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Researchers And Projects Database

To find researcher / project please complete one (or more) of the fields below.

Name City Country Institution Disease(s) Project
Renné
Thomas
Würtzburg Germany

University Hospital Würzburg
Institute for Clinical Biochemistry and Pathobiochemistry

Hereditary angioedema type III HAE III
Hennies
Hans Christian
Köln Germany

Cologne Center for Genomic
Division of Dermatogenetics

Hereditary angioedema type III, congenital rare skin diseases
Bork
Konrad
Mainz Germany

University of Mainz
Department of Dermatology

Hereditary angioedema type III HAE III
Drouet
Christian
Grenoble France

University Joseph Fourier Grenoble
National Centre for Angioedema

Hereditary angioedema type III HAE III
Colombo
Roberto
Milano Italy

IRCCS Don Carlo Gnocchi
Foundation Laboatory of Molecular Medicine and Biotechnologies

Hereditary angioedema type III HAE III
Muratori
Luigi
Bologna Italy
University of Bologna
Sant'Orsola-Malpighi Hospital
Department of Internal Medicine, Cardioangiology, Hepatology
Autoimmune liver diseases Epinostics
Lyonnet
Stanislas
Paris France

Inserm/ University of Paris V

Hirschprung disease, Craniofacial malformations
Akarsu
Nurten
Ankara Turkey

Hacettepe University

Craniofacial malformations
Kayserili
Hülya
Istanbul Turkey

Istanbul Medical Faculty

Craniofacial malformations
Piskin
Erhan
Ankara Turkey

Hacettepe University

craniofacial malformations CRANIRARE
Wieczorek
Dagmar
Essen Germany

University Medical Faculty Essen, University Duisburg-Essen

Craniofacial malformations
Wollnik
Bernd
Cologne Germany
University of Cologne, Center for Molecular Medicine Cologne (CMMC)
Institute of Human Genetics
 
Craniofacial malformations
Thiesen
Hans-Jürgen
Rostock Germany
University of Rostock
Institute of Immunology
Autoimmune liver diseases Epinostics
Bogdanos
Dimitrios
London UK
King's College London
Institute of Liver Studies, Division of Gene and Cell Based Therapy
Denmark Hill Campus
Autoimmune liver diseases Epinostics
Pares
Albert
Barcelona Spain
Hospital Clinic, IDIBAPS
University of Barcelona
Liver Unit, Digestive Diseases Institute
Autoimmune liver diseases Epinostics
Dalekos
George
Larissa Greece

Centre for Research and Technology & University of Thessaly Medical School

Autoimmune liver diseases Epinostics
Blank
Miri
Ramat Gan Israel
Sheba Medical Center
Center of Autoimmune Diseases
Autoimmune liver diseases Epinostics
Gougeon
Marie-Lise
Paris France
Infection and Immunity Department
Istitut Pasteur
 
Autoimmune liver diseases Epinostics
Villa
Anna
Milano Italy
University of Milan
Wiskott Aldrich Group at Telethon Institute for Gene Therapy
Autoimmune liver diseases Epinostics
Rieux-Laucat
Frédéric
Paris France
ISERM Unit 768
Hôpital Necker
Autoimmune liver diseases
Glocker
Michael O.
Rostock Germany

Proteome Center Rostock Institute of Immunology

Autoimmune liver diseases; spinocerebellar ataxia
Cilio
Maria Roberta
Rome Italy

IRCCS Bambino Gesù Children's Hospital

Benign familial neonatal seizures EUROBFNS
Villaroel
Alvaro
Leioa Spain
Universidad del Pais Vasco
Unidad de Biofisica CSIC-UPV/EHU
Benign familial neonatal seizures EUROBFNS
Lerche
Holger
Ulm Germany
University of Ulm
Neurological Clinic and Institute of Applied Physiology
Benign familial neonatal seizures EUROBFNS
Nabbout
Rima
Paris France
Hôpital Necker-Enfants Malades
University of Paris V
Benign familial neonatal seizures EUROBFNS
Villard
Laurent
Marseille France
INSERM U491
Faculté de Médecin de la Timone
Rett Syndrome EuroRETT
Bienvenu
Thierry
Paris France
Institut Cochin
INSERM U567
Rett Syndrome EuroRETT
Broccoli
Vania
Milano Italy
San Raffaele Scientific Istitute
DIBIT
Rett Syndrome EuroRETT
Cardoso
M. Cristina
Berlin Germany

Max Delbrück Center Molecular Medicine

Rett Syndrome EuroRETT
Esteller
Manel
Madrid Spain
Spanish National Cancer Centre (CNIO)
Molecular Pathology Programme,
Cancer Epigenetics Laboratory
Rett Syndrome EuroRETT
Gak
Eva
Tel Hashomer Israel
Sheba Medical Center
Genetics Institute
Rett Syndrome EuroRETT
Huppke
Peter
Göttingen Germany
Georg August University
Pediatrics and Pediartic Neurology
Rett Syndrome EuroRETT
Laviola
Giovanni
Rome Italy

Instituto Superiore di Sanita

Rett Syndrome EuroRETT
Levi
Giovanni
Paris France
UMR166 CNRS/MNHN
RDDM
Rett Syndrome EuroRETT
Russo
Silvia
Milano Italy
Instituto Auxologico Italiano
Laboratorio di Biologia Molecolare
Rett Syndrome EuroRETT
Brice
Alexis
Paris France
INSERM, Unit 679
Pitié-Salpêtrière Hospital
Spastic paraplegias EUROSPA
Schöls
Ludger
Tübingen Germany
University of Tübingen
Department of Neurology and Hertie-Institute for Clinical Brain
Spastic paraplegias, non-Friedreich ataxias
Santorelli
Fillipo M.
Rome Italy
IRCCS Children's Hospital Bambino Gesù
Molecular Medicine
Spastic paraplegias EUROSPA
Lossos
Alexander
Jerusalem Israel
Hadassah-Hebrew University
Medical Center, Neurology
Spastic paraplegias EUROSPA
Cichon
Sven
Bonn Germany
University of Bonn, Life & Brain Center
Department of Genomics
 
Hereditary angioedema type III HAE III
Ceccherini
Isabella
Genova Italy
IRCCS - Instituto Giannina Gaslini
Laboratorio di Genetica Molecolare
Hirschprung disease HSCR
Borrego
Salud
Seville Spain
Hospitales Universitarios Virgen del Rocio (HUVR)
Unidad Clinica de Genética y Reproduccion
 
Hirschprung disease HSCR
Hofstra
Robert
Groningen The Netherlands
University Medical Center Groningen
University of Groningen
 
Hirschprung disease HSCR
Chakravarti
Aravinda
Baltimore USA
Johns Hopkins University School of Medicine
McKusick-Nathans Institute of Genetic Medicine
Hirschprung disease HSCR
Kwong Hang Tam
Paul
Hong Kong China
The University of Hong Kong
Surgery
Hirschprung disease HSCR
Bruckner-Tuderman
Leena
Freiburg Germany
University Medical Center Freiburg
Dermatology
Epidermolysis bullosa; Kindler syndrome
Zambruno
Giovanna
Rome Italy
Instituto Dermatologico Dell'Immacolata - IRCCS
Laboratory of Molecular and Cell Biology
Kindler syndrome Kindlernet
Fischer
Judith
Evry France
Centre National de Génotypage
CNRG componente CNG
Kindler syndrome Kindlernet
Fässler
Reinhard
Martinsried Germany
Max Planck Institute of Biochemistry
Molecular Medicine
Kindler syndrome Kindlernet
Bruckner
Peter
Münster Germany
University Hospital Münster
Physiological Chemistry and Pathobiochemistry
Kindler syndrome Kindlernet
Laporte
Jocelyn
Illkrich France
IGBMC-ISERM U596 - UMR7104
Université Louis Pasteur
Department of Molecular Biology
Myotubularinopathies
Bolino
Alessandra
Milano Italy
Fondazione Centro San Raffaele del Monte Tabor
DIBIT
Myotubularinopathies
Payrastre
Bernard
Toulouse France
ISERM U563 - CPTP - IFT30
Université Paul Sabatier
Myotubularinopathies MTMPathies
Ugazio
Alberto Giovanni
Rome Italy
Ospedale Pediatrico Bambino Gesù
Medicina Pediatrica
Osteopetrosis OSTEOPETR
de Vernejoul
Marie Christine
Paris France

Istitut National de la Recherche Médicale, U606

Osteopetrosis OSTEOPETR
Kornak
Uwe
Berlin Germany
Cherité Universitaetsmedizin Berlin
Institute of Medical Genetics
Osteopetrosis; congenital disorders of glycosylation
Amling
Michael
Hamburg Germany
University Medical Center Hamburg
Department of Trauma, Hand and Reconstructive Surgery
Osteopetrosis OSTEOPETR
Schulz
Ansgar
Ulm Germany

Universitätsklinik für Kinder Jugendmedizin

Osteopetrosis OSTEOPETR
Schaefer
Franz
Heidelberg Germany
Heidelberg University Hospital
Division of Pediatric Nephrology
Center for Pediatric and Adolescent
Hereditary diseases of the podocite PodoNet
Antignac
Corinne
Paris France
Hôpital Necker - Enfants Malades
INSERM U574 and Department of Genetics
Hereditary diseases of the podocite PodoNet
Bakkaloglu
Aysin
Ankara Turkey
Hacettepe University
Faculty of Medicine
Pediatric Nephrology
Hereditary diseases of the podocite PodoNet
Emma
Francesco
Rome Italy
Ospedale Pediatrico Bambino Gesù
Pediatric Nephorlogy and Dialysis
Hereditary diseases of the podocite PodoNet
Ghiggeri
Gian Marco
Genova Italy
Instituto Giannina Gaslini
Laboratory of Physiopahology of Uremia
Hereditary diseases of the podocite PodoNet
Remuzzi
Giuseppe
Bergamo Italy
Mario Negri Institute
Clinical Research Centre for Rare Diseases "Aldo e cele dacco"
Hereditary diseases of the podocite PodoNet
Klockgether
Thomas
Bonn Germany
University Hospital Bonn
Department of Neurology
Spinocerebellar ataxia RISCA
Berciano
José
Santander Spain
University Hospital Marqués de Valdecilla
Department of Neurology
Spinocerebellar ataxia RISCA
Dürr
Alexandra
Paris France
Hôpital de la Pitié-Salpêtrière
ISERM U679
Department of Genetics
Spinocerebellar ataxia RISCA
Mariotti
Caterina
Milano Italy
Fondazione IRCCS- Instituto Neurologico Carlo Besta
Division of Biochemistry and Genetics
Spinocerebellar ataxia RISCA
Schöls
Lufger
Tübingen Germany
University of Tübingen
Department of Neurology and Hertie-Institute for Clinical Brain Research
Spinocerebellar ataxia RISCA
Riess
Olaf
Tübingen Germany
University of Tübingen
Department of Medical Genetics
Spinocerebellar ataxia RISCA
Schulz
Jörg
Göttingen Germany
University of Göttingen
Department of Neurodegeneration and Restorative Research
Spinocerebellar ataxia RISCA
Tezenas du Montcel
Sophie
Paris France
University Pierre et Marie Curie
EA 3974 Modeling Clinical Research
Spinocerebellar ataxia RISCA
Viola
Antonella
Rozzano Italy
Instituto Clinico Humanitas, IRCCS - Humanitas Mirasole SpA
Adaptive Immunity
WHIM syndrome WHIMPath
Manes
Santos
Madrid Spain
Consejo Superior de Investigaciones Cientificas
Immunology and Oncolgy
WHIM syndrome WHIMPath
Bachelerie
Françoise
Paris France
Institut Pasteur
Department of Virology
WHIM syndrome
Bosch
Assumpcio
Barcelona Spain
Universitat Autònoma de Bracelona
Biochemistry and Molecular Biology
CBATEG, Campus UAB
Mucopolysaccharidosis CAV-4-MPS
Kremer
Eric
Montpellier France
Istitut de Génétique Moleculaire de Montpellier
UMR5535
Mucopolysaccharidosis CAV-4-MPS
Verdier
Jean-Michel
Montpellier France
Ecole Pratique des Hautes Etudes
Biology & Health
Mucopolysaccharidosis CAV-4-MPS
Schwarz
Johannes
Leipzig Germany
Universität Leipzig
Klinik für Neurologie
Mucopolysaccharidosis CAV-4-MPS
Dierssen
Mara
Barcelona Spain
Center for Genomic Regulation
Genes and Disease Program
Fragile X syndrome Cure-FXS
Diana
Giovanni
Rome Italy
Istituto Superiore de Sanita
Department of Therapeutic Research and Medicines Evaluation
Fragile X syndrome Cure-FXS
Ramakers
Gerard
Amsterdam The Netherlands
University of Amsterdam
Department of Developmental Psychology
Fragile X syndrome Cure-FXS
Stork
Oliver
Magdeburg Germany
Otto von Guericke University Magdeburg
Insitute of Biology
Department of Genetics & Molecular Neurobiology
Fragile X syndrome Cure-FXS
Bardoni
Barbara
Valbonne France

IMPC-CNRS, UMR6097

Fragile X syndrome Cure-FXS
Welte
Karl H.
Hannover Germany
Hannover Medical School
Molecular Hematopoiesis
Congenital neutropenia ELA2-CN
Zeidler
Cornelia
Hannover Germany
Hannover Medical School
Molecular Hematopoiesis
Congenital neutropenia ELA2-CN
Touw
Ivo
Rotterdam The Netherlands
Erasmus University Medical Center
Hematology Office H EE13-30c
Congenital neutropenia ELA2-CN
Coffer
Paul J.
Ultrech The Netherlands
University Medical Center
Molecular Immunology Lab
Department of Immunology & Pediatrics
Congenital neutropenia; chronic granulomatous disease
Yilmaz Karapinar
Deniz
Bomova-Izmir Turkey
Ege University Faculty of Medicine
Childrens Hospital
Department of Pediatric Hematology
Congenital neutropenia ELA2-CN
Tamary
Hannah
Petah Tikva Israel
Schneider Children's Medical Center of Israel
Pediatric Hematology
Congenital neutropenia ELA2-CN
Bonneau
Dominique
Angers France
Biochemistry and Genetics
CHU Angers
Mendelian inherited optic neuropathy ERMION
Wissinger
Bernd
Tübingen Germany
Eberhard Karls Universität Tübingen
Centre for Ophtalmology
Molecular Genetics Laboratory
Mendelian inherited optic neuropathy ERMION
Matrinuzzi
Andrea
Conegliano Italy
E. medea Scientific Institute
Department of Genetics
Mendelian inherited optic neuropathy ERMION
Lenaers
Guy
Montpellier France
Institut des Neurosciences de Montpellier et INSERM U583
CHU St Eloi
Mendelian inherited optic neuropathy ERMION
Luisetti
Maurizio
Pavia Italy
Fondazione IRCCS Policlinico San Matteo
Clina Malattie Apparato Respratiorio
Pulmonary alveolar proteinosis EuPAPNet
Costabel
Ulrich
Essen Germany
Ruhrlandklinik
Abteilung Pneumologie/Allergologie
Pulmonary alveolar proteinosis EuPAPNet
Grutters
Jan C.
Nieuwegein The Netherlands
St Antionius Hospital
Department of Pulmonology
Pulmonary alveolar proteinosis EuPAPNet
Griese
Matthias
Munich Germany
University of Munich
Children's Hospital
 
Pulmonary alveolar proteinosis EuPAPNet
Prohaska
Reiner
Vienna Austria
Medical University of Vienna
Max F. Perutz Laboratories
Neuroacanthocytosis EMINA
Bosman
Giel
Nijmegen The Netherlands
Radboud University Medical Center
Biochemistry
 
Neuroacanthocytosis EMINA
Sibon
Ody
Groningen The Netherlands
University Medical Center Groningen (UMCG)
Cell Biology, Radiation and Stress Cell Biology
Neuroacanthocytosis EMINA
Tison
François
Pessac France
Centre Hospitalier Universitaire de Bordeaux
Service Neurologie
Neuroacanthocytosis EMINA
Yapici
Zuhal
Istanbul Turkey
Istanbul Faculty of Medicine
Department of Neurology
Neuroacanthocytosis EMINA
Aiuti
Alessandro
Milano Italy
Fondazione Centro San raffaele del Monte Tabor
HSR-TIGET
Chronic granulomatous disease EURO-CGD
Roos
Dirk
Amsterdam The Netherlands
Sanquin Research and University of Amsterdam
Blood Cell Research
Chronic granulomatous disease EURO-CGD
Rossi
Paolo
Rome Italy
IRCCS Ospedale Pediatrico Bambino Gesù
Medicina Pediatrica
Chronic granulomatous disease EURO-CGD
Grez
Manuel
Frankfurt Germany
Institute for Biomedical Research - Georg-Speyer-Haus
Applied Virology and Gene Therapy
Chronic granulomatous disease EURO-CGD
Köker
M. Yavuz
Kayseri Turkey
University of Erciyes
Immunology laboratory, Cappadocia Transplant Centre,
Hematology-Immunology division
Chronic granulomatous disease EURO-CGD
Vaxillaire
Martine
Lille France
CNRS
Genomic and Molecular Physiology of Metabolic Diseases
Biologie de Lille-Institut
Pancreatic Beta-cell insufficiency EuroGeBeta
Bellane-Echantelot
Christine
Paris France
AP.MP Groupe Hospitalier Pitié-Salpêtrière
Department of Genetics
Pancreatic Beta-cell insufficiency EuroGeBeta
Polak
Michel
Paris France
Hôpital Necker - Enfants Malades
ISERM U845
Pediatric Endocrinology
Pancreatic Beta-cell insufficiency EuroGeBeta
Cuesta-Munoz
Antonio Luis
Malaga Spain
IMABIS Foundation Hospital Carlos Haya
Center for the Study of Pancreatic B-Cell Disease
Pancreatic Beta-cell insufficiency EuroGeBeta
Phillip
Moshe
Petah Tikva Israel
Schneider Children Medical Center
Lea Shafer Institute of Endocrinology and Diabetes
Pancreatic Beta-cell insufficiency EuroGeBeta
Barbetti
Fabrizio
Rome Italy
Bambino Gesù Pediatric Hospital, IRCCS
Laboratory of Molecular Endocrinology and Metabolism
 
Pancreatic Beta-cell insufficiency EuroGeBeta
Anagnou
Nicholas
Athens Greece
University of Athens School of Medicine and Foundation
for Biomedical Research of the Academy of Athens
Basic Medical Sciences
Thalassemia GETHERTHAL
Cosset
François-Loïc
Lyon France
ISERM U758
Human Virology
Thalassemia GETHERTHAL
von Kalle
Christof
Heidelberg Germany
DKFZ/NCT Heidelberg
Translational Oncology
Thalassemia GETHERTHAL
Beaumont
Carole
Paris France
INSERM U773
University Paris Diderot, Site Bichat
Microcytic hypochromic anemias HMA-IRON
Camaschella
Clara
Milano Italy
IRCCS San Raffaele
Genetics and Biology

 

 

Microcytic hypochromic anemias HMA-IRON
Muckenthier
Martina
Heidelberg Germany
Universitätsklinikum Heidelberd
Department of Pediatric Hematology, Oncology and Immunology
Microcytic hypochromic anemias HMA-IRON
del Carmen Sanchez
Maria
Barcelona Spain
Institut de Medicina Predictiva I Personalitzada des Cancer (IMPPC)
Genetics and Epigenetics of Cancer
Microcytic hypochromic anemias HMA-IRON
Estévez
Raul
L'Hospitalet de Llobregat Spain
IDIBELL
Ciencias Fisiologiques II
Megalencephalic leukoencephalopathy with subcortical cysts MLC-Team
van der Knaap
Marjo S.
Amsterdam The Netherlands
VU University Medical Center
Child Neurology
Megalencephalic leukoencephalopathy with subcortical cysts MLC-Team
Mansvelder
Huibert
Amsterdam The Netherlands
VU University Medical Center
Integrative Neurophysiology
Megalencephalic leukoencephalopathy with subcortical cysts MLC-Team
Verheijen
Mark
Amsterdam The Netherlands
Center for Neurogenomics and Cognitive Research
Molecular and Cellular Neurobiology
Megalencephalic leukoencephalopathy with subcortical cysts MLC-Team
Bendahan
David
Marseille France
CNRS
Center for Magnetic Resonance in Biology and Medicine (CRMBM)
Médicine de Marseille
Nemaline myopathy NEMMYOP
Ottenheijm
Coen
Amsterdam The Netherlands
VU University Medical Center
Laboratory for Physiology
Institute for Cardiovascular Research
Nemaline myopathy NEMMYOP
Labeit
Siegfried
Mannheim Germany
Medical Faculty Mannheim
University of Heidelberg
Integrative Pathology
Nemaline myopathy NEMMYOP
Klein
Christoph
Hannover Germany
Hannover Medical School
Pediatric Hematology/Oncology
Inherited disorders of myeloid cells NEUTRO-NET
Donadieu
Jean
Paris France
Hôpital Trousseau AP HP
Registre Français des Neutropénies Congénitales
Service d'Hémato-Oncologie Pédiatrique
Inherited disorders of myeloid cells NEUTRO-NET
Kutukculer
Necil
Izmir Turkey
Ege University School of Medicine
Pediatrics, Division of Pediatric Immunology
Inherited disorders of myeloid cells NEUTRO-NET
Herbomel
Philippe
Paris France
Institut Pasteur and CNRS
Developmental Biology
Inherited disorders of myeloid cells NEUTRO-NET
Penninger
Josef
Vienna Austria
Institute of Molecular Biotechnology (IMBA)
of the Austrian Academy of Science
Inherited disorders of myeloid cells NEUTRO-NET
Tartaglia
Marco
Rome Italy
Instituto Superiore di Sanita
Ematologia, Oncologia e Medicina Molecolare
Noonan syndrome NsEuroNet
Zenker
Martin
Erlangen Germany
University Hospital of Erlangen
University of Erlangen-Nuremberg
Noonan syndrome NsEuroNet
Ahmadian
Reza
Düsseldorf Germany
Heinrich Heine Medical Center
Biochemistry and Molecular Biology II (IMBM)
Noonan syndrome NsEuroNet
Cavé
Hélène
Paris France
CHU Robert Debré
Université Denis Diderot Paris VII
Genetics
Noonan syndrome NsEuroNet
Elgersma
Ype
Rotterdam The Netherlands
Erasmus University Center (EMC)
Neuroscience
Noonan syndrome NsEuroNet
Raynal
Patrick
Toulouse France
INSERM U563
Centre de Physiopathologie de Toulouse-Purpan
Noonan syndrome NsEuroNet
Jonkman
Marcel
Groningen The Netherlands
University Medical Center Groningen
Dermatology
Epidermolysis bullosa EB
Delrio
Marcela
Madrid Spain
Energéticas, Medioambivalentes y Tecnologicas and Centro de Investigaciones
Biomédicas en Red en Enfermedades Raras
Epithelial Cell Division
Basic Research Department U714
 
Epidermolysis bullosa EB
Audo
Isabelle
Paris France
Centre de Recherche Institut de Vision (IdV) UMRS 968
INSERM - Université Pierre et Marie Curie
CIC 503 Inserm
Department of Genetics
Rod-cone dystrophies RHORCOD
Banin
Eyal
Jerusalem Israel
Hadassah - Hebrew University Medical School
Ophtalmology
Rod-cone dystrophies RHORCOD
Zrenner
Eberhart
Tübingen Germany
University of Tübingen
Center for Ophtalmology
Institute of Ophtalmic Research
Rod-cone dystrophies RHORCOD
Macaluso
Claudio
Parma Italy
Regione Emilia Romagna
Ophtalmology, University Hospital of Parma
Rod-cone dystrophies RHORCOD
Anheit
Peter
Vienna Austria
Medical University of Vienna
Physiology
Rod-cone dystrophies RHORCOD
Danek
Adrian
Munich Germany
Ludwig-Maximilians University Munich
Klinikum Grosshadern
Department of Neurology
Neuroacanthocytosis EMINA
Silva
Eduardo
Coimbra Portugal
IBILI- Faculty of Medicine
University of Coimbra
Rod-cone dystrophies RHORCOD
Chelly
Jamel
Paris France

Institut Cochin

Department of Genetics and Development

INSERM

Malformations of cortical development TUB-GENCODEV
Guerrini
Renzo
Pisa Italy

Research, IRCCS Stella Maris Foundation

Calambrone

Malformations of cortical development TUB-GENCODEV
Keays
David
Vienna Austria

Laboratory for the Molecular Basis of Migration, Research

Institute of Molecular Pathology

Malformations of cortical development TUB-GENCODEV
Simons
Mikael
Göttingen Germany

Department of Neurology

University of Göttingen

Myotubularinopathies MTMPathies2
Aberdam
Daniel
Nice France

Stem Cells, Development and Cancer

INSERM, Nice

Congenital rare skin diseases SkinDev
Sprecher
Eli
Tel Aviv Israel

Dermatology

Tel Aviv Sourasky Medical Center

Congenital rare skin diseases SkinDev
Missero
Caterina
Napoli Italy

CEINGE Biotecnologie Avanzate

Congenital rare skin diseases SkinDev
Marignier
Romain
Lyon France

Service de Neurologie A

Hopital Neurologique Pierre Wertheimer

Groupement Hospitalier Est

Lyon Neurosciences

Devic's neuromyelitis optica EDEN
Lassmann
Hans
Vienna Austria

Department of Neuroimmunology

Center for Brain Research

Medical University of Vienna

Devic's neuromyelitis optica EDEN
Hartung
Hans-Peter
Düsseldorf Germany

Department of Neurology

Heinrich-Heine-University

Devic's neuromyelitis optica EDEN
Siva
Aksel
Istanbul Turkey

Department of Neurology

Istanbul University

Cerrahpasa School of Medicine

Devic's neuromyelitis optica EDEN
Wandinger
Klaus-Peter
Lübeck Germany

CNS Research & Development

EUROIMMUN Medizinische Labordiagnostika AG

Devic's neuromyelitis optica EDEN
Vincent
Angela
Oxford UK

Nuffoeld department of Clinical Neurosciences

The Chancellor, Masters and Scholars of the University of Oxford

Devic's neuromyelitis optica EDEN
Sozzani
Silvano
Rozzano Italy

Instituto Clinico Humanitas

WHIM syndrome WHIM-Thernet
Galzi
Jean-Luc
Illkrich France

Biotechnologie et Signalisation Cellulaire

Ecole Supérieure de Biotechnologie

WHIM syndrome WHIM-Thernet
Münch
Jan
Ulm Germany

Insitute of Molecular Virology

Ulm University Medical Center

WHIM syndrome WHIM-Thernet
Scherman
Daniel
Paris France

Pharmacologie Chimique et Genetique et d'Imagerie

CNRS

von WIllebrand disease TRANSPOSMART
Vanhoorelbeke
Karen
Kortrijk Belgium

Laboratory for Thrombosis Research

KU Leuven Campus Kortrijk

von WIllebrand disease TRANSPOSMART
Izsvak
Zsuzsanna
Berlin Germany

Cardiovascular, Max Delbruck Center for Molecular Medicine

von WIllebrand disease TRANSPOSMART
Ehrhard
Anja
Munich Germany

Department of Virology

Ludwig-Maximilians-University of Munich

Max von Pettenkofer Institute

von WIllebrand disease TRANSPOSMART
Athanassiadou
Aglaia
Patras Greece

Department of Biology

University of Patras

Medical School

von WIllebrand disease TRANSPOSMART
Galun
Eithan
Jerusalem Israel

Hadassah Hebrew University Hospital

Goldyne Savad Institute for Gene Therapy

von WIllebrand disease TRANSPOSMART
Koenig
Michel
Illkrich France

Department of Translational Medicine and Neurogenetics

Institut de Genetique et de Biologie Moleculaire et Cellulaire

non-Friedreich ataxias Euro-SCAR
Pandolfo
Massimo
Brussels Belgium

Laboratoire de Neurologie Expérimentale-CP601

Université Libre de Bruxelles

non-Friedreich ataxias Euro-SCAR
Topaloglu
Haluk
Ankara Turkey

Department of Pediatrics

Hacettepe University

CHildrens Hospital

non-Friedreich ataxias Euro-SCAR
Meiner
Vardiella
Jerusalem Israel

Department of Genetics and Metabolic Diseases

Hadassah-Hebrew University Hospital

non-Friedreich ataxias Euro-SCAR
Taroni
Franco
Milano Italy

Fondazione IRCCS Instituto Neurologico Carlo Besta

Department of Research and Applied Technology

non-Friedreich ataxias Euro-SCAR
Meitinger
Thomas
Munich Germany

Institute of Human Genetics

Technical University of Munich

Mitochondrial disorders GENOMIT
Zeviani
Massimo
Milano Italy

Molecular Genetics

Fondazione IRCCS, Instituto Neurologico Carlo Besta

Mitochondrial disorders GENOMIT
Rötig
Agnes
Paris France

INSERM U781

Insitut National de la Santé et de la Recherche Médicale

Mitochondrial disorders GENOMIT
Edvardson
Simon
Jerusalem Israel

Department of Pediatrics

Neuropediatrics Unit

Hadassah Medical Center - Hebrew University Jerusalem

Mitochondrial disorders GENOMIT
Sperl
Wolfgang
Salzburg Austria

Department of Pediatrics

Paracelsus Medical University

Salzburger Landeskliniken (SALK)

Mitochondrial disorders GENOMIT
Muller
Marc
Liège Belgium

GIGA-R, University of Liège

Unit for Molecular Biology and Genetic Engineering

Mitochondrial disorders GENOMIT
Barquinero
Jorge
Barcelona Spain

Gene and Cell Therapy

Vall d'Hebron Research Institute

Hemophilia HEMO-iPS
Weber
Anne
Paris France

INSERM U972

Le Kremlin Bicetre

Hemophilia HEMO-iPS
Schinco
Piercarla
Torino Italy

A.Re.S.S. Piemonte-Azienda Ospedaliera Universitaria S. Giovanni Battista-Molinette

Dipartimento di Oncologia e Ematologia Malattie Trombotiche ed Emorragiche

 

Hemophilia HEMO-iPS
Vidal
Francisco
Barcelona Spain

Diagnostic and Moleculat Therapy Unit

Blood and Tissue Bank

Hemophilia HEMO-iPS
Moeller
Marcus
Aachen Germany

Division of Nephrology and Immunology

University Hospital of the Aachen Technical University (RWTH)

Glomerular diseases Rare-G
Endlich
Nicole
Greifswald Germany

Anatomy and Cell Biology

Ernst Moritz Arndt University

Glomerular diseases Rare-G
Kerjaschki
Dontscho
Vienna Austria

Chair of the Department of Pathology

Medical University of Vienna

Glomerular diseases Rare-G
Tharaux
Pierre-Louis
Paris France

PARCC, INSERM and Université Paris-Descartes

Glomerular diseases Rare-G
Matthijs
Gert
Leuven Belgium

Center for Human Genetics

University of Leuven

Congenital Disorder of Glycosylation EURO-CDG
Van Schaftingen
Emile
Brussels Belgium

Laboratory of Physiological Chemistry

de Duve Institute

Université Catholique de Louvain

Congenital Disorder of Glycosylation EURO-CDG
Seta
Nathalie
Paris France

Biochemistry Department

Hopital Bichat-Claude Bernard

Congenital Disorder of Glycosylation EURO-CDG
Körner
Christian
Heidelberg Germany

Center for Child and Adolescent Medicine

Center for Metabolic Diseases

University Children's Hospital Heidelberg

Congenital Disorder of Glycosylation EURO-CDG
Foulquier
François
Lille France

CNRS, Structural and Functional Glycobiology Unit

Université de Lille

Villeneuve d'Ascq

Congenital Disorder of Glycosylation EURO-CDG
Prasse
Antje
Freiburg Germany

Pneumology, Albert Ludwigs University Freiburg

University Medical centre

Idiopathic Pulmonary Fibrosis IPF-AE
Königshoff
Melanie
Munich Germany

Comprehensive Pneumology Center

Ludwig Maximillian University and

Helmholtz Zentrum Munich

Idiopathic Pulmonary Fibrosis IPF-AE
Papakonstantinou
Eleni
Thessaloniki Greece

Lab of Pharmacology

School of Medicine

Aristotle University of Thessaloniki

Idiopathic Pulmonary Fibrosis IPF-AE
Poletti
Venerino
Forli Italy

Regione Emilia Romagna-Ospedale GB Morgagni

Department of Diseases of the Thorax

 

Idiopathic Pulmonary Fibrosis IPF-AE
Rottoli
Paola
Siena Italy

Regione Toscana-Le Scotte Hospital

Respiratory Diseases Section Depertment of Clinical Medicine and Immunology Sciences

 

Idiopathic Pulmonary Fibrosis IPF-AE
Valeyre
Dominique
Bobigny France

Université Paris Nord

PRES Sorbonne Paris Cité and

Avicenne Universitary Hospital

Service de Pneumologie

Idiopathic Pulmonary Fibrosis IPF-AE
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