Results 151 to 160 of about 429,050 (291)

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

Study of neutrino production in the Cannonball model of Gamma ray bursts (Possibility of observation of these neutrinos with the ANTARES neutrinos telescope, and study of the optical background recorded with the prototype sector line)

, 2004
Sophie Ferry, RACCA, Chantal
openalex   +1 more source

A hierarchical Bayesian model for background variation in radiation source localization

, 2021
Isaac Michaud, Kathleen Schmidt, Ralph C. Smith, Carolyn Mattingly   +3 more
openalex   +2 more sources

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi, Lara Basovic, Christopher Michael McGraw   +2 more
wiley   +1 more source

Complex Background Subtraction by Pursuing Dynamic Spatio-Temporal Models [PDF]

, 2014
Liang Lin, Yuanlu Xu, Xiaodan Liang, Jianhuang Lai   +3 more
openalex   +1 more source

Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein, Maximilian Mönch, Meret Herdick, Frauke Stascheit, Sarah Hoffmann, Hannah Preßler, Philipp Mergenthaler, Carla Dusemund, Paolo Doksani, Haoqi Sun, Pushpa Narayanaswami, Andreas Meisel, Lea Gerischer, Sophie Lehnerer   +13 more
wiley   +1 more source

Image reconstruction and elongation artifact reduction for a dual-panel dedicated prostate PET scanner. [PDF]

Med Phys
Saberi Manesh A, Amini M, Salimi Y, Doroud K, Williams C, Williams T, Arabi H, Zaidi H.   +7 more
europepmc   +1 more source

Impact of Demographic Backgrounds by Humanities and Social Sciences Students on Their Psychological of Emotional Intelligence Skill: Structural Equation Multiple Cause and Multiple Indicator (SEM-MIMIC) Model

Jetnipit Kunchai
openalex   +2 more sources

Holographic model for hadrons in deformed AdS5 background [PDF]

, 2005
Kazuo Ghoroku, Nobuhito Maru, Motoi Tachibana, Masanobu Yahiro   +3 more
openalex   +1 more source

Predicting Loss of Ambulation in Limb Girdle Muscular Dystrophy R9

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Limb girdle muscular dystrophy type R9 (LGMDR9) results from biallelic variants in FKRP. There is limited data to predict loss of ambulation (LOA) among those with LGMDR9. Methods Participants in an ongoing dystroglycanopathy natural history study (NCT00313677) with FKRP variants who had achieved ambulation and were more than 3 ...
Chandra L. Miller, Lauren N. Coffey, Shelley R. H. Mockler, Katie M. Laubscher, Carrie M. Stephan, M. Bridget Zimmerman, Katherine D. Mathews   +6 more
wiley   +1 more source