Results 11 to 20 of about 97,313 (319)

Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome

American Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023
Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings, Lois Janelle Starr   +1 more
wiley   +1 more source

Understanding the dynamics of support seeking in women with lived experience of non‐physical intimate partner violence (IPV) and the service responses—A qualitative study

Australian Journal of Social Issues, Volume 57, Issue 4, Page 861-879, December 2022., 2022
Abstract Non‐physical abuse is a form of intimate partner violence (IPV), which negatively impacts physical and mental well‐being. The study objectives were to understand the process of support seeking amongst women who experience non‐physical IPV. Interviews were conducted with women who have experience of non‐physical IPV and support workers.
Karishma Doolabh, Colleen Fisher, Melissa O'Donnell   +2 more
wiley   +1 more source

Neuroimaging for differential diagnosis of transient neurological attacks

Brain and Behavior, Volume 12, Issue 12, December 2022., 2022
Abstract Background Rapid yet comprehensive neuroimaging protocols are required for patients with suspected acute stroke. However, stroke mimics can account for approximately one in five clinically diagnosed acute ischemic strokes and the rate of thrombolyzed mimics can be as high as 17%.
Ying Wang, Hao Zha
wiley   +1 more source

Microglial/macrophage activation in the cerebrospinal fluid of neuromyelitis optica spectrum disorders

Brain and Behavior, Volume 12, Issue 12, December 2022., 2022
Abstract Aim The aims of this pilot study were to investigate the levels of biomarkers of microglial/macrophage activation—YKL‐40, sCD163, and sCD14—in patients with neuromyelitis optica spectrum disorder (NMOSD) and determine the possible associations between these biomarkers and Expanded Disability Status Scale (EDSS) scores.
Jinghong Li, Yan He, Honghao Wang, Jinyu Chen   +3 more
wiley   +1 more source

Prevalence and correlates of diagnosed and undiagnosed epilepsy and migraine headache among people with severe psychiatric disorders in Ethiopia.

PLoS ONE, 2020
BackgroundThere is a paucity of research on the prevalence of diagnosed as well as undiagnosed neurological disorders with episodic manifestations such as epilepsy and migraine headaches in people with severe psychiatric disorders (SPD).
Getinet Ayano, Sileshi Demelash, Zegeye Yohannes, Kibrom Haile, Light Tsegay, Abel Tesfaye, Kelemua Haile, Mikias Tulu, Belachew Tsegaye, Melat Solomon, Getahun Hibdye, Dawit Assefa, Berihun Assefa Dachew   +12 more
doaj   +1 more source

Simulation‐based team‐training in acute stroke: Is it safe to speed up?

Brain and Behavior, Volume 12, Issue 12, December 2022., 2022
Abstract Background In acute ischemic stroke (AIS), rapid treatment with intravenous thrombolysis (IVT) is crucial for good clinical outcome. Weekly simulation‐based team‐training of the stroke treatment team was implemented, resulting in faster treatment times.
Liv Jorunn Høllesli, Soffien Chadli Ajmi, Martin W. Kurz, Thomas Bailey Tysland, Morten Hagir, Ingvild Dalen, Sigrun Anna Qvindesland, Hege Ersdal, Kathinka D. Kurz   +8 more
wiley   +1 more source

Prevalence of Psychiatric Comorbidities in Patients with Migraine: A Cross-sectional Study [PDF]

Indian Journal of Private Psychiatry
Aim: To evaluate the prevalence of psychiatric comorbidity in migraine patients. Materials and methods: A total of 60 patients diagnosed with migraine according to the International Classification of Headache Disorders (ICHD-3) were included in the study
Hina Bano, Kushagra Varma, Jai Singh, Mohammad Aleem Siddiqui, Abdul Qadir Jilani   +4 more
doaj   +1 more source

Migraine and Neuroticism: A Scoping Review

Behavioral Sciences, 2022
Headache is the first cause of consultation in neurology, and one of the most frequent reasons for consultation in general medicine. Migraine is one of the most common, prevalent, and socioeconomically impactful disabling primary headache disorders ...
Carmen M. Galvez-Sánchez, Casandra I. Montoro Aguilar   +1 more
doaj   +1 more source

SCN 1A /Na V 1.1 channelopathies: Mechanisms in expression systems, animal models, and human iPSC models [PDF]

Epilepsia, Wiley, 2019, 60 (S3), 2022
Pathogenic SCN1A/NaV1.1 mutations cause well defined epilepsies, including Genetic Epilepsy with Febrile Seizures Plus (GEFS+) and the severe epileptic encephalopathy Dravet syndrome. In addition, they cause a severe form of migraine with aura, Familial Hemiplegic Migraine.
arxiv   +1 more source

Migraine in university students: A systematic review and meta‐analysis

European Journal of Pain, Volume 27, Issue 1, Page 14-43, January 2023., 2023
Abstract Background Migraine is a complex, neurobiological disorder usually presenting as a unilateral, moderate to severe headache accompanied by sensory disturbances. Migraine prevalence has risen globally, affecting 14% of individuals and 16% of students and carries many negative impacts in both cohorts.
Orla Flynn, Brona M. Fullen, Catherine Blake   +2 more
wiley   +1 more source