Mots-clés
> MYOBASE > SOCIETE > démographie > épidémiologie > morbidité > prévalence
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)
|
Documents disponibles dans cette catégorie (673)
trié(s) par (Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) | Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de recherche
Etendre la recherche sur niveau(x) vers le bas
Article
Article
Article
Article
Chen G ; Sharif B ; Gerber B ; Farris MS ; Cowling T ; Cabalteja C ; Wu JW ; Maturi B ; Klein-Panneton K ; Jean K Mah | England | 11/2021Article
Article
Alharbi N ; Shosha E ; Cupler E ; Al Hindi H ; Murad H ; Alhomud I ; Alshehri A ; Almohazee M ; Monies D ; Abohlega S | Italy | 08/2021Article
Tankink M ; Horlings CGC ; Voermans N ; van der Sluijs B ; Kessels RPC ; van Engelen B ; Raaphorst J | Netherlands | 28/07/2021Article
Pinal Fernandez I ; Pak K ; Gil-Vila A ; Baucells A ; Plotz B ; Casal-Dominguez M ; Derfoul A ; Angeles Martinez M ; Selva-O Callaghan A ; Sabbagh S ; Casciola-Rosen L ; Albayda J ; Paik J ; Tiniakou E ; Danoff SK ; Lloyd TE ; Miller FW ; Rider LG ; Christopher Stine L ; Mammen AL | United States | 27/07/2021Article
Last Update: July 8, 2021. (previous version July 8, 2021)Article
Leckie JN ; Joel MM ; Martens K ; King A ; King M ; Korngut LW ; de Koning APJ ; Pfeffer G ; Schellenberg KL | 07/07/2021Article
Article
Weber F | 01/07/2021Initial Posting: July 18, 2003; Last Update: July 1, 2021. Clinical characteristics. Hyperkalemic periodic paralysis (hyperPP) is characterized by attacks of flaccid limb weakness (which may also include weakness of the muscles of the eyes[...]Article
Aoki M ; Takahashi T | 27/05/2021Initial Posting: February 5, 2004; Last Update: May 27, 2021. Clinical characteristics. Dysferlinopathy includes a spectrum of muscle disease characterized by two major phenotypes: Miyoshi muscular dystrophy (MMD) and limb-girdle muscular [...]Article
Rodrigues Filho JC ; Neves DD ; Moreira GA ; Viana ADC Jr ; Araújo-Melo MH | Netherlands | 24/05/2021Article
Barsotti S ; Cavazzana I ; Zanframundo G ; Neri R ; Taraborelli M ; Cioffi E ; Cardelli C ; Tripoli A ; Codullo V ; Tincani A ; Cavagna L ; Franceschini F ; Mosca M | Netherlands | 05/2021Article
Initial Posting: June 11, 2015; Last Update: April 8, 2021 Clinical description. Riboflavin transporter deficiency (RTD), comprising RTD2 and RTD3 (caused by biallelic pathogenic variants in SLC52A2 and SLC52A3, respectively) is a rare neu[...]Article
Foley AR ; Mohassel P ; Donkervoort S ; Bolduc V ; Bonnemann CG | 11/03/2021Initial Posting: June 25, 2004; Last Update: March 11, 2021. Clinical characteristics. Collagen VI-related dystrophies (COL6-RDs) represent a continuum of overlapping clinical phenotypes with Bethlem muscular dystrophy at the milder end, U[...]Article
Azzedine H ; Salih MA | 11/03/2021Initial Posting: March 31, 2008; Last Update: March 11, 2021. Clinical characteristics. SH3TC2-related hereditary motor and sensory neuropathy (SH3TC2-HMSN) is a demyelinating neuropathy characterized by severe spine deformities (scoliosis[...]Article
Initial Posting: August 3, 2005; Last Update: February 25, 2021. Clinical characteristics. Myotonia congenita is characterized by muscle stiffness present from childhood; all striated muscle groups including the extrinsic eye muscles, faci[...]Article
Velez-Bartolomei F ; Lee C ; Enns G | 07/01/2021Initial Posting: June 3, 2003; Last Update: January 7, 2021. Clinical characteristics. MERRF (myoclonic epilepsy with ragged red fibers) is a multisystem disorder characterized by myoclonus (often the first symptom) followed by generalized[...]Article
Hov B ; Andersen T ; Toussaint M ; Vollsaeter M ; Mikalsen IB ; Indrekvam S ; Hovland V | England | 03/01/2021Article
Prior TW ; Leach ME ; Finanger E | 3/12/2020Initial Posting: February 24, 2000; Last Revision: December 3, 2020. Clinical characteristics. Spinal muscular atrophy (SMA) is characterized by muscle weakness and atrophy resulting from progressive degeneration and irreversible loss of t[...]