1. Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene. Issue 3 (17th June 2015) Authors: Praschberger, Roman; Balint, Bettina; Mencacci, Niccolo E.; Hersheson, Joshua; Rubio‐Agusti, Ignacio; Kullmann, Dimitri M.; Bettencourt, Conceição; Bhatia, Kailash; Houlden, Henry Journal: Movement disorders clinical practice Issue: Volume 2:Issue 3(2015) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Functional (psychogenic) symptoms in Parkinson's disease. Issue 12 (4th June 2013) Authors: Pareés, Isabel; Saifee, Tabish A.; Kojovic, Maja; Kassavetis, Panagiotis; Rubio‐Agusti, Ignacio; Sadnicka, Anna; Bhatia, Kailash P.; Edwards, Mark J. Journal: Movement disorders Issue: Volume 28:Issue 12(2013) Page Start: 1622 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study. Issue 14 (25th September 2014) Authors: Gómez‐Garre, Pilar; Huertas‐Fernández, Ismael; Cáceres‐Redondo, María Teresa; Alonso‐Canovas, Araceli; Bernal‐Bernal, Inmaculada; Blanco‐Ollero, Alberto; Bonilla‐Toribio, Marta; Burguera, Juan Andrés; Carballo, Manuel; Carrillo, Fatima; José Catalán‐Alonso, M.; Escamilla‐Sevilla, Francisco; Espin... Journal: Movement disorders Issue: Volume 29:Issue 14(2014) Page Start: 1825 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Movement Disorders in Adult Patients With Classical Galactosemia. Issue 6 (11th February 2013) Authors: Rubio‐Agusti, Ignacio; Carecchio, Miryam; Bhatia, Kailash P.; Kojovic, Maja; Parees, Isabel; Chandrashekar, Hoskote S.; Footitt, Emma J.; Burke, Derek; Edwards, Mark J.; Lachmann, Robin H.L.; Murphy, Elaine Journal: Movement disorders Issue: Volume 28:Issue 6(2013) Page Start: 804 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The phenotypic spectrum of DYT24 due to ANO3 mutations. Issue 7 (17th January 2014) Authors: Stamelou, Maria; Charlesworth, Gavin; Cordivari, Carla; Schneider, Susanne A.; Kägi, Georg; Sheerin, Una‐Marie; Rubio‐Agusti, Ignacio; Batla, Amit; Houlden, Henry; Wood, Nicholas W.; Bhatia, Kailash P. Journal: Movement disorders Issue: Volume 29:Issue 7(2014) Page Start: 928 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The syndrome of deafness‐dystonia: Clinical and genetic heterogeneity. Issue 6 (15th February 2013) Authors: Kojovic, Maja; Pareés, Isabel; Lampreia, Tania; Pienczk‐Reclawowicz, Karolina; Xiromerisiou, Georgia; Rubio‐Agusti, Ignacio; Kramberger, Milica; Carecchio, Miryam; Alazami, Anas M.; Brancati, Francesco; Slawek, Jaroslaw; Pirtosek, Zvezdan; Valente, Enza Maria; Alkuraya, Fowzan S.; Edwards, Mark J... Journal: Movement disorders Issue: Volume 28:Issue 6(2013) Page Start: 795 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Transcranial magnetic stimulation follow‐up study in early Parkinson's disease: A decline in compensation with disease progression?. Issue 8 (5th March 2015) Authors: Kojovic, Maja; Kassavetis, Panagiotis; Bologna, Matteo; Pareés, Isabel; Rubio‐Agusti, Ignacio; Beraredelli, Alfredo; Edwards, Mark J.; Rothwell, John C.; Bhatia, Kailash P. Journal: Movement disorders Issue: Volume 30:Issue 8(2015) Page Start: 1098 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗