Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Imogen Newsom-Davis"'
Autor:
Maria Escolar, Jessica Bradshaw, Valerie Tharp Byers, Roberto Giugliani, Lynn Golightly, Charles Marques Lourenço, Kimberly McDonald, Nicole Muschol, Imogen Newsom-Davis, Cara O’Neill, Holly L. Peay, Jennifer Siedman, Martha L. Solano, Tessa Wirt, Tim Wood, Lonnie Zwaigenbaum
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 8 (2020)
Abstract Mucopolysaccharidosis III (MPS III) is a rare inherited metabolic disease primarily affecting the central nervous system, leading to developmental and/or speech regression. Early diagnosis of the disease is important to introduce appropriate
Externí odkaz:
https://doaj.org/article/86edb4b4702e4fd7b7906c6b0e95342f
Autor:
Tim Wood, Tessa Wirt, Cara O’Neill, Holly L. Peay, Valerie Tharp Byers, Roberto Giugliani, Nicole Muschol, Charles Marques Lourenço, Jennifer Siedman, Kimberly McDonald, Imogen Newsom-Davis, Lonnie Zwaigenbaum, Martha Solano, Lynn Golightly, Maria L. Escolar, Jessica Bradshaw
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 8 (2020)
Journal of Inborn Errors of Metabolism and Screening v.8 2020
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening, Volume: 8, Article number: e20200002, Published: 15 JUN 2020
Journal of Inborn Errors of Metabolism and Screening v.8 2020
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening, Volume: 8, Article number: e20200002, Published: 15 JUN 2020
Mucopolysaccharidosis III (MPS III) is a rare inherited metabolic disease primarily affecting the central nervous system, leading to developmental and/or speech regression. Early diagnosis of the disease is important to introduce appropriate manageme
Autor:
Dora Steel, Christina Hawkins, Andreas Brunklaus, Samuel Gittins, Imogen Newsom-Davis, Sarah E. Aylett
Publikováno v:
Epilepsybehavior : EB. 88
Sturge–Weber syndrome (SWS) is a neurocutaneous disorder characterized by the combination of a facial naevus flammeus and pial angioma, often associated with learning difficulties and/or epilepsy. Here, we report on the neuropsychological character
Autor:
Imogen Newsom-Davis, Laura H. Goldstein, Peter Leigh, Vanessa Bryant, Michael Brammer, Andrew Simmons
Publikováno v:
Journal of Neurology
Since amyotrophic lateral sclerosis (ALS) can be accompanied by executive dysfunction, it is hypothesised that ALS patients will have impaired performance on tests of cognitive inhibition. We predicted that ALS patients would show patterns of abnorma
Publikováno v:
Seizure. (2):101-106
Despite the wealth of epidemiological evidence showing the comorbidity of epilepsy with various forms of psychopathology, there has been little systematic investigation of its relationship with affective disorders. This study aims to explore the phen
Autor:
Wright K; Department of Psychology, Institute of Psychiatry, Kings College London., Lam D; Department of Psychology, Institute of Psychiatry, Kings College London., Newsom-Davis I; Imogen Newsom- Davis, Neurosciences Unit, Institute of Child Health.
Publikováno v:
Journal of abnormal psychology [J Abnorm Psychol] 2005 Nov; Vol. 114 (4), pp. 689-696.