Paraskevas Iatropoulos

发表

Next-generation sequencing for new gene identification and for diagnosis in steroid-resistant nephrotic syndrome

P. Iatropoulos, Paraskevas Iatropoulos, 2017 .

MYO1E mutations and childhood familial focal segmental glomerulosclerosis.

G. Remuzzi, F. Macciardi, A. Benigni, 2011, The New England journal of medicine.

Disruption of PTPRO causes childhood-onset nephrotic syndrome.

A. Bakkaloğlu, F. Schaefer, N. Akarsu, 2011, American journal of human genetics.

Variations of the angiotensin II type 1 receptor gene are associated with extreme human longevity

D. Mari, G. Remuzzi, A. Benigni, 2013, AGE.

Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia

P. Iatropoulos, E. Sacchetti, C. Magri, 2009, Psychiatric genetics.

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

A. Anarat, G. Ardissino, G. Ghiggeri, 2013, Kidney international.

Direct Reprogramming of Human Bone Marrow Stromal Cells into Functional Renal Cells Using Cell-free Extracts

G. Remuzzi, A. Benigni, M. Goligorsky, 2015, Stem cell reports.

CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

G. Remuzzi, A. Benigni, P. Iatropoulos, 2021, Frontiers in Genetics.

Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN

G. Remuzzi, A. Benigni, P. Iatropoulos, 2018, Front. Immunol..

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome.

G. Remuzzi, E. Daina, P. Iatropoulos, 2016, Molecular immunology.

Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant

G. Remuzzi, A. Benigni, P. Iatropoulos, 2020, Frontiers in Medicine.

Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS

G. Remuzzi, A. Benigni, A. Amoroso, 2019, Front. Immunol..

Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutation

G. Remuzzi, E. Daina, P. Iatropoulos, 2012, Pediatric Nephrology.

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.

G. Remuzzi, E. Daina, P. Iatropoulos, 2017, Journal of the American Society of Nephrology : JASN.

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.

G. Remuzzi, R. Lifton, Mathieu Lemaire, 2015, Clinical journal of the American Society of Nephrology : CJASN.

Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM‐IV‐TR schizophrenia: A pilot case‐control association study in an Italian sample

P. Iatropoulos, E. Sacchetti, C. Magri, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genotype-phenotype associations in WT1 glomerulopathy.

K. Tory, G. Caridi, P. Iatropoulos, 2014, Kidney international.

Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome

D. Taruscio, F. Brancati, A. Ferlini, 2018, European Journal of Human Genetics.