Results 61 to 70 of about 15,738 (237)
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
New H-ALPHA Emission Stars in A Region to the East of the T-Association Near Rho Ophiuci
The result of a survey of H-alpha emission objects in an area of approximately 25 square degrees centered on the star CD -24°12765 (R.A.=16h38.m5; Dec.=-24°22';1950), is presented.
Pik Sin The, Ham Keng Lim
doaj
An organisation’s inability to generate adequate income to sustain its business activities poses a significant challenge to maintaining profitability. Employing revenue-maximisation strategies is crucial to securing necessary resources and ensuring the ...
John Adanse +2 more
doaj +1 more source
The SFA Start Charts are designed to work anywhere on Earth. Instructions are included on the last two pages. The constellations lines are based in part on those in a book called The Stars by H. A. Rey. These constellation patterns were adopted by Google
Bruton, W D
core
ABSTRACT Objective Intravenous thrombolysis (IVT) before thrombectomy for ischemic stroke may alter clot structure and procedural performance. We investigated how IVT relates to thrombectomy metrics across stroke etiologies. Methods We performed a time‐to‐event analysis of consecutive patients with anterior circulation large vessel occlusion (acLVO ...
Annahita Sedghi +8 more
wiley +1 more source
Communicating finite-state machines, first-order logic, and star-free propositional dynamic logic
International audienceMessage sequence charts (MSCs) naturally arise as executions of communicating finite-state machines (CFMs), in which finite-state processes exchange messages through unbounded FIFO channels.
Fortin, Marie +2 more
core +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Includes text, 9 insets, and color illustrations.; On verso with text: National Geographic Map of the heavens with monthly star charts for both hemispheres.;Color;(Decl. +90° to -90°).
National Geographic Society (U.S.). Cartographic Division.
core
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Choroid Plexus Enlargement and USPIO‐Based Inflammatory Feature in Cerebral Small Vessel Disease
ABSTRACT Objective The choroid plexus (CP) is a key component of the blood–cerebrospinal fluid barrier (BCSFB), but its mechanism of action in cerebral small vessel disease (CSVD) remains unclear. This study investigated CP volume (CPV) alterations and their association with conventional imaging markers in CSVD and explored the underlying role of ...
Yongqiang Qu +11 more
wiley +1 more source

