Results 171 to 180 of about 6,069 (199)
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Polymicrogyria and schizencephaly

2011
The porphyrias are a group of conditions in which there are deficiencies in one of the eight enzymes of the heme biosynthetic pathway (the porphyrin pathway): four of the enzymes are located in the mitochondria and the other four in the cytosol. There are three acute porphyrias which cause epilepsy and other neurological symptoms: acute intermittent ...
Guerrini R., Barba C.
openaire   +2 more sources

Neuropathological basis of polymicrogyria

2004
Rationale: Polymicrogyria (PMG) is a relatively common malformation of cortical development. However, the pathogenesis, epileptogenesis and anatomo-clinical correlation of PMG require further clarification. We aim to 1. study the extent and type of pathological changes in polymicrogyric lesions as well as in adjacent non-polymicrogyric tissue 2.
Jansen, Anna   +8 more
openaire   +2 more sources

Clinical, MRI, and Pathological Features of Polymicrogyria in Chromosome 22q11 Deletion Syndrome

American Journal of Medical Genetics, Part A, 2004
Fiona Stewart   +2 more
exaly  

Megalencephaly, Polymicrogyria, and Hydrocephalus (MPPH) Syndrome: A New Case With Syndactyly

Journal of Child Neurology, 2008
Tiziana Pisano   +2 more
exaly  

Polymicrogyria Associated With 17p13.3p13.2 Duplication: Case Report and Review of the Literature

European Journal of Medical Genetics, 2020
Chloe Cunningham   +2 more
exaly  

Prenatal Ultrasound Detection of Bilateral Focal Polymicrogyria

Prenatal Diagnosis, 2004
Maria Angela Rustico   +2 more
exaly  

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