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Last Update: July 7, 2021. [Previous update: February 13, 2021]Article
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Sansa A ; Hidalgo I ; Miralles MP ; de la Fuente S ; Perez-Garcia MJ ; Munell F ; Soler RM ; Garcera A | 03/07/2021Article
Oury J ; Zhang W ; Leloup N ; Koide A ; Corrado AD ; Ketavarapu G ; Hattori T ; Koide S ; Burden SJ | England | 07/2021Article
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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
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Van Lent J ; Verstraelen P ; Asselbergh B ; Adriaenssens E ; Mateiu L ; Verbist C ; De Winter V ; Eggermont K ; van den Bosch L ; De Vos WH ; Timmerman V | England | 15/06/2021Article
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Creary LE ; Gangavarapu S ; Caillier SJ ; Cavalcante P ; Frangiamore R ; Lie BA ; Bengtsson M ; Harbo HF ; Brauner S ; Hollenbach JA ; Oksenberg JR ; Bernasconi P ; Maniaol AH ; Hammarström L ; Mantegazza R ; Fernández-Viña MA | 07/06/2021Publication AFM
Myoinfo, Auteur ; Bonne G, Validateur ; Ben Yaou R, Validateur | AFM-TELETHON | Savoir & Comprendre | 06/2021Les dystrophies musculaires d’Emery-Dreifuss sont des maladies rares, d'origine génétique. Elles se manifestent par une faiblesse et une atrophie musculaires progressives, des rétractions musculo-tendineuses (raccourcissement et perte d'élastici[...]Article
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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
Malacarne C ; Galbiati M ; Giagnorio E ; Cavalcante P ; Salerno F ; Andreetta F ; Cagnoli C ; Taiana M ; Nizzardo M ; Corti S ; Pensato V ; Venerando A ; Gellera C ; Fenu S ; Pareyson D ; Masson R ; Maggi L ; Dalla Bella E ; Lauria G ; Mantegazza R ; Bernasconi P ; Poletti A ; Bonanno S ; Marcuzzo S | 26/05/2021Article
Ababneh NA ; Barham R ; Al-Kurdi B ; Ali D ; Sharar N ; Al Hadidi S ; Alatoom RM ; Zalloum S ; Gharandouq MH ; Makahleh L ; Alnsour LN ; Alshahwan H ; El-Khateeb M ; Awidi A | England | 11/05/2021Article
Coppens S ; Barnard AM ; Puusepp S ; Pajusalu S ; Õunap K ; Vargas-Franco D ; Bruels CC ; Donkervoort S ; Pais L ; Chao KR ; Goodrich JK ; England EM ; Weisburd B ; Ganesh VS ; Gudmundsson S ; O'Donnell-Luria A ; Nigul M ; Ilves P ; Mohassel P ; Siddique T ; Milone M ; Nicolau S ; Maroofian R ; Houlden H ; Hanna MG ; Quinlivan R ; Beiraghi Toosi M ; Ghayoor Karimiani E ; Costagliola S ; Deconinck N ; Kadhim H ; Macke E ; Lanpher BC ; Klee EW ; Łusakowska A ; Kostera-Pruszczyk A ; Hahn A ; Schrank B ; Nishino I ; Ogasawara M ; El Sherif R ; Stojkovic T ; Nelson I ; Bonne G ; Cohen E ; Boland-Augé A ; Deleuze JF ; Meng Y ; Topf A ; Vilain C ; Pacak CA ; Rivera-Zengotita ML ; Bonnemann CG ; Straub V ; Handford PA ; Draper I ; Walter GA ; Kang PB | United States | 06/05/2021Correction : A form of muscular dystrophy associated with pathogenic variants in JAG2 Error in the spelling of an author's name Late Breaking Abstracts 2020 : A novel form of muscular dystrophy associated with mutations in JAG2Article
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
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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
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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
Weiss L ; Jung KM ; Nalbandian A ; Llewellyn K ; Yu H ; Ta L ; Chang I ; Migliore M ; Squire E ; Ahmed F ; Piomelli D ; Kimonis V | 25/02/2021Article
Bora G ; Hensel N ; Rademacher S ; Koyunoğlu D ; Sunguroğlu M ; Aksu Menges E ; Balcı-Hayta B ; Claus P ; Erdem-Yurter H | England | 25/02/2021Article
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
Ventura F ; Williams E ; Ikeya M ; Bullock AN ; Ten Dijke P ; Goumans MJ ; Sanchez-Duffhues G | 19/02/2021Article
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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
Kohlschmidt N ; Elbracht M ; Czech A ; Häusler M ; Phan V ; Topf A ; Huang KT ; Bartok A ; Eggermann K ; Zippel S ; Eggermann T ; Freier E ; Gross C ; Lochmuller H ; Horvath R ; Hajnoczky G ; Weis J ; Roos A | England | 11/01/2021Article
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Trollet C ; Boulinguiez A ; Roth F ; Stojkovic T ; Butler Browne G ; Evangelista T ; Lacau St Guily J ; Richard P | 22/10/2020Initial Posting: March 8, 2001; Last Update: October 22, 2020. Clinical characteristics. Oculopharyngeal muscular dystrophy (OPMD) is characterized by ptosis and dysphagia due to selective involvement of the muscles of the eyelids and phar[...]Article
McCray BA ; Schindler A ; Hoover-Fong JE ; Sumner CJ | 17/09/2020Initial Posting: May 15, 2014; Last Update: September 17, 2020. Clinical characteristics. The autosomal dominant TRPV4 disorders (previously considered to be clinically distinct phenotypes before their molecular basis was discovered) are n[...]Article
Initial Posting: April 2, 2009; Last Update: September 17, 2020. Clinical characteristics. Most individuals with classic GBE1 adult polyglucosan body disease (GBE1-APBD) present after age 40 years with unexplained progressive neurogenic bl[...]Article
Oliveira J ; Parente Freixo J ; Santos M ; Coelho T | 17/09/2020Initial Posting: June 7, 2012; Last Update: September 17, 2020. Clinical characteristics. The clinical manifestations of LAMA2 muscular dystrophy (LAMA2-MD) comprise a continuous spectrum ranging from severe congenital muscular dystrophy t[...]Article
Chrestian N | 27/08/2020Initial Posting: September 28, 1998; Last Update: August 27, 2020. Clinical characteristics. Hereditary neuropathy with liability to pressure palsies (HNPP) is characterized by recurrent acute sensory and motor neuropathy in a single or mu[...]Article
Dermatomyositis is a rare acquired immune-mediated muscle disease characterized by muscle weakness and skin rash. It is classified as one of the idiopathic inflammatory myopathies (IIM). Although all idiopathic inflammatory myopathies share the [...]Article
McElhanon KE ; Young N ; Hampton J ; Paleo BJ ; Kwiatkowski TA ; Beck EX ; Capati A ; Jablonski K ; Gurney T ; Perez MAL ; Aggarwal R ; Oddis CV ; Jarjour WN ; Weisleder N | 03/08/2020Article
Van Pelt DW ; Kharaz YA ; Sarver DC ; Eckhardt LR ; Dzierzawski JT ; Disser NP ; Piacentini AN ; Comerford E ; McDonagh B ; Mendias CL | 15/07/2020Article
Ferreira C ; Pierre G ; Thompson R ; Vernon H | 09/07/2020nitial Posting: October 9, 2014; Last Update: July 9, 2020. Clinical characteristics. Barth syndrome is characterized in affected males by cardiomyopathy, neutropenia, skeletal myopathy, prepubertal growth delay, and distinctive facial ges[...]Article
Deng J ; Yu J ; Li P ; Luan X ; Cao L ; Zhao J ; Yu M ; Zhang W ; Lv H ; Xie Z ; Meng L ; Zheng Y ; Zhao Y ; Gang Q ; Wang Q ; Liu J ; Zhu M ; Guo X ; Su Y ; Liang Y ; Liang F ; Hayashi T ; Maeda MH ; Sato T ; Ura S ; Oya Y ; Ogasawara M ; Iida A ; Nishino I ; Zhou C ; Yan C ; Yuan Y ; Hong D ; Wang Z | United States | 07/2020Article
Garcia-Rodriguez R ; Hiller M ; Jimenez-Gracia L ; van der Pal Z ; Balog J ; Adamzek K ; Aartsma Rus A ; Spitali P | United States | 07/2020Article
Wurmser M ; Chaverot N ; Madani R ; Sakai H ; Negroni E ; Demignon J ; Saint-Pierre B ; Mouly V ; Amthor H ; Tapscott S ; Birchmeier C ; Tajbakhsh S ; Le Grand F ; Sotiropoulos A ; Maire P | 26/06/2020Article
Prasun P | 18/06/2020Clinical characteristics. Multiple acyl-CoA dehydrogenase deficiency (MADD) represents a clinical spectrum in which presentations can be divided into type I (neonatal onset with congenital anomalies), type II (neonatal onset without congenita[...]Article
Rietveld A ; van Gaalen J ; Saris C ; Okkersen K ; Kusters B ; van de Warrenburg B ; van Engelen B ; Sacconi S ; Raaphorst J | England | 06/2020Publication AFM
La maladie de Kennedy (ou amyotrophie bulbo-spinale liée à l’X) est une maladie rare d’origine génétique. Elle se manifeste à l'âge adulte par une faiblesse musculaire progressive et des troubles hormonaux. Elle est caractérisée par une dégénére[...]Publication AFM
Myoinfo, Auteur ; Strochlic L, Validateur ; Godard-Bauche S, Validateur | AFM-TELETHON | Savoir & Comprendre | 06/2020Les syndromes myasthéniques congénitaux sont des maladies rares, d'origine génétique. Ils se caractérisent par une faiblesse musculaire, localisée ou généralisée. Elle évolue de manière plus ou moins fluctuante, avec une tendance nette à s’aggr[...]Article
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Zhou Y ; Borchelt D ; Bauson JC ; Fazio S ; Miles JR ; Tavori H ; Notterpek L | United States | 06/2020Article
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Osman EY ; Van Alstyne M ; Yen PF ; Lotti F ; Feng Z ; Ling KK ; Ko CP ; Pellizzoni L ; Lorson CL | United States | 06/2020Article
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Sawade L ; Grandi F ; Mignanelli M ; Patino-Lopez G ; Klinkert K ; Langa-Vives F ; Di Guardo R ; Echard A ; Bolino A ; Haucke V | 06/2020Article
Abstract from publisher web site : Facioscapulohumeral muscular dystrophy (FSHD) is the third most common form of muscular dystrophy. The disease is named by the initial pattern of weakness, with patients developing facial weakness, scapular wi[...]Article
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Chen K ; Birkinshaw RW ; Gurzau AD ; Wanigasuriya I ; Wang R ; Iminitoff M ; Sandow JJ ; Young SN ; Hennessy PJ ; Willson TA ; Heckmann DA ; Webb AI ; Blewitt ME ; Czabotar PE ; Murphy JM | United States | 06/2020Article
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Ferry A ; Messéant J ; Parlakian A ; Lemaitre M ; Roy P ; Delacroix C ; Lilienbaum A ; Hovhannisyan Y ; Furling D ; Klein A ; Li Z ; Agbulut O | England | 06/2020Article
Zuchner S | 14/05/2020Initial Posting: February 18, 2005; Last Update: May 14, 2020. Clinical characteristics. MFN2 hereditary motor and sensory neuropathy (MFN2-HMSN) is a classic axonal peripheral sensorimotor neuropathy, inherited in either an autosomal domi[...]Article
Dupont C ; Novak K ; Denman K ; Myers JH ; Sullivan JM ; Walker PV 2nd ; Brown NL ; Ladle DR ; Bogdanik L ; Lutz CM ; Voss A ; Sumner CJ ; Rich MM | United States | 05/2020Article
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Morioka S ; Sakaguchi H ; Mohri H ; Taniguchi-Ikeda M ; Kanagawa M ; Suzuki T ; Miyagoe-Suzuki Y ; Toda T ; Saito N ; Ueyama T | 05/2020Article
Carrillo N ; Malicdan MC ; Huizing M | 09/04/2020Initial Posting: March 26, 2004; Last Update: April 9, 2020. Clinical characteristics. GNE myopathy is a slowly progressive muscle disease that typically presents between age 20 and 40 years with bilateral foot drop caused by anterior tibial[...]Article
Kim H ; Gunter-Rahman F ; McGrath JA ; Lee E ; de Jesus AA ; Targoff IN ; Huang Y ; O'Hanlon TP ; Tsai WL ; Gadina M ; Miller FW ; Goldbach-Mansky R ; Rider LG | 04/2020Article
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Knottnerus SJG ; Mengarelli I ; Wust RCI ; Baartscheer A ; Bleeker JC ; Coronel R ; Ferdinandusse S ; Guan K ; Ijlst L ; Li W ; Luo X ; Portero VM ; Ulbricht Y ; Visser G ; Wanders RJA ; Wijburg FA ; Verkerk AO ; Houtkooper RH ; Bezzina CR | 04/2020Article
Geroldi A ; Prada V ; Veneri F ; Trevisan L ; Origone P ; Grandis M ; Schenone A ; Gemelli C ; Lanteri P ; Fossa P ; Mandich P ; Bellone E | United States | 04/2020Article
Stunnenberg B ; LoRusso S ; Arnold WD ; Barohn RJ ; Cannon SC ; Fontaine B ; Griggs RC ; Hanna MG ; Matthews E ; Meola G ; Sansone VA ; Trivedi JR ; van Engelen B ; Vicart S ; Statland JM | United States | 04/2020Article
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Schoser B | 19/03/2020Initial Posting: September 21, 2006; Last Update: March 19, 2020. Clinical characteristics. Myotonic dystrophy type 2 (DM2) is characterized by myotonia and muscle dysfunction (proximal and axial weakness, myalgia, and stiffness), and less[...]Article
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Acta neuropathologica Intracellular calcium leak as a therapeutic target for RYR1-related myopathies
Kushnir A ; Todd JJ ; Witherspoon JW ; Yuan Q ; Reiken S ; Lin H ; Munce RH ; Wajsberg B ; Melville Z ; Clarke OB ; Wedderburn-Pugh K ; Wronska A ; Razaqyar MS ; Chrismer IC ; Shelton MO ; Mankodi A ; Grunseich C ; Tarnopolsky MA ; Tanji K ; Hirano M ; Riazi S ; Kraeva N ; Voermans NC ; Gruber A ; Allen C ; Meilleur KG ; Marks AR | Germany | 03/2020Article
Harandi VM ; Oliveira BMS ; Allamand V ; Friberg A ; Fontes-Oliveira CC ; Durbeej M | Switzerland | 03/2020Article
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Bertrand AT ; Brull A ; Azibani F ; Benarroch L ; Chikhaoui K ; Stewart CL ; Medalia O ; Ben Yaou R ; Bonne G | Switzerland | 03/2020Article
Perego MGL ; Galli N ; Nizzardo M ; Govoni A ; Taiana M ; Bresolin N ; Comi GP ; Corti S | Switzerland | 03/2020Article
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Harr JC ; Schmid CD ; Munoz-Jimenez C ; Romero-Bueno R ; Kalck V ; Gonzalez-Sandoval A ; Hauer MH ; Padeken J ; Askjaer P ; Mattout A ; Gasser SM | United States | 03/2020Article
Torres-Ruiz J ; Carrillo-Vazquez DA ; Padilla-Ortiz DM ; Vazquez-Rodriguez R ; Nunez-Alvarez C ; Juarez-Vega G ; Gomez-Martin D | 03/2020Article
Suarez-Calvet X ; Alonso Perez J ; Castellví I ; Carrasco-Rozas A ; Fernandez-Simon E ; Zamora C ; Martinez-Martinez L ; Alonso-Jimenez A ; Rojas Garcia R ; Turon J ; Querol L ; de Luna N ; Milena-Millan A ; Corominas H ; Castillo D ; Cortes Vicente E ; Illa I ; Gallardo E ; Diaz-Manera J | United States | 03/2020Article
Ciszewski L ; Lu Nguyen N ; Slater A ; Brennan A ; Williams HEL ; Dickson G ; Searle MS ; Popplewell L | England | 03/2020Article
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Cerquone Perpetuini A ; Giuliani G ; Reggio A ; Cerretani M ; Santoriello M ; Stefanelli R ; Palma A ; Vumbaca S ; Harper S ; Castagnoli L ; Bresciani A ; Cesareni G | 03/2020Article
Mishra R ; Amanullah A ; Upadhyay A ; Dhiman R ; Dubey AR ; Singh S ; Prasad A ; Mishra A | Netherlands | 03/2020Article
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Sullivan JM ; Motley WW ; Johnson JO ; Aisenberg WH ; Marshall KL ; Barwick KE ; Kong L ; Huh JS ; Saavedra-Rivera PC ; McEntagart MM ; Marion MH ; Hicklin LA ; Modarres H ; Baple EL ; Farah MH ; Zuberi AR ; Lutz CM ; Gaudet R ; Traynor BJ ; Crosby AH ; Sumner CJ | United States | 03/2020Thèse/Mémoire
Britson KA | 03/2020The absence of an animal model for sporadic Inclusion Body Myositis (IBM) has hindered progress in the field including an incomplete understanding of pathogenesis and a lack of effective therapies. We have developed a novel xenograft model of IB[...]Article
Abrams CK | 20/02/2020Initial Posting: June 18, 1998; Last Update: February 20, 2020. Clinical characteristics. GJB1 disorders are typically characterized by peripheral motor and sensory neuropathy with or without fixed CNS abnormalities and/or acute, self-limite[...]Article
Conte E ; Bresciani E ; Rizzi L ; Cappellari O ; de Luca A ; Torsello A ; Liantonio A | 13/02/2020Article
Preston MK ; Tawil R ; Wang LH | 06/02/2020Initial Posting: March 8, 1999; Last Update: February 6, 2020. Clinical characteristics. Facioscapulohumeral muscular dystrophy (FSHD) typically presents with weakness of the facial muscles, the stabilizers of the scapula, or the dorsiflexor[...]Article
Kinder TB ; Heier CR ; Tully CB ; Van der Muelen JH ; Hoffman EP ; Nagaraju K ; Fiorillo AA | United States | 02/2020Article
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Ono H ; Suzuki N ; Kanno SI ; Kawahara G ; Izumi R ; Takahashi T ; Kitajima Y ; Osana S ; Nakamura N ; Akiyama T ; Ikeda K ; Shijo T ; Mitsuzawa S ; Nagatomi R ; Araki N ; Yasui A ; Warita H ; Hayashi YK ; Miyake K ; Aoki M | United States | 02/2020Article
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Rosenberg H ; Sambuughin N ; Riazi S ; Dirksen R | 16/01/2020Initial Posting: December 19, 2003; Last Update: January 16, 2020. Clinical characteristics. Malignant hyperthermia susceptibility (MHS) is a pharmacogenetic disorder of skeletal muscle calcium regulation associated with uncontrolled skeleta[...]Article
Initial Posting: February 17, 2005; Last Update: January 2, 2020. Clinical characteristics. Udd distal myopathy – tibial muscular dystrophy (UDM-TMD) is characterized by weakness of ankle dorsiflexion and inability to walk on the heels aft[...]Article
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Villar-Quiles RN ; Catervi F ; Cabet E ; Juntas-Morales R ; Genetti CA ; Gidaro T ; Koparir A ; Yuksel A ; Coppens S ; Deconinck N ; Pierce-Hoffman E ; Lornage X ; Durigneux J ; Laporte J ; Rendu J ; Romero NB ; Beggs AH ; Servais L ; Cossee M ; Olive M ; Bohm J ; Duband-Goulet I ; Ferreiro A | United States | 2020Article
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Das M ; Karnam A ; Stephen-Victor E ; Gilardin L ; Bhatt B ; Kumar Sharma V ; Rambabu N ; Patil V ; Lecerf M ; Kasermann F ; Bruneval P ; Narayanaswamy Balaji K ; Benveniste O ; Kaveri SV ; Bayry J | England | 01/2020Article
Chivet M ; Marchioretti C ; Pirazzini M ; Piol D ; Scaramuzzino C ; Polanco MJ ; Romanello V ; Zuccaro E ; Parodi S ; D'Antonio M ; Rinaldi C ; Sambataro F ; Pegoraro E ; Soraru G ; Pandey UB ; Sandri M ; Basso M ; Pennuto M | Switzerland | 01/2020Article
Kaplan FS, Auteur | 01/2020January, 2020 [Revised: Pages 105, 106] // June, 2019 [Revised: Pages 3, 6, 54, 101, 106] From The International Clinical Council on FOP (ICC) & Consultants: Kaplan FS, Al Mukaddam M, Baujat G, Brown M, Cali A, Cho T-J, Crowe C, De Cunto C[...]Article
Tripoli A ; Marasco E ; Cometi L ; De Stefano L ; Marcucci E ; Furini F ; Barsotti S ; Cavagna L | Italy | 01/2020Article
Al Tanoury Z ; Rao J ; Tassy O ; Gobert B ; Gapon S ; Garnier JM ; Wagner E ; Hick A ; Hall A ; Gussoni E ; Pourquié O | 2020Article
Fernandes SA ; Almeida CF ; Souza LS ; Lazar M ; Onofre-Oliveira P ; Yamamoto GL ; Nogueira L ; Tasaki LY ; Cardoso RR ; Pavanello RCM ; Silva HCA ; Ferrari MFR ; Bigot A ; Mouly V ; Vainzof M | 2020Article
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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
Morales F ; Vasquez M ; Corrales E ; Vindas-Smith R ; Santamaria-Ulloa C ; Zhang B ; Sirito M ; Estecio MR ; Krahe R ; Monckton DG | England | 2020Article
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Antoine M ; Patrick KL ; Soret J ; Duc P ; Rage F ; Cacciottolo R ; Nissen KE ; Cauchi RJ ; Krogan NJ ; Guthrie C ; Gachet Y ; Bordonne R | United States | 01/2020Article
Seto N ; Torres-Ruiz JJ ; Carmona-Rivera C ; Pinal Fernandez I ; Pak K ; Purmalek MM ; Hosono Y ; Fernandes-Cerqueira C ; Gowda PC ; Arnett N ; Gorbach A ; Benveniste O ; Gomez-Martin D ; Selva-O Callaghan A ; Milisenda JC ; Grau-Junyent JM ; Christopher Stine L ; Miller FW ; Lundberg IE ; Kahlenberg JM ; Schiffenbauer AI ; Mammen AL ; Rider LG ; Kaplan MJ | United States | 01/2020Article
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Earle AJ ; Kirby TJ ; Fedorchak GR ; Isermann P ; Patel J ; Iruvanti S ; Moore SA ; Bonne G ; Wallrath LL ; Lammerding J | England | 2020Article
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Vernerova L ; Horvathova V ; Kropackova T ; Vokurkova M ; Klein M ; Tomcik M ; Oreska S ; Spiritovic M ; Storkanova H ; Hermankova B ; Kubinova K ; Krystufkova O ; Mann H ; Ukropec J ; Ukropcova B ; Vencovsky J | England | 01/2020Article
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Bengoechea R ; Findlay AR ; Bhadra AK ; Shao H ; Stein KC ; Pittman SK ; Daw J ; Gestwicki JE ; True HL ; Weihl CC | United States | 2020Article
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Auxerre-Plantie E ; Nakamori M ; Renaud Y ; Huguet A ; Choquet C ; Dondi C ; Miquerol L ; Takahashi MP ; Gourdon G ; Junion G ; Jagla T ; Zmojdzian M ; Jagla K | England | 12/2019Article
Ates S ; Deistung A ; Schneider R ; Prehn C ; Lukas C ; Reichenbach JR ; Schneider-Gold C ; Bellenberg B | Switzerland | 12/2019Article
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