C. Pangalos

Novel SCN1A and GABRA1 Gene Mutations With Diverse Phenotypic Features and the Question on the Existence of a Broader Spectrum of Dravet Syndrome

C. Konialis, A. Papavasiliou, M. Gontika, 2017, Child neurology open.

Pregnancy following preimplantation genetic diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

C. Konialis, C. Pangalos, G. Kokkali, 2007, Prenatal diagnosis.

The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis

K. Spengos, S. Shim, C. Konialis, 2005, Prenatal diagnosis.

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.

M. McInnis, A. Chakravarti, S. Antonarakis, 1992, American journal of human genetics.