C. Konialis

Dilemmas in Prenatal Chromosomal Diagnosis Revealed Through a Single Center's 30 Years' Experience and 90,000 Cases

C. Konialis, C. Pangalos, InterGenetics, 2015, Fetal Diagnosis and Therapy.

Birth of a Healthy Histocompatible Sibling following Preimplantation Genetic Diagnosis for Chronic Granulomatous Disease at the Blastocyst Stage Coupled to HLA Typing

C. Konialis, C. Pangalos, K. Pantos, 2008, Fetal Diagnosis and Therapy.

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.

First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects

C. Konialis, C. Pangalos, K. Lilakos, 2016, PeerJ.

Prenatal diagnosis of X‐linked myopathy associated with a VMA21 gene mutation afforded through a novel targeted exome sequencing strategy applied in fetuses with abnormal ultrasound findings

E. Assimakopoulos, A. Sotiriadis, C. Konialis, 2017, Clinical case reports.

Successful hematopoietic stem cell transplantation in 2 children with X-linked chronic granulomatous disease from their unaffected HLA-identical siblings selected using preimplantation genetic diagnosis combined with HLA typing.

V. Kitra, C. Konialis, C. Pangalos, 2010, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Human embryo twinning with proof of monozygocity

C. Konialis, C. Pangalos, K. Illmensee, 2011 .

Middle East Fertility Society Middle East Fertility Society

C. Konialis, C. Pangalos, K. Illmensee, 2011 .

Human embryo splitting: proof of homozygosity

C. Konialis, C. Pangalos, K. Illmensee, 2010 .

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.

Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non‐selective application of a MLPA‐based extended prenatal panel in routine prenatal diagnosis

C. Konialis, C. Pangalos, B. Hagnefelt, 2011, Prenatal diagnosis.

Routine application of a novel MLPA-based first-line screening test uncovers clinically relevant copy number aberrations in haematological malignancies undetectable by conventional cytogenetics

J. Schouten, K. Zoi, S. Savola, 2014, Hematology.

A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation – case report and review of the literature

C. Konialis, C. Pangalos, Christos Aravidis, 2014, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

The APOE E4 Allele Confers Increased Risk of Ischemic Stroke Among Greek Carriers.

K. Vemmos, K. Spengos, E. Gialafos, 2016, Advances in clinical and experimental medicine : official organ Wroclaw Medical University.