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3. Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

4. Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia

8. The Added Value of Coronary Calcium Score in Predicting Cardiovascular Events in Familial Hypercholesterolemia

9. Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

10. Efficacy and Safety of a new Low-Volume PEG with Citrate and Simethicone bowel preparation for pediatric elective colonoscopy: a phase 3 RCT

11. Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

14. Recurrent "outsider" intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb.

15. A European Survey on Digestive Perianastomotic Ulcerations, a Rare Crohn-like Disorder Occurring in Children and Young Adults

17. Clinical Remission and Psychological Management are Major Issues for the Quality of Life in Pediatric Crohn Disease

19. Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood

22. Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia

24. Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

25. Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis

28. Impact of diet on sensory processing in early childhood: summary of an interactive webconference / expert roundtable discussion.

30. Membrane progestin receptors: beyond the controversy, can we move forward?

31. The Added Value of Coronary Calcium Score in Predicting Cardiovascular Events in Familial Hypercholesterolemia

32. Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form

33. Implication of Heterozygous Variants in Genes of the Leptin–Melanocortin Pathway in Severe Obesity

35. Feeding disorders in children with oesophageal atresia: a cross-sectional study

38. Feeding disorders in children with oesophageal atresia: a cross-sectional study.

40. Clinical Remission and Psychological Management are Major Issues for the Quality of Life in Pediatric Crohn Disease

42. Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

43. Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome

44. Contractile forces at tricellular contacts modulate epithelial organization and monolayer integrity

46. Microbiote et obésité.

47. Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis.

48. Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form

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