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Leena Mewasingh

Observed names: L D Mewasingh, L Duvika Mewasingh, L Mewasingh, L. Mewasingh, L.D MEWASINGH, L.D. Mewasingh, LD Mewasingh, Leena D Mewasingh, Leena D. Mewasingh, Leena Duvika Mewasingh, Mewasingh, Leena
Observed institutions: National Health Service, Leeds General Infirmary, Université Libre de Bruxelles, Imperial College Healthcare NHS Trust, Great Ormond Street Hospital, Leicester Royal Infirmary, Great Ormond Street Hospital for Children NHS Foundation Trust, University Hospitals of Leicester NHS Trust, Birmingham Children's Hospital, St Mary's Hospital, Queen Fabiola Children's University Hospital, University College London, Imperial College London, Newcastle University
ORCID: 0000-0002-0340-302X
Observed ORCID: 0000-0002-0340-302X
OpenAlex ID: A5045285802
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome
2007 · Gillian Rice, Teresa Patrick, et al. · The American Journal of Human Genetics · 455
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Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial
2018 · Finbar J K O'Callaghan, Stuart W Edwards, et al. · The Lancet Child & Adolescent Health · 170
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Febrile seizures:
2015 · Nikhil Patel, Dipak Ram, et al. · BMJ · 158
TBC1D24 genotype–phenotype correlation
2016 · Simona Balestrini, Mathieu Milh, et al. · Neurology · 127
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Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya
2018 · Sara C. Tho-Calvi, Dominic Thompson, et al. · Neurology · 119
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Oral ketamine in paediatric non-convulsive status epilepticus
2003 · L.D MEWASINGH, T SÉKHARA, et al. · Seizure · 98
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Current understanding of febrile seizures and their long‐term outcomes
2020 · Leena D Mewasingh, Richard F M Chin, et al. · Developmental Medicine & Child Neurology · 88
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Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet
2013 · Wilhelmina G. Leen, Leena Mewasingh, et al. · Movement Disorders · 56
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian Sibship
2009 · Anne-Hélène Lebrun, Stephan Storch, et al. · Human Mutation · 55
Hyponatraemia associated with lamotrigine in cranial diabetes insipidus
2000 · Leena Mewasingh, S Aylett, et al. · The Lancet · 55
Nonsurgical cerebellar mutism (anarthria) in two children
2003 · Leena D Mewasingh, Hazim Kadhim, et al. · Pediatric Neurology · 53
Postinfectious immune-mediated encephalitis after pediatric herpes simplex encephalitis
2004 · Xavier De Tiège, Corinne De Laet, et al. · Brain and Development · 49
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children
2009 · J D Stewart, S Tennant, et al. · Journal of Medical Genetics · 47
Pediatric phantom vision (Charles Bonnet) syndrome
2002 · Leena D Mewasingh, Charles Kornreich, et al. · Pediatric Neurology · 37
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Febrile seizures.
2014 · Leena D Mewasingh · Europe PMC (PubMed Central) · 34
Pediatric SUNCT Syndrome
2005 · Tayeb Sékhara, Karine Pelc, et al. · Pediatric Neurology · 34
Predictive value of electrophysiology in children with hypoxic coma
2003 · Leena D. Mewasingh, Catherine Christophe, et al. · Pediatric Neurology · 31
Benign intracranial hypertension: atypical presentation of Miller Fisher syndrome?
2002 · Leena D Mewasingh, Tayeb Sékhara, et al. · Pediatric Neurology · 27
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Crossed cerebellar diaschisis secondary to refractory frontal seizures in childhood
2002 · L.D MEWASINGH, F CHRISTIAENS, et al. · Seizure · 25
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Motor strategies in standing up in children with hemiplegia
2004 · Leena Duvika Mewasingh, Tayeb Sékhara, et al. · Pediatric Neurology · 21
Guillain‐Barré syndrome associated with CASPR2 antibodies: two paediatric cases
2014 · Richard E. Rosch, Alasdair Bamford, et al. · Journal of the Peripheral Nervous System · 20
Motor strategies in standing up in leukomalacic spastic diplegia
2002 · Leena D Mewasingh, Audrey Demil, et al. · Brain and Development · 20
Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease
2018 · A. Papandreou, S. Rahman, et al. · Journal of Inherited Metabolic Disease · 17
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Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature
2023 · Gabriella Gazdagh, David Hunt, et al. · American Journal of Medical Genetics Part A · 14
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Autoimmune cortical encephalitis in two children with anti-myelin oligodendrocyte glycoprotein (MOG) antibody
2020 · D. Doig, C. McNamara, et al. · Journal of Neurology · 14
Works count: 61
Citation count: 2,003
H-index: 21
I10-index: 29
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