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Akesson LS ; Savarirayan R | 2020Clinical characteristics. Fibrodysplasia ossificans progressiva (FOP) is characterized by congenital bilateral hallux valgus malformations and early-onset heterotopic ossification, which may be spontaneous or precipitated by trauma including [...]Article
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Peto A ; Kosa D ; Feher P ; Ujhelyi Z ; Sinka D ; Vecsernyes M ; Szilvassy Z ; Juhasz B ; Csanadi Z ; Vigh L ; Bacskay I | Switzerland | 01/2020Article
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Wadman RI ; van der Pol WL ; Bosboom WM ; Asselman FL ; van den Berg LH ; Iannaccone ST ; Vrancken AF | England | 01/2020MAIN RESULTS: The review authors found 10 randomised, placebo-controlled trials of treatments for SMA types II and III for inclusion in this review, with 717 participants. We added four of the trials at this update. The trials investigated creat[...]Article
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Polido GJ ; de Miranda MMV ; Carvas N ; Mendonça RH ; Caromano FA ; Reed UC ; Zanoteli E ; Voos MC | Brazil | 12/2019Article
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Iolascon G ; Vitacca M ; Carraro E ; Chisari C ; Fiore P ; Messina S ; Mongini T ; Moretti A ; Sansone VA ; Toscano A ; Siciliano G | Italy | 12/2019Article
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Messina S, Auteur ; Frongia AL ; Antonaci L ; Pera MC ; Coratti G ; Pane M ; Pasternak A ; Civitello M ; Montes J ; Mayhew A ; Finkel R ; Muntoni F ; Mercuri E | England | 12/2019Article
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Wadman RI ; van der Pol WL ; Bosboom WM ; Asselman FL ; van den Berg LH ; Iannaccone ST ; Vrancken AF | England | 12/2019Résumé extrait de la "Cochrane Library" Background Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletion in combination with a point mutation in [...]Article
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Labrador E ; Weinstein DA | 27/11/2019Initial Posting: April 23, 2009; Last Update: November 27, 2019. Clinical characteristics. Glycogen storage disease type VI (GSD VI) is a disorder of glycogenolysis caused by deficiency of hepatic glycogen phosphorylase. This critical enzy[...]Article
Des mutations récessives dans le gène PYROXD1 ont été récemment décrites chez des patients présentant un tableau de myopathie congénitale ou de dystrophie musculaire des ceintures [1-4]. PYROXD1 (PYRidine nucleotide-disulfide OXidoreductase Doma[...]Article
Les 19 et 20 juin 2019, la conférence internationale sur la recherche dans la dystrophie facio-scapulo-humérale (FSHD) a eu lieu à Marseille. La rencontre rassemblant 180 participants, médecins, scientifiques et patients était organisée au Palai[...]Article
Les dermatomyosites (DM) sont des maladies auto-immunes rares du groupe des myopathies inflammatoires idiopathiques, définies par une atteinte cutanée caractéristique. Elles peuvent survenir dans l’enfance, ou chez l’adulte. Il existe des variat[...]Article
L’analyse histologique du tissu musculaire est un élément déterminant pour le diagnostic et la compréhension physiopathologique des myopathies. Le développement d’outils numériques et informatiques permet des analyses d’images quantifiées à gran[...]Article
Une révolution est actuellement en cours dans le domaine des maladies neuromusculaires avec l’arrivée de nouvelles thérapies. L’amyotrophie spinale (SMA ou spinal muscular atrophy) est parmi les maladies pionnières de ce bouleversement thérapeut[...]Article
Il est bien établi que le nombre réduit de patients atteints d’une maladie rare (MR), la dispersion géographique de ceux-ci ainsi que le nombre réduit d’experts constituent des obstacles au diagnostic, à l’accès aux soins, à la recherche et au p[...]Article
Pons C ; Barrière A ; Bertrand G ; Morard MD ; Lilien C ; Vuillerot C | AFM-TELETHON | Les cahiers de myologie | 11/2019À l’heure des nouvelles thérapeutiques chez les personnes présentant une amyotrophie spinale antérieure ou spinal muscular atrophy (SMA), la mesure régulière, précise et fiable des capacités motrices est devenue indispensable. Différents outils [...]Article
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Robert-Paganin J, Auteur ; Pylypenko O ; Kikuti C ; Sweeney HL ; Houdusse A | United States | 11/2019Article
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Selva-O Callaghan A, Auteur ; Gil-Vila A ; Simo-Perdigo M ; Trallero-Araguas E ; Alvarado-Cardenas M ; Pinal Fernandez I | United States | 11/2019Article
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Nieuwenhuis S ; Okkersen K ; Widomska J ; Blom P ; 't Hoen PAC ; van Engelen B ; Glennon JC | Switzerland | 11/2019Article
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Llavero F ; Arrazola Sastre A ; Luque Montoro M ; Galvez P ; Lacerda HM ; Parada LA ; Zugaza JL | Switzerland | 11/2019Article
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Salabarria SM ; Nair J ; Clément N ; Smith BK ; Raben N ; Fuller DD ; Byrne BJ ; Corti M | Netherlands | 11/2019Article
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Bellotti AS, Auteur ; Andreoli L ; Ronchi D ; Bresolin N ; Comi GP ; Corti S | United States | 11/2019Article
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Warman-Chardon J, Auteur ; Diaz-Manera J ; Tasca G ; Bonnemann CG ; Gomez-Andres D ; Heerschap A ; Mercuri E ; Muntoni F ; Pichiecchio A ; Ricci E ; Walter MC ; Hanna M ; Jungbluth H ; Morrow JM ; Torron RF ; Udd B ; Vissing J ; Yousry T ; Quijano Roy S ; Straub V ; Carlier RY | England | 11/2019Article
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Wang H, Auteur ; Kacar Bayram A ; Sprute R ; Ozdemir O ; Cooper E ; Pergande M ; Efthymiou S ; Nedic I ; Mazaheri N ; Stumpfe K ; Azizi Malamiri R ; Shariati G ; Zeighami J ; Bayram N ; Naghibzadeh SK ; Tajik M ; Yasar M ; Sami Guven A ; Bibi F ; Sultan T ; Salpietro V ; Houlden H ; Per H ; Galehdari H ; Shalbafan B ; Jamshidi Y ; Cirak S | Switzerland | 10/2019Article
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Kimonis V | 12/09/2019Initial Posting: May 25, 2007; Last Update: September 12, 2019. Clinical characteristics. Inclusion body myopathy associated with Paget disease of bone (PDB) and/or frontotemporal dementia (IBMPFD) is characterized by adult-onset proximal [...]Article
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Penttila S ; Vihola A ; Palmio J ; Udd B | 22/08/2019Initial Posting: November 29, 2012; Last Update: August 22, 2019. Clinical characteristics. The spectrum of ANO5 muscle disease is a continuum that ranges from asymptomatic hyperCKemia and exercise-induced myalgia to proximal and/or distal m[...]Article
Bonne G ; Leturcq F ; Ben Yaou R | 15/08/2019Initial Posting: September 29, 2004; Last Update: August 15, 2019. Clinical characteristics. Emery-Dreifuss muscular dystrophy (EDMD) is characterized by the clinical triad of: joint contractures that begin in early childhood; slowly progr[...]Article
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Hellebrekers DMJ, Auteur ; Lionarons JM ; Faber CG ; Klinkenberg S ; Vles JSH ; Hendriksen JGM | United States | 08/2019Article
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Schoser B, Auteur ; Montagnese F ; Bassez G ; Fossati B ; Gamez J ; Heatwole C ; Hilbert J ; Kornblum C ; Kostera-Pruszczyk A ; Krahe R ; Lusakowska A ; Meola G ; Moxley R 3rd ; Thornton C ; Udd B ; Formaker P | United States | 08/2019Article
Boehler JF, Auteur ; Ricotti V ; Gonzalez JP ; Soustek-Kramer M ; Such L ; Brown KJ ; Schneider JS ; Morris CA | England | 08/2019Article
Bosgra S, Auteur ; Sipkens J ; De Kimpe S ; den Besten C ; Datson N ; van Deutekom J | United States | 08/2019Article
Saito K | 03/07/2019Initial Posting: January 26, 2006; Last Update: July 3, 2019. Clinical characteristics. Fukuyama congenital muscular dystrophy (FCMD) is characterized by hypotonia, symmetric generalized muscle weakness, and CNS migration disturbances that[...]Article
Gras-Champel V, Auteur ; Masmoudi I ; Batteux B ; Merle PE ; Liabeuf S ; Masmoudi K | France | 07/2019Article
Initial Posting: April 19, 2006; Last Update: June 20, 2019. Clinical characteristics. Glycogen storage disease type V (GSDV, McArdle disease) is a metabolic myopathy characterized by exercise intolerance manifested by rapid fatigue, myalgia[...]Article
Initial Posting: June 20, 2019. Clinical characteristics. STAC3 disorder is characterized by congenital myopathy, musculoskeletal involvement of the trunk and extremities, feeding difficulties, and delayed motor milestones. Most affected ind[...]Article
Initial Posting: August 5, 2008; Last Update: June 6, 2019. The purpose of this overview is to increase clinician awareness of the genetic basis of hypertrophic cardiomyopathy (HCM) and the benefits of early diagnosis and management to indivi[...]Article
Jumah MA ; Muhaizea MA ; Rumayyan AA ; Saman AA ; Shehri AA ; Cupler E ; Jan M ; Madani AA ; Fathalla W ; Kashyape P ; Kodavooru G ; Thihli KA ; Bastaki L ; Mégarbané A ; Skrypnyk C ; Zamani G ; Tuffery-Giraud S ; Urtizberea JA ; Ortez Gonzalez CI | England | 06/2019Article
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Bethesda (MD) 05/20192012 [Last Update: May 15, 2019] LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012-. Amifampridine. [Updated 2019 May 15]. A[...]Article
Hackman P ; Savarese M ; Carmignac V ; Udd B ; Salih MA | 11/04/2019Initial Posting: January 12, 2012; Last Update: April 11, 2019. Clinical characteristics. Salih myopathy is characterized by muscle weakness (manifest during the neonatal period or in early infancy) and delayed motor development; children ac[...]Article
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Erratum in : Corrigendum to "Recently Identified Congenital Myopathies" [Semin Pediatr Neurol 29 (2019) 83-90].Article
Wieser T | 03/01/2019Initial Posting: August 27, 2004; Last Revision: January 3, 2019. Clinical characteristics. Carnitine palmitoyltransferase II (CPT II) deficiency is a disorder of long-chain fatty-acid oxidation. The three clinical presentations are lethal n[...]Article
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Pushpakom S ; Iorio F ; Eyers PA ; Escott KJ ; Hopper S ; Wells A ; Doig A ; Guilliams T ; Latimer J ; McNamee C ; Norris A ; Sanseau P ; Cavalla D ; Pirmohamed M | England | 01/2019Article
Johnson NE, Auteur ; Aldana EZ ; Angeard N ; Ashizawa T ; Berggren KN ; Marini Bettolo C ; Duong T ; Ekstrom AB ; Sansone V ; Tian C ; Hellerstein L ; Campbell C | 2019Article
Ashizawa T, Auteur ; Gagnon C ; Groh WJ ; Gutmann L ; Johnson NE ; Meola G ; Moxley R 3rd ; Pandya S ; Rogers MT ; Simpson E ; Angeard N ; Bassez G ; Berggren KN ; Bhakta D ; Bozzali M ; Broderick A ; Byrne JLB ; Campbell C ; Cup E ; Day JW ; De Mattia E ; Duboc D ; Duong T ; Eichinger K ; Ekstrom AB ; van Engelen B ; Esparis B ; Eymard B ; Ferschl M ; Gadalla SM ; Gallais B ; Goodglick T ; Heatwole C ; Hilbert J ; Holland V ; Kierkegaard M ; Koopman WJ ; Lane K ; Maas D ; Mankodi A ; Mathews KD ; Monckton DG ; Moser D ; Nazarian S ; Nguyen L ; Nopoulos P ; Petty R ; Phetteplace J ; Puymirat J ; Raman S ; Richer L ; Roma E ; Sampson J ; Sansone V ; Schoser B ; Sterling L ; Statland J ; Subramony SH ; Tian C ; Trujillo C ; Tomaselli G ; Turner C ; Venance S ; Verma A ; White M ; Winblad S | 12/2018Article
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
Herbert M ; Goldstein JL ; Rehder C ; Austin S ; Kishnani PS ; Bali DS | 01/11/2018Initial Posting: May 31, 2011; Last Update: November 1, 2018. Clinical characteristics. Phosphorylase kinase (PhK) deficiency causing glycogen storage disease type IX (GSD IX) results from deficiency of the enzyme phosphorylase b kinase, whi[...]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
Veerapandiyan A ; Statland JM ; Tawil R | 07/06/2018Initial Posting: November 22, 2004; Last Update: June 7, 2018. Clinical characteristics. Andersen-Tawil syndrome (ATS) is characterized by a triad of: episodic flaccid muscle weakness (i.e., periodic paralysis); ventricular arrhythmias and p[...]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
June CH ; June CH ; O'Connor RS ; Kawalekar OU ; Ghassemi S ; Milone MC | United States | 23/03/2018Article
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Michelson D, Auteur ; Ciafaloni E ; Ashwal S ; Lewis E ; Narayanaswami P ; Oskoui M ; Armstrong MJ | 2018Article
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Birnkrant DJ ; Bushby K ; Bann CM ; Apkon SD ; Blackwell A ; Brumbaugh D ; Case L ; Clemens PR ; Hadjiyannakis S ; Pandya S ; Street N ; Tomezsko J ; Wagner KR ; Ward LM ; Weber DR | 2018Comment in: Evidence-based care in Duchenne muscular dystrophy. [Lancet Neurol. 2018]Article
Birnkrant DJ ; Bushby K ; Bann CM ; Alman BA ; Apkon SD ; Blackwell A ; Case L ; Cripe L ; Hadjiyannakis S ; Olson AK ; Sheehan DW ; Bolen J ; Weber DR ; Ward LM | 2018Comment in: Evidence-based care in Duchenne muscular dystrophy. [Lancet Neurol. 2018]Article
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Mercuri E ; Finkel RS ; Muntoni F ; Wirth B ; Montes J ; Main M ; Mazzone ES ; Vitale M ; Snyder B ; Quijano Roy S ; Bertini E ; Davis RH ; Meyer OH ; Simonds AK ; Schroth MK ; Graham RJ ; Kirschner J ; Iannaccone ST ; Crawford TO ; Woods S ; Qian Y ; Sejersen T | 23/11/2017Article
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El-Hattab AW ; Scaglia F | 18/05/2017Initial Posting: May 26, 2009; Last Revision: May 18, 2017. Clinical characteristics. SUCLA2-related mitochondrial DNA (mtDNA) depletion syndrome, encephalomyopathic form with methylmalonic aciduria is characterized by onset of the following[...]Article
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Bird TD | 30/03/2017Initial Posting: May 11, 2004; Last Update: March 30, 2017. Clinical characteristics. GDAP1-related hereditary motor and sensory neuropathy (GDAP1-HMSN) is a peripheral neuropathy (also known as a subtype of Charcot-Marie-Tooth disease) th[...]Article
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Miyatake S, Auteur ; Mitsuhashi S ; Hayashi YK ; Purevjav E ; Nishikawa A ; Koshimizu E ; Suzuki M ; Yatabe K ; Tanaka Y ; Ogata K ; Kuru S ; Shiina M ; Tsurusaki Y ; Nakashima M ; Mizuguchi T ; Miyake N ; Saitsu H ; Kawai M ; Towbin J ; Nonaka I ; Nishino I ; Matsumoto N | 2017Article