Zobrazeno 1 - 10
of 1 700
pro vyhledávání: '"Clinical course"'
Autor:
Sakyo Hirai, Shigeru Nemoto, Kyohei Fujita, Shinji Yamamoto, Jun Karakama, Fuga Ayabe, Shoko Fujii, Hiroto Yamaoka, Masataka Yoshimura, Kazutaka Sumita
Publikováno v:
Journal of Neuroendovascular Therapy. 16:339-345
Autor:
Wouter M. Sluis, Marijke Linschoten, Julie E. Buijs, J. Matthijs Biesbroek, Heleen M. den Hertog, Tessa Ribbers, Dennis J. Nieuwkamp, Reinier C. van Houwelingen, Andreas Dias, Ingeborg W.M. van Uden, Joost P. Kerklaan, H. Paul Bienfait, Sarah E. Vermeer, Sonja W. de Jong, Mariam Ali, Marieke J.H. Wermer, Marieke T. de Graaf, Paul J.A.M. Brouwers, Folkert W. Asselbergs, L. Jaap Kappelle, H. Bart van der Worp, Annemijn M. Algra, Richard C.J.M. Donders, D. Martijn O. Pruissen, Aaf F.M. Kuijper, Clara E.E. van Ofwegen-Hanekamp, Rik S. Hermanides, Hortence E. Haerkens-Arends, Rutger L. Anthonio, Mireille E. Emans, René A. Tio, Jur M. ten Berg, Björn E. Groenemeijer, Ron Pisters, P. Marc van der Zee, Hans-Marc J. Siebelink, Derk O. Verschure, Matthijs F.L. Meijs, Astrid Schut, Robert G. Tieleman, Wanda Hermans-van Ast, Jeroen Schaap, Lucia S. Jewbali, Peter C. Smits, Pim van der Harst, Maarten van Smeden, Wiek H. van Gilst
Publikováno v:
Stroke, 52(12), 3978-3986. LIPPINCOTT WILLIAMS & WILKINS
Stroke, 52(12), 3978-3986. Lippincott Williams and Wilkins
Stroke, 52(12), 3978-3986. Lippincott Williams & Wilkins
Stroke, 52(12), 3978-3986. Lippincott Williams and Wilkins
Stroke, 52(12), 3978-3986. Lippincott Williams & Wilkins
Background and Purpose: The frequency of ischemic stroke in patients with coronavirus disease 2019 (COVID-19) varies in the current literature, and risk factors are unknown. We assessed the incidence, risk factors, and outcomes of acute ischemic stro
Autor:
Katherine E. Kunigelis, Bette K. Kleinschmidt-DeMasters, D. Ryan Ormond, A. Samy Youssef, Kevin O. Lillehei
Publikováno v:
World Neurosurgery. 155:e229-e235
Objective Pineal parenchymal tumors of intermediate differentiation (PPTID) are rare tumors of the pineal gland. Their treatment is often heterogeneous due to the lack of literature to compile standardized treatments. Although no single institution h
Publikováno v:
Journal of Pediatric Neurology. 20:129-132
Congenital brain stem gliomas are rare in neonates and are difficult to diagnose given their subtle clinical presentation. They are usually associated with poor prognosis by their location and behavior. However, there are few reports of spontaneous r
Autor:
Anne M. Meehan, Darrell R. Schroeder, Juraj Sprung, Diana J Valencia Morales, Toby N. Weingarten, Mariana L. Laporta
Publikováno v:
Pain Medicine. 23:878-886
Background We describe the clinical course of medical and surgical patients who received naloxone on general hospital wards for suspected opioid-induced respiratory depression (OIRD). Methods From May 2018 through October 2020, patients who received
Autor:
Fatma Ece Çetin, Hatice Karasoy
Publikováno v:
Türk Nöroloji Dergisi, Vol 27, Iss 3, Pp 263-269 (2021)
Objective: Myasthenia gravis (MG) is a chronic autoimmune disease with fluctuating non-specific symptoms, and symptoms are exacerbated by stress. Many psychiatric disorders, especially depression, may accompany MG. This study aimed to determine the p
Autor:
Cyprian Popescu
Publikováno v:
Case Reports in Neurology
Case Reports in Neurology, Vol 13, Iss 3, Pp 668-671 (2021)
Case Reports in Neurology, Vol 13, Iss 3, Pp 668-671 (2021)
There is emerging evidence of a broad spectrum of neurological manifestations in COVID-19 patients. We report a case of a patient diagnosed with COVID-19 who presented bilateral lesions of the basal ganglia related to a severe acute respiratory distr
Publikováno v:
Seizure. 91:425-436
Epilepsy is a common, often severe, feature of LAMA2-related muscular dystrophy (LAMA2-RD) and could represent its onset and main manifestation, even in the absence of overt muscle involvement. To date, there is no systematic characterization of epil
Autor:
Parayil Sankaran Bindu, Periyasamy Govindaraj, Doniparthi V. Seshagiri, Madhu Nagappa, Sumanth Shivaram, Sanjib Sinha, Arun B Taly, Jitender Saini
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49:708-712
Vanishing white matter disease (VWMD) due to eIF2B mutations is a common leukodystrophy characterised by childhood onset, autosomal recessive inheritance, and progressive clinical course with episodic worsening. There are no reports of genetically co
Autor:
Hesna Bektas, Ebru Bilge Dirik, Gorkem Tutal Gursoy, Rahmet Guner, Levent Yamanel, Hatice Yuksel, Ozlem Ozturk Tan
Publikováno v:
Neurology Asia. 26:521-526
Background: Coronavirus disease 2019 (COVID-19) has affected a rapidly growing patient population worldwide. To effectively manage the disease, physicians need tests or methods that classify patients according to their risks. Our aim is to determine