Results 41 to 50 of about 1,972 (155)

Genomic Surveillance of SARS‐CoV‐2 in Rio de Janeiro (2020–2021): Temporal Distribution of Viral Variants During the Early Pandemic Genomic Surveillance of SARS‐CoV‐2 in Brazil

Advances in Virology, Volume 2026, Issue 1, 2026.
Genomic surveillance of SARS‐CoV‐2 is essential for monitoring the emergence and spread of variants in complex urban settings such as Rio de Janeiro, one of the epicenters of Coronavirus disease 2019 (COVID‐19) in Brazil. This retrospective observational study aimed to describe the temporal distribution of SARS‐CoV‐2 variants between October 2020 and ...
Priscila de Jesus Fajardo, Léo Freitas Corrêa, Thays Cristine dos Santos Vieira, Carlos Otávio Brandão, Rodrigo Pratte-Santos, Olga Morozova   +5 more
wiley   +1 more source

Alternating Hypotropia with Pseudoptosis: A New Phenotype of Congenital Cranial Dysinnervation Disorder

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, Toby Y.B. Chan, Inas Makar   +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

Spasmodic Dysphonia

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

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

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, Chiao-Wen Hwang, Ping-Hong Lai, Chu-Chin Chen   +3 more
doaj   +1 more source

Kidney injury in patients with heart failure‐related cardiogenic shock: Results from an international, multicentre cohort study

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, Caroline Kellner, Benedikt N. Beer, Lisa Besch, Angela Dettling, Letizia Fausta Bertoldi, Stefan Blankenberg, Jeroen Dauw, Dennis Eckner, Ingo Eitel, Tobias Graf, Patrick Horn, Joanna Jozwiak‐Nozdrzykowska, Paulus Kirchhof, Stefan Kluge, Axel Linke, Ulf Landmesser, Enzo Lüsebrink, Nicolas Majunke, Norman Mangner, Sven Möbius Winkler, Peter Nordbeck, Martin Orban, Federico Pappalardo, Matthias Pauschinger, Michal Pazdernik, Alastair Proudfoot, Matthew Kelham, Tienush Rassaf, Hermann Reichenspurner, Clemens Scherer, P. Christian Schulze, Robert H.G. Schwinger, Carsten Skurk, Marek Sramko, Guido Tavazzi, Holger Thiele, Luca Villanova, Nuccia Morici, Ephraim B. Winzer, Dirk Westermann, Benedikt Schrage   +41 more
wiley   +1 more source

Piebaldism-Moebius and prenatal exposure to misoprostol: a case report

Iatreia, 2016
Piebaldism is a rare congenital disease with prevalence of 1/100.000, characterized by patchy depigmentation of the skin and the presence of a white forelock. Its course is static and otherwise patients are healthy.
Mendoza-Urbano, Diana Marcela, Ramírez-Cheyne, Julián, Saldarriaga-Gil, Wilmar   +2 more
doaj   +1 more source

Fatal Recrudescence of Malignant Hyperthermia in an Infant with Moebius Syndrome

Brazilian Journal of Anesthesiology, 2013
Background and objectives: Malignant hyperthermia (MH) is a pharmacogenetic skeletal muscle disorder characterized by a hypermetabolic state after anesthesia with succinylcholine and/or volatile anesthetics. Various neuromuscular syndromes are associated
Cláudia Regina Fernandes, Washington Aspiculeta Pinto Filho, Lia Cavalcante Cezar, Josenília Maria Alves Gomes, Glauco Kleming Florencio da Cunha   +4 more
doaj   +1 more source

Superior Rectus Transposition Surgery: Safety, Efficacy, and Place in Therapy

Clinical Ophthalmology, 2022
Mohammad Reza Akbari, Babak Masoomian, Motahhareh Sadeghi, Arash Mirmohammadsadeghi Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, IranCorrespondence: Arash Mirmohammadsadeghi, Farabi Eye Hospital, Ghazvin Square,
Akbari MR, Masoomian B, Sadeghi M, Mirmohammadsadeghi A   +3 more
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