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Effect of longacting somatostatin analogue on kidney and cyst growth in autosomal dominant polycystic kidney disease (ALADIN): a randomised, placebo-controlled, multicentre trial

The Lancet (British edition), 2013-11, Vol.382 (9903), p.1485-1495

2013

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Octreotide-LAR in later-stage autosomal dominant polycystic kidney disease (ALADIN 2): A randomized, double-blind, placebo-controlled, multicenter trial

PLoS medicine, 2019-04, Vol.16 (4), p.e1002777

2019

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Sirolimus Therapy to Halt the Progression of ADPKD

Journal of the American Society of Nephrology, 2010-06, Vol.21 (6), p.1031-1040

2010

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Measuring and estimating GFR and treatment effect in ADPKD patients: results and implications of a longitudinal cohort study

PloS one, 2012-02, Vol.7 (2), p.e32533-e32533

2012

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A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals

iScience, 2023-10, Vol.26 (10), p.107629-107629, Article 107629

2023

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Early detection of diabetic kidney disease by urinary proteomics and subsequent intervention with spironolactone to delay progression (PRIORITY): a prospective observational study and embedded randomised placebo-controlled trial

The lancet. Diabetes & endocrinology, 2020-04, Vol.8 (4), p.301-312

2020

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Paricalcitol for secondary hyperparathyroidism in renal transplantation

Journal of the American Society of Nephrology, 2015-05, Vol.26 (5), p.1205-1214

2015

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Effect of Sirolimus on Disease Progression in Patients with Autosomal Dominant Polycystic Kidney Disease and CKD Stages 3b-4

Clinical journal of the American Society of Nephrology, 2016-05, Vol.11 (5), p.785-794

2016

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Octreotide-LAR in later-stage autosomal dominant polycystic kidney disease

PLoS medicine, 2019-04, Vol.16 (4)

2019

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Moderate salt restriction with or without paricalcitol in type 2 diabetes and losartan-resistant macroalbuminuria (PROCEED): a randomised, double-blind, placebo-controlled, crossover trial

The lancet. Diabetes & endocrinology, 2018-01, Vol.6 (1), p.27-40

2018

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Integrating Personalized and Accessible Itineraries in MaaS Ecosystems Through Microservices

Mobile networks and applications, 2018-02, Vol.23 (1), p.167-176

2018

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Gamifying cultural experiences across the urban environment

Multimedia tools and applications, 2019-02, Vol.78 (3), p.3341-3364

2019

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COVID-19 in rheumatic diseases in Italy: first results from the Italian registry of the Italian Society for Rheumatology (CONTROL-19)

Clinical and experimental rheumatology, 2020-07, Vol.38 (4), p.748

2020

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Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak–like primary immunodeficiency syndrome

Blood, 2012-03, Vol.119 (13), p.3185-3187

2012

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Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism

Orphanet journal of rare diseases, 2013-10, Vol.8 (1), p.168-168, Article 168

2013

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A Service-Oriented Approach to Crowdsensing for Accessible Smart Mobility Scenarios

Mobile information systems, 2016-01, Vol.2016, p.1-14

2016

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Effects of Sevelamer Carbonate in Patients With CKD and Proteinuria: The ANSWER Randomized Trial

American journal of kidney diseases, 2019-09, Vol.74 (3), p.338-350

2019

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Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy

Human molecular genetics, 2005-03, Vol.14 (5), p.657-665

2005

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Drug–drug interactions involving CYP3A4 and p-glycoprotein in hospitalized elderly patients

European journal of internal medicine, 2019-07, Vol.65, p.51-57

2019

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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 21 as a milder allelic variant of congenital muscular dystrophy MDC1C

Human molecular genetics, 2001-12, Vol.10 (25), p.2851-2859

2001

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Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis

American journal of respiratory cell and molecular biology, 2016-11, Vol.55 (5), p.645-656

2016

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I want to ride my bicycle: A microservice-based use case for a MaaS architecture

2017 IEEE Symposium on Computers and Communications (ISCC), 2017, p.18-22

2017

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Mutations in the Fukutin-Related Protein Gene ( FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

American journal of human genetics, 2001, Vol.69 (6), p.1198-1209

2001

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Effect of longacting somatostatin analogue on kidney and cyst growth in autosomal dominant polycystic kidney disease (ALADIN): a randomised, placebo-controlled, multicentre trial

Octreotide-LAR in later-stage autosomal dominant polycystic kidney disease (ALADIN 2): A randomized, double-blind, placebo-controlled, multicenter trial

Sirolimus Therapy to Halt the Progression of ADPKD

Preventing microalbuminuria with benazepril, valsartan, and benazepril–valsartan combination therapy in diabetic patients with high-normal albuminuria: A prospective, randomized, open-label, blinded endpoint (PROBE) study

Measuring and estimating GFR and treatment effect in ADPKD patients: results and implications of a longitudinal cohort study

A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals

Early detection of diabetic kidney disease by urinary proteomics and subsequent intervention with spironolactone to delay progression (PRIORITY): a prospective observational study and embedded randomised placebo-controlled trial

Paricalcitol for secondary hyperparathyroidism in renal transplantation

Preventing microalbuminuria with benazepril, valsartan, and benazepril-valsartan combination therapy in diabetic patients with high-normal albuminuria: A prospective, randomized, open-label, blinded endpoint

Effect of Sirolimus on Disease Progression in Patients with Autosomal Dominant Polycystic Kidney Disease and CKD Stages 3b-4

Octreotide-LAR in later-stage autosomal dominant polycystic kidney disease

Moderate salt restriction with or without paricalcitol in type 2 diabetes and losartan-resistant macroalbuminuria (PROCEED): a randomised, double-blind, placebo-controlled, crossover trial

Integrating Personalized and Accessible Itineraries in MaaS Ecosystems Through Microservices

Gamifying cultural experiences across the urban environment

COVID-19 in rheumatic diseases in Italy: first results from the Italian registry of the Italian Society for Rheumatology (CONTROL-19)

Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak–like primary immunodeficiency syndrome

Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism

A Service-Oriented Approach to Crowdsensing for Accessible Smart Mobility Scenarios

Effects of Sevelamer Carbonate in Patients With CKD and Proteinuria: The ANSWER Randomized Trial

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy

Drug–drug interactions involving CYP3A4 and p-glycoprotein in hospitalized elderly patients

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 21 as a milder allelic variant of congenital muscular dystrophy MDC1C

Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis

I want to ride my bicycle: A microservice-based use case for a MaaS architecture

Mutations in the Fukutin-Related Protein Gene ( FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

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