Results 51 to 60 of about 1,407 (200)
Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy
South African Journal of Radiology, 2017 Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar +4 more
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Cerebellum: an explanation for dystonia? [PDF]
, 2017 Dystonia is a movement disorder that is characterized by involuntary muscle contractions, abnormal movements and postures, as well as by non-motor symptoms, and is due to abnormalities in different brain areas.
Berardelli, Alfredo, Bologna, Matteo
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Dyke-Davidoff-Masson syndrome: A case report
Medical Journal of Dr. D.Y. Patil University, 2014 Dyke-Davidoff-Masson Syndrome (DDMS), also called as cerebral hemiatrophy, is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties.
Biswajyoti Rath +3 more
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Annals of Pediatric Cardiology, 2021 We report a case of 8-year-old boy with unexplained desaturation and clubbing. Echocardiography showed anomalous drainage of right superior vena cava into left atrium. He did not have any neurological symptoms preoperatively.
Nilanjan Dutta +7 more
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Proof of concept: Portable ultra-low-field magnetic resonance imaging for the diagnosis of epileptogenic brain pathologies. [PDF]
EpilepsiaAbstract Objective High‐field magnetic resonance imaging (MRI) is a standard in the diagnosis of epilepsy. However, high costs and technical barriers have limited adoption in low‐ and middle‐income countries. Even in high‐income nations, many individuals with epilepsy face delays in undergoing MRI.
Bauer T +15 more
europepmc +2 more sources
Síndrome de moyamoya associada a neurofibromatose tipo I em paciente pediátrico [PDF]
, 2011 CONTEXT: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder among humans. Moyamoya disease is a cerebral vasculopathy that is only rarely observed in association with NF-1, particularly in the pediatric age range ...
DARRIGO JÚNIOR, Luiz Guilherme +5 more
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Trudności diagnostyczne objawów napadowych u chłopca z zespołem Parry'ego-Romberga [PDF]
, 1970 Parry-Romberg syndrome is characterized by progressive unilateral facial atrophy affecting subcutaneous tissue, cartilage and bone structures. Headache attacks and epilepsy are commonly associated with this syndrome but the underlying pathophysiology is ...
Biedroń, Agnieszka +3 more
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Intracranial yolk sac tumor in an adult patient: MRI, diffusion-weighted imaging and 1H MR spectroscopy features [PDF]
, 2012 Introduction. Yolk sac tumors represent only 5%-7% of intracranial germ cell tumors, which comprise about 1% of all primary brain tumors in adults. Literature data about nonspecific imaging characteristics of these tumors are scant.
Gavrilović Svetlana +7 more
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A case of hippocampal sclerosis diagnosed as cortical dysplasia due to preoperative brain MRI finding [PDF]
, 2010 Hippocampal sclerosis (HS) is one of the most common features of intractable temporal lobe epilepsy. Generally it can be identified through brain magnetic resonance imaging (MRI) with high degree of sensitivity and specificity. Typical brain MRI findings
Barkovich +31 more
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Progressive facial hemiatrophy (Parry-Romberg syndrome) with ipsilateral cerebral hemiatrophy [PDF]
Neurology, 2010 The authors report a case of Progressive facial hemiatrophy (Parry-Romberg syndrome) with ipsilateral cerebral hemiatrophy; they underline how the clinical aspect of atrophy is concordant with MRI of the brain and soft tissue that shows cerebral omolateral atrophy and lack of the ipsilateral soft facial tissue.
RESTIVO D. A, MILONE, Pietro
openaire +3 more sources