Cargando…
May PEHO Syndrome be a Clinical Entity Associated with Early Onset Encephalopathies?
Autores principales: | Ekici, Arzu, Yılmaz, İlyas, Görükmez, Orhan, Orcan, Cengiz Gökhan, Dorum, Sevil |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313604/ https://www.ncbi.nlm.nih.gov/pubmed/32606555 http://dx.doi.org/10.4103/aian.AIAN_331_19 |
Ejemplares similares
-
The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders
por: Salpietro, Vincenzo, et al.
Publicado: (2017) -
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases
por: Yiş, Uluç, et al.
Publicado: (2011) -
Intravenous Immunoglobulin: A Good Choice for Acute Cerebellar Ataxia Associated with Varicella
por: Kılavuz, Fatma G, et al.
Publicado: (2018) -
Acute Encephalopathy Following Measles Vaccination: A Novel Entity
por: Kasinathan, Ananthanarayanan, et al.
Publicado: (2021) -
CCDC88A mutations cause PEHO-like syndrome in humans and mouse
por: Nahorski, Michael S., et al.
Publicado: (2016)