Results 81 to 90 of about 442,861 (243)

Life‐Threatening Bradycardia in Anti‐NMDA‐Receptor Encephalitis and a Novel Use for Permanent Pacing

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Pediatric anti‐NMDA receptor encephalitis (pNMDARE) is an autoantibody‐mediated disorder that can cause severe autonomic dysfunction, including symptomatic bradycardia and asystole. Dysautonomia can last for years, making it very challenging to manage.
Sarah Tucker   +9 more
wiley   +1 more source

Critique of Mulla Sadra’s Version of “Individual Unity of Existence” [PDF]

open access: yesحکمت صدرایی, 2016
Mulla Sadra Presents "Individual unity of existence" theory as his final vision in discussion of the associating of the diversity to the Unite. In this view, the only actual existence is God and others are his manifestations. Here is where the "Cause and
maryam aghamohammadreza   +1 more
doaj  

Cognitive Status in People With Epilepsy in the Republic of Guinea: A Prospective, Case–Control Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective People with epilepsy (PWE) may experience cognitive deficits but fail to undergo formal evaluation. This study compares cognitive status between PWE and healthy controls in the West African Republic of Guinea. Methods A cross‐sectional, case–control study was conducted in sequential recruitment phases (July 2024–July 2025) at Ignace ...
Maya L. Mastick   +14 more
wiley   +1 more source

Manifest

open access: yes, 2012
Item does not contain ...
Wilthagen, A.C.J.M.   +4 more
openaire   +3 more sources

Research progress on cancerrelated cognitive impairment

open access: yesHuli yanjiu, 2017
This article reviewed the manifestations,evaluation methods and influencing factors of cognitive impairment in cancer patients and introduced the existing intervention measures of cancerrelated cognitive impairment,in order to provide direction and ...
张扬   +4 more
doaj  

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron   +5 more
wiley   +1 more source

THE SYSTEM OF DIVINE MANIFESTATION IN IBN ‘ARABI’S SCHOOL OF THOUGHT [PDF]

open access: yesReligious Inquiries, 2012
One of the fundamental problems of theoretical mysticism is how to explain the difference between God and the world on the basis of the idea of wahdat al-wujud (the unity of existence).
Seyyed Ahmad Fazeli
doaj  

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

The Origin of Islamic Mysticism in the Light of the Personal Unity of Existence [PDF]

open access: yesReligious Inquiries, 2016
The question of the origin of Islamic mysticism has been one of the major concerns of many researchers in the field of mysticism in the recent decades. Some have maintained that Islamic mysticism is an imported product: a combination of Eastern spiritual
Ebrahim Rezaei, Jafar Shanazari
doaj  

Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein   +13 more
wiley   +1 more source

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