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#	Item
191	Int J Clin Exp Med 2014;7(12):www.ijcem.com /ISSN:IJCEM0002859 Case Report Gastrointestinal symptom due to lupus peritonitis: a rare form of onset of SLE Add to Reading List Source URL: www.emergencyultrasoundteaching.com - Date: 2016-08-31 10:54:44
192	Job Description Country Medical Director Company Background Amicus Therapeutics (NASDAQ:FOLD) is a biopharmaceutical company at the forefront of therapies for rare and orphan diseases. The Company has a robust pipeline o Add to Reading List Source URL: www.amicusrx.co.uk - Date: 2016-10-27 09:42:56
193	EURORDIS Template email for Patient Organisations to share with members Oggetto: Registrati a Rare Barometer Voices EURORDIS, l’Organizzazione Europea per le Malattie Rare, sta lanciando un nuovo progetto chiamato Rar Add to Reading List Source URL: www.eurordis.org - Date: 2016-02-23 10:22:06
194	Identification of Rare & Novel Senses Using Translations in a Parallel Corpus ¨ ∗ , Fabienne Martin† , Achim Stein† Richard Schwarz∗ , Hinrich Schutze ∗ Institute for Natural Language Processing, Universit¨a Add to Reading List Source URL: www.lrec-conf.org - Date: 2010-06-28 09:24:32
195	Policy and Legislative Update: Budgetary Agreement and Policy in 2015 Joshua Stewart Assistant Director of Policy Budgetary Agreement – the “CRomnibus” On December 13, in a rare Saturday session, the Senate voted t Add to Reading List Source URL: www.nchv.org - Date: 2016-03-29 17:48:28
196	Négationnisme économique : quand la « science » pète les plombs Michel Husson, A l’encontre, 16 septembre 2016 Le livre de Pierre Cahuc et André Zylberberg1 (C&Z dans ce qui suit), est une attaque d’une rare vi Add to Reading List Source URL: hussonet.free.fr - Date: 2016-11-17 06:57:49
197	The BASES Expert Statement on Genetic Research and Testing in Sport and Exercise Science Left: Eero Mantyranta, multiple Olympic medal winner, had a rare mutation in his EPOR gene Add to Reading List Source URL: www.bases.org.uk - Date: 2012-03-16 11:42:50
198	Addressing the Rare Word Problem in Neural Machine Translation Minh-Thang Luong† ∗ Stanford Ilya Sutskever† Add to Reading List Source URL: cs224d.stanford.edu - Date: 2016-05-12 22:27:25
199	Dear Primary Care Provider, Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease characterized by weakness of the skeletal and respiratory muscles. SMA is a rare disorder occurring approximately 1 in 10,000 b Add to Reading List Source URL: www.curesma.org - Date: 2015-05-01 10:28:22
200	Clinical Study Start-up Time Lines for Rare Orphan Diseases: Can We Do Better? The Example of Primary Biliary Cholangitis 1 Varga , 2 Add to Reading List Source URL: content.equisolve.net - Date: 2016-11-11 08:32:19

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