1. A thrombopoietin receptor agonist to rescue an unusual platelet transfusion-induced reaction in a p.V1316M-associated von Willebrand disease type 2B patient. (February 2022) Authors: Casari, Caterina; Favier, Remi; Legendre, Paulette; Kauskot, Alexandre; Adam, Frederic; Picard, Veronique; Lenting, Peter J.; Denis, Cecile V.; Proulle, Valerie Journal: Therapeutic advances in hematology Issue: Volume 13(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders. (21st April 2015) Authors: Civaschi, Elisa; Klersy, Catherine; Melazzini, Federica; Pujol‐Moix, Nuria; Santoro, Cristina; Cattaneo, Marco; Lavenu‐Bombled, Cécile; Bury, Loredana; Minuz, Pietro; Nurden, Paquita; Cid, Ana R.; Cuker, Adam; Latger‐Cannard, Véronique; Favier, Remi; Nichele, Ilaria; Noris, Patrizia; the European... Journal: British journal of haematology Issue: Volume 170:Number 4(2015:Aug.) Page Start: 559 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clonal evolution in hereditary thrombocytosis with MPL T487A mutation. Issue 2 (4th August 2022) Authors: Vasseur, Loic; Favier, Remi; Kim, Rathana; Rabian, Florence; Cabannes‐Hamy, Aurelie; Cassinat, Bruno; Maslah, Nabih; Vasquez, Nadia; Clappier, Emmanuelle; Kiladjian, Jean‐Jacques; Boissel, Nicolas Journal: Pediatric blood & cancer Issue: Volume 70:Issue 2(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Eltrombopag to Treat Thrombocytopenia During Last Month of Pregnancy in a Woman With MYH9-Related Disease: A Case Report. Issue 1 (1st January 2018) Authors: Favier, Remi; De Carne, Celine; Elefant, Elisabeth; Lapusneanu, Ruxanda; Gkalea, Vasiliki; Rigouzzo, Agnès Journal: A & A practice Issue: Volume 10:Issue 1(2018:Jan. 01) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Eltrombopag to Treat Thrombocytopenia During Last Month of Pregnancy in a Woman With MYH9-Related Disease: A Case Report. Issue 1 (1st January 2018) Authors: Favier, Remi; De Carne, Celine; Elefant, Elisabeth; Lapusneanu, Ruxanda; Gkalea, Vasiliki; Rigouzzo, Agnès Journal: A & A case reports Issue: Volume 10:Issue 1(2018:Jan. 01) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders. Issue 1 (December 2016) Authors: Latger-Cannard, Veronique; Philippe, Christophe; Bouquet, Alexandre; Baccini, Veronique; Alessi, Marie-Christine; Ankri, Annick; Bauters, Anne; Bayart, Sophie; Cornillet-Lefebvre, Pascale; Daliphard, Sylvie; Mozziconacci, Marie-Joelle; Renneville, Aline; Ballerini, Paola; Leverger, Guy; Sobol, Ha... Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Jacobsen syndrome: Advances in our knowledge of phenotype and genotype. (18th August 2015) Authors: Favier, Remi; Akshoomoff, Natacha; Mattson, Sarah; Grossfeld, Paul; Cody, Jannine DeMars; Battaglia, Agatino; Hale, Daniel Esten Journal: American journal of medical genetics Issue: Volume 169:Number 3(2015:Jul.) Page Start: 239 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α‐granules. Issue 2 (17th November 2017) Authors: Favier, Marie; Bordet, Jean‐Claude; Favier, Remi; Gkalea, Vasiliki; Pillois, Xavier; Rameau, Philippe; Debili, Najet; Alessi, Marie‐Christine; Nurden, Paquita; Raslova, Hana; Nurden, Alan Journal: American journal of hematology Issue: Volume 93:Issue 2(2018:Feb.) Page Start: 195 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. MYH9‐related disease mutations cause abnormal red blood cell morphology through increased myosin‐actin binding at the membrane. Issue 6 (17th April 2019) Authors: Smith, Alyson S.; Pal, Kasturi; Nowak, Roberta B.; Demenko, Anastasiya; Zaninetti, Carlo; Da Costa, Lydie; Favier, Remi; Pecci, Alessandro; Fowler, Velia M. Journal: American journal of hematology Issue: Volume 94:Issue 6(2019:Jun.) Page Start: 667 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension. Issue 21 (21st November 2017) Authors: Hadinnapola, Charaka; Bleda, Marta; Haimel, Matthias; Screaton, Nicholas; Swift, Andrew; Dorfmüller, Peter; Preston, Stephen D.; Southwood, Mark; Hernandez-Sanchez, Jules; Martin, Jennifer; Treacy, Carmen; Yates, Katherine; Bogaard, Harm; Church, Colin; Coghlan, Gerry; Condliffe, Robin; Corris, P... Journal: Circulation Issue: Volume 136:Issue 21(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗