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42 results on '"de Lucas-Collantes C"'

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1. TLR7 gain-of-function genetic variation causes human lupus

7. Neumonía sarampionosa

9. Minimal Change Disease Is Associated With Endothelial Glycocalyx Degradation and Endothelial Activation

10. Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-Linked hypophosphataemia: rationale and description

11. Molecular Mechanisms of Proteinuria in Minimal Change Disease

12. β1-Integrin blockade prevents podocyte injury in experimental models of minimal change disease.

13. DECTIN-1: A modifier protein in CTLA-4 haploinsufficiency.

14. Hypercapnia in hospitalized children and adolescents with anorexia nervosa as a predictive marker for readmission: a prospective study.

15. The International X-Linked Hypophosphatemia (XLH) Registry: first interim analysis of baseline demographic, genetic and clinical data.

17. Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries.

18. Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-linked hypophosphataemia: rationale and description.

19. TLR7 gain-of-function genetic variation causes human lupus.

20. Fanconi Syndrome Secondary to Sodium Valproate Therapy: Experience and Literature Review.

21. Molecular Mechanisms of Proteinuria in Minimal Change Disease.

22. Minimal Change Disease Is Associated With Endothelial Glycocalyx Degradation and Endothelial Activation.

24. [Tuberous sclerosis complex: analysis of areas of involvement, treatment progress and translation to routine clinical practice in a cohort of paediatric patients].

25. Lupus nephritis in children.

27. Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.

29. Systemic lupus erythematosus presenting as thrombotic thrombocytopaenic purpura in a child: a diagnostic challenge.

31. Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus.

32. Nutritional status of iodine in children: When appropriateness relies on milk consumption and not adequate coverage of iodized salt in households.

33. Ulcerative Colitis and Atypical Hemolytic-Uremic Syndrome: An Unusual But Potentially Life-threatening Complication.

34. FGF23 and its role in X-linked hypophosphatemia-related morbidity.

35. Mitochondrial Disease in Children: The Nephrologist's Perspective.

39. [Imerslund-Gräsbeck syndrome: megaloblastic anaemia with proteinuria].

40. [Urinary tract infections: antibiotic resistance and clinical follow up].

42. [Measles pneumonia].

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