Results 51 to 60 of about 1,423,846 (344)

Diagnosis by behavioral observationHome-Videosomnography – A Rigorous Ethnographic Approach to Sleep of Children with Neurodevelopmental Conditions

Frontiers in Psychiatry, 2015
Introduction Advanced video technology is available for sleep-laboratories. However, low-cost equipment for screening in the home setting has not been identified and tested, nor has a methodology for analysis of video recordings been suggested.MethodsWe ...
Osman Sevket Ipsiroglu, Osman Sevket Ipsiroglu, Osman Sevket Ipsiroglu, Yi-Hsuan Amy Hung, Forson eChan, Michelle eRoss, Dorothee eVeer, Sonja eSoo, Gloria eHo, Mai eBerger, Graham eMcAllister, Heinrich eGarn, Heinrich eGarn, Gerhard eKloesch, Adriano Vilela Barbosa, Sylvia eStockler, Sylvia eStockler, William eMcKellin, William eMcKellin, Eric eVatikiotis-Bateson   +19 more
doaj   +1 more source

TronicBoards: An Accessible Electronics Toolkit for People with Intellectual Disabilities [PDF]

, 2022
Hashini Senaratne, Swamy Ananthanarayan, Kirsten Ellis   +2 more
openalex   +1 more source

Overprotection in the lives of people with intellectual disability in Malta: knowing what is control and what is enabling support

Disability & Society, 2019
A study of overprotection in the lives of persons with intellectual disability in Malta was carried out on the principles of inclusive research. Focus groups were held with people with intellectual disability, parents of people with intellectual ...
A. Callus, Isabel Bonello, Charmaine Mifsud, Rosanne Fenech   +3 more
semanticscholar   +1 more source

Applying an Ethical Lens to the Treatment of People With Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The practice of neurology requires an understanding of clinical ethics for decision‐making. In multiple sclerosis (MS) care, there are a wide range of ethical considerations that may arise. These involve shared decision‐making around selection of a disease‐modifying therapy (DMT), risks and benefits of well‐studied medications in comparison to
Methma Udawatta, Farrah J. Mateen
wiley   +1 more source

RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour [PDF]

, 2021
Maria Lidia Mignogna, Stefano Musardo, Giulia Ranieri, Susanna Gelmini, Pedro Espinosa, Paolo Marra, Sara Belloli, Valentina Murtaj, Rosa Maria Moresco, Camilla Bellone, Patrizia D’Adamo   +10 more
openalex   +1 more source

Characterization of Clinical Phenotype to Glial Fibrillary Acidic Protein Concentrations in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine the concentration of glial fibrillary acidic protein (GFAP) in cerebrospinal fluid (CSF) and plasma in Alexander disease (AxD) and whether GFAP levels are predictive of disease phenotypes. Methods CSF and plasma were collected (longitudinally when available) from AxD participants and non‐AxD controls.
Amy T. Waldman, Asako Takanohashi, Joshua Y. Joung, Geraldine W. Liu, Kaley Arnold, Amy Pizzino, Walter Faig, Sarah Woidill, Sona Narula, Adeline L. Vanderver   +9 more
wiley   +1 more source

Association of Borderline Intellectual Functioning and Adverse Childhood Experience with adult psychiatric morbidity. Findings from a British birth cohort

BMC Psychiatry, 2019
Background To examine whether Borderline Intellectual Functioning (BIF) and Adverse Childhood Experiences independently predict adult psychiatric morbidity.
Angela Hassiotis, Emma Brown, James Harris, David Helm, Kerim Munir, Luis Salvador-Carulla, Marco Bertelli, Amaria Baghdadli, Jannelien Wieland, Ramon Novell-Alsina, Jordi Cid, Laura Vergés, Rafael Martínez-Leal, Tuba Mutluer, Fuad Ismayilov, Eric Emerson   +15 more
doaj   +1 more source

Listening to the experts: person-centred approaches to supporting autistic people and people with an intellectual disability in the mental health system [PDF]

, 2023
Alexis Quinn, Alicia Wood, Keri-Michèle Lodge, Sheila Hollins   +3 more
openalex   +1 more source

Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda, Hyo‐Min Kim, Nicole Battaglia, Joshua Rong, Amy Tam, Enrique Gonzalez Saez‐Diez, Cornelius F. Boerkoel, Afshin Saffari, Vicente Quiroz, Luca Schierbaum, Zainab Zaman, Katerina Bernardi, Darius Ebrahimi‐Fakhari   +12 more
wiley   +1 more source

Evaluation of the child with global developmental delay and intellectual disability.

Paediatrics & child health, 2018
Global developmental delay (GDD) and intellectual disability (ID) are common concerns in the paediatric setting. Etiologies of both conditions are highly heterogeneous. The American Academy of Pediatrics, the American Academy of Neurology and the British
S. Bélanger, Joannie Caron
semanticscholar   +1 more source