Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Emily A. Innes"'
Autor:
Jingya Yan, Kavitha Kothur, Emily A. Innes, Velda X. Han, Hannah F. Jones, Shrujna Patel, Erica Tsang, Richard Webster, Sachin Gupta, Christopher Troedson, Manoj P. Menezes, Jayne Antony, Simone Ardern-Holmes, Esther Tantsis, Shekeeb Mohammad, Louise Wienholt, Ananda S. Pires, Benjamin Heng, Gilles J. Guillemin, Anna Guller, Deepak Gill, Sushil Bandodkar, Russell C. Dale
Publikováno v:
EBioMedicine, Vol 84, Iss , Pp 104280- (2022)
Summary: Background: Epileptic (previously infantile) spasms is the most common epileptic encephalopathy occurring during infancy and is frequently associated with abnormal neurodevelopmental outcomes. Epileptic spasms have a diverse range of known (
Externí odkaz:
https://doaj.org/article/a996c30a8b944c29b682c22fe3ffea37
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⟩
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
Autor:
Emily A. Innes, Robert Goetti, Neil Mahant, Gladys Ho, Laura Williams, Deepak Gill, Russell C. Dale, Shekeeb S. Mohammad
Publikováno v:
Parkinsonism & Related Disorders. 99:76-78
This is a unique case of SPG11 mutation presenting as childhood onset dystonic tremor without weakness or spastic paraplegia. Hereditary spastic paraplegia is the most common phenotype of SPG11 mutation though there are reports of an extended phenoty
Autor:
Khoa L Nguyen, Daniel McGurty, Emily A Innes, Robert Goetti, Terrence Thomas, Sameer Dal, Sushil Bandodkar, Jingya Yan, Melanie Wong, Russell C Dale, Shekeeb S Mohammad
Publikováno v:
Journal of Paediatrics and Child Health. 58:1688-1690
Autor:
Alexandra M. Johnson, Emily Amy Innes
Publikováno v:
Journal of International Child Neurology Association, Pp 10-10 (2019)
Background: Valproate (VPA) has been previously described to cause reversible cerebral atrophy and cognitive decline, but few cases are reported and neuropsychological data is lacking. We report a case of VPA induced encephalopathy in an 11-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e80232cca097812716354d52fa4315f
https://jicna.org/index.php/journal/article/view/118
https://jicna.org/index.php/journal/article/view/118
Autor:
Hartwig Klinker, Eva Schulte-Kemna, Xiaoying Sun, Ekkehard Werner Zöllner, Sara H. Browne, Richard Haubrich, Margaret van Niekerk, Mark F. Cotton, Sonia Jain, Emily Ryan Innes, Clair Edson, Helena Rabie, Steve Innes
Publikováno v:
The Pediatric infectious disease journal. 32(6)
BACKGROUND The prevalence of potentially stigmatizing lipoatrophy in children receiving antiretroviral therapy in Southern Africa is high, affecting around a third of children. Early diagnosis of lipoatrophy is essential for effective intervention to