H
Hadi Manji
Researcher at UCL Institute of Neurology
Publications - 22
Citations - 1394
Hadi Manji is an academic researcher from UCL Institute of Neurology. The author has contributed to research in topics: Chronic inflammatory demyelinating polyneuropathy & Peripheral neuropathy. The author has an hindex of 10, co-authored 22 publications receiving 865 citations. Previous affiliations of Hadi Manji include University College London.
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Journal ArticleDOI
Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study.
Aravinthan Varatharaj,Aravinthan Varatharaj,Naomi Thomas,Mark Ellul,Mark Ellul,Mark Ellul,Nicholas W. S. Davies,Thomas A Pollak,Elizabeth L Tenorio,Mustafa Sultan,Ava Easton,Gerome Breen,Michael S. Zandi,Jonathan P. Coles,Hadi Manji,Rustam Al-Shahi Salman,David K. Menon,Timothy R Nicholson,Laura A Benjamin,Laura A Benjamin,Alan Carson,Craig J. Smith,Martin R Turner,Tom Solomon,Tom Solomon,Tom Solomon,Rachel Kneen,Rachel Kneen,Sarah Pett,Ian Galea,Ian Galea,Rhys H. Thomas,Rhys H. Thomas,Benedict D Michael,Benedict D Michael,Benedict D Michael,Claire Allen,Neil Archibald,James Arkell,Peter Arthur-Farraj,Mark R. Baker,Harriet A. Ball,Verity Bradley-Barker,Zoe Brown,Stefania Bruno,Lois Carey,Christopher Carswell,Annie Chakrabarti,James Choulerton,Mazen Daher,Ruth Davies,Rafael Di Marco Barros,Sofia Dima,Rachel Dunley,Dipankar Dutta,Richard James Booth Ellis,Alex Everitt,Joseph Fady,Patricia Fearon,Leonora Fisniku,Ivie Gbinigie,Alan Gemski,Emma Gillies,Effrossyni Gkrania-Klotsas,Julie Grigg,Hisham Hamdalla,Jack Hubbett,Neil Hunter,Anne-Catherine Huys,Ihmoda Ihmoda,Sissi Ispoglou,Ashwani Jha,Ramzi Joussi,Dheeraj Kalladka,Hind Khalifeh,Sander Kooij,Guru Kumar,Sandar Kyaw,Lucia Li,Edward Littleton,Malcolm R. Macleod,Mary Joan MacLeod,Barbara Madigan,Vikram Mahadasa,Manonmani Manoharan,Richard Marigold,Isaac Marks,Paul M. Matthews,Michael Mccormick,Caroline Mcinnes,Antonio Metastasio,Philip Milburn-McNulty,Clinton Mitchell,Duncan Mitchell,Clare Morgans,Huw R. Morris,Jasper M. Morrow,Ahmed Mubarak Mohamed,Paula Mulvenna,Louis Murphy,Robert Namushi,Edward J Newman,Wendy Phillips,Ashwin Pinto,David A Price,Harald Proschel,Terry Quinn,Deborah Ramsey,Christine Roffe,Amy L Ross Russell,Neshika Samarasekera,Stephen Sawcer,Walee Sayed,Lakshmanan Sekaran,Jordi Serra-Mestres,Victoria K. Snowdon,Gayle Strike,James Sun,Christina Tang,Mark Vrana,Ryckie G. Wade,Chris Wharton,Lou Wiblin,Iryna Boubriak,Katie Herman,Gordon T. Plant +125 more
TL;DR: This is the first nationwide, cross-specialty surveillance study of acute neurological and psychiatric complications of COVID-19 and provides valuable and timely data that are urgently needed by clinicians, researchers, and funders.
Journal ArticleDOI
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort
Gabrielle L. Davidson,Sinéad M. Murphy,James M. Polke,Matilde Laura,M. A. Mohamed Salih,Francesco Muntoni,Julian Blake,Sebastian Brandner,NP Davies,Rita Horvath,S. Price,Michael Donaghy,Mark Roberts,Nicola Foulds,Gita Ramdharry,Doriette Soler,Michael P. Lunn,Hadi Manji,Mary B. Davis,Henry Houlden,Mary M. Reilly +20 more
TL;DR: Mutations in the known genes for HSAN are rare suggesting that further HSAN genes are yet to be identified, and the p.Cys133Trp mutation in SPTLC1 is the most common cause of HSAN.
Journal ArticleDOI
Tremor in inflammatory neuropathies
Tabish A. Saifee,Petra Schwingenschuh,Petra Schwingenschuh,Mary M. Reilly,Michael P. Lunn,Petra Katschnig,Petra Katschnig,Panagiotis Kassavetis,Isabel Pareés,Hadi Manji,Kailash P. Bhatia,John C. Rothwell,Mark J. Edwards +12 more
TL;DR: Evidence that tremor may add to disability in patients with inflammatory neuropathy is provided and it is demonstrated for the first time that although tremor severity correlates with F wave latency, it is not sufficient to distinguish those with, from those without, tremor.
Journal ArticleDOI
RFC1 expansions are a common cause of idiopathic sensory neuropathy.
Riccardo Currò,Alessandro Salvalaggio,Stefano Tozza,Chiara Gemelli,Natalia Dominik,Valentina Galassi Deforie,Francesca Magrinelli,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. Lunn,Elena Pegoraro,Lucio Santoro,Marina Grandis,Emilia Bellone,Nicholas J. Beauchamp,Marios Hadjivassiliou,Diego Kaski,Diego Kaski,Adolfo M. Bronstein,Henry Houlden,Mary M. Reilly,Paola Mandich,Angelo Schenone,Fiore Manganelli,Chiara Briani,Andrea Cortese,Andrea Cortese +43 more
TL;DR: In this article, the authors reported that RFC1 expansions could underlie a fraction of idiopathic sensory neuropathies also diagnosed as chronic axonal polyneuropathy, referred to a sensory or sensory-motor, axonal, slowly progressive neuropathy of unknown origin.
Journal ArticleDOI
Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease.
Alejandro Horga,Matilde Laura,Zane Jaunmuktane,Nivedita U. Jerath,Michael A. Gonzalez,James M. Polke,Roy Poh,Julian Blake,Yo Tsen Liu,Yo Tsen Liu,Sarah Wiethoff,Conceição Bettencourt,Michael P. Lunn,Hadi Manji,Michael G. Hanna,Henry Houlden,Sebastian Brandner,Stephan Züchner,Michael E. Shy,Michael E. Shy,Mary M. Reilly +20 more
TL;DR: NEFL-related CMT is clinically and genetically heterogeneous and mutational hotspots and relevant clinical–genetic associations that may be helpful in the evaluation of NEFL sequence variants and the differential diagnosis with other forms of CMT are proposed.