1. A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia. (4th December 2020) Authors: Smaili, Imane; Hajjaj, Imane; Razine, Rachid; Tibar, Houyam; Salmi, Ayyoub; Bouslam, Naima; Moussa, Ahmed; Regragui, Wafa; Bouhouche, Ahmed Other Names: Mittal Balraj Academic Editor. Journal: Case reports in genetics Issue: Volume 2020(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Availability of Therapies and Services for Parkinson's Disease in Africa: A Continent‐Wide Survey. Issue 10 (3rd June 2021) Authors: Hamid, Eman; Ayele, Biniyam A.; Massi, Daniel Gams; Ben Sassi, Samia; Tibar, Houyam; Djonga, Emmanuel Epenge; El‐Sadig, Sarah Misbah; AMER EL KHEDOUD, Wahiba; Razafimahefa, Julien; Kouame‐Assouan, Ange Eric; Ben‐Adji, Djibrilla; Lengané, Yilédoma Thierry Modeste; Musubire, Abdu Kisekka; Mohamed, ... Journal: Movement disorders Issue: Volume 36:Issue 10(2021) Page Start: 2393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing. (15th November 2018) Authors: Bouhouche, Ahmed; Tibar, Houyam; Kriouale, Yamna; Jiddane, Mohammed; Smaili, Imane; Bouslam, Naima; Benomar, Ali; Yahyaoui, Mohamed; El Fahime, Elmostafa Other Names: Dmitrzak-Weglarz Monika Academic Editor. Journal: Case reports in genetics Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease. (30th March 2017) Authors: Bouhouche, Ahmed; Tibar, Houyam; Ben El Haj, Rafiqua; El Bayad, Khalil; Razine, Rachid; Tazrout, Sanaa; Skalli, Asmae; Bouslam, Naima; Elouardi, Loubna; Benomar, Ali; Yahyaoui, Mohammed; Regragui, Wafa Other Names: Berwick Daniel Academic Editor. Journal: Parkinson's disease Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Management of rare movement diseases in different world regions. (March 2023) Authors: Painous, Celia; Martí, Maria J.; Graessner, Holm; Camargo, Andrea Paola; El-Jaafary, Shaimaa Ibrahim; Martínez-Ramírez, Daniel; Ojo, Oluwadamilola O.; Taiwo, Funmilola T.; Rajan, Roopa; Cornejo-Olivas, Mario; Ayele, Biniyam A.; Tibar, Houyam; Kearney, Mary; Gatto, Emilia; Tijssen, Marina AJ. Journal: Parkinsonism & related disorders Issue: Volume 108(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Myokymia revealing multiple sclerosis. (January 2016) Authors: Tibar, Houyam; Ait Benhaddou, Elhachmia; Regragui, Wafa; Benomar, Ali; Yahyaoui, Mohamed; Birouk, Nezha; Jiddane, Mohamed Journal: Parkinsonism & related disorders Issue: Volume 22(2016)Supplement 2 Page Start: e131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Task Force Consensus on Nosology and Cut‐Off Values for Axial Postural Abnormalities in Parkinsonism. Issue 5 (9th May 2022) Authors: Tinazzi, Michele; Geroin, Christian; Bhidayasiri, Roongroj; Bloem, Bastiaan R.; Capato, Tamine; Djaldetti, Ruth; Doherty, Karen; Fasano, Alfonso; Tibar, Houyam; Lopiano, Leonardo; Margraf, Nils G.; Merello, Marcelo; Moreau, Caroline; Ugawa, Yoshikazu; Artusi, Carlo Alberto Journal: Movement disorders clinical practice Issue: Volume 9:Issue 5(2022) Page Start: 594 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗