First Page | Document Content | |
---|---|---|
Date: 2013-04-14 20:11:00Hereditary hemorrhagic telangiectasia Cavernous hemangioma Center for Cerebrovascular Research Neurology Comorbidity KRIT1 Biomarker Rare disease Medicine Health Neurological disorders | The Journal of Rare Disorders Brain Vascular Malforma on Consor um: Overview, Progress, and Future Direc ons Amy L. Akers, PhD1; Karen L. Ball, BS2; Marianne Clancy, BS3; Anne M. Comi, MD4; MAdd to Reading ListSource URL: www.journalofraredisorders.comDownload Document from Source WebsiteFile Size: 804,16 KBShare Document on Facebook |
The Journal of Rare Disorders Brain Vascular Malforma on Consor um: Overview, Progress, and Future Direc ons Amy L. Akers, PhD1; Karen L. Ball, BS2; Marianne Clancy, BS3; Anne M. Comi, MD4; MDocID: 1aiC8 - View Document | |
Bacteria in sputum of stable severe asthma and increased airway wall thicknessDocID: 15WBd - View Document | |
UNIVERSITY OF PENNSYLVANIA GENETIC DIAGNOSTIC LABORATORY IMAGe Beckwith-Wiedemann SyndromeDocID: 12D12 - View Document | |
Erratum: Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia Michael Benzinou, Frederic F. Clermont, Tom G.W. Letteboer, Jai-hyun Kim, Silvia Espejel, KellDocID: X9kO - View Document | |
Microsoft Word - HAE[removed]new figure 2 _230508_.docDocID: N26y - View Document |