D. Iancu

发表

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

Johann M B Simbürger, P. Oefner, A. Hammers, 2018, Journal of the American Society of Nephrology : JASN.

ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature

N. Brunetti‐Pierri, M. Mansukhani, F. Santos-Simarro, 2021, American journal of medical genetics. Part A.

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

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

C. Gheorghe, M. Diculescu, R. Iacob, 2013, Journal of Crohn's & colitis.

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

R. Kleta, Simona Dumitriu, R. Coletta, 2017, Oral surgery, oral medicine, oral pathology and oral radiology.

Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation

Ellard, M. Weedon, N. Sebire, 2017 .

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

K. Dahan, P. Houillier, X. Jeunemaître, 2019, Kidney international.

Contribution of High-throughput sequencing to the Diagnosis of tubulopathies and Familal Hypercalcemia Hypocalciuria in Adults

Favero, K. Dahan, P. Houillier, 2019 .

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

P. Hawkins, R. Kleta, H. Stanescu, 2017, Rheumatology.

Clinical and diagnostic features of Bartter and Gitelman syndromes

R. Kleta, D. Bockenhauer, L. Jenkins, 2017, Clinical kidney journal.

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

A. Vénisse, K. Dahan, X. Jeunemaître, 2018, Kidney international.

Hypolipemiant besides antileukemic effect of imatinib mesylate.

G. Constantinescu, D. Georgescu, R. Gologan, 2009, Leukemia research.

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

K. Tullus, D. Iancu, Georgia Malakasioti, 2020, Pediatric Nephrology.

Management of children with congenital nephrotic syndrome: challenging treatment paradigms.

A. Edefonti, J. Bacchetta, G. Ariceta, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Challenging DNA samples solved with MiniSTR analysis. Brief overview

C. Iancu, E. Neagu, L. Bărbării, 2012 .

Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients

Shih-Hua Lin, D. Bockenhauer, S. Walsh, 2022, Kidney international reports.

Diagnostic Strategies to Identify Patients with Genetic Salt-Losing Tubulopathies

Shih-Hua Lin, D. Bockenhauer, S. Walsh, 2021, medRxiv.

Molecular signatures of cardiac stem cells.

S. Hostiuc, D. Dermengiu, M. Rusu, 2015, Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie.

Inherited Renal Tubulopathies—Challenges and Controversies

E. Ashton, D. Iancu, 2020, Genes.

Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome

R. Kleta, D. Bockenhauer, H. Stanescu, 2016, Molecular genetics & genomic medicine.