Francesca Magrinelli

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 57

Top Venues

Movement disorders clinical practice

Movement disorders : official journal of the Movement Disorder Society

NPJ Parkinson's disease

medRxiv : the preprint server for health sciences

University College London

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University College London Mar 04 2019

United Kingdom

Honorary Research Associate :: Clinical and Movement Sciences

Universita' degli Studi di VERONA Oct 01 2017

Italy

Dottorandi :: DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO

Università degli Studi di Verona Oct 01 2017

Italy

PhD Candidate :: Neuroscienze, Biomedicina e Movimento

Universita' degli Studi di VERONA Sep 15 2012 - Jul 16 2013

Italy

Assegnisti :: EX-DIPARTIMENTO DI SCIENZE NEUROLOGICHE E DEL MOVIMENTO-(2000/2015)

Publications

Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Alvarez, Pau Pastor, Alessio di Fonzo, Kailash P Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek P Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockman, Huw R Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean-Christophe Corvol, null null
Genotype-phenotype correlation in PRKN-associated Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Alvarez, Pau Pastor, Alessio di Fonzo, Kailash P Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek P Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockman, Huw R Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean-Christophe Corvol, null null
Genotype-phenotype correlation in PRKN-associated Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Bettina Balint, Shermyn Xiumin Neo, Francesca Magrinelli, Eoin Mulroy, Anna Latorre, Maria Stamelou, Huw R Morris, Amit Batla, Kailash P Bhatia
Ethnic Differences in Atypical Parkinsonism-is South Asian PSP Different? Movement disorders clinical practice (2024)
Shermyn Xiumin Neo, Francesca Magrinelli, Carla Cordivari, Kailash P Bhatia
Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B-Related Spinocerebellar Ataxia. Movement disorders clinical practice 11 (5) (2024)
Sara Nagy, Aisling Carr, Magdalena Mroczek, Simon Rinaldi, Riccardo Curro, Natalia Dominik, Nicole Japzon, Francesca Magrinelli, Michael P T Lunn, Hadi Manji, Mary M Reilly, Andrea Cortese, Henry Houlden
Pathologic RFC1 repeat expansions do not contribute to the development of inflammatory neuropathies. Brain communications 6 (4) (2024)
Shermyn Xiumin Neo, Francesca Magrinelli, Carla Cordivari, Kailash P Bhatia
Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B-Related Spinocerebellar Ataxia. Movement disorders clinical practice (2024)
Sara Nagy, Aisling Carr, Magdalena Mroczek, Simon Rinaldi, Riccardo Curro, Natalia Dominik, Nicole Japzon, Francesca Magrinelli, Michael P T Lunn, Hadi Manji, Mary M Reilly, Andrea Cortese, Henry Houlden
Pathologic RFC1 repeat expansions do not contribute to the development of inflammatory neuropathies. Brain communications 6 (4) (2024)
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Alvarez, Pau Pastor, Alessio di Fonzo, Kailash P Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek P Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockman, Huw R Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean-Christophe Corvol, null null
Genotype-phenotype correlation in PRKN-associated Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Shermyn Xiumin Neo, Francesca Magrinelli, Carla Cordivari, Kailash P Bhatia
Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B-Related Spinocerebellar Ataxia. Movement disorders clinical practice 11 (5) (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Alvarez, Pau Pastor, Alessio di Fonzo, Kailash P Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek P Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockman, Huw R Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean-Christophe Corvol, null null
Genotype-phenotype correlation in PRKN-associated Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Shermyn Xiumin Neo, Francesca Magrinelli, Carla Cordivari, Kailash P Bhatia
Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B-Related Spinocerebellar Ataxia. Movement disorders clinical practice 11 (5) (2024)
Sara Nagy, Aisling Carr, Magdalena Mroczek, Simon Rinaldi, Riccardo Curro, Natalia Dominik, Nicole Japzon, Francesca Magrinelli, Michael P T Lunn, Hadi Manji, Mary M Reilly, Andrea Cortese, Henry Houlden
Pathologic RFC1 repeat expansions do not contribute to the development of inflammatory neuropathies. Brain communications 6 (4) (2024)
Andrea Quattrone, Anna Latorre, Francesca Magrinelli, Eoin Mulroy, Roopa Rajan, Ray Jen Neo, Aldo Quattrone, John C Rothwell, Kailash P Bhatia
A Reflection on Motor Overflow, Mirror Phenomena, Synkinesia and Entrainment. Movement disorders clinical practice 10 (9) (2023)
Robin Wijngaard, German Demidov, Luke O'Gorman, Jordi Corominas-Galbany, Burcu Yaldiz, Wouter Steyaert, Elke de Boer, Lisenka E L M Vissers, Erik-Jan Kamsteeg, Rolph Pfundt, Hilde Swinkels, Amber den Ouden, Iris B A W Te Paske, Richarda M de Voer, Laurence Faivre, Anne Sophie Denommé-Pichon, Yannis Duffourd, Antonio Vitobello, Martin Chevarin, Volker Straub, Ana Topf, Anneke J van der Kooi, Francesca Magrinelli, Clarissa Rocca, Michael G Hanna, Jana Vandrovcova, null null, Stephan Ossowski, Steven Laurie, Christian Gilissen
Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples. European journal of human genetics : EJHG (2023)
Ray Jen Neo, Arpan R Mehta, Mikail Weston, Francesca Magrinelli, Andrea Quattrone, Sonia Gandhi, Eileen M Joyce, Kailash P Bhatia
Neuropsychiatric Presentation of Anti-DPPX Progressive Encephalomyelitis with Rigidity and Myoclonus. Movement disorders clinical practice 11 (1) (2023)
Simeona Jacinto, Anna Latorre, Francesca Magrinelli, Kailash P Bhatia
Parkinsonism Following SARS-CoV-2 Infection Unmasks a Genetic Twist. Movement disorders clinical practice 10 (7) (2023)
Ray Jen Neo, Arpan R Mehta, Mikail Weston, Francesca Magrinelli, Andrea Quattrone, Sonia Gandhi, Eileen M Joyce, Kailash P Bhatia
Neuropsychiatric Presentation of Anti-DPPX Progressive Encephalomyelitis with Rigidity and Myoclonus. Movement disorders clinical practice 11 (1) (2023)
Robin Wijngaard, German Demidov, Luke O'Gorman, Jordi Corominas-Galbany, Burcu Yaldiz, Wouter Steyaert, Elke de Boer, Lisenka E L M Vissers, Erik-Jan Kamsteeg, Rolph Pfundt, Hilde Swinkels, Amber den Ouden, Iris B A W Te Paske, Richarda M de Voer, Laurence Faivre, Anne Sophie Denommé-Pichon, Yannis Duffourd, Antonio Vitobello, Martin Chevarin, Volker Straub, Ana Topf, Anneke J van der Kooi, Francesca Magrinelli, Clarissa Rocca, Michael G Hanna, Jana Vandrovcova, null null, Stephan Ossowski, Steven Laurie, Christian Gilissen
Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples. European journal of human genetics : EJHG (2023)
Ray Jen Neo, Arpan R Mehta, Mikail Weston, Francesca Magrinelli, Andrea Quattrone, Sonia Gandhi, Eileen M Joyce, Kailash P Bhatia
Neuropsychiatric Presentation of Anti-DPPX Progressive Encephalomyelitis with Rigidity and Myoclonus. Movement disorders clinical practice 11 (1) (2023)
Maria Bejerholm Christensen, Amanda M Levy, Nazanin A Mohammadi, Marcello Niceta, Rauan Kaiyrzhanov, Maria Lisa Dentici, Chadi Al Alam, Viola Alesi, Valérie Benoit, Kailash P Bhatia, Tatjana Bierhals, Christian Malte Boßelmann, Julien Buratti, Bert Callewaert, Berten Ceulemans, Perrine Charles, Matthias De Wachter, Mohammadreza Dehghani, Erika D'haenens, Martine Doco-Fenzy, Michaela Geßner, Cyrielle Gobert, Ulviyya Guliyeva, Tobias B Haack, Trine B Hammer, Tilman Heinrich, Maja Hempel, Theresia Herget, Ute Hoffmann, Judit Horvath, Henry Houlden, Boris Keren, Christina Kresge, Candy Kumps, Damien Lederer, Alban Lermine, Francesca Magrinelli, Reza Maroofian, Mohammad Yahya Vahidi Mehrjardi, Mahdiyeh Moudi, Amelie J Müller, Anna J Oostra, Beth A Pletcher, David Ros-Pardo, Shanika R Samarasekera, Tartaglia Marco, Kristof Van Schil, Julie Vogt, Evangeline Wassmer, Juliane Winkelmann, Maha Saad Zaki, Michael Zech, Holger Lerche, Francesca Clementina Radio, Paulino Gómez-Puertas, Rikke Steensjerre Moller, Zeynep Tümer
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Clinical genetics 102 (2) (2022)
Maria João Malaquias, Francesca Magrinelli, Andrea Quattrone, Ray Jen Neo, Anna Latorre, Eoin Mulroy, Kailash P Bhatia
Presynaptic Hemiparkinsonism Following Cerebral Toxoplasmosis: Case Report and Literature Review. Movement disorders clinical practice 10 (2) (2022)
Francesca Magrinelli, Niccolò Emanuele Mencacci
Digging into the Unknowns of the Human Genome Sequence: The T2T-CHM13 Reference Assembly Release. Movement disorders : official journal of the Movement Disorder Society 37 (11) (2022)
Elena Antelmi, Lorenzo Rocchi, Anna Latorre, Daniele Belvisi, Francesca Magrinelli, Kailash P Bhatia, Michele Tinazzi
Restless Legs Syndrome: Known Knowns and Known Unknowns. Brain sciences 12 (1) (2022)
Shahedah Koya Kutty, Francesca Magrinelli, Anna Vera Milner, Kailash P Bhatia
Abnormal DaTscan in GM1-Gangliosidosis Type III Manifesting with Dystonia-Parkinsonism. Movement disorders clinical practice 9 (6) (2022)
Francesca Magrinelli, Elisa Cali, Vinícius Lopes Braga, Uluç Yis, Hoda Tomoum, Hanan Shamseldin, Julian Raiman, Christoph Kernstock, Flavio Moura Rezende Filho, Orlando Graziani Povoas Barsottini, Robert W Taylor, Elsebet Østergaard, Abdullah Tamim, Karin Schäferhoff, Juliana Maria Ferraz Sallum, Maha S Zaki, Fernando Kok, Kailash P Bhatia, Bernd Wissinger, Kate Sergeant, Tobias B Haack, Rita Horvath, Semra Hiz, Fowzan S Alkuraya, Henry Houlden, José Luiz Pedroso, Reza Maroofian
Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. Movement disorders clinical practice 9 (2) (2022)
Francesca Magrinelli, Kailash P Bhatia, Mehran Beiraghi Toosi, Fatemeh Arab, Ehsan Ghayoor Karimiani, Sahar Sedighzadeh, Behnaz Ansari, Maedeh Neshatdoust, Clarissa Rocca, Henry Houlden, Reza Maroofian
Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Movement disorders clinical practice 10 (1) (2022)
Francesca Magrinelli, Kailash P Bhatia, Mehran Beiraghi Toosi, Fatemeh Arab, Ehsan Ghayoor Karimiani, Sahar Sedighzadeh, Behnaz Ansari, Maedeh Neshatdoust, Clarissa Rocca, Henry Houlden, Reza Maroofian
Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Movement disorders clinical practice 10 (1) (2022)
Ishani Rajapakshe, Eoin Mulroy, Francesca Magrinelli, Chulika Makawita, Kailash P Bhatia, Bimsara Senanayake
Cranial Dystonia as an Isolated Presentation of DJ-1 Disease: Case Report and Literature Review. Movement disorders clinical practice 10 (2) (2022)
Francesca Magrinelli, Kailash P Bhatia, Mehran Beiraghi Toosi, Fatemeh Arab, Ehsan Ghayoor Karimiani, Sahar Sedighzadeh, Behnaz Ansari, Maedeh Neshatdoust, Clarissa Rocca, Henry Houlden, Reza Maroofian
Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Movement disorders clinical practice 10 (1) (2022)
Francesca Magrinelli, Katja Lohmann
PRKRAP1 and Other Pseudogenes in Movement Disorders: The Troublemakers in Genetic Analyses Are More Than Genomic Fossils. Movement disorders clinical practice 9 (5) (2022)
Ishani Rajapakshe, Eoin Mulroy, Francesca Magrinelli, Chulika Makawita, Kailash P Bhatia, Bimsara Senanayake
Cranial Dystonia as an Isolated Presentation of DJ-1 Disease: Case Report and Literature Review. Movement disorders clinical practice 10 (2) (2022)
Francesca Magrinelli, Ishani Rajapaksha, Christopher Kobylecki, Anna Latorre, Eoin Mulroy, Carlos Estevez-Fraga, Henry Houlden, Michele Tinazzi, Kailash P Bhatia
Reply to: Juvenile PLA2G6-parkinsonism due to Indian 'Asian' p.R741Q mutation, and response to STN DBS. Movement disorders : official journal of the Movement Disorder Society 37 (3) (2022)
Maria João Malaquias, Francesca Magrinelli, Andrea Quattrone, Ray Jen Neo, Anna Latorre, Eoin Mulroy, Kailash P Bhatia
Presynaptic Hemiparkinsonism Following Cerebral Toxoplasmosis: Case Report and Literature Review. Movement disorders clinical practice 10 (2) (2022)
Maria João Malaquias, Francesca Magrinelli, Kailash P Bhatia
Breakthrough News in Adenoviral Vector-Mediated AADC Gene Therapy: Lessons from the Success in AADC Deficiency and Possible Future Applications. Movement disorders clinical practice 9 (6) (2022)
Francesca Magrinelli, Clarissa Rocca, Roberto Simone, Riccardo Zenezini Chiozzi, Zane Jaunmuktane, Niccolò Emanuele Mencacci, Michele Tinazzi, Sandeep Jayawant, Andrea H Nemeth, German Demidov, Henry Houlden, Kailash P Bhatia
Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2-1-Related Disorder. Movement disorders : official journal of the Movement Disorder Society (2022)
Riccardo Currò, Alessandro Salvalaggio, Stefano Tozza, Chiara Gemelli, Natalia Dominik, Valentina Galassi Deforie, Francesca Magrinelli, Francesca Castellani, Elisa Vegezzi, Pietro Businaro, Ilaria Callegari, Anna Pichiecchio, Giuseppe Cosentino, Enrico Alfonsi, Enrico Marchioni, Silvia Colnaghi, Simone Gana, Enza Maria Valente, Cristina Tassorelli, Stephanie Efthymiou, Stefano Facchini, Aisling Carr, Matilde Laura, Alexander M Rossor, Hadi Manji, Michael P T Lunn, Elena Pegoraro, Lucio Santoro, Marina Grandis, Emilia Bellone, Nicholas J Beauchamp, Marios Hadjivassiliou, Diego Kaski, Adolfo M Bronstein, Henry Houlden, Mary M Reilly, Paola Mandich, Angelo Schenone, Fiore Manganelli, Chiara Briani, Andreas Cortese
RFC1 expansions are a common cause of idiopathic sensory neuropathy. Brain : a journal of neurology 144 (5) (2021)
Francesca Magrinelli, Dalila Moualek, Meriem Tazir, Lamia Ali Pacha, Alice Verghese, Kailash P Bhatia, Reza Maroofian, Henry Houlden
Heterozygous EIF2AK2 Variant Causes Adolescence-Onset Generalized Dystonia Partially Responsive to DBS. Movement disorders clinical practice 9 (2) (2021)
Francesca Magrinelli, Sara Mariotto, Gianpaolo Nadali, Giuseppe Todeschini, Massimiliano Lanzafame, Tiziana Cavallaro, Salvatore Monaco, Sergio Ferrari
A 58-year-old man with B-cell chronic lymphocytic leukemia and multiple strokes. Brain pathology (Zurich, Switzerland) 31 (6) (2021)
Niccolò Emanuele Mencacci, Dora Steel, Francesca Magrinelli, Jerry Hsu, Ignacio Juan Keller Sarmiento, Mónica Troncoso Schifferli, Daniela Muñoz, Leonidas Stefanis, Steven J Lubbe, Nicholas W Wood, Manju A Kurian, Maria Stamelou
Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant. Movement disorders : official journal of the Movement Disorder Society 36 (6) (2021)
Eoin Mulroy, Andreea Ilinca, Cristina Gonzalez-Robles, Francesca Magrinelli, Andreas Puschmann, Kailash P Bhatia
Throat-Clearing Vocalizations in Primary Brain Calcification Syndromes. Movement disorders clinical practice 8 (4) (2021)
Giulia Di Lazzaro, Francesca Magrinelli, Carlos Estevez-Fraga, Enza Maria Valente, Antonio Pisani, Kailash P Bhatia
X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity. Movement disorders : official journal of the Movement Disorder Society 36 (7) (2021)
Francesca Magrinelli, Bettina Balint, Kailash P Bhatia
Challenges in Clinicogenetic Correlations: One Gene - Many Phenotypes. Movement disorders clinical practice 8 (3) (2021)
Carlos Estevez-Fraga, Francesca Magrinelli, Davina Hensman Moss, Eoin Mulroy, Giulia Di Lazzaro, Anna Latorre, Melissa Mackenzie, Henry Houlden, Sarah J Tabrizi, Kailash P Bhatia
Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions. Neurology. Genetics 7 (2) (2021)
Eoin Mulroy, Francesca Baschieri, Francesca Magrinelli, Anna Latorre, Pietro Cortelli, Kailash P Bhatia
Movement Disorders and Liver Disease. Movement disorders clinical practice 8 (6) (2021)
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, Anna Latorre, Mark J Edwards, Bettina Balint, Purba Basu, Christopher Kobylecki, Sergiu Groppa, Anaita Hegde, Eoin Mulroy, Carlos Estevez-Fraga, Anshita Arora, Hrishikesh Kumar, Susanne A Schneider, Patrick A Lewis, Zane Jaunmuktane, Tamas Revesz, Sonia Gandhi, Nicholas W Wood, John A Hardy, Michele Tinazzi, Vivek Lal, Henry Houlden, Kailash P Bhatia
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism. Movement disorders : official journal of the Movement Disorder Society (2021)
Giulia Di Lazzaro, Francesca Magrinelli, Christos Ganos, Kailash P Bhatia
The Need to Tic. Movement disorders clinical practice 7 (7) (2020)
Bettina Balint, Joana Damasio, Francesca Magrinelli, Rita Guerreiro, Jose Bras, Kailash P Bhatia
Psychiatric Manifestations of ATP13A2 Mutations. Movement disorders clinical practice 7 (7) (2020)
Shahedah Koya Kutty, Giulia Di Lazzaro, Francesca Magrinelli, Eoin Mulroy, Anna Latorre, Kailash P Bhatia
Late-Onset Chorea in JAK2-Associated Essential Thrombocythemia. Movement disorders clinical practice 8 (1) (2020)
Daniele Belvisi, Roberta Pellicciari, Andrea Fabbrini, Matteo Costanzo, Sara Pietracupa, Maria De Lucia, Nicola Modugno, Francesca Magrinelli, Carlo Dallocchio, Tommaso Ercoli, Claudio Terravecchia, Alessandra Nicoletti, Paolo Solla, Giovanni Fabbrini, Michele Tinazzi, Alfredo Berardelli, Giovanni Defazio
Risk factors of Parkinson disease: Simultaneous assessment, interactions, and etiologic subtypes. Neurology 95 (18) (2020)
Francesca Magrinelli, Michele Tinazzi, Kailash P Bhatia
Toward an Early Real-Time Quaking-Induced Conversion-Based Diagnostic Biomarker for Lewy Body-Related Synucleinopathies. Movement disorders clinical practice 7 (7) (2020)
Francesca Magrinelli, Eoin Mulroy, Susanne A Schneider, Anna Latorre, Giulia Di Lazzaro, Anita Hennig, Stephanie Grünewald, Darryl C De Vivo, Kailash P Bhatia
Criss-cross gait: A clue to glucose transporter type 1 deficiency syndrome. Neurology 95 (11) (2020)
Eoin Mulroy, Anna Latorre, Francesca Magrinelli, Kailash P Bhatia
Ciliary Dysfunction: The Hairy Explanation of Normal Pressure Hydrocephalus? Movement disorders clinical practice 7 (1) (2019)
Francesca Magrinelli, Ruggero Bacchin, Michele Tinazzi, Mattia Gambarin
Twelve-year Follow-up of A Large Italian Family with Atypical Phenotypes of DYT1-dystonia. Movement disorders clinical practice 6 (2) (2018)
Francesca Magrinelli, Alessandro Picelli, Pierluigi Tocco, Angela Federico, Laura Roncari, Nicola Smania, Giampietro Zanette, Stefano Tamburin
Pathophysiology of Motor Dysfunction in Parkinson's Disease as the Rationale for Drug Treatment and Rehabilitation. Parkinson's disease 2016 (2016)

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Francesca Magrinelli