Results 41 to 50 of about 261,143 (157)

Developmental Trajectories of Hand Movements in Typical Infants and Those at Risk of Developmental Disorders: An Observational Study of Kinematics during the First Year of Life

open access: yesFrontiers in Psychology, 2018
HighlightsThe kinematics of hand movements (spatial use, curvature, acceleration, and velocity) of infants with their mothers in an interactive setting are significantly associated with age in cohorts of typical and at-risk infantsdiffer significantly at
Lisa Ouss   +15 more
doaj   +1 more source

Oral findings in West syndrome – A Case Report

open access: yesBrazilian Dental Science, 2017
West syndrome is a severe form of epilepsy syndrome which is characterized by triad of infantile spasms, EEG findings (hypsarrhythmia) and developmental delay.
Sheetal Dilip Badnaware   +3 more
doaj   +1 more source

First‐choice hormonal therapies for children with infantile epileptic spasms syndrome in South Asia: A network meta‐analysis of randomized controlled trials

open access: yesEpilepsia Open
Considering the peculiar challenges with infantile epileptic spasms syndrome (IESS) in South Asia and a wide variation in the usage of hormonal therapies, we compared the efficacy and safety of various hormonal therapies for children with IESS in South ...
Nagita Devi   +5 more
doaj   +1 more source

Development of West Syndrome in Infants with Epileptic Discharges

open access: yesPediatric Neurology Briefs, 2007
Of 45 infants having epileptic discharges on the EEG in early infancy, 26 developed West syndrome (WS), in a study at Okayama University, Japan.
J Gordon Millichap
doaj   +1 more source

Epileptic spasms relapse is associated with response latency but not conventional attributes of post‐treatment EEG

open access: yesEpilepsia Open
Objective Relapse of epileptic spasms after initial treatment of infantile epileptic spasms syndrome (IESS) is common. However, past studies of small cohorts have inconsistently linked relapse risk to etiology, treatment modality, and EEG features upon ...
Emmi Deckard   +7 more
doaj   +1 more source

Congenital Cytomegalovirus Infection and Risk of Epilepsy

open access: yesPediatric Neurology Briefs, 2008
The clinical, laboratory and neuroradiological findings in 19 children with congenital cytomegalovirus (CMV) infection were retrospectively reviewed for features of epilepsy in 7 (37%), in a study at Osaka Medical Center, Japan.
J Gordon Millichap
doaj   +1 more source

West syndrome: ethiology, management, long-term outcomes

open access: yesБюллетень сибирской медицины, 2009
The article is based on long-term observation of 27 patients with West syndrome, age of onset, etiology of symptomatic forms, neurological status, efficiency of hormone therapy and antiepileptic drugs.
L. S. Krayeva   +2 more
doaj   +1 more source

Epileptic Syndromes With Possible Immunological Mechanisms (Rasmussen Encephalitis, FIRES, West Syndrome, Landau-Kleffner Syndrome)

open access: yesArchives of Epilepsy, 2016
Some of childhood epileptic syndromes reminds immunological etiologies with their good response to immuno-therapy and histopathological findings. These syndromes, such as Rasmussen encephalitis, FIRES, West syndrome, and Landau-Kleffner syndrome each of ...
Demet KINAY, Pınar TEKTÜRK
doaj   +1 more source

Combination Therapy With Vigabatrin and Prednisolone Versus Vigabatrin Alone for Infantile Spasms

open access: yesAnnals of Clinical and Translational Neurology
Objective The study evaluated the effectiveness of combination therapy with vigabatrin and prednisolone versus vigabatrin alone for treating infantile epileptic spasms syndrome (IESS).
Rachata Boonkrongsak   +6 more
doaj   +1 more source

Low-Dose ACTH Therapy for Infantile Spasms

open access: yesPediatric Neurology Briefs, 1999
The lowest effective ACTH dose, with fewest adverse effects, for the treatment of West syndrome (WS) was determined in a comparative, randomly assigned, controlled study involving 25 patients with cryptogenic (CWS, n=9) or symptomatic (SWS, n=16) WS, at ...
J Gordon Millichap
doaj   +1 more source

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