Nucleotide Variations in the <i>NPHS2</i> Gene in Greek Children with Steroid-Resistant Nephrotic Syndrome
Spyridon Megremis(University of Leicester), Joanne Traeger‐Synodinos(National and Kapodistrian University of Athens), Artemis G. Mitsioni(Panagiotis & Aglaia Kyriakou Children's Hospital), Sofia Kitsiou-Tzelli(Iaso Children’s Hospital), Irene Fylaktou(Children's Hospital Agia Sophia), Constantinos J. Stefanidis(Panagiotis & Aglaia Kyriakou Children's Hospital), Emmanuel Kanavakis(Athens State University), Andromachi Mitsioni(Panagiotis & Aglaia Kyriakou Children's Hospital)
Cited by 19
Related Papers
The interaction of α thalassaemia with heterozygous β thalassaemia
|British Journal of Haematology|1982|103
Successful long-term immunologic reconstitution by allogeneic hematopoietic stem cell transplantation cures patients with autosomal dominant hyper-IgE syndrome
|Journal of Allergy and Clinical Immunology|2010|78
Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia
|British Journal of Haematology|1983|74
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA
|Journal of the Neurological Sciences|2018|44