Zobrazeno 1 - 10 of 87 pro vyhledávání: '"Shekeeb S Mohammad"'
1
Akademický článek
Improving epilepsy control among children with cerebral palsy in rural Bangladesh: a prospective cohort-based study
Autor: Nadia Badawi, Shekeeb S Mohammad, Mohammad Muhit, Gulam Khandaker, Tasneem Karim, Manik Chandra Das
Publikováno v: BMJ Open, Vol 12, Iss 4 (2022)
Objective To define the prevalence and seizure subtypes among children with cerebral palsy (CP) in rural Bangladesh and explore barriers to optimum epilepsy control.Design Prospective cohort study.Setting The study was conducted in Shahjadpur, a rura
Externí odkaz: https://doaj.org/article/72d25d5b453b421ba59b0dbebb407a67
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2
Akademický článek
Utility of CSF Cytokine/Chemokines as Markers of Active Intrathecal Inflammation: Comparison of Demyelinating, Anti-NMDAR and Enteroviral Encephalitis.
Autor: Kavitha Kothur, Louise Wienholt, Shekeeb S Mohammad, Esther M Tantsis, Sekhar Pillai, Philip N Britton, Cheryl A Jones, Rajeshwar R Angiti, Elizabeth H Barnes, Timothy Schlub, Sushil Bandodkar, Fabienne Brilot, Russell C Dale
Publikováno v: PLoS ONE, Vol 11, Iss 8, p e0161656 (2016)
BACKGROUND:Despite the discovery of CSF and serum diagnostic autoantibodies in autoimmune encephalitis, there are still very limited CSF biomarkers for diagnostic and monitoring purposes in children with inflammatory or autoimmune brain disease. The
Externí odkaz: https://doaj.org/article/89052ec324e24c089b85e826143faec2
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4
Akademický článek
Maternal acute and chronic inflammation in pregnancy is associated with common neurodevelopmental disorders: a systematic review
Autor: Velda X. Han, Shrujna Patel, Hannah F. Jones, Timothy C. Nielsen, Shekeeb S. Mohammad, Markus J. Hofer, Wendy Gold, Fabienne Brilot, Samantha J. Lain, Natasha Nassar, Russell C. Dale
Publikováno v: Translational Psychiatry, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Inflammation is increasingly recognized as a cause or consequence of common problems of humanity including obesity, stress, depression, pollution and disease states such as autoimmunity, asthma, and infection. Maternal immune activation (MIA
Externí odkaz: https://doaj.org/article/c22563d0167e48929f5f14fb25cecc6a
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5
The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders
Autor: Belén Pérez‐Dueñas, 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
Publikováno v: Scientia
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Background and Objective: The objective of this study was to better delineate the genetic landscape and key clinical characteristics of complex, early-onset, monogenic hyperkinetic movement disorders. Methods: Patients were recruited from 14 internat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e52a833a18ac97e7e86869c9abdc0d05
https://doi.org/10.1002/mds.29182
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6
Efficacy of Caffeine in ADCY5 ‐Related Dyskinesia: A Retrospective Study
Autor: Aurélie Méneret, Shekeeb S. Mohammad, Laura Cif, Diane Doummar, Claudio DeGusmao, Mathieu Anheim, Magalie Barth, Philippe Damier, Nathalie Demonceau, Jennifer Friedman, Cécile Gallea, Domitille Gras, Juliana Gurgel‐Giannetti, Emily A. Innes, Ján Necpál, Florence Riant, Sandrine Sagnes, Catherine Sarret, Yury Seliverstov, Vijayashankar Paramanandam, Kuldeep Shetty, Christine Tranchant, Mohamed Doulazmi, Marie Vidailhet, Tamara Pringsheim, Emmanuel Roze
Publikováno v: Movement Disorders
Movement Disorders, 2022, 37 (6), pp.1294-1298. ⟨10.1002/mds.29006⟩
ADCY5-related dyskinesia is characterized by early-onset movement disorders. There is currently no validated treatment, but anecdotal clinical reports and biological hypotheses suggest efficacy of caffeine.The aim is to obtain further insight into th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5004457db37435320917da63dab35f2
https://doi.org/10.1002/mds.29006
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7
Rapid onset functional tic‐like behaviours in children and adolescents during COVID ‐19: Clinical features, assessment and biopsychosocial treatment approach
Autor: Velda X Han, Kasia Kozlowska, Kavitha Kothur, Michelle Lorentzos, Wui Kwan Wong, Shekeeb S Mohammad, Blanche Savage, Catherine Chudleigh, Russell C Dale
Publikováno v: Journal of Paediatrics and Child Health. 58:1181-1187
To report the prevalence and clinical characteristics of children with rapid onset functional tic-like behaviours during the COVID-19 pandemic.Single centre, retrospective cohort study of children (18 years) referred to the tic clinic from January 20
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca0ff937c010a07d9c56808cb9cb343
https://doi.org/10.1111/jpc.15932
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8
A case of QARS1 associated epileptic encephalopathy and review of epilepsy in aminoacyl-tRNA synthetase disorders
Autor: Joëlle Rudinger-Thirion, Denise L. Chan, Kavitha Kothur, Shekeeb S. Mohammad, Lisa G. Riley, Gladys Ho, Magali Frugier
Publikováno v: Brain and Development. 44:142-147
Introduction Mutations in QARS1, which encodes human glutaminyl-tRNA synthetase, have been associated with epilepsy, developmental regression, progressive microcephaly and cerebral atrophy. Epilepsy caused by variants in QARS1 is usually drug-resista
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3195cbae06cfab80b97a0910e352be82
https://doi.org/10.1016/j.braindev.2021.10.009
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9
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition
Autor: Elizabeth E. Palmer, Michael Pusch, Alessandra Picollo, Caitlin Forwood, Matthew H. Nguyen, Vanessa Suckow, Jessica Gibbons, Alva Hoff, Lisa Sigfrid, Andre Megarbane, Mathilde Nizon, Benjamin Cogné, Claire Beneteau, Fowzan S. Alkuraya, Aziza Chedrawi, Mais O. Hashem, Hannah Stamberger, Sarah Weckhuysen, Arnaud Vanlander, Berten Ceulemans, Sulekha Rajagopalan, Kenneth Nunn, Stéphanie Arpin, Martine Raynaud, Constance S. Motter, Catherine Ward-Melver, Katrien Janssens, Marije Meuwissen, Diane Beysen, Nicola Dikow, Mona Grimmel, Tobias B. Haack, Emma Clement, Amy McTague, David Hunt, Sharron Townshend, Michelle Ward, Linda J. Richards, Cas Simons, Gregory Costain, Lucie Dupuis, Roberto Mendoza-Londono, Tracy Dudding-Byth, Jackie Boyle, Carol Saunders, Emily Fleming, Salima El Chehadeh, Marie-Aude Spitz, Amelie Piton, Bénédicte Gerard, Marie-Thérèse Abi Warde, Gillian Rea, Caoimhe McKenna, Sofia Douzgou, Siddharth Banka, Cigdem Akman, Jennifer M. Bain, Tristan T. Sands, Golder N. Wilson, Erin J. Silvertooth, Lauren Miller, Damien Lederer, Rani Sachdev, Rebecca Macintosh, Olivier Monestier, Deniz Karadurmus, Felicity Collins, Melissa Carter, Luis Rohena, Marjolein H. Willemsen, Charlotte W. Ockeloen, Rolph Pfundt, Sanne D. Kroft, Michael Field, Francisco E. R. Laranjeira, Ana M. Fortuna, Ana R. Soares, Vincent Michaud, Sophie Naudion, Sailaja Golla, David D. Weaver, Lynne M. Bird, Jennifer Friedman, Virginia Clowes, Shelagh Joss, Laura Pölsler, Philippe M. Campeau, Maria Blazo, Emilia K. Bijlsma, Jill A. Rosenfeld, Christian Beetz, Zöe Powis, Kirsty McWalter, Tracy Brandt, Erin Torti, Mikaël Mathot, Shekeeb S. Mohammad, Ruth Armstrong, Vera M. Kalscheuer
Publikováno v: Molecular Psychiatry, 28, 668-697
Molecular psychiatry, Vol. 28, no. 2, p. 668-697 (2022)
Molecular psychiatry
Molecular Psychiatry
MOLECULAR PSYCHIATRY
CLCN4 concortium 2023, ' Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition ', Molecular psychiatry, vol. 28, no. 2, pp. 668-697 . https://doi.org/10.1038/s41380-022-01852-9
Molecular Psychiatry, 28, 2, pp. 668-697
Molecular Psychiatry, 28, 668-697. SPRINGERNATURE
Missense and truncating variants in the X-chromosome-linked CLCN4 gene, resulting in reduced or complete loss-of-function (LOF) of the encoded chloride/proton exchanger ClC-4, were recently demonstrated to cause a neurocognitive phenotype in both mal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39edfb04a13ae9bc854e89ef1416ed62
http://hdl.handle.net/2066/290784
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