1. A 58‐year‐old man with B‐cell chronic lymphocytic leukemia and multiple strokes. (30th July 2021) Authors: Magrinelli, Francesca; Mariotto, Sara; Nadali, Gianpaolo; Todeschini, Giuseppe; Lanzafame, Massimiliano; Cavallaro, Tiziana; Monaco, Salvatore; Ferrari, Sergio Journal: Brain pathology Issue: Volume 31:Number 6(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A geroscience approach for Parkinson's disease: Conceptual framework and design of PROPAG-AGEING project. (March 2021) Authors: Pirazzini, Chiara; Azevedo, Tiago; Baldelli, Luca; Bartoletti-Stella, Anna; Calandra-Buonaura, Giovanna; Dal Molin, Alessandra; Dimitri, Giovanna Maria; Doykov, Ivan; Gómez-Garre, Pilar; Hägg, Sara; Hällqvist, Jenny; Halsband, Claire; Heywood, Wendy; Jesús, Silvia; Jylhävä, Juulia; Kwiatkowska, K... Journal: Mechanisms of ageing and development Issue: Volume 194(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A new family with GLRB-related hyperekplexia showing chorea in homo- and heterozygous variant carriers. (October 2020) Authors: Estevez-Fraga, Carlos; Magrinelli, Francesca; Latorre, Anna; Cordivari, Carla; Houlden, Henry; Tinazzi, Michele; Hemingway, Cheryl; Tabrizi, Sarah J.; Bhatia, Kailash P. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Abnormal DaTscan in GM1‐Gangliosidosis Type III Manifesting with Dystonia‐Parkinsonism. Issue 6 (10th July 2022) Authors: Koya Kutty, Shahedah; Magrinelli, Francesca; Milner, Anna Vera; Bhatia, Kailash P. Journal: Movement disorders clinical practice Issue: Volume 9:Issue 6(2022) Page Start: 825 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy. Issue 2 (3rd January 2022) Authors: Magrinelli, Francesca; Cali, Elisa; Braga, Vinícius Lopes; Yis, Uluç; Tomoum, Hoda; Shamseldin, Hanan; Raiman, Julian; Kernstock, Christoph; Rezende Filho, Flávio Moura; Barsottini, Orlando Graziani Povoas; Taylor, Robert W.; Østergaard, Elsebet; Tamim, Abdullah; Schäferhoff, Karin; Sallum, Julia... Journal: Movement disorders clinical practice Issue: Volume 9:Issue 2(2022) Page Start: 218 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Issue 2 (8th June 2022) Authors: Christensen, Maria B.; Levy, Amanda M.; Mohammadi, Nazanin A.; Niceta, Marcello; Kaiyrzhanov, Rauan; Dentici, Maria Lisa; Al Alam, Chadi; Alesi, Viola; Benoit, Valérie; Bhatia, Kailash P.; Bierhals, Tatjana; Boßelmann, Christian M.; Buratti, Julien; Callewaert, Bert; Ceulemans, Berten; Charles, P... Journal: Clinical genetics Issue: Volume 102:Issue 2(2022) Page Start: 98 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Breakthrough News in Adenoviral Vector‐Mediated AADC Gene Therapy: Lessons from the Success in AADC Deficiency and Possible Future Applications. Issue 6 (25th June 2022) Authors: Malaquias, Maria João; Magrinelli, Francesca; Bhatia, Kailash P. Journal: Movement disorders clinical practice Issue: Volume 9:Issue 6(2022) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes. Issue 3 (2nd March 2021) Authors: Magrinelli, Francesca; Balint, Bettina; Bhatia, Kailash P. Journal: Movement disorders clinical practice Issue: Volume 8:Issue 3(2021) Page Start: 299 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Childhood‐Onset Chorea Caused by a Recurrent De Novo DRD2 Variant. Issue 6 (18th June 2021) Authors: Mencacci, Niccolò E.; Steel, Dora; Magrinelli, Francesca; Hsu, Jerry; Keller Sarmiento, Ignacio Juan; Troncoso Schifferli, Mónica; Muñoz, Daniela; Stefanis, Leonidas; Lubbe, Steven J.; Wood, Nicholas W.; Kurian, Manju A.; Stamelou, Maria Journal: Movement disorders Issue: Volume 36:Issue 6(2021) Page Start: 1472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Issue 1 (23rd August 2022) Authors: Magrinelli, Francesca; Bhatia, Kailash P.; Beiraghi Toosi, Mehran; Arab, Fatemeh; Karimiani, Ehsan Ghayoor; Sedighzadeh, Sahar; Ansari, Behnaz; Neshatdoust, Maedeh; Rocca, Clarissa; Houlden, Henry; Maroofian, Reza Journal: Movement disorders clinical practice Issue: Volume 10:Issue 1(2023) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗