Results 81 to 90 of about 5,265,871 (311)
ObjectiveTo enhance clinicians' awareness of pulmonary arterial hypertension (PAH) complicating chronic active Epstein–Barr virus infection (CAEBV) in pediatric patients.MethodClinical data of a pediatric patient diagnosed with CAEBV complicated by PAH ...
Meng Zhang +6 more
doaj +1 more source
Gaucher’s disease: orphan disease in pediatric practice
Approaches to diagnostics and treatment of Gaucher’s disease in children were considered. A clinical case is given.
T. A. Bokova
doaj
Bogen, Aaron and Louis (Box 90, Folder 10)
Series VIII: Audiocassettes features informal oral histories about the Hebrew Orphan Asylum and its alumni.Digital recordingDigital finding ...
Hebrew Orphan Asylum of New York
core
Abstract Aims Amyloid cardiomyopathy is caused by the deposition of light chain (AL) or transthyretin amyloid (ATTR) fibrils, that leads to a restrictive cardiomyopathy, often resulting in heart failure (HF) with preserved or reduced ejection fraction.
Robin Willixhofer +25 more
wiley +1 more source
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare genetic disorder inherited in an autosomal dominant manner. The FOP development is caused by a mutation in the ACVR1 gene, which encodes a receptor for bone morphogenetic protein, leading ...
E. G. Gasymov +5 more
doaj +1 more source
Schorr, Dave (Box 91, Folder 14)
Series VIII: Audiocassettes features informal oral histories about the Hebrew Orphan Asylum and its alumni.Digital recordingDigital finding ...
Hebrew Orphan Asylum of New York
core
Childhood tuberculosis : no longer an orphan disease? [PDF]
CITATION: Beyers, N. & Gie, R. 2013. Childhood tuberculosis : no longer an orphan disease? Public Health Action, 3(3):190-190, doi:10.5588/pha.13.0076.At the start of the twenty-first century, children were not regarded as important to tuberculosis (TB)
Beyers, Nulda, Gie, Robert
core +1 more source
Transcriptomic analysis reveals distinct expression patterns in focal cortical dysplasia
Abstract Objective Focal cortical dysplasia (FCD) is a common cause of drug‐resistant epilepsy in children and adults and exhibits substantial clinical and histopathological heterogeneity. However, morphological classification alone does not fully explain variability in epileptogenicity, disease severity, or treatment response.
Shivani Sonawane +20 more
wiley +1 more source
Anaesthesia management in anti-synthetase syndrome, a rare orphan disease - A case study. [PDF]
Pruthi G, Samagh N, Utkarsh, Grewal A.
europepmc +1 more source
Baron, Shirley in her home (Box 90, Folder 6)
Series VIII: Audiocassettes features informal oral histories about the Hebrew Orphan Asylum and its alumni.Digital recordingDigital finding ...
Hebrew Orphan Asylum of New York
core

