Results 141 to 150 of about 2,000,070 (348)
Factor IX administration in the skin primes inhibitor formation and sensitizes hemophilia B mice to systemic factor IX administration. [PDF]
Sherman A +4 more
europepmc +1 more source
ABSTRACT Objective This analysis evaluates the effect of successful reperfusion on functional outcomes after MT, stratified by admission National Institutes of Health Stroke Scale (NIHSS) and Alberta Stroke Program Early CT Score (ASPECTS) as surrogates for clinical‐core mismatch, using multicenter registry data.
Felix Schlicht +53 more
wiley +1 more source
Se reevaluó el rango de referencia del tiempo parcial de tromboplastina activada (TPTA). Se obtuvo un rango de referencia de 29 a 40 seg. con una media () de 34,01 seg.
Alina Díaz Concepción +2 more
doaj
Biodistribution of recombinant factor IX, extended half-life recombinant factor IX Fc fusion protein, and glycoPEGylated recombinant factor IX in hemophilia B mice. [PDF]
van der Flier A +9 more
europepmc +1 more source
An intragenic deletion of the factor IX gene in a family with hemophilia B. [PDF]
S.-H. Chen +6 more
openalex +1 more source
Fusion of engineered albumin with factor IX Padua extends half‐life and improves coagulant activity
Silvia Lombardi +8 more
openalex +2 more sources
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
Endogenous atrial natriuretic factor and airway control [PDF]
ix, 82 leaves : ill. ; 30 cm.This thesis describes two experiments investigating the role of endogenous atrial natriuretic factor (ANF) in the modulation of airway calibre and bronchial hyperresponsiveness in humans under normal physiological conditions.
Homan, Sean David Robert
core
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source

