Zobrazeno 1 - 10
of 8 171
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:
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:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 43(1)
Objective We aimed to investigate the clinical features of cochlear nerve deficiency (CND), and in particular, the long-term course of hearing disability and audiogram shapes. Study design Retrospective observational nonrandomized group study. Settin
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:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 92
Introduction Nelson’s syndrome (NS) is a rare complication involving enlargement of an adrenocorticotropic hormone (ACTH) producing tumor in the pituitary following bilateral adrenalectomy in Cushing’s syndrome. Here, we explore the epidemiology,
Publikováno v:
The Journal of hand surgery, European volume. 45(5)
In this retrospective study, we report a series of 80 Arpe prostheses for trapeziometacarpal osteoarthritis in 63 patients. Twenty-seven prostheses (20 patients) were lost to follow-up. Twenty-one were revised, eight of them during the first year aft
Publikováno v:
The American journal of the medical sciences. 363(4)
Background Broncholithiasis is a rare disease defined as the presence of calcified material (broncholith) within the tracheobronchial tree. We described our experience in broncholithiasis to provide a more effective clinical basis for the management
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
Autor:
Frediano Inzani, Andrea Imperatori, Lorenzo Dominioni, Mauro Papotti, Pierluigi Granone, Silvia Uccella, Fausto Sessa, Roberta Maragliano, Alessandra Siciliani, Nicola Rotolo, Ida Rapa, Carlo Capella, Stefano La Rosa, Guido Rindi, Marco Volante
Publikováno v:
Virchows Archiv, vol. 475, no. 5, pp. 587-597
Adrenocorticotropic hormone (ACTH)-secreting lung carcinoids represent the principal cause of ectopic Cushing syndrome, but the prevalence of ACTH expression and the association between ACTH production and Cushing syndrome in lung carcinoids have sca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63c6e41aa369a7f2485ffeac2fa88b5c
https://serval.unil.ch/notice/serval:BIB_73364EEDBA89
https://serval.unil.ch/notice/serval:BIB_73364EEDBA89