[HTML][HTML] Dyke-Davidoff-Masson syndrome

MR Behera, S Patnaik, AK Mohanty - Journal of Neurosciences in …, 2012 - ncbi.nlm.nih.gov
A 14-month-old male child presented with recurrent generalized seizures, spastic
hemiplegia, microcephaly and had developmental delay in motor and speech domains. CT …

[HTML][HTML] Adult presentation of Dyke-Davidoff-Masson syndrome: a case report

U Roy, A Panwar, A Mukherjee, D Biswas - Case Reports in Neurology, 2016 - karger.com
Abstract Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically
characterized by hemiparesis, seizures, facial asymmetry, and mental retardation. The …

Radiological imaging findings of Dyke–Davidoff–Masson syndrome

E Gökçe, M Beyhan, R Sade - Acta Neurologica Belgica, 2017 - Springer
Abstract Radiological findings of Dyke–Davidoff–Masson syndrome (DDMS) in patients with
different etiologies are presented in our study. The study included 12 patients (seven …

Two cases of neurogenic paralysis in medieval skeletal samples from Croatia

M Novak, M Čavka, M Šlaus - International Journal of Paleopathology, 2014 - Elsevier
Osteological changes consistent with neurogenic paralysis were observed in one male and
one female skeleton recovered from two Croatian medieval sites–Virje and Zadar. Both …

Arterial spin labeling hyperperfusion in Rasmussen's encephalitis: is it due to focal brain inflammation or a postictal phenomenon?

S Kumar, CP Nagesh, B Thomas… - Journal of …, 2018 - Elsevier
Background and purpose The study evaluated the utility of arterial spin labeling (ASL)
perfusion imaging in Rasmussen's encephalitis (RE). Material and methods The hospital …

Possible neurogenic disorder in a female buried in the monastic cemetery at Ghazali (ca. 670–1270 CE), northern Sudan

JA Ciesielska, RJ Stark - International Journal of …, 2020 - Wiley Online Library
During the archaeological excavations of a Christian monastic cemetery in northern Sudan,
a double‐vaulted tomb was discovered housing the remains of three individuals, among …

Dyke-Davidoff-Masson syndrome: a delayed diagnosis of an acquired variant

TS Kumar, A Vipul, R Yadav - Journal of Medical Research and …, 2018 - jmrionline.com
Abstract Dyk-Davidof-Masson Syndrome (DDMS) is an important cause of intractable and
drug-resistant seizures. It has varied clinical presentation and history with distinct …

[PDF][PDF] Long-term effect of rituximab in a case with late-onset Rasmussens encephalitis with anti-ganglioside IgGQ1b and anti-GAD antibodies positivity

G Timárová, I Lisá, P Kukumberg - Neuroendocrinology Letters, 2016 - researchgate.net
Rasmussens encephalitis is a rare autoimmune encephalitis usually involving one brain
hemisphere, presenting with refractory epileptic seizures, and neurological and cognitive …

[HTML][HTML] Dyke-Davidoff-Masson Syndrome as a Rare Cause of Cerebral Hemiatrophy: Insights From a Case Series

PK Sharma, A Faizal, ALR Prabhu, I Misbah - Cureus, 2024 - ncbi.nlm.nih.gov
Abstract Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological condition
marked by changes in the skeletal structure, cerebral hemiatrophy, and ventriculomegaly …

Hemiatrophy and seizures: a case of adult-onset Rasmussen encephalitis

J Cosgrove, M Busby - Practical neurology, 2013 - pn.bmj.com
A 21-year-old man with no medical history presented in 2007 with a generalised tonic-clonic
seizure. Over the previous 2 months he had experienced intermittent episodes of left-sided …