Results 1 to 10 of about 4,546 (149)

MRI-based spectral analysis of fetal brain gyrification in typical development and in lissencephaly and polymicrogyria [PDF]

open access: yesScientific Reports
Cortical gyrification is a key marker of fetal brain development and is typically assessed qualitatively on ultrasound or MRI. While previous quantitative approaches have characterized gestational trajectories in typically developing (TD) fetuses, only a
Bossmat Yehuda   +6 more
doaj   +2 more sources

Histopathology of Polymicrogyria

open access: yesPediatric Neurology Briefs, 2015
Investigators from Sainte Justine Hospital (Montreal), Montreal Neurological Hospital and Institute, King's College Hospital (London), and John Radcliffe Hospital (Oxford) retrospectively reviewed medical records, autopsy reports, and genetic studies ...
Iga Fudyma, Nitin R. Wadhwani
doaj   +4 more sources

Genetic Profiling of Polymicrogyria in a South Indian Cohort [PDF]

open access: yesAnnals of Indian Academy of Neurology
Polymicrogyria (PMG) represents a complex disorder involving malformation of the cortex. There have not been any comprehensive genetic studies of PMG from India.
Mary Iype   +3 more
doaj   +2 more sources

Current concepts of polymicrogyria [PDF]

open access: yesNeuroradiology, 2010
Polymicrogyria is one of the most common malformations of cortical development. It has been known for many years and its clinical and MRI manifestations are well described. Recent advances in imaging, however, have revealed that polymicrogyria has many different appearances on MR imaging, suggesting that is may be a more heterogeneous malformation than
Anthony James Barkovich
exaly   +6 more sources

The genetic landscape of polymicrogyria

open access: yesAnnals of Indian Academy of Neurology, 2022
Polymicrogyria (PMG) is a relatively common complex malformation with cortical development, characterized by an exorbitant number of abnormally tiny gyri separated by shallow sulci. It is a neuronal migration disorder.
Jesmy James   +4 more
doaj   +3 more sources

Polymicrogyria-Associated Epilepsy

open access: yesPediatric Neurology Briefs, 2013
Investigators from the Boston Children's Hospital, New York University, Brown University, and Birmingham School of Medicine, AL, studied the clinical epilepsy and imaging features of 87 patients with polymicrogyria (PMG) and epilepsy, recruited through ...
J Gordon Millichap
doaj   +3 more sources

A Prenatal Ultrasound Study of Cerebral Cortical Sulci and Gyri Development in Fetuses With Overgrowth Syndrome and/or Cerebral Malformations due to Abnormalities in MTOR Pathway Genes [PDF]

open access: yesMolecular Genetics & Genomic Medicine
Objectives To investigate the abnormal development of cerebral cortical sulci and gyri in fetuses with Overgrowth Syndrome and/or Cerebral Malformations Due to mTOR Pathway Gene Abnormalities (OCMMPG), focusing on prenatal imaging correlates of mTOR ...
Hui Wang   +8 more
doaj   +2 more sources

Time‐Frequency Fingerprint Analysis in SEEG Source‐Space to Identify the Epileptogenic Zone [PDF]

open access: yesAnnals of Clinical and Translational Neurology
This case study highlights the application of seizure fingerprint analysis in the source‐space of stereo‐EEG (SEEG) data to accurately localize the epileptogenic zone (EZ) in patients with complex cortical malformations.
Yash Shashank Vakilna   +10 more
doaj   +2 more sources

A Neonate Diagnosed with Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome with Mutation [PDF]

open access: yesNeonatal Medicine, 2023
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP) is a rare genetic disorder characterized by megalencephaly, polymicrogyria, body overgrowth, and cutaneous capillary malformations. It has been reported recently that MCAP is related to
Young Mi Park   +3 more
doaj   +1 more source

Epilepsy Secondary to Polymicrogyria. [PDF]

open access: yesJ Community Hosp Intern Med Perspect
Putta Y, Miller SB, Bandaru SK.
europepmc   +3 more sources

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