Results 201 to 210 of about 8,222,439 (341)
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
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 +5 more
wiley +1 more source
Assessing muscle morphology and mechanics: one protocol does not fit all. [PDF]
Kissane RWP.
europepmc +1 more source
Predicting Loss of Ambulation in Limb Girdle Muscular Dystrophy R9
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 +6 more
wiley +1 more source
Compressibility characteristics and coefficient of consolidation determination for unsaturated sand treated with micro silica. [PDF]
Shwan BJ.
europepmc +1 more source
ABSTRACT Objective To investigate the value of constructing models based on habitat radiomics and pathomics for predicting the risk of progression in high‐grade gliomas. Methods This study conducted a retrospective analysis of preoperative magnetic resonance (MR) images and pathological sections from 72 patients diagnosed with high‐grade gliomas (52 ...
Yuchen Zhu +14 more
wiley +1 more source
Joint attention GAN for medical report generation with clinical style preservation. [PDF]
Tang Z, Liu X, Bie J, Xu L, Xu S.
europepmc +1 more source
An Active Learning Algorithm for Ranking from Pairwise Preferences with an Almost Optimal Query Complexity [PDF]
Nir Ailon
openalex +1 more source
An Almost Optimal Algorithm for Unbounded Search with Noisy Information
Dariusz Dereniowski +2 more
openalex +2 more sources
ABSTRACT Objective To determine the concentration of glial fibrillary acidic protein (GFAP) in cerebrospinal fluid (CSF) and plasma in Alexander disease (AxD) and whether GFAP levels are predictive of disease phenotypes. Methods CSF and plasma were collected (longitudinally when available) from AxD participants and non‐AxD controls.
Amy T. Waldman +9 more
wiley +1 more source

