PEHO syndrome: the endpoint of different genetic epilepsies
M Chitre, MS Nahorski, K Stouffer… - Journal of Medical …, 2018 - jmg.bmj.com
Background Progressive encephalopathy, hypsarrhythmia and optic atrophy (PEHO) has
been described as a clinically distinct syndrome. It has been postulated that it is an …
been described as a clinically distinct syndrome. It has been postulated that it is an …
Optic atrophy in children
MC Brodsky, MC Brodsky - Pediatric Neuro-Ophthalmology, 2016 - Springer
Optic atrophy is a morphologic sequel to a multitude of anterior visual pathway insults that
culminate in the loss of retinal ganglion cell axons [631, 771, 822]. Histopathologically, it is …
culminate in the loss of retinal ganglion cell axons [631, 771, 822]. Histopathologically, it is …
[HTML][HTML] Clinical and genetic features of PEHO and PEHO-Like syndromes: A scoping review
H Sabaie, NK Ahangar, S Ghafouri-Fard… - Biomedicine & …, 2020 - Elsevier
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO)
syndrome is a genetic neurological condition characterized by extreme cerebellar atrophy …
syndrome is a genetic neurological condition characterized by extreme cerebellar atrophy …
[HTML][HTML] Neuroimaging of pediatric cerebellum in inherited neurodegenerative diseases
L Chiapparini, M Moscatelli - Applied Sciences, 2021 - mdpi.com
In the study of cerebellar degenerative diseases, morphologic imaging (computed
tomography, CT and magnetic resonance imaging, MRI) is the most common examination …
tomography, CT and magnetic resonance imaging, MRI) is the most common examination …
Advanced MR brain imaging. Why?
TAGM Huisman, A Tekes - Pediatric radiology, 2008 - Springer
The discovery of X-rays has been a revolution in medicine allowing physicians to study
human anatomy in vivo. The medical specialty initially known as roentgenology, later to be …
human anatomy in vivo. The medical specialty initially known as roentgenology, later to be …
PEHO syndrome: a study of five Argentinian patients
RH Caraballo, AN Pozo, M Gomez, M Semprino - Pediatric neurology, 2011 - Elsevier
We describe two familial and three nonfamilial cases from Argentina, examined between
February 1, 1990-July 31, 2008, who met the diagnostic criteria of progressive …
February 1, 1990-July 31, 2008, who met the diagnostic criteria of progressive …
Частная дерматоонкология
ВД Елькин, ЛС Митрюковский, ТГ Седова - 2018 - elibrary.ru
Предлагаемая читателям монография является продолжением предыдущей («Частная
дерматоонкология. Опухоли, опухолеподобные образования и пороки развития …
дерматоонкология. Опухоли, опухолеподобные образования и пороки развития …
[PDF][PDF] Diffusion magnetic imaging applied to epilepsy
S Vulliémoz, R Meuli, P Maeder, M Seeck, J Delavelle… - Epileptologie, 2007 - epi.ch
Diffusion imaging is a new imaging method based on Magnetic Resonance Imaging (MRI)
that allows in vivo measurement of local diffusion properties of water molecules in the brain …
that allows in vivo measurement of local diffusion properties of water molecules in the brain …
A Case of PEHO Syndrome.
HK Moon - Journal of the Korean Child Neurology Society, 2007 - annchildneurol.org
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO)
syndrome was first described in 1991 by Salonen. It is a rare, autosomal recessive, and …
syndrome was first described in 1991 by Salonen. It is a rare, autosomal recessive, and …
Anaesthetic management of a child with PEHO syndrome
B Marshall, M Turner, S Lobo - Anaesthesia Cases, 2013 - Wiley Online Library
Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy (PEHO)
syndrome is a rare neurodegenerative disorder of probable autosomal recessive …
syndrome is a rare neurodegenerative disorder of probable autosomal recessive …