Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Diana Bronshteyn"'
Autor:
Arielle Hershkovich, Erica F Weiss, John McGinley, Diana Bronshteyn, David Masur, Ronda Facchini
Publikováno v:
Archives of Clinical Neuropsychology. 37:1429-1429
Objective: The KCNQ2 gene mutations (KCNQ2), a known cause of neuronal potassium channel dysfunction in brain cells, causes susceptibility to seizures beginning within the first days of life. Seizure semiology, severity and cognitive sequela can vary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8318ff794ca0b9c18a80bd60dc8b1dd
https://doi.org/10.1093/arclin/acac060.278
https://doi.org/10.1093/arclin/acac060.278
Publikováno v:
Archives of Clinical Neuropsychology. 37:1318-1318
Objective: We present the neuropsychological profile of a 9-year-old girl with a history of waxing and waning ataxia, initially diagnosed at 18 months of age, with Acute Disseminated Encephalomyelitis (ADEM), later thought to be axonal motor sensory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce44d0dc07ce8a25c0513818f76c1e5
https://doi.org/10.1093/arclin/acac060.163
https://doi.org/10.1093/arclin/acac060.163
Publikováno v:
Archives of Clinical Neuropsychology. 36:1099-1099
Objective Antiphospholipid Antibody Syndrome (APS), also known as Hughes Syndrome, is an autoimmune condition linked to various adverse medical and neurological outcomes affecting 5 in 100,000. APS results from antibodies (aPL) that attack blood prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::951f6680519901ee4a93febf0e08a9ea
https://doi.org/10.1093/arclin/acab062.75
https://doi.org/10.1093/arclin/acab062.75
Publikováno v:
Archives of Clinical Neuropsychology. 36:1082-1082
Objective Developmental Discoordination Disorder (DCD) is an often overlooked and seldom diagnosed neurodevelopmental condition marked by impairments in motor skills. Lacking identifiable medical or neurological etiology, children with DCD often have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d17403ca372cbaca1d60c7305f9f7773
https://doi.org/10.1093/arclin/acab062.59
https://doi.org/10.1093/arclin/acab062.59
Publikováno v:
Archives of Clinical Neuropsychology. 36:1126-1126
Objective Spinocerebellar ataxia 29 (SCA29) is a rare autosomal dominant disorder resulting in infantile-onset hypertonia, gross motor delay and cognitive impairment. SCA29 causes cerebellar dysfunction and atrophy manifested by poor hand coordinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78b19b9f14fdf7c877d3c282e46f8a71
https://doi.org/10.1093/arclin/acab062.99
https://doi.org/10.1093/arclin/acab062.99