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Progetti di ricerca

Factors associated with chronic and severe status of rare disease and health-related quality of life among rare disease patients Korea National Institute of Health

Integrative study of epigenetic variations in rare diseases Korea National Institute of Health

Establishment and operation of the clinical research network for rare glomerular diseases Yonsei University College of Medicine

Establishment of a scalable semantic data architecture for study of chronic disease Trinity College Dublin ADAPT Centre

Ensemble 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

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 y trasplante renal

Deciphering the mechanisms of PLA2R-specific B-cell autoimmunity in primary membranous nephropathy (PMN) (BCELL-MEM) Hospital Universitari de Bellvitge Servicio de Nefrología

Role on Nonmuscle Myosin II in membrane trafficking and organ function Faculty of Medicine and University Hospital Motol Department of Pediatrics

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

Molecular signature of convertase activation in complement-dependent glomerulopathies Centre de Recherches des Cordeliers (CRC) Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

Constitutive hematologic diseases: clinical and therapeutic research, molecular biology GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis Service d'hématologie pédiatrique

A prospective, international, multicentre cohort study (observational study) study on patients with profound combined immunodeficiency (P-CID) CCI am Universitätsklinikum Freiburg Centrum für Chronische Immundefizienz

C3G_ECUL: Eculizumab for the treatment of C3 glomerulopathy Universitätsklinikum Freiburg Klinik für Innere Medizin IV - Nephrologie und Allgemeinmedizin

European Alport Therapy Registry - European Initiative Towards Delaying Renal Failure in Alport Syndrome Universitätsmedizin Göttingen Klinik für Nephrologie und Rheumatologie

Role of the interaction of slit membrane, podocyte and glomerular basement membrane in pathogenesis of glomerular kidney diseases such as Alport's syndrome Universitätsmedizin Göttingen Klinik für Nephrologie und Rheumatologie

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

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

Primary CoQ deficiency zebrafish models for the study of the establishment of the disease during development and drug screening Centro Andaluz de Biología del Desarrollo (CABD) Grupo de Biología celular y Biotecnología

Role of Apolipoprotein A-Ib in the idiopathic nephrotic syndrome Vall d'Hebron Institut de Recerca VHIR Grupo de investigación en nefrología y trasplante renal

Host-microbiota interactions and defective gut mucosal integrity triggering glomerular damage in idiopathic nephrotic syndrome Instituto de Investigación Biomédica de Lleida (IRBLLEIDA) Instituto de Investigación Biomédica de Lleida - IRBLLEIDA

Stem Cell Factor, a Potential Biological Marker of Skin Involvement in Systemic Sclerosis? CHU Brugmann Service de rhumatologie - CHU Brugmann

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE CHU de Liège - Domaine universitaire du Sart Tilman Rhumatologie

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE VIB headquarters VIB (vlaams instituut voor biotechnologie) headquarters

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE UZ Leuven - Campus Gasthuisberg Pediatric Rheumatology

The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis Hospital for Sick Children, Research Institute

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

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

Systematic assessment of MEFV coding sequence variants pathogenicity-A new methodology applied to two autoinflammatory diseases Centre International de Recherche en Infectiologie (CIRI) Inflammasome, infections bactériennes et autoinflammation

Characterization of the mechanisms underlying perifascicular muscle fiber abnormalities in patients with dermatomyositis Institution: Information not provided - FR

Evaluation and treatement of scleroderma AP-HP.Sorbonne Université - Hôpital Saint-Antoine Service de médecine interne

PLA2R-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"

Models of AL amyloidosis for a better understanding of the disease and therapeutic investigations UMR 7276 Faculté de Médecine Centre de Biologie et Recherche en Santé (CBRS) Développement lymphocytaire B terminal et pathologies associées aux immunoglobulines monoclonales

Exome sequencing of inflammatory amyloidosis of unknown cause (AAx) CHU de Montpellier - Hôpital Arnaud de Villeneuve Laboratoire de génétique des maladies rares et autoinflammatoires

Dynamics 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"

ReDox: Repurposing doxycycline in the treatment of AL amyloidosis - DE Zentrum für Innere Medizin (Krehl-Klinik) Medizinische Klinik V - Hämatologie, Onkologie und Rheumatologie

Tübingen Registry for Adamantiades-Behcet's disease Interdisziplinäres Rheumazentrum (INDIRA) Zentrum für Interdisziplinäre Rheumatologie, klinische Immunologie und Autoimmunerkrankungen

STOP-FSGS: Soluble factors in FSGS Internistisches Zentrum des Universitätsklinikums Erlangen Medizinische Klinik 4 - Nephrologie und Hypertensiologie

Relevance of serum biomarkers in the therapy of ventricular arrhythmias in cardiac sarcoidosis Helios Klinikum München West Klinik für Kardiologie und Internistische Intensivmedizin

The Influence of Extracorporeal Photopheresis on Skin Sclerosis - an Exploratory Clinical Study Charité - Universitätsmedizin Berlin (CCM) Clinical Research Center for Hair and Skin Science

Fabry_VS_amyloidosis: regional biventricular and biatrial strain for differentiation of Fabry disease and amyloidosis with cardiac involvement Charité - Universitätsmedizin Berlin (CCM) Medizinische Klinik mit Schwerpunkt Kardiologie und Angiologie

ActiMON: Activity monitoring in adolescents and young adults with inflammatory rheumatic musculoskeletal diseases Deutsches Rheuma-Forschungszentrum Berlin Forschungsbereich Epidemiologie

Systematic retrospective evaluation of patients with sarcoidosis treated with the Havelhöher Sarcoidosis Therapy Protocol (HSP) Forschungsinstitut Havelhöhe gGmbH

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

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project Universitätsklinikum Frankfurt Klinik für Dermatologie, Venerologie und Allergologie

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project Medizinische Hochschule Hannover Klinik für Dermatologie, Allergologie und Venerologie

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

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

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project Universitätsklinikum Köln Klinik und Poliklinik für Dermatologie und Venerologie

Vasculitis Registry RLP/S: Prospective investigation of the diagnosis and therapy of vasculitides in Rhineland-Palatinate/Saarland Klinikum der Stadt Ludwigshafen gGmbH Klinik für Innere Medizin, Hämato-Onkologie, Nephrologie, Infektiologie und Rheumatologie

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

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

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

Investigation of Adult Still's disease in precision medicine to create evidences that facilitate the revision of diagnostic criteria through nation-wide clinical research network Nagasaki University Graduate School of Biomedical Sciences Department of Immunology and Rheumatology

Sviluppo di trattamenti e prevenzione della cardiopatia grave nella sclerosi sistemica AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani Divisione di Reumatologia

Sviluppo di trattamenti e prevenzione dell'ipertensione polmonare nella sclerosi sistemica AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani Divisione di Reumatologia

Prevenzione e trattamento delle ulcere digitali nella sclerosi sistemica AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani Divisione di Reumatologia

Comprendere il ruolo delle alterazioni del gene di PAX2 nello sviluppo di glomerulosclerosi focale segmentaria IRCCS Mario Negri - Centro Anna Maria Astori Dipartimento Medicina Molecolare

Identificazione di nuovi geni associati alla sindrome nefrosica steroido-resistente Istituto di Ricerche Farmacologiche Mario Negri Centro di Ricerche Cliniche per le Malattie Rare

Sviluppo di trattamenti e prevenzione della cardiopatia grave nella sclerosi sistemica AOU Careggi S.O.D. di Reumatologia

Sviluppo di trattamenti e prevenzione dell'ipertensione polmonare nella sclerosi sistemica AOU Careggi S.O.D. di Reumatologia

Prevenzione e trattamento delle ulcere digitali nella sclerosi sistemica AOU Careggi S.O.D. di Reumatologia

Prediction of response to immunosuppressive treatment in Systemic sclerosis (Precise) Oslo University Hospital Avdeling for revmatologi, hud- og infeksjonssykdommer

'The Norwegian, nationwide Systemic Sclerosis cohort; a novel tool for cardiopulmonary, gastro-intestinal and cancer risk evaluation; (NORSE Care study) from beside to bench' Oslo University Hospital Avdeling for revmatologi, hud- og infeksjonssykdommer

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

Pathogenic mechanisms and effects of treatment in chronic, idiopathic inflammatory myopathies, myositis University of Cambridge Department of Medicine

Sub-phenotyping in juvenile dermatomyositis (JDM), a rare and serious autoimmune childhood disorder, within the UK JDM Cohort and Biomarker Study: from phenotype to stratified treatments GOSH NHS Foundatin Trust Juvenile Dermatomyositis Research Centre

Exploring the Immunology of Sarcoidosis Castle Hill Hospital

Genetics of adult-onset familial focal segmental glomerulosclerosis (FSGS) - implications for individualized therapy and successful kidney transplantation University Hospital Motol Department of Biology and Medical Genetics

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome Instituto de Investigación Germans Trias i Pujol Grupo de investigación en Mecanismos epigenéticos del cáncer y diferenciación celular

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome Fundació Puigvert Servicio de Nefrología

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome Universitat Politècnica de Catalunya Departamento de Ingeniería de Sistemas, Automática e Informática Industrial

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome Hospital Universitario Fundación Jiménez Díaz Servicio de Nefrología e Hipertensión

Gene expression in nonspecific orbital inflammatory disease University Of California Berkeley Ophthalmology

Fiber design and assessment for development of a novel biomimetic medical device Institution: Information not provided - US

Juvenile myositis Institution: Information not provided - US

Genetic analysis of complex inflammatory disorders Institution: Information not provided - US

Factors associated with chronic and severe status of rare disease and health-related quality of life among rare disease patients
Korea National Institute of Health

Integrative study of epigenetic variations in rare diseases
Korea National Institute of Health

Establishment and operation of the clinical research network for rare glomerular diseases
Yonsei University College of Medicine

Establishment of a scalable semantic data architecture for study of chronic disease
Trinity College Dublin

ADAPT Centre

Ensemble 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

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 y trasplante renal

Deciphering the mechanisms of PLA2R-specific B-cell autoimmunity in primary membranous nephropathy (PMN) (BCELL-MEM)
Hospital Universitari de Bellvitge

Servicio de Nefrología

Role on Nonmuscle Myosin II in membrane trafficking and organ function
Faculty of Medicine and University Hospital Motol

Department of Pediatrics

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

Molecular signature of convertase activation in complement-dependent glomerulopathies
Centre de Recherches des Cordeliers (CRC)

Centre de Recherche des Cordeliers (CRC) - INSERM UMRS 1138

Constitutive hematologic diseases: clinical and therapeutic research, molecular biology
GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis

Service d'hématologie pédiatrique

A prospective, international, multicentre cohort study (observational study) study on patients with profound combined immunodeficiency (P-CID)
CCI am Universitätsklinikum Freiburg

Centrum für Chronische Immundefizienz

C3G_ECUL: Eculizumab for the treatment of C3 glomerulopathy
Universitätsklinikum Freiburg

Klinik für Innere Medizin IV - Nephrologie und Allgemeinmedizin

European Alport Therapy Registry - European Initiative Towards Delaying Renal Failure in Alport Syndrome
Universitätsmedizin Göttingen

Klinik für Nephrologie und Rheumatologie

Role of the interaction of slit membrane, podocyte and glomerular basement membrane in pathogenesis of glomerular kidney diseases such as Alport's syndrome
Universitätsmedizin Göttingen

Klinik für Nephrologie und Rheumatologie

Alport Syndrome: Clinical and molecular study of Portuguese families
Faculdade de Medicina da Universidade do Porto

Unidade de Investigação e Desenvolvimento de Nefrologia

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

Primary CoQ deficiency zebrafish models for the study of the establishment of the disease during development and drug screening
Centro Andaluz de Biología del Desarrollo (CABD)

Grupo de Biología celular y Biotecnología

Role of Apolipoprotein A-Ib in the idiopathic nephrotic syndrome
Vall d'Hebron Institut de Recerca VHIR

Grupo de investigación en nefrología y trasplante renal

Host-microbiota interactions and defective gut mucosal integrity triggering glomerular damage in idiopathic nephrotic syndrome
Instituto de Investigación Biomédica de Lleida (IRBLLEIDA)

Instituto de Investigación Biomédica de Lleida - IRBLLEIDA

Stem Cell Factor, a Potential Biological Marker of Skin Involvement in Systemic Sclerosis?
CHU Brugmann

Service de rhumatologie - CHU Brugmann

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE
CHU de Liège - Domaine universitaire du Sart Tilman

Rhumatologie

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE
VIB headquarters

VIB (vlaams instituut voor biotechnologie) headquarters

ImmunAID: Immunome Project Consortium for Autoinflammatory Disorders - BE
UZ Leuven - Campus Gasthuisberg

Pediatric Rheumatology

The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis
Hospital for Sick Children, Research Institute

Genetic transmission of familial forms of sarcoidosis
CHU de Lyon HCL - GH Est

Unité Médicale de Génétique des Cancers et des Maladies Multifactorielles

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

Service de pneumologie

Systematic assessment of MEFV coding sequence variants pathogenicity-A new methodology applied to two autoinflammatory diseases
Centre International de Recherche en Infectiologie (CIRI)

Inflammasome, infections bactériennes et autoinflammation

Characterization of the mechanisms underlying perifascicular muscle fiber abnormalities in patients with dermatomyositis
Institution: Information not provided - FR

Evaluation and treatement of scleroderma
AP-HP.Sorbonne Université - Hôpital Saint-Antoine

Service de médecine interne

PLA2R-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"

Models of AL amyloidosis for a better understanding of the disease and therapeutic investigations
UMR 7276 Faculté de Médecine Centre de Biologie et Recherche en Santé (CBRS)

Développement lymphocytaire B terminal et pathologies associées aux immunoglobulines monoclonales

Exome sequencing of inflammatory amyloidosis of unknown cause (AAx)
CHU de Montpellier - Hôpital Arnaud de Villeneuve

Laboratoire de génétique des maladies rares et autoinflammatoires

Dynamics 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"

ReDox: Repurposing doxycycline in the treatment of AL amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)

Medizinische Klinik V - Hämatologie, Onkologie und Rheumatologie

Tübingen Registry for Adamantiades-Behcet's disease
Interdisziplinäres Rheumazentrum (INDIRA)

Zentrum für Interdisziplinäre Rheumatologie, klinische Immunologie und Autoimmunerkrankungen

STOP-FSGS: Soluble factors in FSGS
Internistisches Zentrum des Universitätsklinikums Erlangen

Medizinische Klinik 4 - Nephrologie und Hypertensiologie

Relevance of serum biomarkers in the therapy of ventricular arrhythmias in cardiac sarcoidosis
Helios Klinikum München West

Klinik für Kardiologie und Internistische Intensivmedizin

The Influence of Extracorporeal Photopheresis on Skin Sclerosis - an Exploratory Clinical Study
Charité - Universitätsmedizin Berlin (CCM)

Clinical Research Center for Hair and Skin Science

Fabry_VS_amyloidosis: regional biventricular and biatrial strain for differentiation of Fabry disease and amyloidosis with cardiac involvement
Charité - Universitätsmedizin Berlin (CCM)

Medizinische Klinik mit Schwerpunkt Kardiologie und Angiologie

ActiMON: Activity monitoring in adolescents and young adults with inflammatory rheumatic musculoskeletal diseases
Deutsches Rheuma-Forschungszentrum Berlin

Forschungsbereich Epidemiologie

Systematic retrospective evaluation of patients with sarcoidosis treated with the Havelhöher Sarcoidosis Therapy Protocol (HSP)
Forschungsinstitut Havelhöhe gGmbH

International Inceptions cohort for Juvenile Systemic Sclerosis (jSSc)
Schön Klinik Hamburg Eilbek

Hamburger Zentrum für Kinder- und Jugendrheumatologie

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project
Universitätsklinikum Frankfurt

Klinik für Dermatologie, Venerologie und Allergologie

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project
Medizinische Hochschule Hannover

Klinik für Dermatologie, Allergologie und Venerologie

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

Institut für Humangenetik

Alterations of slit diaphragm signaling as a cause of FSGS
Universitätsklinikum Köln

Klinik II für Innere Medizin - Nephrologie, Rheumatologie, Diabetologie und allgemeine Innere Medizin

Immunohistochemical analysis of transcription intermediary factor-1gamma (TIF1-gamma) antibodies expression in the skin of adult anti-TIF1-gamma positive dermatomyositis patients - TIF1-gamma project
Universitätsklinikum Köln

Klinik und Poliklinik für Dermatologie und Venerologie

Vasculitis Registry RLP/S: Prospective investigation of the diagnosis and therapy of vasculitides in Rhineland-Palatinate/Saarland
Klinikum der Stadt Ludwigshafen gGmbH

Klinik für Innere Medizin, Hämato-Onkologie, Nephrologie, Infektiologie und Rheumatologie

Epidemiology of Behcet disease in Germany
Städtisches Klinikum Dessau

Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

Prognostic criteria of Behcet disease
Städtisches Klinikum Dessau

Klinik für Dermatologie, Venerologie und Allergologie / Immunologisches Zentrum

Generation and characterization of an antibody-based mouse model for systemic sclerosis
Universitätsklinikum Schleswig-Holstein - Campus Lübeck

Klinik für Rheumatologie und Klinische Immunologie

Investigation of Adult Still's disease in precision medicine to create evidences that facilitate the revision of diagnostic criteria through nation-wide clinical research network
Nagasaki University Graduate School of Biomedical Sciences

Department of Immunology and Rheumatology

Sviluppo di trattamenti e prevenzione della cardiopatia grave nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani

Divisione di Reumatologia

Sviluppo di trattamenti e prevenzione dell'ipertensione polmonare nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani

Divisione di Reumatologia

Prevenzione e trattamento delle ulcere digitali nella sclerosi sistemica
AOU Università degli Studi della Campania "Luigi Vanvitelli"- Cappella Cangiani

Divisione di Reumatologia

Comprendere il ruolo delle alterazioni del gene di PAX2 nello sviluppo di glomerulosclerosi focale segmentaria
IRCCS Mario Negri - Centro Anna Maria Astori

Dipartimento Medicina Molecolare

Identificazione di nuovi geni associati alla sindrome nefrosica steroido-resistente
Istituto di Ricerche Farmacologiche Mario Negri

Centro di Ricerche Cliniche per le Malattie Rare

Sviluppo di trattamenti e prevenzione della cardiopatia grave nella sclerosi sistemica
AOU Careggi

S.O.D. di Reumatologia

Sviluppo di trattamenti e prevenzione dell'ipertensione polmonare nella sclerosi sistemica
AOU Careggi

S.O.D. di Reumatologia

Prevenzione e trattamento delle ulcere digitali nella sclerosi sistemica
AOU Careggi

S.O.D. di Reumatologia

Prediction of response to immunosuppressive treatment in Systemic sclerosis (Precise)
Oslo University Hospital

Avdeling for revmatologi, hud- og infeksjonssykdommer

'The Norwegian, nationwide Systemic Sclerosis cohort; a novel tool for cardiopulmonary, gastro-intestinal and cancer risk evaluation; (NORSE Care study) from beside to bench'
Oslo University Hospital

Avdeling for revmatologi, hud- og infeksjonssykdommer

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

Longcentrum

Pathogenic mechanisms and effects of treatment in chronic, idiopathic inflammatory myopathies, myositis
University of Cambridge

Department of Medicine

Sub-phenotyping in juvenile dermatomyositis (JDM), a rare and serious autoimmune childhood disorder, within the UK JDM Cohort and Biomarker Study: from phenotype to stratified treatments
GOSH NHS Foundatin Trust

Juvenile Dermatomyositis Research Centre

Exploring the Immunology of Sarcoidosis
Castle Hill Hospital

Genetics of adult-onset familial focal segmental glomerulosclerosis (FSGS) - implications for individualized therapy and successful kidney transplantation
University Hospital Motol

Department of Biology and Medical Genetics

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Instituto de Investigación Germans Trias i Pujol

Grupo de investigación en Mecanismos epigenéticos del cáncer y diferenciación celular

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Fundació Puigvert

Servicio de Nefrología

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Universitat Politècnica de Catalunya

Departamento de Ingeniería de Sistemas, Automática e Informática Industrial

Use of artificial intelligence and systems biology for diagnosis and personalized risk assessment for inherited kidney diseases, focusing on Alport syndrome
Hospital Universitario Fundación Jiménez Díaz

Servicio de Nefrología e Hipertensión

Gene expression in nonspecific orbital inflammatory disease
University Of California Berkeley

Ophthalmology

Fiber design and assessment for development of a novel biomimetic medical device
Institution: Information not provided - US

Juvenile myositis
Institution: Information not provided - US

Genetic analysis of complex inflammatory disorders
Institution: Information not provided - US

Genetics; natural history; and pathophysiology of behcet's disease
Institution: Information not provided - US

Genetics; pathophysiology; and treatment of recessive autoinflammatory diseases
Institution: Information not provided - US

Genetic; cellular and molecular mechanisms in autoimmunity to retina
Institution: Information not provided - US

Immunogenetic mechanisms in behcet's disease
Institution: Information not provided - US