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Progetti di ricerca

IRLANDA

County Dublin
DUBLIN

Finanziato da un ente associato a IRDiRCEnsemble averaging for complex disease prediction in the large p small n domain from multiple data sources
Trinity College Dublin
School of Computer Science and Statistcs - O'Reilly Institute

COREA DEL SUD

KOREA, REPUBLIC OF
KOREA

COREA DEL SUD

KOREA, REPUBLIC OF
SEOUL

FRANCIA

ILE-DE-FRANCE
PARIS

Predisposition factors in hemolytic uremic syndrome, atypical form, and in thrombotic microangiopathies
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
Laboratoire d'Immunologie biologique

GERMANIA

Baden-Württemberg
FREIBURG

SFB 1140 (KIDGEM) : Identification of TULP3-mutations in patients with cystic kidney disease and related ciliopathies
Zentrum für Klinische Forschung am Universitätsklinikum Freiburg
Nephro Lab

GERMANIA

Baden-Württemberg
HEIDELBERG

Finanziato da un ente associato a IRDiRCNEOCYST: Multidisciplinary network to study the pathogenesis, clinical presentation and prognosis of hereditary cystic kidney disease in childhood
Zentrum für Kinder- und Jugendmedizin - Angelika-Lautenschläger-Klinik
Klinik für Kinderheilkunde I - Sektion Pädiatrische Nephrologie

GERMANIA

Nordrhein-Westfalen
KÖLN

GERMANIA

Nordrhein-Westfalen
MÜNSTER

Finanziato da un ente associato a IRDiRCNEOCYST: Multidisciplinary network to study the pathogenesis, clinical presentation and prognosis of hereditary cystic kidney disease in childhood
KfH Kuratorium für Dialyse und Nierentransplantation e.V.
KfH-Nierenzentrum für Kinder und Jugendliche

SPAGNA

Galicia
SANTIAGO DE COMPOSTELA

STATI UNITI

South Dakota
SIOUX FALLS

BELGIO

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

EUNEFRON: rare disorders of the distal convoluted tubule (WP4)
Cliniques universitaires Saint-Luc - UCLouvain
Laboratory of Nephrology

BELGIO

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

FRANCIA

AUVERGNE-RHONE-ALPES
GRENOBLE

Physiopathological studies of Lowe's syndrome and Dent's disease, two clinical entities with common molecular basis?
CHU de Grenoble et des Alpes - Institut de biologie et de pathologie
Laboratoire de Génétique Moléculaire: maladies héréditaires et oncologie

FRANCIA

ILE-DE-FRANCE
PARIS

EUNEFRON: rare disorders of the distal convoluted tubule (WP4)
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
Service de génétique

FRANCIA

ILE-DE-FRANCE
PARIS

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCIdentification of New Molecular Mechanisms involved in Bartter Syndrome
Centre de Recherches des Cordeliers (CRC)
Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCPLA2R-negative extramembranous glomerulopathies: antigens, models and patients
Groupe hospitalier AP-HP.6 - Hôpital Tenon
INSERM UMRS 1155 "Des maladies rénales aux maladies fréquentes, remodelage et réparation"

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCStudy of the rupture of tubular homeostasis in polycystic kidney disease
Hôpital Necker-Enfants Malades
Néphropathies héréditaires et rein en développement

FRANCIA

OCCITANIE
MONTPELLIER

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
VALBONNE

Finanziato da un ente associato a IRDiRCDynamics of anti-PLA2R1 and anti-THSD7A autoantibodies in patients with extramembranous glomerulonephritis: from early stages to active disease
IPMC - Institut de Pharmacologie Moléculaire et Cellulaire
Equipe "Physiopathologie moléculaire des phospholipases A2 & de leurs médiateurs"

GERMANIA

Baden-Württemberg
FREIBURG

The role of CCL2 in nephronophthisis and autosomal dominant polycystic kidney disease (ADPKD)
Zentrum für Klinische Forschung am Universitätsklinikum Freiburg
Nephro Lab

GERMANIA

Baden-Württemberg
FREIBURG

GERMANIA

Nordrhein-Westfalen
KÖLN

The German ADPKD Tolvaptan Treatment Registry is a Prospective, Observational, Multicentric Study of Patients Suffering From ADPKD That Are Considered for Tolvaptan Treatment
Universitätsklinikum Köln
Klinik II für Innere Medizin - Nephrologie, Rheumatologie, Diabetologie und allgemeine Innere Medizin

GERMANIA

Sachsen
LEIPZIG

High-throughput mutation analysis for known and novel single-gene causes of kidney stones and related disorders
Universitätsklinikum Leipzig AöR
Klinik und Poliklinik für Endokrinologie, Nephrologie, Rheumatologie

GERMANIA

Sachsen
LEIPZIG

Genetic determinants of kidney stone formation in ADPKD
Universitätsklinikum Leipzig AöR
Klinik und Poliklinik für Endokrinologie, Nephrologie, Rheumatologie

GIAPPONE

JAPAN
KYOTO

GIAPPONE

JAPAN
TOKYO

Finanziato da un ente associato a IRDiRCDevelopment of novel therapeutic drugs for congenital nephrogenic diabetes insipidus
Tokyo Medical and Dental University
Department of Nephrology

GIAPPONE

JAPAN
TOKYO

Finanziato da un ente associato a IRDiRCScreening of novel therapeutics for intellectual disability and autism in tuberous sclerosis complex
Tokyo Metropolitan Institute of Medical Science
Department of Brain Development and Neural Regeneration

NORVEGIA

Østlandet
OSLO

Effectiveness and safety of mTOR-inhibitor in patients with tuberous sclerosis complex
Oslo University Hospital, Ullevaal
NevSom - Nasjonalt kompetansesenter for nevroutviklingsforstyrrelser og hypersomier

REGNO UNITO; GRAN BRETAGNA

West Midlands
BIRMINGHAM

EURO-WABB: EURO-Rare Diabetes Project (coordination)
Birmingham Children's Hospital NHS Foundation Trust
Diabetes Unit

SPAGNA

Canarias
LAS PALMAS DE GRAN CANARIA

Finanziato da un ente associato a IRDiRCInvestigation of therapeutic strategies for Dent-1 disease and adaptation of RenalTube to the needs of patients with primary tubulopathies
Hospital Universitario de Gran Canaria Dr. Negrín
FIISC: Fundación Canaria Instituto de Investigación Sanitaria de Canarias

SPAGNA

Cataluña
BARCELONA

Finanziato da un ente associato a IRDiRCPrediction models in autosomal dominant hereditary nephropathies
Fundació Puigvert
Servicio de Nefrología

SPAGNA

Cataluña
BARCELONA

Deciphering the mechanisms of PLA2R-specific B-cell autoimmunity in primary membranous nephropathy (PMN) (BCELL-MEM)
Vall d'Hebron Institut de Recerca VHIR
Grupo de investigación en nefrología

SPAGNA

Cataluña
L'HOSPITALET DE LLOBREGAT

Finanziato da un ente associato a IRDiRCCystinuria: Validation of a new cystine lithiasis biomarker in patients and design of a new treatment based on cystine lithiasis modulators identified in mouse models
IDIBELL - Instituto de Investigación Biomédica de Bellvitge
Instituto de Investigación Biomédica de Bellvitge

SPAGNA

Galicia
VIGO

Finanziato da un ente associato a IRDiRCMolecular mechanisms in ciliopathies
Universidade de Vigo
Grupo de Enfermedades raras

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCHuman biochemical genetics
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCMechanisms of retinal degeneration in inherited diseases
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCMechanotransduction and the regulation of skeletal muscle mass
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCZfp423 mechanisms in joubert syndrome and related disorders
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCFilamin a in tsc
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCMechanisms of synapse remodeling in tsc
Institution: Information not provided - US

SVEZIA

Region Skåne
LUND

Bacterial virulence factors, innate immunity and prothrombotic mechanisms in renal disease
Skånes Universitetssjukhus
Department of Clinical Sciences, Division of Pediatrics

SVEZIA

Region Stockholm
STOCKHOLM

Understanding Genetic Mechanisms in Disorders and Development of Diagostic Methods
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery

SVIZZERA

Suisse Alémanique
BERN

Thrombotic thrombocytopenic purpura - role of ADAMTS13 and long-term outcome
University Hospital Inselspital
Department of Hematology and Central Hematology Laboratory

AUSTRIA

TIROL
INNSBRUCK

Structure of the Neurofibromatosis Type 1 Protein
Medizinische Universität Innsbruck
Sektion für Biologische Chemie

BELGIO

VLAAMS BRABANT
LEUVEN

Molecular and functional pathogenesis in NF1 and related diseases
UZ Leuven - Campus Gasthuisberg
Centrum Menselijke Erfelijkheid - UZ Leuven

CANADA

Ontario
TORONTO

FINLANDIA

Finland
TURKU

Clinical research study on neurofibromatosis type 1 in Finland
University of Turku
Institute of Biomedicine

FRANCIA

AUVERGNE-RHONE-ALPES
PRAGUE

Finanziato da un ente associato a IRDiRCNeurofibromatosis type 1 Disease Model
Faculty of Medicine and University Hospital Motol
Department of Pediatrics

FRANCIA

AUVERGNE-RHONE-ALPES
PRAGUE

Finanziato da un ente associato a IRDiRCRole on Nonmuscle Myosin II in membrane trafficking and organ function
Faculty of Medicine and University Hospital Motol
Department of Pediatrics

FRANCIA

CENTRE-VAL DE LOIRE
ORLÉANS

Finanziato da un ente associato a IRDiRCFirst preclinical validation of LOOK / ROCK inhibitors for the treatment of neurofibromatosis type 1
UPR4301 Centre de biophysique moléculaire (CBM)
Equipe signalisation cellulaire et neurofibromatose

FRANCIA

GRAND-EST
STRASBOURG

Bernard-Soulier Syndrome and MYH9 associated diseases: study of blood platelets anomalies and of the thrombopoïesis, correction by genetic therapy
Établissement Français du Sang - Grand Est
UR U311 - Biologie et pharmacologie de l'hémostase et de la thrombose

FRANCIA

ILE-DE-FRANCE
PARIS

Implementation of non-invasive prenatal diagnosis of rare and severe monogenic diseases
CHU Paris Centre - Hôpital Cochin, Site Cochin
Service de génétique et biologie moléculaires

FRANCIA

ILE-DE-FRANCE
PARIS

Constitutive hematologic diseases: clinical and therapeutic research, molecular biology
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
Service d'hématologie pédiatrique

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCMolecular signature of convertase activation in complement-dependent glomerulopathies
Centre de Recherches des Cordeliers (CRC)
Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

FRANCIA

NORMANDIE
CAEN

Genetic lesions of the GS alpha protein (GNAS1) in Albright osteodystrophy and pseudohypoparathyroïdism type 1A and 1B
Faculté de médecine de Caen
Mobilités : Attention, Orientation et Chronobiologie (COMETE)

FRANCIA

OCCITANIE
TOULOUSE

Structure-function relationship of the TSH receptor and of the related receptors
CHU de Toulouse - Hôpital Rangueil
Institut des Maladies Métaboliques et Cardiovasculaires

FRANCIA

PAYS DE LA LOIRE
ANGERS

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
VALBONNE

Finanziato da un ente associato a IRDiRCMNaims : Molecular dissection of PLA2R1-related membranous nephropathy: towards a portfolio of new clinical biomarkers - FR
IPMC - Institut de Pharmacologie Moléculaire et Cellulaire
Equipe "Physiopathologie moléculaire des phospholipases A2 & de leurs médiateurs"

GERMANIA

Baden-Württemberg
ULM

Finanziato da un ente associato a IRDiRCGeNeRARe: German Network for RASopathies
Institute of Comparative Molecular Endocrinology der Universität Ulm
Cirstea Lab

GERMANIA

Berlin
BERLIN

CLC Cl- channels and transporters in basic cellular processes and pathological states
Leibniz-Institut für Molekulare Pharmakologie
Department Physiology and Pathology of Ion Transport

GERMANIA

Berlin
BERLIN

Molecular genetics of autosomal-dominant hypertension with brachydactyly type E
Max-Delbrück-Centrum für Molekulare Medizin
AG Luft - Genetik und Pathophysiologie des Herz - Kreislaufsystems

GERMANIA

Hamburg
HAMBURG

Finanziato da un ente associato a IRDiRCGeNeRARe: German Network for RASopathies
UKE - Universitätsklinikum Hamburg-Eppendorf
Institut für Humangenetik

GERMANIA

Mecklenburg-Vorpommern
GREIFSWALD

Mutational spectra and clinical manifestation in patients with congenital haemophilia
Institut für Humangenetik der Universitätsmedizin Greifswald
Institut für Humangenetik

GERMANIA

Niedersachsen
GÖTTINGEN

European Alport therapy registry
Universitätsmedizin Göttingen
Klinik für Nephrologie und Rheumatologie

GERMANIA

Niedersachsen
GÖTTINGEN

Finanziato da un ente associato a IRDiRCGeNeRARe: German Network for RASopathies
Universitätsmedizin Göttingen
Klinik für Thorax-, Herz- und Gefäßchirurgie

GERMANIA

Nordrhein-Westfalen
BAD OEYNHAUSEN

Molekular diagnosis and pathomechanism in pseudoxanthoma elasticum
Ruhr-Universität Bochum
Institut für Laboratoriums- und Transfusionsmedizin

GERMANIA

Nordrhein-Westfalen
DÜSSELDORF

Finanziato da un ente associato a IRDiRCGeNeRARe: German Network for RASopathies
Heinrich-Heine-Universität Düsseldorf
Institut für Biochemie und Molekularbiologie II

GERMANIA

Sachsen-Anhalt
MAGDEBURG

Finanziato da un ente associato a IRDiRCGeNeRARe: German Network for RASopathies
Otto-von-Guericke-Universität Magdeburg
Abteilung Genetik & Molekulare Neurobiologie

GIAPPONE

JAPAN
FUKUOKA

Finanziato da un ente associato a IRDiRCEstablishment of high evidence level for revision of guideline ofAllied Disorders of Hirschsprung's disease
Kyushu University Faculty of Medical Sciences
Department of Pediatric Surgery

GIAPPONE

JAPAN
TOKYO

ITALIA

EMILIA ROMAGNA
MODENA

Pseudoxantoma elstico: dalla comprensione dei meccanismi patogenetici verso prospettive terapeutiche
Università degli Studi di Modena e Reggio Emilia
LabGen - Laboratorio Sequenziamento Genomico

ITALIA

LIGURIA
GENOVA

PAESI BASSI

Gelderland
NIJMEGEN

HNF1ß: master regulator of cilia formation and electrolyte homeostasis in ADTKD-HNF1ß patients
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

PORTOGALLO

NORTE
PORTO

Alport Syndrome: Clinical and molecular study of Portuguese families
Faculdade de Medicina da Universidade do Porto
Unidade de Investigação e Desenvolvimento de Nefrologia

PORTOGALLO

NORTE
PORTO

LIMP-2 studies: from clinical genetics to functional genomics and back (studies in action myoclonus-renal failure syndrome (AMRF))
Instituto de Biologia Molecular e Celular
Unidade de Biologia do Lisossoma e do Peroxissoma

PORTOGALLO

SUL
LISBOA

Functional and genetic analysis of WNK protein kinases involved in Gordon syndorme
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Unidade de Investigação e Desenvolvimento

REGNO UNITO; GRAN BRETAGNA

Tyne & Wear
NEWCASTLE UPON TYNE

Finanziato da un ente associato a IRDiRCThe Role of Membrane Attack Complex in Atypical Haemolytic Uraemic Syndrome
Institute of Cellular Medicine, Newcastle University, Medical School
Institute of Cellular Medicine

SPAGNA

Andalucía
SEVILLA

Mathematical models of disease mechanisms to reformulate drugs for rare diseases
Fundación Progreso y Salud
Área de bioinformática clínica

SPAGNA

Asturias
OVIEDO

Finanziato da un ente associato a IRDiRCApplication of RenalTube to patients needs and clinical and experimental research on distal renal tubular acidosis and hypophosphatemic rickets linked to the X chromosome
Fundación para la Investigación Biosanitaria del Principado de Asturias
FINBA: Fundación para la Investigación Biosanitaria del Principado de Asturias

SPAGNA

Cataluña
BADALONA

Finanziato da un ente associato a IRDiRCImpact of cellular, genetic and epigenetic heterogeneity in the progression and treatment of peripheral nervous system tumors associated to Neurofibromatosis type 1
Instituto de Investigación Germans Trias i Pujol
Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol

SPAGNA

Madrid
MADRID

Finanziato da un ente associato a IRDiRCQuantitative profiles of complement FH/FHR proteins as biomarkers of disease predisposition and evolution in primary and secondary haemolytic uraemic syndrome
IdiPAZ - Instituto de Investigación Sanitaria del Hospital Universitario La Paz
Laboratorio de Inmunopatología del Complemento

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCTargeting tumors with nf1 loss
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCClinical and genetic studies of vacterl association
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCMechanisms of nf1 pathophysiology underlying hyperactivity
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCSocial competence in youth with neurofibromatosis type 1
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 1: gene networks for social cognition in williams syndrome
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 2: modeling williams syndrome using human neurons
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 3: cellular architectonics and local circuits
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 4: neuroimaging of social circuitry
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 5: characterization of social phenotype
Institution: Information not provided - US

SVIZZERA

Suisse Alémanique
ZÜRICH

SVIZZERA

Suisse Romande
GENÈVE

Non-cell-autonomous circadian regulation of brain function
UNIGE
Département de Génétique et Evolution

SVIZZERA

Suisse Romande
LAUSANNE

AUSTRIA

WIEN
WIEN

Systems medicine analysis of sarcoidosis by targeting mTOR in a co-clinical trial in patients and mice
Allgemeines Krankenhaus der Stadt Wien
Universitätsklinik für Dermatologie

CANADA

Ontario
TORONTO

FRANCIA

AUVERGNE-RHONE-ALPES
BRON

Genetic transmission of familial forms of sarcoidosis
CHU de Lyon HCL - GH Est
Unité Médicale de Génétique des Cancers et des Maladies Multifactorielles

FRANCIA

AUVERGNE-RHONE-ALPES
BRON

Genetic transmission of familial forms of sarcoidosis
CHU de Lyon HCL - GH Est-Hôpital Louis Pradel
Service de pneumologie

FRANCIA

ILE-DE-FRANCE
MONTROUGE

Finanziato da un ente associato a IRDiRCVasorin: Role of Vasorin in the kidney, bone and arterial crosstalk - FR
Université Paris Descartes - UFR Odontologie
Laboratoire "Pathologie, Imagerie et Biothérapies orofaciales" - EA2496

FRANCIA

ILE-DE-FRANCE
PARIS

Evaluation and treatement of scleroderma
CHU Paris Est - Hôpital Saint-Antoine
Service de médecine interne

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCFMFgeneToDiag : Familial Mediterranean Fever (FMF) and FMF-like diseases: From genetics to functional diagnostic tests - FR
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Physiopathologie Des Maladies Génétiques d'Expression Pédiatrique - Inserm UMRS_933

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCT-JUST: Tight junctions: from structure to treatment - FR
Centre de Recherches des Cordeliers (CRC)
Equipe "Métabolisme et Physiologie Rénale"

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCGenetransnephrose: Genetic and translational studies in patients with steroid sensitive nephrotic syndrome - FR
Groupe hospitalier AP-HP.6 - Hôpital Tenon
INSERM UMRS 1155 "Des maladies rénales aux maladies fréquentes, remodelage et réparation"

GERMANIA

Baden-Württemberg
HEIDELBERG

Finanziato da un ente associato a IRDiRCReDox: Repurposing doxycycline in the treatment of AL amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

GERMANIA

Baden-Württemberg
TÜBINGEN

ESPED-study: Omphaloceles and Associated Malformations in Preterm and Term Newborns
Universitätsklinik für Kinder- und Jugendmedizin Tübingen
Abteilung für Neonatologie

GERMANIA

Bayern
ERLANGEN

Finanziato da un ente associato a IRDiRCSTOP-FSGS: Soluble factors in FSGS
Internistisches Zentrum des Universitätsklinikums Erlangen
Medizinische Klinik 4 - Nephrologie und Hypertensiologie

GERMANIA

Bayern
MÜNCHEN

Role of kinase-coupled TRP channels in Mg2+ homeostasis: From mouse models to human disease (TRR 152: P15)
Walther-Straub-Institut für Pharmakologie und Toxikologie der LMU München
Walther-Straub-Institut für Pharmakologie und Toxikologie

GERMANIA

Berlin
BERLIN

Finanziato da un ente associato a IRDiRCActiMON: Activity monitoring in adolescents and young adults with inflammatory rheumatic musculoskeletal diseases
Deutsches Rheuma-Forschungszentrum Berlin
Forschungsbereich Epidemiologie

GERMANIA

Hamburg
HAMBURG

International Inceptions cohort for Juvenile Systemic Sclerosis (jSSc)
Schön Klinik Hamburg Eilbek
Hamburger Zentrum für Kinder- und Jugendrheumatologie

GERMANIA

Nordrhein-Westfalen
KÖLN

Genomic profiling and epigenetic biomarker discovery in steroid-resistant nephrotic syndrome
Institut für Humangenetik am Universitätsklinikum Köln
Institut für Humangenetik

GERMANIA

Nordrhein-Westfalen
KÖLN

Alterations of slit diaphragm signaling as a cause of FSGS
Universitätsklinikum Köln
Klinik II für Innere Medizin - Nephrologie, Rheumatologie, Diabetologie und allgemeine Innere Medizin

GERMANIA

Sachsen-Anhalt
DESSAU

Diagnostic criteria of Behcet disease
Städtisches Klinikum Dessau
Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

GERMANIA

Sachsen-Anhalt
DESSAU

Epidemiology of Behcet disease in Germany
Städtisches Klinikum Dessau
Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

GERMANIA

Sachsen-Anhalt
DESSAU

Prognostic criteria of Behcet disease
Städtisches Klinikum Dessau
Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

GERMANIA

Schleswig-Holstein
LÜBECK

Generation and characterization of an antibody-based mouse model for systemic sclerosis
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Rheumatologie und Klinische Immunologie

GIAPPONE

JAPAN
AICHI

Finanziato da un ente associato a IRDiRCThe establishment of novel diagnostic methods for adult nephrotic syndrome.
Nagoya University Graduate School of Medicine
Division of Nephrology

GIAPPONE

JAPAN
KUMAMOTO

Finanziato da un ente associato a IRDiRCThe investigation on the efficacy of new low molecular compound for systemic sclerosis
Faculty of Life Sciences, Kumamoto University
Department of Dermatology and Plastic Surgery

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCSviluppo di trattamenti e prevenzione della cardiopatia grave nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCSviluppo di trattamenti e prevenzione dell'ipertensione polmonare nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCPrevenzione e trattamento delle ulcere digitali nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani
Divisione di Reumatologia

ITALIA

LOMBARDIA
BERGAMO

Finanziato da un ente associato a IRDiRCComprendere il ruolo delle alterazioni del gene di PAX2 nello sviluppo di glomerulosclerosi focale segmentaria
IRCCS Mario Negri - Centro Anna Maria Astori
Dipartimento Medicina Molecolare

ITALIA

LOMBARDIA
RANICA

Finanziato da un ente associato a IRDiRCIdentificazione di nuovi geni associati alla sindrome nefrosica steroido-resistente
Istituto di Ricerche Farmacologiche Mario Negri
Centro di Ricerche Cliniche per le Malattie Rare

ITALIA

TOSCANA
FIRENZE

PAESI BASSI

Gelderland
NIJMEGEN

The magnesium journey through the renal cell: how to get out?
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

PAESI BASSI

Gelderland
NIJMEGEN

PAESI BASSI

Utrecht
NIEUWEGEIN

Genetic predisposition to interstitital lung diseases and disease phenotypes
St. Antonius Ziekenhuis, locatie Nieuwegein
Longcentrum

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
CAMBRIDGE

SPAGNA

Andalucía
GRANADA

Finanziato da un ente associato a IRDiRCUrinary biomarkers for the non-invasive diagnosis of kidney disease in systemic autoimmune diseases
GENYO - Genómica e Investigación Oncológica
Grupo de Genética de enfermedades complejas

SPAGNA

Andalucía
SEVILLA

Finanziato da un ente associato a IRDiRCAutophagy and inflammation: model in classic autoinflammatory syndromes and Behçet's disease
IBIS - Instituto de Biomedicina de Sevilla
Grupo de Inmunología

SPAGNA

Cataluña
MARTORELL

SPAGNA

Madrid
ALCORCÓN

Finanziato da un ente associato a IRDiRCDeciphering the role of factor-H related proteins in complement-related kidney diseases
Hospital Universitario Fundación Alcorcón
Servicio de Nefrología

SPAGNA

Madrid
MADRID

Finanziato da un ente associato a IRDiRCDeciphering the role of factor-H related proteins in complement-related kidney diseases
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en Nefrología Clínica

SPAGNA

País Vasco
BARAKALDO

SPAGNA

País Vasco
DERIO

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCJuvenile myositis
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCGenetic analysis of complex inflammatory disorders
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCGenetics; natural history; and pathophysiology of behcet's disease
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCImmunogenetic mechanisms in behcet's disease
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCPathogenesis of behcet's disease and still's disease
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 1: systemic sclerosis skin biomarkers & therapeutics
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCProject 3: targeting pro-fibrotic e3 ligases in systemic sclerosis
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

SVEZIA

Region Stockholm
STOCKHOLM

Molecular and clinical studies of bladder exstrophy and congenital adrenal hyperplasia
Karolinska Institutet - Solna
Department of Women's and Children's Health

FRANCIA

ILE-DE-FRANCE
PARIS

Model contribution in the microeconomic assessment of therapeutic strategies in Wegener granulomatosis
CHU Paris Centre - Hôpital Cochin, Site Cochin
Service de Santé publique : Gestion des risques et qualité

GERMANIA

Bayern
MÜNCHEN

Establishment of surface plasmon resonance (SPR) tests for improved diagnostics of autoimmune diseases
Klinikum rechts der Isar der Technischen Universität München
Arbeitsgruppe Biosensorik

ITALIA

PUGLIA
BARI

Fisiopatologia della Vasculite Crioglobulinemica HCV-correlata: analisi molecolare, immunologica e clinica
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Unità di Epatologia - Sezione di Medicina Interna e Oncologia Clinica

REGNO UNITO; GRAN BRETAGNA

West Yorkshire
LEEDS

GCA Consortium - Clinical and immunogenetic characterization of Giant Cell Arteritis (GCA) and polymyalgia rheumatica (PMR)
Leeds Institute of Rheumatic and Musculoskeletal Medicine
Molecular Rheumatology Group

REGNO UNITO; GRAN BRETAGNA

West Yorkshire
LEEDS

REGNO UNITO; GRAN BRETAGNA

West Yorkshire
LEEDS

REGNO UNITO; GRAN BRETAGNA

West Yorkshire
LEEDS

SPAGNA

Andalucía
ARMILLA

Finanziato da un ente associato a IRDiRCIdentification of functionally relevant genetic variants associated with GCA - ES
Instituto de Parasitología y Biomedicina "López-Neyra"
Bases genéticas de las enfermedades autoinmunes

SPAGNA

Andalucía
ARMILLA

Finanziato da un ente associato a IRDiRCIdentification of pathogenic mechanisms involved in the development of giant cell arteritis through individual T-cell transcriptome sequencing
Instituto de Parasitología y Biomedicina "López-Neyra"
Bases fisiopatología y terapéutica médica

SPAGNA

Andalucía
CÓRDOBA

Finanziato da un ente associato a IRDiRCIdentification of molecular heterogeneity associated with cardiovascular disease, clinical course and therapeutic response in systemic autoimmune diseases
IMIBIC - Instituto Maimónides de Investigación Biomédica de Córdoba
GC05 - Grupo de investigación en enfermedades autoinmunes inflamatorias sistémicas y crónicas del aparato locomotor

SPAGNA

Cantabria
SANTANDER

Finanziato da un ente associato a IRDiRCCharacterization of molecular bases of IgA-mediated vasculitis
IDIVAL: Instituto de Investigación Marqués de Valdecilla
Grupo de Epidemiología genética y arterioesclerosis en enfermedades inflamatorias sistémicas

SPAGNA

Cataluña
BARCELONA

Finanziato da un ente associato a IRDiRCMultimodal imaging study for the diagnosis and prognosis of patients with systemic lupus erythematosus
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Institut d'Investigacions Biomèdiques August Pi i Sunyer

SPAGNA

Cataluña
BARCELONA

Finanziato da un ente associato a IRDiRCFunctional characterisation of inflammation and vascular remodelling pathways in GCA - ES
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Grupo de investigación en enfermedades autoinmunes sistémicas

SPAGNA

Cataluña
BARCELONA

Finanziato da un ente associato a IRDiRCChimeric autoantigen receptor T cells (CAAR-Tcell) as a new targeted therapy for lupus nephritis
Vall d'Hebron Institut de Recerca VHIR
Grupo de investigación en reumatología

SPAGNA

Comunidad Valenciana
VALENCIA

Finanziato da un ente associato a IRDiRCProfile of exosomal microRNAs and their long-term prognostic value in systemic lupus erythematosus. Association with established markers of kidney damage
INCLIVA - Facultad de Medicina de la Universidad de Valencia
Grupo de estudio de riesgo cardiometabólico y renal

SPAGNA

Madrid
MADRID

Finanziato da un ente associato a IRDiRCStudy of the relevance of PSGL-1/P-selectin interaction in the cellular proteostasis and implication in the pathogenesis of scleroderma and lupus
IIS Princesa - Instituto de Investigación del Hospital de La Princesa
Fundación Biomédica del Hospital de La Princesa

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCCharacterizing the takayasu arteritis genetic risk in rps9/lilrb3
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

SVIZZERA

Suisse Alémanique
BASEL

SVIZZERA

Suisse Romande
LAUSANNE

Restoration of IL-2 response and cytotoxic capacity of CD8+ T cell and NK cell from systemic lupus erythematosus patients
Centre Hospitalier Universitaire Vaudois CHUV
Service d'immunologie et d'allergologie

Progetti di ricerca multicentrici