K. Salavoura

Juvenile idiopathic arthritis-type disease associated with chromosomal aberrations.

C. Sofocleous, A. Mavrou, A. Kolialexi, 2008, Clinical and experimental rheumatology.

Potential prevention of thromboembolism by genetic counseling and testing for two common thrombophilia mutations.

E. Vairaktaris, C. Yapijakis, T. Antoniadi, 2012, In vivo.

Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.

G. Tsangaris, E. Kanavakis, S. Kitsiou-Tzeli, 2004, In vivo.

Successful HLA‐identical hematopoietic stem cell transplantation in a patient with purine nucleoside phosphorylase deficiency

S. Grafakos, J. Peristeri, G. Vessalas, 2007, Pediatric transplantation.

Rituximab in the treatment of high responding inhibitors in severe haemophilia A

F. Tzortzatou-Stathopoulou, M. Moschovi, H. Platokouki, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).

G. Tsangaris, C. Sofocleous, A. Mavrou, 2006, In vivo.

The Hygiene Hypothesis and the Participation of Chemical Products

K. Salavoura, 2018 .

Development of cancer in patients with primary immunodeficiencies.

Ariadni Mavrou, G. Tsangaris, A. Kolialexi, 2008, Anticancer research.

A case of Ehlers Danlos syndrome type VI.

A. Mavrou, A. Kolialexi, M. Valari, 2006, Genetic counseling.