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2. A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

4. MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset

5. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

8. Systematic and combined endobronchial and endoscopic ultrasound (EBUS-EUS) for diagnosis and staging in lung cancer: experience from a tertiary center

10. Endoscopic full-thickness resection of duodenal neuroendocrine tumors using the Full-Thickness Resection Device (FTRD): Results from a large, retrospective, multicenter study

11. BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status

16. Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy

18. Safety and efficacy of salvage endoscopic submucosal dissection for Barrett’s neoplasia recurrence after radiofrequency ablation

21. Penetrance and Prognosis of MYH7Variant-Associated Cardiomyopathies

22. A deep learning system for detection of early Barrett's neoplasia: a model development and validation study

24. A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects

25. ENETS standardized (synoptic) reporting for endoscopy in neuroendocrine tumors

44. 789 CALY-002, AN ANTI-IL-15 ANTIBODY, PREVENTS GLUTEN CHALLENGEINDUCED MUCOSAL DAMAGE AND INFLAMMATION: RESULTS FROM A PHASE 1A/B STUDY.

45. Western outcomes of circumferential endoscopic submucosal dissection for early esophageal squamous cell carcinoma.

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