Results 61 to 70 of about 2,263,401 (204)
Transplant Infectious Disease, Volume 28, Issue 1, January/February 2026.A sudden increase in EBV DNAemia appears to be a better predictor of PTLD and EBV end‐organ disease than persistent and stable levels of EBV DNAemia. Most HCT recipients with EBV DNAemia did not require rituximab, and immunosuppression reduction was sufficient to control most episodes of EBV reactivation.
Anna Beatriz Coelho de Souza +12 more
wiley +1 more source
Decoder for the Triangular Color Code by Matching on a Möbius Strip
PRX Quantum, 2022 The color code is remarkable for its ability to perform fault-tolerant logic gates. This motivates the design of practical decoders that minimize the resource cost of color-code quantum computation.
Kaavya Sahay, Benjamin J. Brown
doaj +1 more source
World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 11, Issue 4, Page 548-567, December 2025.ABSTRACT Spasmodic dysphonia is a laryngeal dystonia that can present as adductor, abductor, or mixed types, with or without tremor. The etiology is not understood fully. Comprehensive evaluation is required to establish the diagnosis. Treatments include voice therapy, medications, botulinum toxin injection, laryngeal surgery, deep brain stimulation ...
Aaron J. Jaworek, Robert T. Sataloff
wiley +1 more source
The axillary approach to raising the latissimus dorsi free flap for facial re-animation: a descriptive surgical technique [PDF]
, 2015 The latissimus dorsi flap is popular due to the versatile nature of its applications. When used as a pedicled flap it provides a robust solution when soft tissue coverage is required following breast, thoracic and head and neck surgery.
Butler, D, Grobbelaar, A, Leckenby, J
core +2 more sources
A Genealogy of Neurodiversity and Its Entangled Politics
Journal of Social Issues, Volume 81, Issue 4, December 2025.ABSTRACT This article will outline a genealogy of neurodiversity, highlighting the power structures and systems that brought about the neurodiversity movement and their implications. Understanding the neurodiversity paradigm from the politicized perspective of genealogy, it builds on this to conduct an intersectional analysis of the categories of ...
Tom Walters
wiley +1 more source
Orphanet Journal of Rare Diseases, 2022 Background Congenital cranial dysinnervation disorders (CCDDs) are a group of diseases with high clinical and genetic heterogeneity. Clinical examinations combined with Magnetic resonance imaging (MRI) and whole exome sequencing (WES) were performed to ...
Hongyan Jia +12 more
doaj +1 more source
European Journal of Heart Failure, Volume 27, Issue 11, Page 2397-2409, November 2025.Kidney injury in heart failure‐related cardiogenic shock. AKI, acute kidney injury; CI, confidence interval; eCPR, extracorporeal cardiopulmonary resuscitation; eGFR, estimated glomerular filtration rate; HR, hazard ratio; OR, odds ratio; VA‐ECMO, veno‐arterial extracorporeal membrane oxygenation.
Jonas Sundermeyer +41 more
wiley +1 more source
Case Reports in Ophthalmology, 2018 Congenital cranial dysinnervation disorders, also known as CCDDs, are characterized by aberrant innervation to extraocular and facial muscles resulting in unusual forms of incomitant strabismus.
Fady Sedarous +2 more
doaj +1 more source
Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay [PDF]
Korean Journal of Pediatrics, 2017 PurposeRecent advancements in molecular techniques have greatly contributed to the discovery of genetic causes of unexplained developmental delay. Here, we describe the results of array comparative genomic hybridization (CGH) and the clinical features of
Kyung Yeon Lee, Eunsim Shin
doaj +1 more source
Möbius Syndrome as a Syndrome of Rhombencephalic Maldevelopment: A Case Report
Pediatrics and Neonatology, 2009 Möbius syndrome is a rare congenital disorder characterized by congenital facial weakness with impairment of ocular abduction. It is considered as a rhombencephalic disorder, and is often accompanied with hypoplasia of the pons and cerebellum.
Hsueh-Ting Huang +3 more
doaj +1 more source