1. 98. AbobotulinumtoxinA (Dysport) in the treatment of adults with upper limb spasticity in a randomized, double-blind, placebo-controlled study. (January 2015) Authors: Gracies, Jean-Michel; Lejeune, Thierry; Boyer, Francois; Kocer, Serdar; Marque, Philippe; Csanyi, Attila; Denes, Zoltan; Vecchio, Michele; Kaminska, Anna; Rudzinska, Monika; Timerbaeva, Sofia L.; Brashear, Allison; O'Dell, Michael; Vilain, Claire; Picaut, Philippe Journal: Toxicon Issue: Volume 93(2015)Supplement Page Start: S30 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An Association Between Migraines and Heart Anomalies—True or False? A Heart Ultrasound Study Using cTTE in Migraine Patients and Control Participants. Issue 12 (5th November 2014) Authors: Domitrz, Izabela; Styczynski, Grzegorz; Wilczko, Justyna; Marczewska, Malgorzata M.; Domitrz, Wojciech; Kaminska, Anna Journal: Pain medicine Issue: Volume 15:Issue 12(2014) Page Start: 2156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Andersen–Tawil syndrome: Report of 3 novel mutations and high risk of symptomatic cardiac involvement. Issue 2 (19th November 2014) Authors: Kostera‐Pruszczyk, Anna; Potulska‐Chromik, Anna; Pruszczyk, Piotr; Bieganowska, Katarzyna; Miszczak‐Knecht, Maria; Bienias, Piotr; szczałuba, krzysztof; Lee, Hsien‐Yang; Quinn, Emily; Ploski, Rafal; Kaminska, Anna; Ptáček, Louis J. Journal: Muscle & nerve Issue: Volume 51:Issue 2(2015:Feb.) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial. Issue 10101 (23rd September 2017) Authors: McDonald, Craig M; Campbell, Craig; Torricelli, Ricardo Erazo; Finkel, Richard S; Flanigan, Kevin M; Goemans, Nathalie; Heydemann, Peter; Kaminska, Anna; Kirschner, Janbernd; Muntoni, Francesco; Osorio, Andrés Nascimento; Schara, Ulrike; Sejersen, Thomas; Shieh, Perry B; Sweeney, H Lee; Topaloglu... Journal: Lancet Issue: Volume 390:Issue 10101(2017) Page Start: 1489 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Benign Neonatal Sleep Myoclonus Evokes Somatosensory Responses. Issue 6 (November 2017) Authors: Losito, Emma; Eisermann, Monika; Vignolo, Patricia; Hovhannisyan, Shushanik; Magny, Jean François; Kaminska, Anna Journal: Journal of clinical neurophysiology Issue: Volume 34:Issue 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019) Authors: Bachoud-Lévi, Anne-Catherine; Bentivoglio, Anna-Rita; Biunno, Ida; Bonelli, Raphael M.; Bronzova, Juliana; Burgunder, Jean-Marc; Dunnett, Stephen B.; Ferreira, Joaquim J.; Frich, Jan; Giuliano, Joe; Handley, Olivia J.; Heiberg, Arvid; Illarioshkin, Sergey; Illmann, Torsten; Klempir, Jiri; Landweh... Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Comprehensive evaluation of EMG and biopsy findings supported by computer simulations – A preliminary study. Issue 8 (August 2018) Authors: Zalewska, Ewa; Kaminska, Anna; Kierdaszuk, Biruta; Szmidt-Salkowska, Elżbieta; Gawel, Małgorzata Journal: Clinical neurophysiology Issue: Volume 129:Issue 8(2018:Aug.) Page Start: 1595 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes. Issue 11 (14th September 2020) Authors: Jaber, Dana; Gitiaux, Cyril; Blesson, Sophie; Marguet, Florent; Buard, David; Varela Salgado, Maritzaida; Kaminska, Anna; Saada, Julien; Fallet-Bianco, Catherine; Martinovic, Jelena; Laquerriere, Annie; Melki, Judith Journal: Journal of medical genetics Issue: Volume 58:Issue 11(2021) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures. Issue 2 (22nd August 2019) Authors: Hubert, Laurence; Cannata Serio, Magda; Villoing-Gaudé, Laure; Boddaert, Nathalie; Kaminska, Anna; Rio, Marlène; Lyonnet, Stanislas; Munnich, Arnold; Poirier, Karine; Simons, Matias; Besmond, Claude Journal: Journal of medical genetics Issue: Volume 57:Issue 2(2020) Page Start: 138 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Do children with Dravet syndrome continue to benefit from stiripentol for long through adulthood?. (22nd August 2018) Authors: Chiron, Catherine; Helias, Marie; Kaminska, Anna; Laroche, Cecile; de Toffol, Bertrand; Dulac, Olivier; Nabbout, Rima; An, Isabelle Journal: Epilepsia Issue: Volume 59:issue 9(2018) Page Start: 1705 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗