Results 31 to 40 of about 5,262 (291)
Penal Substitution in the Construction of British Evangelical Identity: Controversies in the Doctrine of the Atonement in the Mid-2000s [PDF]
, 2011 This thesis examines the controversy surrounding the doctrine of the atonement and penal substitution which occurred within British evangelicalism as a result of the publication of Steve Chalke and Alan Mann‘s book The Lost Message of Jesus (2003).
WOOD, MAXWELL,THOMAS +1 more
core
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Isolated rapid eye movement sleep behavior disorder (iRBD) is a prodromal state for Lewy body disorders and exhibits biological heterogeneity that may influence clinical expression and progression. We examined clinical features in individuals with iRBD and biomarker‐defined synucleinopathy.
Daniel Weintraub +24 more
wiley +1 more source
Beelde vir die kruis van Christus in die vierde en vyfde eeu
HTS Teologiese Studies/Theological Studies, 2002 Images of Christ’s cross in the 4th and 5th centuries The Church Fathers did not have a common theory or system of atonement. Therefore, if one wants to appreciate what they had to say about atonement, one needs to study the rich images that pervade ...
H.F. Stander
doaj +1 more source
A Two‐Stage Questionnaire and Actigraphy Screening for iRBD in a Multicenter Retrospective Cohort
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Isolated rapid‐eye‐movement sleep behavior disorder is a prodromal marker of synucleinopathies. However, most cases remain undiagnosed due to the insufficient predictive value of questionnaires and limited access to confirmatory video‐polysomnography. We assessed a two‐stage screening strategy combining a brief questionnaire on rapid‐
Caleb A. Massimi +17 more
wiley +1 more source
Prominent Movement Disorders in RNU2‐2‐Related Spliceosomopathy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Pediatric movement disorders often overlap with neurodevelopmental diseases, suggesting shared molecular mechanisms. Variants in small nuclear RNA (snRNA) genes encoding spliceosome components have recently been associated with neurodevelopmental disorders, termed “RNUopathies.” We analyzed genome sequencing data from 14 patients with ...
Magdalena Krygier +6 more
wiley +1 more source
Beyond Repair? Ruins and Rubble in Ian McEwan’s Atonement
Études Britanniques Contemporaines, 2012 In his representation of England in the 1930s and of the Second World War, McEwan’s Atonement stages shattered worlds, both public and private, from derelict marriages and ruined relationships to the rubble of the Dunkirk retreat and the soldiers ...
Sylvie Maurel
doaj +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
Auditory Stimulation of Slow‐Wave Sleep Promotes Recovery after Brain Injury in an Animal Model
Annals of Neurology, EarlyView.Objective Traumatic brain injury (TBI) significantly reduces the quality of life for millions of survivors worldwide, causing persistent brain tissue damage and cognitive impairments, with no established therapeutic interventions currently available.
Carlos G. Moreira +9 more
wiley +1 more source
Atoning for Nostalgia in Ian McEwan’s Atonement
Humanities, 2018 Many critics have pointed out the ambiguities of Atonement, a postmodernist anti-nostalgic novel that brings to the fore all the traditional topoi of Englishness in order better to denounce them as sham. In Atonement, the nostalgic longing is linked to the desire of Briony (the protagonist/narrator) for a return to a state of innocence which, I will ...
openaire +2 more sources
Monoallelic POLR3A Variants Cause Early‐Onset Peripheral Neuropathy
Annals of Neurology, EarlyView.Objective Biallelic variants in genes encoding the RNA polymerase III complex (Pol III) cause a spectrum of neurological disorders primarily affecting the central nervous system. Monoallelic variants have been reported in the POLR3B subunit only, associated with neurodevelopmental disorder, epilepsy, and peripheral neuropathy.
Luiza L. P. Ramos +46 more
wiley +1 more source