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International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia

Journal of Medical Genetics · 2009 · Vol. 48(2) · pp. 73–87
Marie E. FaughnanValerie A. PaldaGuadalupe García–TsaoUrban W. GeisthoffJamie McDonaldDeborah D. ProctorJohn C. SpearsDale BrownElisabetta BuscariniMark S. ChesnuttVincent CottinArupa GangulyJames R. GossageAlan E. GuttmacherRobert H. HylandShelley KennedyJoshua R. KorzenikJohannes J. MagerAugustin OzanneJay F. PiccirilloDaniel PicusHenri PlauchuMary PorteousReed E. PyeritzDouglas A. RossCarlo SabbàKaren L. SwansonP. B. TerryM. Christopher WallaceC. J. J. WestermannRobert I. WhiteLawrence H. YoungRoberto Zarrabeitia

Abstract

The outcome of the conference was the generation of 33 recommendations for the diagnosis and management of HHT, with at least 80% agreement amongst the expert panel for 30 of the 33 recommendations.

Vascular Anomalies and TreatmentsTracheal and airway disordersMedicineTelangiectasiaMEDLINEFamily medicineHealth careDiseasePediatricsACVRL1Intensive care medicinePathology

MeSH terms

EndoglinAdultChildEpistaxisGenetic TestingGastrointestinal HemorrhageHumansMagnetic Resonance ImagingMutationReceptors, Cell SurfaceTelangiectasia, Hereditary HemorrhagicAntigens, CDActivin Receptors, Type IISmad4 ProteinVascular Malformations
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