Manju A Kurian (M A Kurian, Manju Kurian)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 52

Top Topics

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Movement disorders clinical practice

Developmental medicine and child neurology

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

Publications

Robert V V Spaull, Audrey K Soo, Spyros Batzios, Emma Footitt, Rebecca Whiteley, Jonathan W Mink, Lucinda Carr, Paul Gissen, Manju A Kurian
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement Therapy. Neurology 103 (3) (2024)
Wing Sum Chu, Joanne Ng, Simon N Waddington, Manju A Kurian
Gene therapy for neurotransmitter-related disorders. Journal of inherited metabolic disease 47 (1) (2024)
Wing Sum Chu, Joanne Ng, Simon N Waddington, Manju A Kurian
Gene therapy for neurotransmitter-related disorders. Journal of inherited metabolic disease 47 (1) (2024)
Jill Cadwgan, Jane Goodwin, Barbara Babcock, Molly Brick, Richard F M Chin, Ava Easton, Ben Green, Siobhan Hannan, Rhys P D Inward, Suzannah Kinsella, Callum King, Manju A Kurian, Phillip Levine, Andrew A Mallick, Jeremy R Parr, Carol Anne Partridge, Sam Amin, Daniel E Lumsden, Judith Helen Cross, Ming J Lim, null null
UK research priority setting for childhood neurological conditions. Developmental medicine and child neurology (2024)
Ainara Salazar-Villacorta, Robert V V Spaull, Samyami Chowdhury, Bina Mukhtyar, Manali Chitre, Ruth Armstrong, Mario Sa, Saleel Chandratre, Usha Kini, Ravi Chinthapalli, Kshitij Mankad, Sniya Sudhakar, Simon Pope, Simon Heales, Manju A Kurian
Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology. Movement disorders clinical practice (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice 11 (6) (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice 11 (6) (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice 11 (6) (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice (2024)
Wing Sum Chu, Joanne Ng, Simon N Waddington, Manju A Kurian
Gene therapy for neurotransmitter-related disorders. Journal of inherited metabolic disease 47 (1) (2024)
Robert V V Spaull, Audrey K Soo, Spyros Batzios, Emma Footitt, Rebecca Whiteley, Jonathan W Mink, Lucinda Carr, Paul Gissen, Manju A Kurian
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement Therapy. Neurology 103 (3) (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice 11 (6) (2024)
Jonna Komulainen-Ebrahim, Salla M Kangas, Estrella López-Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez-Delgado, Outi Kuismin, Maria Suo-Palosaari, Lucinda Carr, Reetta Hinttala, Manju A Kurian, Johanna Uusimaa
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Movement disorders clinical practice 11 (6) (2024)
Blas Couto, Serena Galosi, Dora Steel, Manju A Kurian, Jennifer Friedman, Carolina Gorodetsky, Anthony E Lang
Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Robert V V Spaull, Audrey K Soo, Spyros Batzios, Emma Footitt, Rebecca Whiteley, Jonathan W Mink, Lucinda Carr, Paul Gissen, Manju A Kurian
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement Therapy. Neurology 103 (3) (2024)
Wing Sum Chu, Joanne Ng, Simon N Waddington, Manju A Kurian
Gene therapy for neurotransmitter-related disorders. Journal of inherited metabolic disease 47 (1) (2024)
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, Tiziana Pisano, Laloe Monteiro, Noémie Penaud, Christian M Korff, Joël Fluss, Carla Marini, Elisabetta Cesaroni, Blanca Mercedes Alvarez, Damien Sanlaville, Nicolas Chatron, Alexis A Arzimanoglou, Audrey Labalme, Vishnu Anand Cuddapah, Sarah M Ruggiero, Francois Lecoquierre, Gaël Nicolas, Guerrot Anne Marie, Axel Lebas, Herve O Testard, Katherine L Helbig, Anna Ruiz, Adeline Ngoh, Manju A Kurian, Kimberley Reid, Robert V V Spaull, Pascal Joset, Georgia Ramantani, Katharina Steindl, Martin Krenn, Lucia Gerstl, Silvia Vieker, Dana Craiu, Manuela Pendziwiat, Chad Haldeman-Englert, Ilya V Kanivets, Irina Romanova, Deepa S Rajan, Jill Anne Rosenfeld, Margaret Au, Katheryn Lynn Grand, John M Graham, Arnaud Isapof, Nathalie Villeneuve, Thomas Smol, Roseline Caumes, Pia Zacher, Sonja Neuser, Sigrid Tinschert, Konrad Platzer, Bartolomaeus Tobias, Ines Mohnke, Maximilian Radtke, Rami Abou Jamra, Ingo Helbig, Floortje E Jansen, Klaas Koop, Gabrielle Rudolf, Sébastien Küry, Julien Courchet, Renzo Guerrini, Gaëtan Lesca
Molecular and Phenotypic Characterization of the RORB -Related Disorder. Neurology 102 (2) (2023)
Joanne Ng, Serena Barral, Simon N Waddington, Manju A Kurian
Gene Therapy for Dopamine Dyshomeostasis: From Parkinson's to Primary Neurotransmitter Diseases. Movement disorders : official journal of the Movement Disorder Society (2023)
Simon N Waddington, William H Peranteau, Ahad Abdul Rahim, Ashley K Boyle, Manju A Kurian, Paul Gissen, Jerry K Y Chan, Anna Louise David
Fetal gene therapy. Journal of inherited metabolic disease (2023)
Joanne Ng, Serena Barral, Simon N Waddington, Manju A Kurian
Gene Therapy for Dopamine Dyshomeostasis: From Parkinson's to Primary Neurotransmitter Diseases. Movement disorders : official journal of the Movement Disorder Society (2023)
Philip Harrer, Matej Skorvanek, Volker Kittke, Ivana Dzinovic, Friederike Borngräber, Mirja Thomsen, Vanessa Mandel, Tatiana Svorenova, Miriama Ostrozovicova, Kristina Kulcsarova, Riccardo Berutti, Hauke Busch, Fabian Ott, Robert Kopajtich, Holger Prokisch, Kishore Raj Kumar, Niccolò Emanuele Mencacci, Manju A Kurian, Alessio di Fonzo, Sylvia Boesch, Andrea A Kühn, Ulrike Blümlein, Katja Lohmann, Bernhard Haslinger, David Weise, Robert Jech, Juliane Winkelmann, Michael Zech
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation Dysfunction. Movement disorders : official journal of the Movement Disorder Society (2023)
Tamara M Pringsheim, Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi-Fakhari, Jennifer Friedman, Jean-Pierre Lin, Jonathan W Mink, Alexander Münchau, Daniela Munoz, Nardo Nardocci, Belen Perez-Duenas, Zomer Sardar, Chahnez Charfi Triki, Hilla Ben-Pazi, Laura Silveira-Moriyama, Monica Troncoso-Schifferli, Kyoko Hoshino, Russell C Dale, Victor S C Fung, Manju A Kurian, Emmanuel Roze
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on Pediatrics. Movement disorders clinical practice 10 (5) (2023)
Lisette H Koens, Marrit R Klamer, Deborah A Sival, Bettina Balint, Kailash P Bhatia, Maria Fiorella Contarino, Martje E van Egmond, Roberto Erro, Jennifer Friedman, Victor S C Fung, Christos Ganos, Manju A Kurian, Anthony E Lang, Eavan M McGovern, Emmanuel Roze, Tom J de Koning, Marina A J Tijssen
A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism. Movement disorders : official journal of the Movement Disorder Society (2023)
Tamara M Pringsheim, Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi-Fakhari, Jennifer Friedman, Jean-Pierre Lin, Jonathan W Mink, Alexander Münchau, Daniela Munoz, Nardo Nardocci, Belen Perez-Duenas, Zomer Sardar, Chahnez Charfi Triki, Hilla Ben-Pazi, Laura Silveira-Moriyama, Monica Troncoso-Schifferli, Kyoko Hoshino, Russell C Dale, Victor S C Fung, Manju A Kurian, Emmanuel Roze
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on Pediatrics. Movement disorders clinical practice 10 (5) (2023)
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, Tiziana Pisano, Laloe Monteiro, Noémie Penaud, Christian M Korff, Joël Fluss, Carla Marini, Elisabetta Cesaroni, Blanca Mercedes Alvarez, Damien Sanlaville, Nicolas Chatron, Alexis A Arzimanoglou, Audrey Labalme, Vishnu Anand Cuddapah, Sarah M Ruggiero, Francois Lecoquierre, Gaël Nicolas, Guerrot Anne Marie, Axel Lebas, Herve O Testard, Katherine L Helbig, Anna Ruiz, Adeline Ngoh, Manju A Kurian, Kimberley Reid, Robert V V Spaull, Pascal Joset, Georgia Ramantani, Katharina Steindl, Martin Krenn, Lucia Gerstl, Silvia Vieker, Dana Craiu, Manuela Pendziwiat, Chad Haldeman-Englert, Ilya V Kanivets, Irina Romanova, Deepa S Rajan, Jill Anne Rosenfeld, Margaret Au, Katheryn Lynn Grand, John M Graham, Arnaud Isapof, Nathalie Villeneuve, Thomas Smol, Roseline Caumes, Pia Zacher, Sonja Neuser, Sigrid Tinschert, Konrad Platzer, Bartolomaeus Tobias, Ines Mohnke, Maximilian Radtke, Rami Abou Jamra, Ingo Helbig, Floortje E Jansen, Klaas Koop, Gabrielle Rudolf, Sébastien Küry, Julien Courchet, Renzo Guerrini, Gaëtan Lesca
Molecular and Phenotypic Characterization of the RORB -Related Disorder. Neurology 102 (2) (2023)
Tamara M Pringsheim, Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi-Fakhari, Jennifer Friedman, Jean-Pierre Lin, Jonathan W Mink, Alexander Münchau, Daniela Munoz, Nardo Nardocci, Belen Perez-Duenas, Zomer Sardar, Chahnez Charfi Triki, Hilla Ben-Pazi, Laura Silveira-Moriyama, Monica Troncoso-Schifferli, Kyoko Hoshino, Russell C Dale, Victor S C Fung, Manju A Kurian, Emmanuel Roze
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on Pediatrics. Movement disorders clinical practice 10 (5) (2023)
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, Tiziana Pisano, Laloe Monteiro, Noémie Penaud, Christian M Korff, Joël Fluss, Carla Marini, Elisabetta Cesaroni, Blanca Mercedes Alvarez, Damien Sanlaville, Nicolas Chatron, Alexis A Arzimanoglou, Audrey Labalme, Vishnu Anand Cuddapah, Sarah M Ruggiero, Francois Lecoquierre, Gaël Nicolas, Guerrot Anne Marie, Axel Lebas, Herve O Testard, Katherine L Helbig, Anna Ruiz, Adeline Ngoh, Manju A Kurian, Kimberley Reid, Robert V V Spaull, Pascal Joset, Georgia Ramantani, Katharina Steindl, Martin Krenn, Lucia Gerstl, Silvia Vieker, Dana Craiu, Manuela Pendziwiat, Chad Haldeman-Englert, Ilya V Kanivets, Irina Romanova, Deepa S Rajan, Jill Anne Rosenfeld, Margaret Au, Katheryn Lynn Grand, John M Graham, Arnaud Isapof, Nathalie Villeneuve, Thomas Smol, Roseline Caumes, Pia Zacher, Sonja Neuser, Sigrid Tinschert, Konrad Platzer, Bartolomaeus Tobias, Ines Mohnke, Maximilian Radtke, Rami Abou Jamra, Ingo Helbig, Floortje E Jansen, Klaas Koop, Gabrielle Rudolf, Sébastien Küry, Julien Courchet, Renzo Guerrini, Gaëtan Lesca
Molecular and Phenotypic Characterization of the RORB -Related Disorder. Neurology 102 (2) (2023)
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, Tiziana Pisano, Laloe Monteiro, Noémie Penaud, Christian M Korff, Joël Fluss, Carla Marini, Elisabetta Cesaroni, Blanca Mercedes Alvarez, Damien Sanlaville, Nicolas Chatron, Alexis A Arzimanoglou, Audrey Labalme, Vishnu Anand Cuddapah, Sarah M Ruggiero, Francois Lecoquierre, Gaël Nicolas, Guerrot Anne Marie, Axel Lebas, Herve O Testard, Katherine L Helbig, Anna Ruiz, Adeline Ngoh, Manju A Kurian, Kimberley Reid, Robert V V Spaull, Pascal Joset, Georgia Ramantani, Katharina Steindl, Martin Krenn, Lucia Gerstl, Silvia Vieker, Dana Craiu, Manuela Pendziwiat, Chad Haldeman-Englert, Ilya V Kanivets, Irina Romanova, Deepa S Rajan, Jill Anne Rosenfeld, Margaret Au, Katheryn Lynn Grand, John M Graham, Arnaud Isapof, Nathalie Villeneuve, Thomas Smol, Roseline Caumes, Pia Zacher, Sonja Neuser, Sigrid Tinschert, Konrad Platzer, Bartolomaeus Tobias, Ines Mohnke, Maximilian Radtke, Rami Abou Jamra, Ingo Helbig, Floortje E Jansen, Klaas Koop, Gabrielle Rudolf, Sébastien Küry, Julien Courchet, Renzo Guerrini, Gaëtan Lesca
Molecular and Phenotypic Characterization of the RORB -Related Disorder. Neurology 102 (2) (2023)
Kimberley M Reid, Robert V V Spaull, Smrithi Salian, Katy Barwick, Esther Meyer, Juan Zhen, Hiromi Hirata, Diba Sheipouri, Hind Benkerroum, Kathleen M Gorman, Apostolos Papandreou, Michael A Simpson, Yoshinobu Hirano, Irene Farabella, Andriy Kryshtafovych, Detelina Grozeva, Keren Jacqueline Carss, Martin Smith, Hardev Pall, Peter Lunt, Susanna De Gressi, Erik-Jan Kamsteeg, Tobias B Haack, Lucinda J Carr, Rita Guerreiro, Jose Bras, Eamonn R Maher, Richard H Scott, Robert J Vandenberg, F Lucy Raymond, Wui K Chong, Sniya Valsa Sudhakar, Kshitij Mankad, Maarten E A Reith, Philippe M Campeau, Robert J Harvey, Manju A Kurian
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia. Movement disorders : official journal of the Movement Disorder Society 37 (10) (2022)
Apostolos Papandreou, Ivan Doykov, Justyna Spiewak, Nikita Komarov, Stephanie Habermann, Manju A Kurian, Philippa B Mills, Kevin A Mills, Paul Gissen, Wendy E Heywood, null null
Niemann-Pick type C disease as proof-of-concept for intelligent biomarker panel selection in neurometabolic disorders. Developmental medicine and child neurology 64 (12) (2022)
Dora Batia Dyne Steel, Aikaterini Vezyroglou, Katy Barwick, Martin Smith, Julie Vogt, Frances M Gibbon, J Helen Cross, Manju A Kurian
Both Heterozygous and Homozygous Loss-of-Function JPH3 Variants Are Associated with a Paroxysmal Movement Disorder. Movement disorders : official journal of the Movement Disorder Society (2022)
Amit Batla, Jean-Pierre Lin, Jitendra K Sahu, Jonathan W Mink, Tamara M Pringsheim, Emmanuel Roze, Manju A Kurian, Victor S C Fung
Transition Services for Children and Young Adults with Movement Disorders: A Survey by the MDS Task Force on Pediatrics. Movement disorders clinical practice 9 (7) (2022)
Apostolos Papandreou, Audrey K S Soo, Robert V V Spaull, Kshitij Mankad, Manju A Kurian, Sniya Valsa Sudhakar
Expanding the Spectrum of Early Neuroradiologic Findings in β Propeller Protein-Associated Neurodegeneration. AJNR. American journal of neuroradiology (2022)
Thomas Wirth, Giacomo Garone, Manju A Kurian, Amélie Piton, Emmanuel Roze, Jean-Pierre Lin, Christine Tranchant, Laura Cif, Diane Doummar, Mathieu Anheim
Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype". Movement disorders : official journal of the Movement Disorder Society 37 (12) (2022)
Belen Perez-Duenas, Kathleen Gorman, Anna Marcé-Grau, Juan D Ortigoza-Escobar, Alfons Macaya, Federica R Danti, Katy Barwick, Apostolos Papandreou, Joanne Ng, Esther Meyer, Shekeeb S Mohammad, Martin Smith, Francesco Muntoni, Pinki Munot, Johanna Uusimaa, Päivi Vieira, Eammon Sheridan, Renzo Guerrini, Jan Cobben, Sanem Yilmaz, Elisa De Grandis, Russell C Dale, Roser Pons, Kathryn J Peall, Vincenzo Leuzzi, Manju A Kurian
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders. Movement disorders : official journal of the Movement Disorder Society 37 (11) (2022)
Thomas Wirth, Giacomo Garone, Manju A Kurian, Amélie Piton, Francisca Millan, Aida Telegrafi, Nathalie Drouot, Gabrielle Rudolf, Jamel Chelly, Warren Marks, Lydie Burglen, Diane Demailly, Phillipe Coubes, Mayte Castro-Jimenez, Sylvie Joriot, Jamal Ghoumid, Jérémie Belin, Jean-Marc Faucheux, Lubov Blumkin, Mariam Hull, Mered Parnes, Claudia Ravelli, Gaëtan Poulen, Nadège Calmels, Andrea H Nemeth, Martin Smith, Angela Barnicoat, Claire Ewenczyk, Aurélie Méneret, Emmanuel Roze, Boris Keren, Cyril Mignot, Christophe Beroud, Fernando Acosta, Catherine Nowak, William G Wilson, Dora Steel, Alessandro Capuano, Marie Vidailhet, Jean-Pierre Lin, Christine Tranchant, Laura Cif, Diane Doummar, Mathieu Anheim
Highlighting the Dystonic Phenotype Related to GNAO1. Movement disorders : official journal of the Movement Disorder Society 37 (7) (2022)
Sunwoo Lee, Eguzkine Ochoa, Katy Barwick, Laura Cif, Fay Rodger, France Docquier, Belen Perez-Duenas, Graeme Clark, Ezequiel Martin, Siddharth Banka, Manju A Kurian, Eamonn R Maher
Comparison of methylation episignatures in KMT2B - and KMT2D -related human disorders. Epigenomics 14 (9) (2022)
Laura Cif, Diane Demailly, Xavier Vasques, Delphine de Verbizier, Philippe Coubes, Kathleen Gorman, Manju A Kurian
Freezing of Gait as a Complication of Pallidal Deep Brain Stimulation in DYT- KMT2B Patients with Evidence of Striatonigral Degeneration. Movement disorders clinical practice 9 (7) (2022)
Robert V V Spaull, Dora Steel, Katy Barwick, Prab Prabhakar, Emma Wakeling, Manju A Kurian
STXBP1 Stop-Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy. Movement disorders clinical practice 9 (6) (2022)
César Augusto Pinheiro Ferreira Alves, O Sherbini, F D'Arco, Dora Batia Dyne Steel, Manju A Kurian, F C Radio, Giovanbattista Giovanni Battista Ferrero, Diana Carli, Tartaglia Marco, Tuğçe B Balcı, N N Powell-Hamilton, S A Schrier Vergano, H Reutter, Julia Hoefele, R Günthner, Elizabeth R Roeder, R O Littlejohn, Davor Lessel, Sabine Peters, C Kentros, Kwame Anyane-Yeboa, Claudia B Catarino, Saadet Mercimek-Mahmutoglu, J Denecke, Michael J Lyons, Florentine Radelfahr, Elizabeth Joyce Bhoj, Laura Bryant, Adeline Vanderver
Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors. AJNR. American journal of neuroradiology 43 (7) (2022)
Thomas Wirth, Giacomo Garone, Manju A Kurian, Amélie Piton, Emmanuel Roze, Jean-Pierre Lin, Christine Tranchant, Laura Cif, Diane Doummar, Mathieu Anheim
Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia Phenotype". Movement disorders : official journal of the Movement Disorder Society 37 (12) (2022)
Michael Zech, Kishore R Kumar, Sophie Reining, Janine Reunert, Michel Tchan, Lisa G Riley, Alexander P Drew, Robert J Adam, Riccardo Berutti, Saskia Biskup, Nicolas Derive, Somayeh Bakhtiari, Sheng Chih Jin, Michael C Kruer, Tanya Bardakjian, Pedro Gonzalez-Alegre, Ignacio J Keller Sarmiento, Niccolò Emanuele Mencacci, Steven J Lubbe, Manju A Kurian, Fabienne Clot, Aurélie Méneret, Jean-Madeleine de Sainte Agathe, Victor S C Fung, Marie Vidailhet, Matthias Baumann, Thorsten Marquardt, Juliane Winkelmann, Sylvia Boesch
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb Involvement. Movement disorders : official journal of the Movement Disorder Society (2021)
Jennifer Friedman, Sara Lucas-Del-Pozo, David Moreno-Martinez, Maria Camprodon-Gomez, Daniel Moreno-Martinez, Jorge Hernandez-Vara, Manju A Kurian
Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life. Movement disorders clinical practice 8 (Suppl 1) (2021)
Robert V V Spaull, Audrey K S Soo, Penelope Hogarth, Susan J Hayflick, Manju A Kurian
Towards Precision Therapies for Inherited Disorders of Neurodegeneration with Brain Iron Accumulation. Tremor and other hyperkinetic movements (New York, N.Y.) 11 (2021)
Jenny L Wilson, Allison Gregory, Manju A Kurian, Ittai Bushlin, Fanny Mochel, Lisa Emrick, Laura Adang, null null, Penelope Hogarth, Susan J Hayflick
Consensus clinical management guideline for beta-propeller protein-associated neurodegeneration. Developmental medicine and child neurology 63 (12) (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)
Alice Lepelley, Erika Della Mina, Erika Van Nieuwenhove, Lise Waumans, Sylvie Fraitag, Gillian I Rice, Ashish Dhir, Marie-Louise Frémond, Mathieu Paul Rodero, Luis Seabra, Edwin Carter, Christine Bodemer, Daniela Buhas, Bert Callewaert, Pascale De Lonlay, Lien De Somer, David A Dyment, Fran Faes, Lucy Grove, Simon Holden, Marie Hully, Manju A Kurian, Hugh J Mcmillan, Kristin Suetens, Henna Tyynismaa, Stéphanie Chhun, Timothy Wai, Carine Wouters, Brigitte Bader-Meunier, Yanick J Crow
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A. The Journal of experimental medicine 218 (10) (2021)
Manju A Kurian, Rauan Kaiyrzhanov, Parvin Allahyarova, Ulviyya Guliyeva, Sughra Gulieva, Kamran Salayev, Aytan Mursalova, Matteo P Ferla, Henry Houlden, Francisco Eduardo Costa Cardoso
Commentary: GM1-Gangliosidosis Type III Associated Parkinsonism. Movement disorders clinical practice 8 (Suppl 1) (2021)
Anne Weissbach, Martje G Pauly, Rebecca Herzog, Lisa Hahn, Sara Halmans, Feline Hamami, Christina Bolte, Sarah Camargos, Beomseok Jeon, Manju A Kurian, Thomas Opladen, Norbert Brüggemann, Hans-Jürgen Huppertz, Inke R König, Christine Klein, Katja Lohmann
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review. Movement disorders : official journal of the Movement Disorder Society 37 (2) (2021)
Miriama Ostrozovicova, Robert Jech, Dora Steel, Petra Pavelekova, Vladimir Han, Zuzana Gdovinova, Peter Lichtner, Manju A Kurian, Sarah Wiethoff, Henry Houlden, Petra Havránková, Julianne Winkelmann, Michael Zech, Matej Skorvanek
A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia. Movement disorders : official journal of the Movement Disorder Society 36 (8) (2021)
Audrey K S Soo, Arianna Ferrini, Manju A Kurian
Precision medicine for genetic childhood movement disorders. Developmental medicine and child neurology 63 (8) (2021)
Apostolos Papandreou, Federica Rachele Danti, Robert V V Spaull, Vincenzo Leuzzi, Amy McTague, Manju A Kurian
The expanding spectrum of movement disorders in genetic epilepsies. Developmental medicine and child neurology 62 (2) (2019)