Seltene Erkrankungen sind kein seltenes Phänomen: Jede einzelne Erkrankung betrifft zwar weniger als fünf von 10.000 Menschen, doch die Gesamtzahl der seltenen Erkrankungen wird auf 7.000 bis 8.000 geschätzt. Daher sind alleine in Deutschland rund vier Millionen Menschen betroffen. Seit 2003 fördert das BMBF Forschungsvorhaben, deren Ziel es ist, durch Grundlagen- und Therapieforschung die Diagnostik seltener …
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Forschungsverbünde - Research for Rare | research4rare.de Reviews
https://research4rare.de
Seltene Erkrankungen sind kein seltenes Phänomen: Jede einzelne Erkrankung betrifft zwar weniger als fünf von 10.000 Menschen, doch die Gesamtzahl der seltenen Erkrankungen wird auf 7.000 bis 8.000 geschätzt. Daher sind alleine in Deutschland rund vier Millionen Menschen betroffen. Seit 2003 fördert das BMBF Forschungsvorhaben, deren Ziel es ist, durch Grundlagen- und Therapieforschung die Diagnostik seltener …
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research4rare.de
EB-Net - Research for Rare
http://www.research4rare.de/alumni/eb-net
Research for Rare - Forschung für seltene Erkrankungen. STOP – FSGS. Zentren für seltene Erkrankungen. EB-Net – Netzwerk Epidermolysis bullosa. Die Partner im Netzwerk sind Ärzte und Wissenschaftler an verschiedenen Standorten in Deutschland und in benachbarten Städten in der Schweiz und in Österreich. Die Hauptzielsetzungen. Frühe und präzise Diagnosestellung und professionelle medizinische Betreuung für möglichst. Viele Patienten mit EB. Diese Aktivitäten werden durch das Netzwerk-Sekretariat. Und Komm...
CARPuD 2 - Research for Rare
http://www.research4rare.de/forschungsverbuende/carpud-2
Research for Rare - Forschung für seltene Erkrankungen. STOP – FSGS. Zentren für seltene Erkrankungen. CARPuD 2 – Netzwerk für seltene Lungenerkrankungen. Α1-Antitrypsin Defizienz, Cystische Fibrose und Surfactant Defizienzen sind Erbkrankheiten für die bisher nicht oder nur sehr begrenzt therapeutische Optionen existieren. Die Funktion des menschlichen Atemwegsystems wird durch diese, in der Regel tödlichen, Lungenerkrankungen stark beeinträchtigt. Als therapeutische Maßnahme bei terminalem Orga...Ziel ...
PID NET - Research for Rare
http://www.research4rare.de/forschungsverbuende/pid-net
Research for Rare - Forschung für seltene Erkrankungen. STOP – FSGS. Zentren für seltene Erkrankungen. PID-NET – Netzwerk für Primäre Immundefekte. Genetik von schweren kombinierten Immundefekten (SCID) (Prof. K. Schwarz, Dr. M. Hönig, Ulm). Genetische und immunologische Variabilität beim Autoimmun-Lymphoproliferativen Syndromen (ALPS) (Dr. C. Speckmann, Prof. S. Ehl, Dr. A. Rensing-Ehl, Freiburg). Prof Dr. C. Klein. Dr von Haunersches Kinderspital. Klinikum der Universität München. BMJ Case Rep. 201...
GERAMY - Research for Rare
http://www.research4rare.de/forschungsverbuende/geramy
Research for Rare - Forschung für seltene Erkrankungen. STOP – FSGS. Zentren für seltene Erkrankungen. GERAMY – Netzwek für Leichtketten (AL-) Amyloidose. Prospektiv-randomisierte Studie zur Therapie mit EGCG vs. Placebo bei Patienten mit Herzamyloidose (PD Dr. S. Schönland, Heidelberg). Genomische Analyse monoklonaler Plasmazellen zur Verbesserung des Verständnisses der Amyloid-Genese und Prognose bei Leichtketten-Amyloidose (Prof. A. Jauch, Heidelberg). Identifizierung neuer modulierender Moleküle für ...
Research Networks - Research for Rare
http://www.research4rare.de/en
Research for Rare - Research for rare diseases. STOP – FSGS. German Centers of Expertise for Rare Diseases. Paper of the month:. Zeb2 is essential for Schwann cell differentiation, myelination and nerve repair. Presentation of the German network on Primary Immunodeficiency Diseases. Advances in basic research should speed up the diagnosis and thus rapidly supply the affected people with adequate medical treatment. For further information, please go to the Download-menu. STOP – FSGS.
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A6 Reprogramming platform and induced pluripotent disease models for the development of novel therapeutics for PID
http://www.pid-net.org/subprojects/a6
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
A4 Phenotypic characterization of mutated procaspase-1 variants in autoinflammation
http://www.pid-net.org/subprojects/a4
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
B1 German National Registry for Primary Immunodeficiencies (PID) (Support Code: 01GM1517C)
http://www.pid-net.org/subprojects/b1
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
IonNeurONet | Netzwerk für neurologische und ophthalmologische Ionenkanalerkrankungen
http://www.ionneuronet.de/publikationen.php
Für Patienten and Ärzte. IonNeurONet Flyer zum Download. Nat Genet. 2015 Apr;47(4):393-9. doi: 10.1038/ng.3239. Epub 2015 Mar 9. PubMed PMID: 25751627. * contributed equally. Die Publikation von Ulrike Hedrich aus der Gruppe von Prof. Lerche wurde von Research4Rare. Im Februar 2015 zum. Paper of the month. Gibt es eine Zusammenfassung auf deutsch und englisch als Pdf-Download. Wir gratulieren! Pressemitteilung des Hertie-Instituts für klinische Hirnforschung. Lemke JR, Hendrickx R, Geider K, Laube B, Sch...
IonNeurONet | Netzwerk für neurologische und ophthalmologische Ionenkanalerkrankungen
http://www.ionneuronet.de/links.php
Für Patienten and Ärzte. Homepages der TP Partner:. Zentrum für seltene Erkrankungen Tübingen. Universität Ulm, Divison of Neurophysiology. Zentrum für seltene Erkrankungen Ulm: Myotonien und periodische Paralysen. Universität Ulm, Institut für Humangenetik. Hertie Institut für klinische Hirnforschung. Universität Tübingen, Forschungsinstitut für Augenheilkunde. Ebe epilepsie bundes-elternverband e.v. Und www.epikurier.de. Die Deutsche Gesellschaft für Muskelkranke e.V. (DGM). Die Deutsche Epilepsieverei...
A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity
http://www.pid-net.org/subprojects/a3
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
B1 German National Registry for Primary Immunodeficiencies (PID) (Support Code: 01GM1517C)
http://www.pid-net.org/subprojects/b
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
A7 Development of stem cell gene therapies for patients with PID and colitis
http://www.pid-net.org/subprojects/a7
German Network on Primary Immunodeficiency Diseases. A joint project initiated by the Working Party Pediatric Immunology (API). A1 German Network on Primary Immunodeficiency Diseases Genetic Diagnosis and Therapy of Primary Immunodeficiency Diseases (Support Code: 01GM1517A). A2 Genetics of human (severe) combined immunodeficiency (S)CID. A3 Genetic and immunological variability in patients with lymphoproliferation and autoimmunity. A5 Primary immunodeficiencies predisposing to severe bacterial infections.
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Research4NC
THE UNIVERSITY of NORTH CAROLINA at CHAPEL HILL. Research4NC delivers one-stop access to resources for promoting health in North Carolina. It compiles resources that University of North Carolina researchers have developed for the state's public health and healthcare practitioners. UNC’s Center for Training and Research Translation offers more than 35 interventions to support healthy lifestyles. NAP SACC provides guidance on what foods to serve in child care and how meal times can build healthy habits.
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Local and global news for OU research managers and leaders. Wednesday, August 1, 2012. Government sacrificing future of postgraduate study. Will be offered by West Coast's Tai Poutini Polytechnic. Tertiary Education Board;. Chair of the Ministry for Business, Innovation and Employment Science Board. We've got to make Maori sexy. On a high note. University appoints new Mäori and Pasifika. Pledged to either not publish, review for or do editorial work for Elsevier. OECD: NZ Health Data. Going to be bigger.
research4rabbits.wordpress.com
Research, Rabbits and Roller Coasters | Reflections on Science, Communication and Science Communication
Research, Rabbits and Roller Coasters. Reflections on Science, Communication and Science Communication. 2016 a year when social media bubbles of misinformation and hate have grown and risen to the surface, as much as to change the world, bringing even more sorrows and worry and exposing a fragility of a civilised society. It is tempting go hiding in our own privileged bubbles, unable to take in more evil madness. During 2016, our Physics Education Resource Centre. And at the Euro Amusement Show. And in c...
Forschungsverbünde - Research for Rare
Research for Rare - Forschung für seltene Erkrankungen. Zentren für seltene Erkrankungen. Paper of the month:. Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia. Conference on systemic AL Amyloidosis (GERAMY). Eva Luise Köhler Forschungspreis. Filmbeitrag des Verbundes Primäre Immundefizienzen. Alle Forschungsverbünde im Überblick.
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Research 4 Reptiles, LLC. - Home
Research 4 Reptiles, LLC. Map of Midewin Prairie. Welcome to Research 4 Reptiles. Research 4 Reptiles, LLC. is a privately-owned company, founded by Holly Zak, whose mission is to provide challenging, hands-on, field-based programs for participants ages 10 years to adult to inspire enthusiasm for and understanding of native Illinois reptile and amphibian species. We offer summer outdoor educational classes and internship opportunities at Midewin National Tallgrass Prairie in Wilmington, Illinois. Check o...
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RFR is a research collaborative which works with community-based organizations to facilitate research projects aimed at supporting popular education and organizing efforts. RFR specializes in research relating to law enforcement and the criminal legal system, immigration, workers’ rights and violence against women.
Research for Rosie | Rosie's Toy Box | Spreading joy, hope and sunshine
Rosie's Journey in Pictures. About Rosie's Toy Box. To help support Rosie and her team. While they dance 13.1 hours FOR THE KIDS! Or Join Team Rosie's Rock Star 2013 and you can DANCE WITH US TOO! Chicago Dance Marathon 2013 for Lurie Children's Hospital. Raquo; Donate now! Rosie's Journey in Pictures. Photo slideshow coming soon. Research for Rosie 2012.
Ryan Mission Possible
Avm info and resources. HELP MAKE A DIFFERENCE. DONATE TODAY. Breakdown of where funds are going:. VIEW MORE NEWS and EVENTS. RECEIVE ONGOING UPDATES ON EVENTS AND PROGRESS. AVM Research Foundation is a 501(c)(3) organization EIN: 47-5184837 Texas registration franchise tax number: 32056591004.
