May PEHO Syndrome be a Clinical Entity Associated with Early Onset Encephalopathies?

Samankaltaisia teoksia

• PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies
  Tekijä: Gawlinski, Pawel, et al.
  Julkaistu: (2016)
• Two patients with glutaric aciduria type 3: a novel mutation and brain magnetic resonance imaging findings
  Tekijä: Sevil Dorum, et al.
  Julkaistu: (2020-08-01)
• The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy
  Tekijä: Fehr, Stephanie, et al.
  Julkaistu: (2013)
• The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders
  Tekijä: Salpietro, Vincenzo, et al.
  Julkaistu: (2017)
• Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases
  Tekijä: Yiş, Uluç, et al.
  Julkaistu: (2011)