Monoamine neurotransmitter disorders--clinical advances and future perspectives
Ng, Joanne, Papandreou, Apostolos, Heales, Simon J, Kurian, Manju A
Published in Nature reviews. Neurology (01.10.2015)
Published in Nature reviews. Neurology (01.10.2015)
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Journal Article
Nanotechnology-Assisted Metered-Dose Inhalers (MDIs) for High-Performance Pulmonary Drug Delivery Applications
Kumar, Raj, Mehta, Piyush, Shankar, Konathala Ravi, Rajora, Manju A. K., Mishra, Yogendra Kumar, Mostafavi, Ebrahim, Kaushik, Ajeet
Published in Pharmaceutical research (01.11.2022)
Published in Pharmaceutical research (01.11.2022)
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Journal Article
Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA
Haack, Tobias B., Hogarth, Penelope, Kruer, Michael C., Gregory, Allison, Wieland, Thomas, Schwarzmayr, Thomas, Graf, Elisabeth, Sanford, Lynn, Meyer, Esther, Kara, Eleanna, Cuno, Stephan M., Harik, Sami I., Dandu, Vasuki H., Nardocci, Nardo, Zorzi, Giovanna, Dunaway, Todd, Tarnopolsky, Mark, Skinner, Steven, Frucht, Steven, Hanspal, Era, Schrander-Stumpel, Connie, Héron, Delphine, Mignot, Cyril, Garavaglia, Barbara, Bhatia, Kailash, Hardy, John, Strom, Tim M., Boddaert, Nathalie, Houlden, Henry H., Kurian, Manju A., Meitinger, Thomas, Prokisch, Holger, Hayflick, Susan J.
Published in American journal of human genetics (07.12.2012)
Published in American journal of human genetics (07.12.2012)
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Journal Article
An Update on the Phenotype, Genotype and Neurobiology of ADCY5‐Related Disease
Ferrini, Arianna, Steel, Dora, Barwick, Katy, Kurian, Manju A.
Published in Movement disorders (01.05.2021)
Published in Movement disorders (01.05.2021)
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Journal Article
The role of manganese dysregulation in neurological disease: emerging evidence
Budinger, Dimitri, Barral, Serena, Soo, Audrey K S, Kurian, Manju A
Published in Lancet neurology (01.11.2021)
Published in Lancet neurology (01.11.2021)
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Journal Article
Neurodegeneration with brain iron accumulation
Hayflick, Susan J., Kurian, Manju A., Hogarth, Penelope
Published in Handbook of Clinical Neurology (2018)
Published in Handbook of Clinical Neurology (2018)
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Book Chapter
Journal Article
HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystonia
Monfrini, Edoardo, Zech, Michael, Steel, Dora, Kurian, Manju A, Winkelmann, Juliane, Di Fonzo, Alessio
Published in Brain (London, England : 1878) (22.10.2021)
Published in Brain (London, England : 1878) (22.10.2021)
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Journal Article
Gene Therapy for Dopamine Dyshomeostasis: From Parkinson's to Primary Neurotransmitter Diseases
Ng, Joanne, Barral, Serena, Waddington, Simon N., Kurian, Manju A.
Published in Movement disorders (01.06.2023)
Published in Movement disorders (01.06.2023)
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Journal Article
Correction: Nanotechnology-Assisted Metered-Dose Inhalers (MDIs) for High-Performance Pulmonary Drug Delivery Applications
Kumar, Raj, Mehta, Piyush, Shankar, Konathala Ravi, Rajora, Manju A. K., Mishra, Yogendra Kumar, Mostafavi, Ebrahim, Kaushik, Ajeet
Published in Pharmaceutical research (01.11.2022)
Published in Pharmaceutical research (01.11.2022)
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Journal Article
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis
Trump, Natalie, McTague, Amy, Brittain, Helen, Papandreou, Apostolos, Meyer, Esther, Ngoh, Adeline, Palmer, Rodger, Morrogh, Deborah, Boustred, Christopher, Hurst, Jane A, Jenkins, Lucy, Kurian, Manju A, Scott, Richard H
Published in Journal of medical genetics (01.05.2016)
Published in Journal of medical genetics (01.05.2016)
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Journal Article
The clinical and genetic heterogeneity of paroxysmal dyskinesias
Gardiner, Alice R, Jaffer, Fatima, Dale, Russell C, Labrum, Robyn, Erro, Roberto, Meyer, Esther, Xiromerisiou, Georgia, Stamelou, Maria, Walker, Matthew, Kullmann, Dimitri, Warner, Tom, Jarman, Paul, Hanna, Mike, Kurian, Manju A, Bhatia, Kailash P, Houlden, Henry
Published in Brain (London, England : 1878) (01.12.2015)
Published in Brain (London, England : 1878) (01.12.2015)
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Journal Article
Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation
Dusi, Sabrina, Valletta, Lorella, Haack, Tobias B., Tsuchiya, Yugo, Venco, Paola, Pasqualato, Sebastiano, Goffrini, Paola, Tigano, Marco, Demchenko, Nikita, Wieland, Thomas, Schwarzmayr, Thomas, Strom, Tim M., Invernizzi, Federica, Garavaglia, Barbara, Gregory, Allison, Sanford, Lynn, Hamada, Jeffrey, Bettencourt, Conceição, Houlden, Henry, Chiapparini, Luisa, Zorzi, Giovanna, Kurian, Manju A., Nardocci, Nardo, Prokisch, Holger, Hayflick, Susan, Gout, Ivan, Tiranti, Valeria
Published in American journal of human genetics (02.01.2014)
Published in American journal of human genetics (02.01.2014)
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Journal Article