Results 61 to 70 of about 18,908 (257)
, 2017 Some languages allow the arguments of a verb in a not to be expressed as an overt Pronoun [Lexicon- Section 3.7] or a lexical [Syntax- Chapter 4]. This is the situation in which the term ‘null argument’ is commonly used. Spoken languages vary with respect to whether they allow the arguments of the verbs to be Miller, C. 1994. Simultaneous Constructions
Özsoy A. Sumru, Chiara Branchini
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Introduction Glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs) have demonstrated significant weight‐reducing effects and may offer benefits in idiopathic intracranial hypertension (IIH); however, recent concerns about the risk of non‐arteritic anterior ischemic optic neuropathy (NAION) have emerged.
Faisal A. Al‐Harbi +9 more
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Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos +5 more
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Studies in Generative Grammar, 2010 In this article I explore a variety of languages to show that there is a correlation between two different linguistic phenomena, wh-in-situ and the occurrence of null arguments, and derive a conclusive prediction that languages with D(iscourse)- based null arguments do not move whwords to form a wh-interrogative sentence.
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Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro +6 more
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Fragments vs. null arguments in Korean
Proceedings of the International Conference on Head-Driven Phrase Structure Grammar, 2012 Korean has two types of answers shorter than full sentential answers: Fragments and null argument constructions. Apparently the two constructions have the same interpretative processes. However, there are some cases where the fragment and null argument construction behave differently: e.g., wh-puzzles, sloppy interpretation.
Hee-Don Ahn, Sungeun Cho
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Upper Cervical Cord Area as a Biomarker of Conversion to Secondary Progressive Multiple Sclerosis
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective This study assessed whether upper cervical cord area (UCCA) measured on routine brain MRI can serve as a biomarker of conversion to SPMS. Methods This is a single‐center retrospective cohort study of RRMS patients with cross‐sectional and longitudinal analyses of clinical and MRI data. Future SPMS converters were matched by age, sex,
Nabil K. El Ayoubi +8 more
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About Twistor Spinors with Zero in Lorentzian Geometry
Symmetry, Integrability and Geometry: Methods and Applications, 2009 We describe the local conformal geometry of a Lorentzian spin manifold (M,g) admitting a twistor spinor φ with zero. Moreover, we describe the shape of the zero set of φ.
Felipe Leitner
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives Focal cortical dysplasia (FCD) is the most common etiology of drug‐resistant epilepsy in children. Focal to bilateral tonic–clonic seizures (FBTCS) mark a high risk of drug‐resistant epilepsy and involve thalamocortical circuitry in their generation and propagation.
Hua Xie +8 more
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The Multiple Sclerosis Severity Allele rs10191329A and Cognitive Function: A UK Biobank Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT The genome‐wide association study of Multiple Sclerosis severity linked the genetic variant rs10191329A to long‐term disability and implicated brain resilience as a determinant of outcome. We hypothesised that rs10191329A might influence cognition in other neurological diseases and healthy controls.
Ioanna Zimianiti +5 more
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