Zobrazeno 1 - 10
of 23 834
pro vyhledávání: '"63"'
Autor:
Gideon Marchie du Sarvaas, Rolf M. F. Berger, Alfred Hager, Graziella Eshuis, Julia Hock, Hiske van Duinen, Hans L. Hillege, Rhoia Neidenbach, Freek van den Heuvel
Publikováno v:
Heart, 108(3), 186-193. BMJ PUBLISHING GROUP
ObjectivesThis study aimed to provide a perspective for the interpretation of exercise capacity (peakVO2) in patients with repaired Tetralogy of Fallot (patients with rTOF) by describing the course of peakVO2from patients aged 6–63 years.MethodsA r
Autor:
Deniz Cagdas, Halil Tuna Akar, Karin van Leeuwen, Cagman Tan, Ilhan Tezcan, Yavuz Köker, Saliha Esenboga, Dirk Roos, Begum Ozbek, Sevil Oskay Halacli, Martin de Boer
Publikováno v:
Journal of clinical immunology, 41(5), 992-1003. Springer New York
Background: Chronic granulomatous disease (CGD), one of the phagocytic system defects, is the primary immunodeficiency caused by dysfunction of the NADPH oxidase complex which generates reactive oxygen species (ROS), which are essential for killing p
Autor:
Qian Li, Yueying Pan, Liming Xia, Shuchang Zhou, Hanxiong Guan, Yujin Wang, Tingting Zhu, Qiongjie Hu
Publikováno v:
European Radiology
The purpose of this study was to observe the imaging characteristics of the novel coronavirus pneumonia. Sixty-three confirmed patients were enrolled from December 30, 2019 to January 31, 2020. High-resolution CT (HRCT) of the chest was performed. Th
Autor:
Marie Essig, Cécile-Audrey Durel, David Jayne, Christelle Barbet, Sandrine Hirschi-Santelmo, Thomas Le Gallou, Antoine Bardy, Jean-Jacques Boffa, Sylvain Marchand-Adam, Dimitri Titeca-Beauport, Grégory Pugnet, Xavier Belenfant, Camille Taillé, Xavier Puéchal, Cédric Rafat, Pascal Godmer, Vincent Cottin, Vítor Teixeira, Alexandre Karras, Julien Bouet, Renato Alberto Sinico, Jacques Gaultier, Philippe Guilpain, Daniel Engelbert Blockmans, Yoann Crabol, Christian Agard, Christophe Deligny
Publikováno v:
Rheumatology. 60:359-365
Objective Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic small-vessel vasculitis characterized by asthma, hypereosinophilia and ANCA positivity in 40% of patients. Renal involvement is rare and poorly described, leading to this re
Publikováno v:
World neurosurgery. 151
Objective The potential significance of relationship of atlantoaxial instability with retro-odontoid pseudotumor, pannus, and/or cyst (RPC) is analyzed. Methods We searched the database of patients with craniovertebral junction–related instability
Publikováno v:
Australasian Journal of Dermatology. 62
Autor:
Kojiro Wada, Satoru Takeuchi, Satoshi Tomura, Hajime Arai, Yasuaki Nakao, Terushige Toyooka, Naoki Otani, Takuji Yamamoto, Arata Tomiyama, Kentaro Mori
Publikováno v:
Operative Neurosurgery. 14:95-103
BACKGROUND Treatments for unruptured anterior communicating artery (AcomA) aneurysm have relatively high morbidity. OBJECTIVE To assess the lateral supraorbital keyhole approach for safe and complete clipping of unruptured AcomA aneurysm and evaluate
Autor:
Masoud Houshmand, M. Movahedi, Dabbaghzade A, Alireza Khayatzadeh, Maryam Mahloujirad, Mohammad Gharagozlou, Saba Arshi, Farhad Abolnezhadian, Mohsen Badalzadeh, Mohammad Hossein Eslamian, Mehrnaz Mesdaghi, Maryam Nourizadeh, Zahra Pourpak, Bahraminia E, Fariborz Zandieh, Arij Z, A.A. Hamidieh, Iraj Mohammadzadeh, Lida Atarod, Mohammamd Nabavi, Sadeghi Shabestary M, Mostafa Moin, Seyed Alireza Mahdaviani, Pesaran F, Mohammad Reza Fazlollahi
Publikováno v:
Journal of Investigational Allergology and Clinical Immunology. 27:299-304
BACKGROUND Severe combined immunodeficiency (SCID) is a life-threatening pediatric disease. We report on the clinical evaluation, immunological assessment, molecular analysis, and outcomes of SCID patients in a tertiary referral center in Iran. METHO
Autor:
Francesca Manunza, Andrea Bassi, Anna Belloni Fortina, Teresa Oranges, B Brunetti, Giuseppe Argenziano, V. Di Lernia, Samantha Berti, Vincenzo Piccolo, G. De Bernardis, Carlo Mazzatenta, V. Boccaletti, C. Filippeschi, Vincenzo Claudio Battarra, Isabella Neri
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Autor:
Angeles Garcia-Cazorla, Mari Oppebøen, Stacy K. H. Tay, Manju A. Kurian, Kathrin Jeltsch, Mitsuhiro Kato, Toni S. Pearson, Laura Gilbert, Vincenzo Leuzzi, Mario Mastrangelo, Dora Steel, Kathleen D. Meeks, Roser Pons, Saadet Mercimek-Andrews, Filippo Manti, Thomas Lücke, Thomas Opladen, Jolanta Sykut-Cegielska, Lisa Flint
Publikováno v:
Journal of Inherited Metabolic Disease
Aromatic l‐amino acid decarboxylase deficiency (AADCD) is a rare, autosomal recessive neurodevelopmental disorder characterized by impaired synthesis of dopamine, noradrenaline, adrenaline and serotonin, leading to a complex syndrome of motor, beha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c12c7cab074e95c8f21ecf7086c88fd0
http://hdl.handle.net/11573/1396140
http://hdl.handle.net/11573/1396140