Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Generalized Disease"'
Autor:
Nils Erik Gilhus
Publikováno v:
Neuromuscular Disorders
Myasthenia gravis is characterized by muscle weakness and fatigue. As sustained muscle use increases the weakness, the value of physical training programs has previously been questioned. This is a review to clarify the safety and usefulness of system
Publikováno v:
Journal of Urology. 206
INTRODUCTION AND OBJECTIVE:Local treatment in generalized disease is a controversial strategy in terms of cancer control and complications. The aim of our systematic review is to analyze the availa...
Autor:
Hachulla, Eric, Agard, Christian, Allanore, Yannick, Avouac, Jérôme, Bader-Meunier, Brigitte, Belot, Alexandre, Berezne, Alice, Bouthors, Anne-Sophie, Condette-Wojtasik, Geraldine, Constans, Joël, de Groote, Pascal, Diot, Elisabeth, Dumas, Florence, Jego, Patrick, Joly, Francisca, Launay, David, Le Guern, Veronique, Le Quintrec, Janine-Sophie, Lescaille, Géraldine, Meune, Christophe, Moulin, Bruno, Nguyen, Christelle, Omeish, Nadine, Pene, Frédéric, Richard, Marie-Aleth, Rochefort, Juliette, Roren, Alexandra, Sitbon, Olivier, Sobanski, Vincent, Truchetet, Marie-Elise, Mouthon, Luc, Bayen, Marc, Bergot, Emmanuel, Berthier, Sabine, Bosco, Julia, Bouhnik, Yoram, Chaigne, Benjamin, Cottin, Vincent, Crestani, Bruno, Deligny, Christophe, Descroix, Vianney, Farge, Dominique, Godard, Dominique, Granel, Brigitte, Guilpain, Philippe, Imbert, Bernard, Le Quellec, Alain, Lega, Christophe, Lok, Catherine, Maillard, Hélène, Martin, Thierry, Pugnet, Grégory, Queyrel, Viviane, Raffray, Loïc, Rilliard, Frédéric, Romier, Mélanie, Schuller, Laurence, Servettaz, Amélie
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2021, 16 (S2), pp.322. ⟨10.1186/s13023-021-01844-y⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss S2, Pp 1-61 (2021)
Orphanet Journal of Rare Diseases, 2021, 16 (S2), pp.322. ⟨10.1186/s13023-021-01844-y⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss S2, Pp 1-61 (2021)
Systemic sclerosis (SSc) is a generalized disease of the connective tissue, arterioles, and microvessels, characterized by the appearance of fibrosis and vascular obliteration. There are two main phenotypical forms of SSc: a diffuse cutaneous form th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::504d094b55ec08caf7f7d0091ae61673
https://hal.science/hal-03652133/file/s13023-021-01844-y.pdf
https://hal.science/hal-03652133/file/s13023-021-01844-y.pdf
Publikováno v:
Muscle & Nerve. 61:226-230
Introduction Juvenile myasthenia gravis (JMG), a pediatric autoimmune neuromuscular junction disorder, includes generalized (GMG), and ocular (OMG) variants. We sought to determine whether differences existed between OMG and GMG children regarding de
Publikováno v:
International Journal of Scientific Research in Computer Science, Engineering and Information Technology. :543-546
We are right now facing a daily reality where mobile utilization is developing exponentially. Mobile technology is omnipresent. It offers services that is customized to us � the 21st century user. Innovation has empowered us incredibly, we look for
Publikováno v:
European Journal of Hybrid Imaging
European Journal of Hybrid Imaging, Vol 5, Iss 1, Pp 1-4 (2021)
European Journal of Hybrid Imaging, Vol 5, Iss 1, Pp 1-4 (2021)
Multiple myeloma is characterized by malignant proliferation of clonal plasma cells. Usually, appears as a generalized disease but it can present as solitary bone plasmacytoma or a solitary soft tissue mass or extramedullary plasmacytoma. In the case
Publikováno v:
Acta dermatovenerologica Alpina, Pannonica, et Adriatica. 29(1)
Introduction Vitiligo is a common chronic depigmentation disease. Patients are generally advised to protect themselves from the sun. Methods One hundred fifty-three patients diagnosed with vitiligo and 106 healthy volunteers with no additional dermat
Autor:
Giuliana Galassi, Alessandra Ariatti, Shaniko Kaleci, Franco Valzania, Paolo Frigio Nichelli, Marco Mazzoli
Publikováno v:
Acta Neurologica Belgica. 118:435-443
An unsolved issue remains whether there are clinical and immunological features to predict in a single patient the risk of conversion from ocular Myasthenia Gravis (OMG) to generalized disease (GMG) as 50-60% of patients may progress within 1-2 years
Publikováno v:
Archives of Clinical and Biomedical Research. :31-35
Multiple Myeloma may have extraosseous manifestations in the cranial region. It may be a solitary intracranial tumor (extramedullary plasmacytomas without any other signs of multiple myeloma) or intracranial disease may be a part of generalized disea
Publikováno v:
Advances in Clinical and Experimental Medicine. 26:875-880
Systemic sclerosis is a rare generalized disease with scleroderma, i.e. skin thickening as one of the most common symptoms. The disease has 2 main subsets, diffuse and limited forms. The subset known as systemic sclerosis sine scleroderma (ssSSc) is