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étiologie
Commentaire :
Etude des causes des maladies. (Dictionnaire médical de poche, 25/09/2006)
Synonyme(s)etiology |
Documents disponibles dans cette catégorie (239)
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Bird TD | 14/03/2024Initial Posting: September 28, 1998; Last Revision: March 14, 2024. The purpose of this overview is to increase the awareness of clinicians regarding Charcot-Marie-Tooth (CMT) hereditary neuropathy, its causes, and its management. The followi[...]Article
Beijer D ; Marte S ; Li JC ; De Ridder W ; Chen JZ ; Tadenev ALD ; Miers KE ; Deconinck T ; Macdonell R ; Marques W ; De Jonghe P ; Pratt SL ; Meyer-Schuman R ; Zuchner S ; Antonellis A ; Burgess RW ; Baets J | 08/03/2024Article
Thada PK ; Bhandari J ; Umapathi KK | 30/01/2024Last Update: January 30, 2024 [Previous update: May 29, 2023]Article
Cortese A ; Beecroft SJ ; Facchini S ; Curro R ; Cabrera-Serrano M ; Stevanovski I ; Chintalaphani S ; Gamaarachchi H ; Weisburd B ; Folland C ; Monahan G ; Scriba CK ; Dofash L ; Johari M ; Grosz BR ; Ellis M ; Fearnley LG ; Tankard R ; Read J ; Bahlo M ; Merve A ; Dominik N ; Vegezzi E ; Schnekenberg RP ; Fernandez G ; Masingue M ; Giovannini D ; Delatycki M ; Storey E ; Gardner M ; Amor D ; Nicholson G ; Vucic S ; Henderson RD ; Robertson T ; Dyke J ; Fabian V ; Mastaglia F ; Davis MR ; Kennerson M ; Quinlivan R ; Hammans S ; Tucci A ; McLean CA ; Laing NG ; Stojkovic T ; Houlden H ; Hanna MG ; Deveson I ; Lockhart PJ ; Lamont PJ ; Fahey MC ; Bugiardini E ; Ravenscroft G | 10/10/2023Article
Mathis S ; Sole G ; Damon-Perrière N ; Rouanet-Larrivière M ; Duval F ; Prigent J ; Nadal L ; Pereon Y ; Le Masson G | 25/08/2023Article
Publication AFM
Myoinfo, Auteur ; Malfatti E, Validateur ; Marty I, Validateur ; Nicot AS, Validateur ; Gilby E, Traducteur | AFM-TELETHON | Savoir & Comprendre | 06/2023Congenital myopathies are a heterogenous group of rare diseases characterised by structural abnormalities in muscle fibres which are most often detected at a young age. These abnormalities lead to muscle weakness (hypotonia and impaired motor sk[...]Publication AFM
Myoinfo, Auteur ; Malfatti E, Validateur ; Marty I, Validateur | AFM-TELETHON | Savoir & Comprendre | 06/2023Les myopathies congénitales constituent un groupe hétérogène de maladies rares caractérisées par des anomalies structurelles de la fibre musculaire, anomalies qui sont le plus souvent révélées à un âge précoce. L’atteinte musculaire entraîne une[...]Article
Last Update: May 29, 2023 ( Published : June 24, 2020, Previous update : May 9, 2022)Article
Last Update: May 25, 2023. [Previous version: August 10, 2020]Article
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Last Update: October 10, 2022 [Previous update: July 12, 2021; February 15, 2021]Article
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Last Update: July 18, 2022 (previous version : November 20, 2020)Article
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Les myosites à éosinophiles appartiennent au groupe des myopathies inflammatoires idiopathiques et sont définies par un infiltrat inflammatoire musculaire composé de polynucléaires éosinophiles. Il n’existe pas à ce jour de consensus concernant [...]Article
Last Update: July 8, 2021. (previous version July 8, 2020)Article
Last Update: May 8, 2022 (Previous update : October 10, 2021)Article
Pfeffer G ; Chinnery PF | 14/04/2022Initial Posting: February 27, 2014; Last Update: April 14, 2022. Clinical characteristics. Hereditary myopathy with early respiratory failure (HMERF) is a slowly progressive myopathy that typically begins in the third to fifth decades of l[...]Article
Hershberger RE ; Jordan E | 07/04/2022Initial Posting: July 27, 2007; Last Update: April 7, 2022. The purpose of this overview is to increase clinician awareness of the genetic basis of dilated cardiomyopathy (DCM) and the benefits of early diagnosis and management to individuals[...]Article
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Capitanio D ; Moriggi M ; Barbacini P ; Torretta E ; Moroni I ; Blasevich F ; Morandi L ; Mora M ; Gelfi C | 27/02/2022Article
Last Update: January 9, 2022 (previous version August 14, 2021; August 15, 2020)Article
Abicht A ; Müller J ; Lochmuller H | 23/12/2021Initial Posting: May 9, 2003; Last Update: December 23, 2021. The purpose of this overview is to increase the awareness of clinicians regarding congenital myasthenic syndromes (CMS) and their genetic causes and management. The following ar[...]Article
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Collectif | 10/2021Programme du 26ème congrès de World Muscle Society (WMS), 2021 - The World Muscle Society is a dynamic community that aims to promote, disseminate, and share all aspects of neuromuscular physiology and diseases, from basic science to patient [...]Article
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Jayarangaiah A ; Theetha Kariyanna P | 15/07/2021Last Update: July 15, 2021. (previous version July 15, 2020)Article
Last Update: July 14, 2021. (previous version November 19, 2020)Article
Last Update: July 8, 2021. (previous version July 8, 2021)Article
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Last Update: July 7, 2021. [Previous update: February 13, 2021]Article
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Bos JW ; Groen EJN ; Wadman RI ; Curial CAD ; Molleman NN ; Zegers M ; van Vught PWJ ; Snetselaar R ; Vijzelaar R ; van der Pol WL ; van den Berg LH | 22/06/2021Article
Yalcintepe S ; Gurkan H ; Gungor Dogan I ; Demir S ; Ozemri Sag S ; Manav Kabayegit Z ; Atli EI ; Atli E ; Eker D ; Temel SG | Turkey | 22/02/2021Article
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Lemmers RJLF ; van der Vliet PJ ; Blatnik A ; Balog J ; Zidar J ; Henderson D ; Goselink R ; Tapscott SJ ; Voermans NC ; Tawil R ; Padberg GWAM ; van Engelen BG ; van der Maarel SM | England | 12/01/2021Article