List of works - Daniela Iancu

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration

scientific article

Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic review

scientific article published on 10 July 2020

Challenging DNA samples solved with MiniSTR analysis. Brief overview

Clinical and diagnostic features of Bartter and Gitelman syndromes.

scientific article published on 10 November 2017

Deletion in MEFV resulting in the loss of p.M694 residue as the cause of autosomal dominant familial Mediterranean fever in North Western European Caucasians - a case series and genetic exploration.

scientific article

EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10

scientific article

Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families

article

Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes

scientific article published on 13 October 2016

Erratum: Long-term outcome in inherited nephrogenic diabetes insipidus

scientific article published on 07 December 2020

Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome.

scientific article

Genetics of renovascular hypertension in children

scientific article published on 06 June 2020

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

scientific article published on 13 April 2018

High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults

scientific article published on 16 September 2019

Inflammatory gene expression profiles in Crohn's disease and ulcerative colitis: a comparative analysis using a reverse transcriptase multiplex ligation-dependent probe amplification protocol

scientific article published on 24 September 2012

Long-term outcome in inherited nephrogenic diabetes insipidus

scientific article published on 13 April 2018

Management of children with congenital nephrotic syndrome: challenging treatment paradigms

scientific article published on 01 August 2019

Molecular signatures of cardiac stem cells

scientific article

Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.

scientific article published on 3 April 2017

Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies

scientific article published in February 2018

Spontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesis

scientific article

Transplantation of a Gitelman Syndrome Kidney Ameliorates Hypertension: A Case Report

scientific article published on 07 September 2018

Treatment and long-term outcome in primary distal renal tubular acidosis

scientific article published on 01 June 2019

List of works by Daniela Iancu

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration

Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic review

Challenging DNA samples solved with MiniSTR analysis. Brief overview

Clinical and diagnostic features of Bartter and Gitelman syndromes.

Deletion in MEFV resulting in the loss of p.M694 residue as the cause of autosomal dominant familial Mediterranean fever in North Western European Caucasians - a case series and genetic exploration.

EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10

Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families

Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes

Erratum: Long-term outcome in inherited nephrogenic diabetes insipidus

Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome.

Genetics of renovascular hypertension in children

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults

Inflammatory gene expression profiles in Crohn's disease and ulcerative colitis: a comparative analysis using a reverse transcriptase multiplex ligation-dependent probe amplification protocol

Long-term outcome in inherited nephrogenic diabetes insipidus

Management of children with congenital nephrotic syndrome: challenging treatment paradigms

Molecular signatures of cardiac stem cells

Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.

Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies

Spontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesis

Transplantation of a Gitelman Syndrome Kidney Ameliorates Hypertension: A Case Report

Treatment and long-term outcome in primary distal renal tubular acidosis