16 results on '"Dupuis-Girod, Sophie"'
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2. Ultra-low dose chest CT for the diagnosis of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
3. Antiplatelet and anticoagulant therapies in hereditary hemorrhagic telangiectasia: A large French cohort study (RETROPLACOTEL)
4. European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
5. Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome
6. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations
7. 12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome
8. Peripheral arterial lesions of Marfan’s the disease: Analysis of a multicentric 138 patients cohort
9. Growth hormone deficiency caused by pituitary stalk interruption in Fanconi’s anemia
10. The psychological impact of cryptic chromosomal abnormalities diagnosis announcement
11. Ex vivo study of bevacizumab transport through porcine nasal mucosa
12. 0362 : Marfan syndrome diagnosed during childhood: focus on cardiac events in the French database
13. 0365 : Risk markers of cardiac events in patients with Marfan syndrome diagnosed during childhood
14. 0537: Risk markers of cardiac events in patients with Marfan syndrome diagnosed during childhood
15. 0543: Marfan syndrome diagnosed during childhood: focus on cardiac events in the French database
16. Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Follow-up and Pathophysiologic Considerations
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