1. Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations. Issue 14 (15th October 2013) Authors: Alcalay, Roy N.; Mirelman, Anat; Saunders‐Pullman, Rachel; Tang, Ming‐X; Mejia Santana, Helen; Raymond, Deborah; Roos, Ernest; Orbe‐Reilly, Martha; Gurevich, Tanya; Bar Shira, Anat; Gana Weisz, Mali; Yasinovsky, Kira; Zalis, Maayan; Thaler, Avner; Deik, Andres; Barrett, Matthew James; Cabassa, Jo... Journal: Movement disorders Issue: Volume 28:Issue 14(2013) Page Start: 1966 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. The relationship between obsessive‐compulsive symptoms and PARKIN genotype: The CORE‐PD study. Issue 2 (12th November 2014) Authors: Sharp, Madeleine E.; Caccappolo, Elise; Mejia‐Santana, Helen; Tang, Ming‐X.; Rosado, Llency; Orbe Reilly, Martha; Ruiz, Diana; Louis, Elan D.; Comella, Cynthia; Nance, Martha; Bressman, Susan; Scott, William K.; Tanner, Caroline; Waters, Cheryl; Fahn, Stanley; Cote, Lucien; Ford, Blair; Rezak, Mi... Journal: Movement disorders Issue: Volume 30:Issue 2(2015) Page Start: 278 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗