli +3 more
wiley +1 more source
A Small Mass Causing a Big Problem: Severe Aortic Regurgitation Induced by a Papillary Fibroelastoma. [PDF]
Bajouka J, Afram R, Deshmukh R.
europepmc +1 more source
Purulent Pericarditis Caused by Polymicrobial Periodontal Pathogens (<i>Tannerella forsythia, Fusobacterium nucleatum</i>, and <i>Porphyromonas gingivalis</i>): A Case Report and Literature Review. [PDF]
Wei BH, Da HJ.
europepmc +1 more source
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
Case Report: Persistent fifth aortic arch with coarctation and fourth aortic arch interruption causing infant heart failure - the prenatal and postnatal echocardiographic course. [PDF]
Zhang X +5 more
europepmc +1 more source
ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg +9 more
wiley +1 more source
Abstract INTRODUCTION Subclinical lower cardiac output (volume of blood pumped per minute) cross‐sectionally relates to smaller cerebral gray matter volumes in older adults. This study relates cardiac output to longitudinal gray matter volumes among middle‐aged and older adults over an 11‐year period.
Elizabeth E. Moore +9 more
wiley +1 more source

