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Items: 1 to 50 of 164

1.

Methylation cycle, arginine-creatine pathway and asymmetric dimethylarginine in paediatric renal transplant.

Andrade F, Rodríguez-Soriano J, Prieto JA, Aguirre M, Ariceta G, Lage S, Azcona I, Prado C, Sanjurjo P, Aldámiz-Echevarría L.

Nephrol Dial Transplant. 2011 Jan;26(1):328-36. doi: 10.1093/ndt/gfq404. Epub 2010 Jul 6.

PMID:
20605841
2.

Persistence of essential fatty acid deficiency in cystic fibrosis despite nutritional therapy.

Aldámiz-Echevarría L, Prieto JA, Andrade F, Elorz J, Sojo A, Lage S, Sanjurjo P, Vázquez C, Rodríguez-Soriano J.

Pediatr Res. 2009 Nov;66(5):585-9. doi: 10.1203/PDR.0b013e3181b4e8d3.

PMID:
19851226
3.

Fatty acid deficiency profile in children with food allergy managed with elimination diets.

Aldámiz-Echevarría L, Bilbao A, Andrade F, Elorz J, Prieto JA, Rodríguez-Soriano J.

Acta Paediatr. 2008 Nov;97(11):1572-6. doi: 10.1111/j.1651-2227.2008.00963.x. Epub 2008 Jul 29.

PMID:
18671692
4.

The arginine-creatine pathway is disturbed in children and adolescents with renal transplants.

Andrade F, Rodríguez-Soriano J, Prieto JA, Elorz J, Aguirre M, Ariceta G, Martin S, Sanjurjo P, Aldámiz-Echevarría L.

Pediatr Res. 2008 Aug;64(2):218-22. doi: 10.1203/PDR.0b013e318176180e. Erratum in: Pediatr Res. 2009 Feb;65(2):248.

PMID:
18391841
5.

Inherited renal tubulopathies associated with metabolic alkalosis: effects on blood pressure.

Ariceta G, Rodríguez-Soriano J.

Semin Nephrol. 2006 Nov;26(6):422-33. Review.

PMID:
17275579
6.

Arachidonic acid content in adipose tissue is associated with insulin resistance in healthy children.

Aldámiz-Echevarría L, Prieto JA, Andrade F, Elorz J, Sanjurjo P, Rodríguez Soriano J.

J Pediatr Gastroenterol Nutr. 2007 Jan;44(1):77-83.

PMID:
17204958
7.

Essential fatty acid deficiency profile in patients with nephrotic-range proteinuria.

Aldámiz-Echevarría L, Vallo A, Aguirre M, Sanjurjo P, Gonzalez-Lamuño D, Elorz J, Prieto JA, Andrade F, Rodríguez-Soriano J.

Pediatr Nephrol. 2007 Apr;22(4):533-40. Epub 2006 Nov 23.

PMID:
17123116
8.

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.

Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, Vitzthum H, Suzuki Y, Luk JM, Becker C, Schlingmann KP, Schmid M, Rodriguez-Soriano J, Ariceta G, Cano F, Enriquez R, Juppner H, Bakkaloglu SA, Hediger MA, Gallati S, Neuhauss SC, Nurnberg P, Weber S.

Am J Hum Genet. 2006 Nov;79(5):949-57. Epub 2006 Sep 19.

9.

Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults.

Geller DS, Zhang J, Zennaro MC, Vallo-Boado A, Rodriguez-Soriano J, Furu L, Haws R, Metzger D, Botelho B, Karaviti L, Haqq AM, Corey H, Janssens S, Corvol P, Lifton RP.

J Am Soc Nephrol. 2006 May;17(5):1429-36. Epub 2006 Apr 12.

10.

Effect of docosahexaenoic acid administration on plasma lipid profile and metabolic parameters of children with methylmalonic acidaemia.

Aldámiz-Echevarría L, Sanjurjo P, Elorz J, Prieto JA, Pérez C, Andrade F, Rodríguez-Soriano J.

J Inherit Metab Dis. 2006 Feb;29(1):58-63.

PMID:
16601869
11.

Osteogenesis imperfecta: anthropometric, skeletal and mineral metabolic effects of long-term intravenous pamidronate therapy.

Vallo A, Rodriguez-Leyva F, Rodríguez Soriano J.

Acta Paediatr. 2006 Mar;95(3):332-9.

PMID:
16497645
12.

Fatty acid composition of skeletal muscle and adipose tissue in Spanish infants and children.

Sanjurjo P, Aldámiz-Echevarría L, Prado C, Azcona I, Elorz J, Prieto JA, Ruiz JI, Rodríguez-Soriano J.

Br J Nutr. 2006 Jan;95(1):168-73.

PMID:
16441930
13.

An analysis of renal tubular acidosis by the Stewart method.

Corey HE, Vallo A, Rodríguez-Soriano J.

Pediatr Nephrol. 2006 Feb;21(2):206-11. Epub 2005 Dec 17.

PMID:
16362393
14.

Abnormalities in plasma fatty acid composition in human immunodeficiency virus-infected children treated with protease inhibitors.

Aldámiz-Echevarría L, Pocheville I, Sanjurjo P, Elorz J, Prieto JA, Rodríguez-Soriano J.

Acta Paediatr. 2005 Jun;94(6):672-7.

PMID:
16188767
15.

Bone mineral density and bone turnover in patients with Bartter syndrome.

Rodríguez-Soriano J, Vallo A, Aguirre M.

Pediatr Nephrol. 2005 Aug;20(8):1120-5. Epub 2005 Jun 8.

PMID:
15942790
16.

A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.

Rodríguez-Soriano J, Vallo A, Pérez de Nanclares G, Bilbao JR, Castaño L.

Pediatr Nephrol. 2005 Jul;20(7):891-6. Epub 2005 May 5.

PMID:
15875219
17.

Long-term renal follow-up of extremely low birth weight infants.

Rodríguez-Soriano J, Aguirre M, Oliveros R, Vallo A.

Pediatr Nephrol. 2005 May;20(5):579-84. Epub 2005 Mar 22.

PMID:
15782301
18.

Acidosis increases magnesiuria in children with distal renal tubular acidosis.

Ariceta G, Vallo A, Rodriguez-Soriano J.

Pediatr Nephrol. 2004 Dec;19(12):1367-70.

PMID:
15503178
19.

Influence of diet on atherogenic risk in children with renal transplants.

Aldámiz-Echevarría L, Vallo A, Sanjurjo P, Elorz J, Prieto JA, Ruiz JI, Rodríguez-Soriano J.

Pediatr Nephrol. 2004 Sep;19(9):1039-45. Epub 2004 Jul 16.

PMID:
15258843
20.

Neonatal hypercalcemia.

Rodríguez Soriano J.

J Nephrol. 2003 Jul-Aug;16(4):606-8. Review.

PMID:
14696768
21.

Branchio-oto-renal syndrome.

Rodríguez Soriano J.

J Nephrol. 2003 Jul-Aug;16(4):603-5. Review.

PMID:
14696767
22.

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.

Seri M, Pecci A, Di Bari F, Cusano R, Savino M, Panza E, Nigro A, Noris P, Gangarossa S, Rocca B, Gresele P, Bizzaro N, Malatesta P, Koivisto PA, Longo I, Musso R, Pecoraro C, Iolascon A, Magrini U, Rodriguez Soriano J, Renieri A, Ghiggeri GM, Ravazzolo R, Balduini CL, Savoia A.

Medicine (Baltimore). 2003 May;82(3):203-15.

23.

Genetic and metabolic determinants of increased plasma plasminogen activator inhibitor-1 activity in children with renal transplants.

Aldámiz-Echevarría L, Sanjurjo P, Vallo A, Aguirre M, Pérez-Nanclares G, Gimeno P, Rueda M, Ruiz JI, Rodríguez-Soriano J.

Pediatr Nephrol. 2003 Aug;18(8):749-55. Epub 2003 May 22.

PMID:
12761670
24.

[Renal hereditary tubulopathies: from the clinic to the molecular biology].

Rodríguez Soriano J.

Nefrologia. 2003;23 Suppl 1:71-83. Review. Spanish. No abstract available.

25.

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.

Stover EH, Borthwick KJ, Bavalia C, Eady N, Fritz DM, Rungroj N, Giersch AB, Morton CC, Axon PR, Akil I, Al-Sabban EA, Baguley DM, Bianca S, Bakkaloglu A, Bircan Z, Chauveau D, Clermont MJ, Guala A, Hulton SA, Kroes H, Li Volti G, Mir S, Mocan H, Nayir A, Ozen S, Rodriguez Soriano J, Sanjad SA, Tasic V, Taylor CM, Topaloglu R, Smith AN, Karet FE.

J Med Genet. 2002 Nov;39(11):796-803.

26.

Hyperhomocysteinemia in children with renal transplants.

Aldámiz-Echevarría L, Sanjurjo P, Vallo A, Aquino L, Pérez-Nanclares G, Gimeno P, Rueda M, Ruiz I, Urreizti R, Rodríguez-Soriano J.

Pediatr Nephrol. 2002 Sep;17(9):718-23. Epub 2002 Jun 11.

PMID:
12215824
27.

Renal tubular acidosis: the clinical entity.

Rodríguez Soriano J.

J Am Soc Nephrol. 2002 Aug;13(8):2160-70. Review. No abstract available.

28.

Neonatal hypercalcemia.

Rodríguez SJ.

Pediatr Med Chir. 2002 Mar-Apr;24(2):111-3. No abstract available.

PMID:
11987508
29.

Familial hypercalcemia and hypercalciuria: no mutations in the Ca2+-sensing receptor gene.

Rodríguez-Soriano J, Vallo A, Quintela MJ, Pérez de Nanclares G, Bilbao JR, Castaño L.

Pediatr Nephrol. 2001 Sep;16(9):748-51.

PMID:
11511994
30.

Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene.

Rodríguez-Soriano J, Vallo A, Bilbao JR, Castaño L.

Pediatr Nephrol. 2001 Jul;16(7):550-3.

PMID:
11465802
31.

[Long-term prognosis of childhood IgA nephropathy in adult life].

Ariceta G, Gallego N, López-Fernández Y, Vallo A, Quintela MJ, Rodríguez Soriano J.

Med Clin (Barc). 2001 Mar 17;116(10):361-4. Spanish.

PMID:
11333668
32.

Predictors of final adult height after renal transplantation during childhood: a single-center study.

Rodríguez-Soriano J, Vallo A, Quintela MJ, Málaga S, Loris C.

Nephron. 2000 Nov;86(3):266-73.

PMID:
11096282
33.

New insights into the pathogenesis of renal tubular acidosis--from functional to molecular studies.

Rodríguez-Soriano J.

Pediatr Nephrol. 2000 Oct;14(12):1121-36. Review.

PMID:
11045400
34.

Hypercalcemia in neonatal distal renal tubular acidosis.

Rodríguez-Soriano J, García-Fuentes M, Vallo A, Alvárez-Granda JL.

Pediatr Nephrol. 2000 Apr;14(4):354-5. No abstract available.

PMID:
10775085
35.

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, Casari G, Bettinelli A, Colussi G, Rodriguez-Soriano J, McCredie D, Milford D, Sanjad S, Lifton RP.

Science. 1999 Jul 2;285(5424):103-6.

36.

Bartter's syndrome comes of age.

Rodriguez-Soriano J.

Pediatrics. 1999 Mar;103(3):663-4. No abstract available.

PMID:
10049972
37.

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.

Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP.

Nat Genet. 1999 Jan;21(1):84-90.

PMID:
9916796
38.

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.

Geller DS, Rodriguez-Soriano J, Vallo Boado A, Schifter S, Bayer M, Chang SS, Lifton RP.

Nat Genet. 1998 Jul;19(3):279-81.

PMID:
9662404
39.

Bartter and related syndromes: the puzzle is almost solved.

Rodríguez-Soriano J.

Pediatr Nephrol. 1998 May;12(4):315-27. Review.

PMID:
9655365
40.

A randomized comparison of surfactant dosing via a dual-lumen endotracheal tube in respiratory distress syndrome. The Spanish Surfactant Collaborative Group.

Valls-i-Soler A, Fernández-Ruanova B, López-Heredia y Goya J, Román Etxebarría L, Rodriguez-Soriano J, Carretero V.

Pediatrics. 1998 Apr;101(4):E4.

PMID:
9533371
41.

[Treatment of idiopathic nephrotic syndrome with cyclosporin A].

Ariceta Iraola G, Rodríguez Soriano J, Vallo Boado A, Quintela Pérez MJ, Oliveros Pérez R.

An Esp Pediatr. 1997 Sep;47(3):273-8. Spanish.

PMID:
9499280
42.

[Anales and the impact factor].

Rodríguez Soriano J.

An Esp Pediatr. 1997 Sep;47(3):234. Spanish. No abstract available.

PMID:
9499273
43.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP.

Nat Genet. 1997 Oct;17(2):171-8.

PMID:
9326936
44.
45.

[Contribution of molecular biology to the study of renal tubular diseases].

Rodríguez Soriano J.

An Esp Pediatr. 1997 Jun;Spec No 1:40-2. Spanish. No abstract available.

PMID:
9382265
46.

[The Spanish Pediatric Association and Internet].

Moya M, Rodríguez Soriano J.

An Esp Pediatr. 1997 Jun;46(6):533. Spanish. No abstract available.

PMID:
9297417
47.

Acute and chronic effects of cisplatin therapy on renal magnesium homeostasis.

Ariceta G, Rodriguez-Soriano J, Vallo A, Navajas A.

Med Pediatr Oncol. 1997 Jan;28(1):35-40.

PMID:
8950334
48.

[A 2-year-old child with acute pulmonary process].

Chouza M, Guibert J, Rodríguez Soriano J.

An Esp Pediatr. 1996 Dec;45(6):653-4. Spanish. No abstract available.

PMID:
9133238
49.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP.

Nat Genet. 1996 Oct;14(2):152-6.

PMID:
8841184
50.

Renal magnesium handling in infants and children.

Ariceta G, Rodríguez-Soriano J, Vallo A.

Acta Paediatr. 1996 Sep;85(9):1019-23.

PMID:
8888910

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