Moser: METAPHYSIK EINST UND JETZT/ALBERT EINSTEIN — BRIEFE AN MAURICE SOLOVINE/Knopp: EINFÜHRUNG IN DIE HÖHERE MATHEMATIK/Körner: OBSERVATION AND INTERPRETATION/Westphal: KLEINES LEHRBUCH DER PHYSIK/Riekher: FERNROHRE UND IHRE MEISTER/Jenkins und White: FUNDAMENTALS OF OPTICS/Hardung‐Hardung: CHANCEN IN DER ATOMWIRTSCHAFT/Rautenfels: IMPULSFREIE ELEKTRISCHE RÜCKSTRAHLVERFAHREN [PDF]
Emil Ungerer +6 more
openalex +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Method of numerical solution of first order ordinary differential equations and its application to geometrical optics [PDF]
Bohumil Jurek
openalex +1 more source
Nonlinear Optics with 2D Layered Materials
A. Autere +5 more
semanticscholar +1 more source
ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich +10 more
wiley +1 more source
Basic Optics of a Television Film Chain [PDF]
D. F. Lyman, A. E. Neumer
openalex +1 more source
Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
Nonlinear spatial integration allows the retina to detect the sign of defocus in natural scenes. [PDF]
Goethals S +7 more
europepmc +1 more source
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source

