Results 201 to 210 of about 193,587 (326)
Bounding the A-hat genus using scalar curvature lower bounds and isoperimetric constants [PDF]
Q. M. Ma +3 more
openalex +1 more source
Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz +3 more
wiley +1 more source
Auxin-cytokinin crosstalk and differential growth: complex relationships driving carpel initiation. [PDF]
Kwiatkowska D, Borowska-Wykręt D.
europepmc +1 more source
Compactness and rigidity of Kähler surfaces with constant scalar curvature [PDF]
Hongliang Shao
openalex +1 more source
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu +11 more
wiley +1 more source
Relativistic triangle-curvature computing for federated HIV-1 protein-sequence monitoring. [PDF]
Villalba-Díez J, González-Marcos A.
europepmc +1 more source
Scalar curvature lower bounds on asymptotically flat manifolds [PDF]
Yuqiao Li
openalex +1 more source
ABSTRACT Background Myasthenia gravis (MG) is an autoimmune disorder characterized by antibody‐mediated complement activation. Efgartigimod, a neonatal Fc receptor (FcRn) antagonist, is approved for treating generalized MG (gMG). However, its modulatory effects on upstream innate and adaptive immune cells remain largely unexplored.
Lei Jin +11 more
wiley +1 more source
The Wafold: Curvature-Driven Termination and Dimensional Compression in Black Holes. [PDF]
Viaña J.
europepmc +1 more source
ABSTRACT Objective The Gold Coast criteria permit diagnosis of amyotrophic lateral sclerosis (ALS) even without upper motor neuron (UMN) signs. However, whether ALS patients with UMN signs (ALSwUMN) and those without (ALSwoUMN) share similar characteristics and prognoses remains unclear.
Hee‐Jae Jung +7 more
wiley +1 more source

