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prévalence
Commentaire :
Nombre total de cas d'une maladie dans une population donnée pendant un temps déterminé, sans distinction entre cas anciens et nouveaux. (d'après le MeSH ; 10/08/2005)
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El-Hattab AW ; Almannai M ; Scaglia F | 29/11/2018Initial Posting: February 27, 2001; Last Update: November 29, 2018. Clinical characteristics. MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) is a multisystem disorder with protean manifestations. The vast [...]Article
Brignol TN, Auteur ; Fort PE ; Ventura DF ; Tadayoni R ; Rendon A | 26/09/2018To the Editor: We read with interest the recent article by Rice and colleagues1 reporting on 596 patients with Duchenne muscular dystrophy (DMD) treated with steroid and evaluated for cataract development. The authors reported that the prevalenc[...]Article
Dowling JJ ; Lawlor MW ; Das S | 23/08/2018Initial Posting: February 25, 2002; Last Update: August 23, 2018. Clinical characteristics. X-linked myotubular myopathy (X-MTM), also known as myotubular myopathy (MTM), is characterized by muscle weakness that ranges from severe to mild. [...]Article
Wolfe L ; Jethva R ; Oglesbee D ; Vockley J | 09/08/2018Initial Posting: September 22, 2011; Last Update: August 9, 2018. Clinical characteristics. Most infants with short-chain acyl-CoA dehydrogenase deficiency (SCADD) identified through newborn screening programs have remained well, and asympto[...]Article
Weber F ; Lehmann-Horn F | 26/07/2018Initial Posting: April 30, 2002; Last Update: July 26, 2018. Clinical characteristics. Hypokalemic periodic paralysis (hypoPP) is a condition in which affected individuals may experience paralytic episodes with concomitant hypokalemia (ser[...]Article
Wang J ; El-Hattab AW | 26/07/2018Initial Posting: December 6, 2012; Last Update: July 26, 2018. Clinical characteristics. TK2-related mitochondrial DNA (mtDNA) maintenance defect is a phenotypic continuum that ranges from severe to mild. To date, approximately 107 individua[...]Article
Comment in: Cataract development associated with long-term glucocorticoid therapy in Duchenne muscular dystrophy patients. [J AAPOS. 2018] Reply. [J AAPOS. 2018]Article
DA Dyment ; Bennett SAL ; Medin JA ; Levade T | 29/03/2018Initial Posting: March 29, 2018. Clinical characteristics. The spectrum of ASAH1-related disorders ranges from Farber disease (FD) to spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). Classic FD is characterized b[...]Article
Neurological sciences Autism spectrum disorders are prevalent among patients with dystrophinopathies
Fujino H, Auteur ; Saito T ; Matsumura T ; Shibata S ; Iwata Y ; Fujimura H ; Imura O | 28/03/2018Article
Leborgne C, Auteur ; Latournerie V ; Boutin S ; Desgue D ; Quéré A ; Pignot E ; Collaud F ; Charles S ; Simon-Sola M ; Masat E ; Jouen F ; Boyer O ; Masurier C ; Mingozzi F ; Veron P | 16/03/2018Article
Stunnenberg BC, Auteur ; Raaphorst J ; Deenen JCW ; Links TP ; Wilde AA ; Verbove DJ ; Kamsteeg EJ ; van den Wijngaard A ; Faber CG ; van der Wilt GJ ; van Engelen BGM ; Drost G ; Ginjaar HB | 09/03/2018Article
Yeker RM, Auteur ; Pinal Fernandez I ; Kishi T ; Pak K ; Targoff IN ; Miller FW ; Rider LG ; Mammen AL | 23/01/2018Article
Comment in: Reply to: "Association of hepatitis E virus infection and myasthenia gravis: A pilot study". [J Hepatol. 2018] Comment on: Hepatitis E virus infection and acute non-traumatic neurological injury: A prospective multicentr[...]Article
Estephan EP, Auteur ; Sobreira CFDR ; Dos Santos ACJ ; Tomaselli PJ ; Marques W ; Ortega RPM ; Costa MCM ; da Silva AMS ; Mendonça RH ; Caldas VM ; Zambon AA ; Abath Neto O ; Marchiori PE ; Heise CO ; Reed UC ; Azuma Y ; Topf A ; Lochmuller H ; Zanoteli E | 2018Article
Andrenelli E, Auteur ; Galli FL ; Gesuita R ; Skrami E ; Logullo FO ; Provinciali L ; Capecci M ; Ceravolo MG ; Coccia M | 2018Article
Fayssoil A, Auteur ; Ben Yaou R ; Ogna A ; Chaffaut C ; Leturcq F ; Nardi O ; Wahbi K ; Duboc D ; Lofaso F ; Prigent H ; Clair B ; Crenn P ; Nicolas G ; Laforet P ; Behin A ; Chevret S ; Orlikowski D ; Annane D | 2018Article
van Vliet J, Auteur ; Tieleman AA ; Verrips A ; Timmerman H ; van Dongen RTM ; van Engelen BGM ; Wilder-Smith OHG | 2018Article
Jimenez-Moreno AC, Auteur ; Raaphorst J ; Babacic H ; Wood L ; van Engelen B ; Lochmuller H ; Schoser B ; Wenninger S | 27/12/2017Article
Papadopoulos C, Auteur ; Kekou K ; Xirou S ; Kitsiou-Tzeli S ; Kararizou E ; Papadimas GK | 08/12/2017Comment in: Christmas tree cataract and myotonic dystrophy type 1. [Eye (Lond). 2018]Brève