Università LUM Giuseppe Degennaro - sito della Ricerca Institutional Research Information System

MITROTTI, ADELE
 Distribuzione geografica
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Continente #
Continente sconosciuto - Info sul continente non disponibili 32
NA - Nord America 1
Totale 33
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Nazione #
US - Stati Uniti d'America 1
Totale 1
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Nome #
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes 2
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy 1
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease 1
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing 1
Podocytes: the role of lysosomes in the development of nephrotic syndrome 1
Autoantibodies Targeting Nephrin in Podocytopathies 1
DUPLICATION OF THE SOX3 GENE IN AN SRY-NEGATIVE 46,XX MALE WITH ASSOCIATED CONGENITAL ANOMALIES OF KIDNEYS AND THE URINARY TRACT: CASE REPORT AND REVIEW OF THE LITERATURE 1
Diagnostic Utility of Exome Sequencing for Kidney Disease 1
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 1
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy 1
What Is Hidden in Patients with Unknown Nephropathy? Genetic Screening Could Be the Missing Link in Kidney Transplantation Diagnosis and Management 1
MUSIC THERAPY REDUCES ANXIETY AND PAIN AND IMPROVES SATISFACTION IN PATIENTS UNDERGOING PERCUTANEOUS RENAL BIOPSY 1
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux 1
Effect of music therapy intervention on anxiety and pain during percutaneous renal biopsy: a randomized controlled trial 1
Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789â 802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018)) 1
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis 1
Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis? 1
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis 1
Rituximab in Granulomatosis with Polyangiotis: Challenging equilibrium between Therapeutic efficacy and iatrogenic complications 1
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy 1
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis 1
Terapia della glomerulopatia a lesioni istologiche minime 1
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease 1
The complement system in the pathogenesis and progression of kidney diseases: What doesn’t kill you makes you older 1
The frequency of rare and monogenic diseases in pediatric organ transplant recipients in Italy 1
Medicine and Nephrology from Social Networks 1
Whole-Exome Sequencing in Adults With Chronic Kidney Disease A Pilot Study 1
Sindrome nefrosica e insufficienza renale rapidamente progressiva in paziente con componente monoclonale: un caso clinico 1
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome 1
The copy number variation landscape of congenital anomalies of the kidney and urinary tract 1
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux 1
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome 1
Totale 33
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Categoria #
all - tutte 86
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 86
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2026/202733 0 0 0 0 33 0 0 0 0 0 0 0
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