Zobrazeno 1 - 10
of 49
pro vyhledávání: '"George Vartzelis"'
Autor:
Anastasia Korona, Despoina Maritsi, Aikaterini Markante, Andromachi Stamati, Stella Mouskou, George Vartzelis
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 58, Iss 1, Pp 1-4 (2022)
Abstract Background Parinaud’s syndrome, also known as dorsal midbrain syndrome, is characterized by a combination of signs, including upgaze palsy, convergence–retraction nystagmus, eyelid retraction and pupillary dissociation. It is caused by p
Externí odkaz:
https://doaj.org/article/a1b3654723de45ecad49ce716e69d759
Autor:
Stella Mouskou, MD, PhD, Adiana Stamati, MD, George Sfakianos, MD,PhD, Astero Malama, Maria Gavra, MD, PhD, George Vartzelis, MD, PhD, Anastasia Korona, MD, MSc, Sotiria Mastrogianni, MD, PhD, Kostas Voudris, MD, PhD
Publikováno v:
Interdisciplinary Neurosurgery, Vol 20, Iss , Pp - (2020)
Intracranial dermoid cysts are uncommon lesions with characteristic imaging appearances. Although they are characterized by slow growth rate, they are often associated with serious complications due to the location and pressure of the adjacent struct
Externí odkaz:
https://doaj.org/article/f3b75d69013e489b854edc38404a6c12
Autor:
Eleni Klinaki, Ioanna Argyri, Georgia Amountza, Gerina Ioannidou, Despoina Maritsi, Anastasia Garoufi, George Vartzelis
Publikováno v:
Case Reports in Pediatrics, Vol 2019 (2019)
A 5.5-month-old female infant with tuberous sclerosis complex presented with infantile spasms and was treated with vigabatrin. As her condition did not improve, she was given adrenocorticotropic hormone (ACTH) intramuscularly which stopped the spasms
Externí odkaz:
https://doaj.org/article/f99ce8133da9413dbc99192408897dea
Autor:
George Vartzelis, Despoina Maritsi, Maria Nikolaidou, Anastasia Garoufi, Constantinos Kilidireas
Publikováno v:
Case Reports in Pediatrics, Vol 2019 (2019)
Multiple sclerosis is a chronic, debilitating disease. Almost one in ten patients with MS has a history of disease onset during childhood. Although numerous therapeutic options exist for adult MS, the available treatments for pediatric patients are s
Externí odkaz:
https://doaj.org/article/85b2b80aa3474efd995875158f4b23d8
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
We present a case of a seven-year-old immunocompetent female patient who developed systemic symptoms mimicking an autoimmune rather than an infectious disease. The patient presented with rash, biquotidian fever, night sweats, and arthralgias. There w
Externí odkaz:
https://doaj.org/article/4441032e7cc4474aaa6398c985936dc8
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Williams syndrome is a rare genetic condition with multisystemic involvement, caused by a microscopic deletion in the chromosome band 7q11.23. We describe the first case of a toddler with Williams syndrome who developed Benign Paroxysmal Torticollis
Externí odkaz:
https://doaj.org/article/43b8199f056f486b99b1525784748e7c
Autor:
Ioannis Kopsidas, Foteini Eleni Dasoula, Eleni Kourkouni, Adamantia Krepi, Harry Α. Mystakelis, Nikos Spyridis, George Vartzelis
Publikováno v:
European Journal of Pediatrics.
The purpose of this study was to investigate knowledge, principles, and practices concerning the management of children with febrile seizures among pediatricians in Greece. A cross-sectional study was performed across Greece. Pediatricians completed
Autor:
Dimitra Dimopoulou, Foteini Dasoula, Marianthi Liaska, Irini Eleftheriou, Despoina Maritsi, Maria Tsolia, George Vartzelis
Publikováno v:
Pediatric Infectious Disease Journal. 42:e128-e129
Autor:
Maria Svingou, Argirios Dinopoulos, George Vartzelis, Nikolaos Diamantopoulos, Charalabos Kotsalis, George-Konstantinos Papadimas, Pelagia Vorgia, Vasiliki Koute, Constantinos Papadopoulos, Konstantinos Skiadas, Athanasios Evangeliou, Evangelos Pavlou, George Niotakis, Christalena Sofocleous, Evangelia Nitsa, Joanne Traeger-Synodinos, Marina Katsalouli, Antigoni Papavasiliou, Kyriaki Kekou, Iliada Nakou, George Konstantinidis, Konstantinos A. Voudris, Efstathia Katsarou, Georgios Tsivgoulis, Niki Mourtzi, Roser Pons, Sotiris Youroukos
Publikováno v:
Journal of Neuromuscular Diseases
Background: Promising genetic treatments targeting the molecular defect of severe early-onset genetic conditions are expected to dramatically improve patients’ quality of life and disease epidemiology. Spinal Muscular Atrophy (SMA), is one of these
Publikováno v:
Annals of the rheumatic diseases. 81(4)
Patients with rheumatic and musculoskeletal diseases (RMDs) on immunosuppressants are generally considered to be more prone to infections, and therefore, a vulnerable group for severe COVID-19 infection. However, current data are reassuring, indicati