Results 61 to 70 of about 45,949 (263)
Acute hemiplegia: aetiology and outcome in Nigerian children
The Pan African Medical Journal, 2020 INTRODUCTION: Acute hemiplegia of childhood is a postnatally acquired nonspecific clinical response of the brain to various aetiological insults in a child who was neurologically normal at birth. This study aims at evaluating the aetiology and outcome of
Komomo Eyong +3 more
doaj +1 more source
Journal of Clinical Ultrasound, EarlyView.We present the case of a 55‐year‐old male who experienced a cryptogenic ischemic stroke, likely due to a patent foramen ovale (PFO) in the setting of an incomplete cor triatriatum sinister (CTS) and a 30 mm GORE Cardioform Septal Occluder was successfully implanted.
Anastasios Apostolos +8 more
wiley +1 more source
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2 [PDF]
, 2017 BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated with familial hemiplegic migraine. However, a wide spectrum of phenotypes that include alternating hemiplegia of childhood and epilepsy have been described.
Nelson, Tanya N +28 more
core +1 more source
Journal of Medical Internet ResearchBackgroundTelemedicine has emerged as a critical tool in the management of acute stroke; yet, its impact on clinical decision-making, particularly in the administration of tissue plasminogen activator (tPA), remains underexplored.
Yao Li +3 more
doaj +1 more source
Journal of Medical Radiation Sciences, EarlyView.Health consumer complaints to the New Zealand Health and Disability Commissioner involving sonographers are rare, totalling 15 in the last 31 years and averaging 1.5 cases per year over the last decade. A large proportion of complaints involve an undetected finding, obstetric examination and private setting.
Martin Necas +5 more
wiley +1 more source
Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements
Movement Disorders Clinical Practice, EarlyView.Abstract Background Congenital Mirror Movement Syndrome (CMMS) involves involuntary movements on one side of the body while voluntary movements are performed on the other side. They disrupt left–right coordination and can be caused by a pathogenic variant in the DCC gene.
Nok‐Yeung Law +7 more
wiley +1 more source
Acute Hemiplegia with Chickenpox [PDF]
, 1998 A case of an 18-month-old girl who developed a right hemiplegia 10 days after onset of varicella infection is reported from the Division of Pediatric Neurology, Istanbul University ...
J Gordon Millichap
core +1 more source