Results 71 to 80 of about 4,566 (168)

Polymicrogyria and Congenital Parvovirus B19 Infection

American Journal of Perinatology Reports, 2011
Fetal parvovirus B19 infection causes anemia, hydrops, and pregnancy loss but is generally not considered teratogenic. Nevertheless, disturbances of neuronal migration have been described with congenital parvovirus infection.
Grant S. Schulert, William F. Walsh, Jörn-Hendrik Weitkamp   +2 more
doaj   +1 more source

Perisylvian Polymicrogyria Epileptic Syndrome

Pediatric Neurology Briefs, 1994
The epileptic spectrum and EEG findings in 31 patients with a congenital bilateral perisylvian syndrome are reported from the University of Alabama at Birmingham and the CBPS Multicenter Collaborative Study Group.
J Gordon Millichap
doaj   +1 more source

Nodular Neuronal Heterotopia

Pediatric Neurology Briefs, 1999
Brain tissue from 4 children with intractable epilepsy and subcortical or periventricular nodular heterotopia of different etiologies (megalencephaly, cortical dysplasia, polymicrogyria) was examined at the University of Oxford, Radcliffe Infirmary, UK.
J Gordon Millichap
doaj   +1 more source

Polymicrogyria

, 2008
Frank Gaillard, Ciléin Kearns, Tariq Walizai   +2 more
  +4 more sources

Issue Information

Epilepsia Open, Volume 11, Issue 2, Page 383-389, April 2026.
wiley   +1 more source

Polymicrogyria

, 2021
openaire   +1 more source

ADGRG1-related polymicrogyria syndrome: report on a large consanguineous family with a novel variant and review

Egyptian Journal of Medical Human Genetics
Background Polymicrogyria is a spectrum of complex cortical malformations encompassing multiple subtypes. Of these, bilateral frontoparietal polymicrogyria (BFPP) has been associated with pathogenic variants in the ADGRG1 gene, formerly known as GPR56 ...
Dalida El Khatib, Moussa Hojeij, Sandra Sabbagh, Cybel Mehawej, Eliane Chouery, Seung Woo Ryu, JiHye Kim, Andre Mégarbané   +7 more
doaj   +1 more source

Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children

Orphanet Journal of Rare Diseases
Background Pallister-Killian syndrome (PKS) is a rare genetic disorder caused by mosaic tetrasomy of 12p with wide neurological involvement. Intellectual disability, developmental delay, behavioral problems, epilepsy, sleep disturbances, and brain ...
Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli   +30 more
doaj   +1 more source

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism

The Journal of Clinical Investigation
Reelin (RELN) is a secreted glycoprotein essential for cerebral cortex development. In humans, recessive RELN variants cause cortical and cerebellar malformations, while heterozygous variants were associated with epilepsy, autism, and mild cortical ...
Martina Riva, Sofia Ferreira, Kotaro Hayashi, Yoann Saillour, Vera P. Medvedeva, Takao Honda, Kanehiro Hayashi, Claire Altersitz, Shahad Albadri, Marion Rosello, Julie Dang, Malo Serafini, Frédéric Causeret, Olivia J. Henry, Charles-Joris Roux, Céline Bellesme, Elena Freri, Dragana Josifova, Elena Parrini, Renzo Guerrini, Filippo Del Bene, Kazunori Nakajima, Nadia Bahi-Buisson, Alessandra Pierani   +23 more
doaj   +1 more source

Mexiletine prevents transient heart failure in a polymicrogyria child with an ATP1A3 variant: a case report. [PDF]

Eur Heart J Case Rep
Aida M, Ozawa J, Takahashi Y, Miyatake S, Watanabe K.   +4 more
europepmc   +1 more source