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39 results on '"Madrid, Álvaro"'

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1. Colony stimulating factor-1 receptor drives glomerular parietal epithelial cell activation in focal segmental glomerulosclerosis

2. Metabolic Acidosis Is Associated With an Accelerated Decline of Allograft Function in Pediatric Kidney Transplantation

4. Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children’s Hospital

7. Complement genetic variants and FH desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

8. Overcoming limits: First ABO incompatible living donor paired kidney transplant in an hypersensitized pediatric recipient in Spain

10. CD44-negative parietal–epithelial cell staining in minimal change disease: association with clinical features, response to corticosteroids and kidney outcome

12. Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

13. CD44-negative parietal–epithelial cell staining in minimal change disease: association with clinical features, response to corticosteroids and kidney outcome.

14. Escuela de atletismo: iniciación y formación de un atleta (Combinadas) = School athletics: Initiation and training of an athlete (Combined events)

15. La seguridad en la Unión Europea

16. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

17. Escuela de atletismo: iniciación y formación de un atleta (Combinadas) = School athletics: Initiation and training of an athlete (Combined events)

18. A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases

19. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

20. Escuela de atletismo: iniciación y formación de un atleta (Combinadas) = School athletics: Initiation and training of an athlete (Combined events)

21. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome : mutations in multiple glomerular genes may influence disease severity

22. Manual de entrenamiento de la fuerza en el fútbol. La planificación del trabajo de fuerza en un equipo

23. Correction: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

24. Conoce Europa a través de la música : siglo XX : guía de lectura

25. Manual de entrenamiento de la fuerza en el fútbol. La planificación del trabajo de fuerza en un equipo

26. Acércate a Europa

27. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.

28. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity

31. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.

32. Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

34. Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

35. Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.

36. Conoce Europa a través de la música: siglo XX : guía de lectura

37. Conoce Europa a través de la novela : siglo XX : guía de lectura

38. Acércate a Europa

39. Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

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