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Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study.
Eur J Pediatr. 2015 Oct;174(10):1373-85. doi: 10.1007/s00431-015-2534-4. Epub 2015 Apr 23.
Eur J Pediatr. 2015.
PMID: 25902753
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
Santín S, Tazón-Vega B, Silva I, Cobo MÁ, Giménez I, Ruíz P, García-Maset R, Ballarín J, Torra R, Ars E; FSGS Spanish Study Group.
Santín S, et al.
Clin J Am Soc Nephrol. 2011 Feb;6(2):344-54. doi: 10.2215/CJN.03770410. Epub 2010 Oct 14.
Clin J Am Soc Nephrol. 2011.
PMID: 20947785
Free PMC article.
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Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
Santín S, García-Maset R, Ruíz P, Giménez I, Zamora I, Peña A, Madrid A, Camacho JA, Fraga G, Sánchez-Moreno A, Cobo MA, Bernis C, Ortiz A, de Pablos AL, Pintos G, Justa ML, Hidalgo-Barquero E, Fernández-Llama P, Ballarín J, Ars E, Torra R; FSGS Spanish Study Group.
Santín S, et al. Among authors: hidalgo barquero e.
Kidney Int. 2009 Dec;76(12):1268-76. doi: 10.1038/ki.2009.381. Epub 2009 Oct 7.
Kidney Int. 2009.
PMID: 19812541
Free article.
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[Penile agenesis and syndrome of multiple abnormalities associated with the ingestion of retinoic acid by the mother].
Martínez Tallo ME, Galán Gómez E, Cordero Carrasco JL, Hidalgo Barquero EH, Campo Sampedro FM, Cardesa García JJ.
Martínez Tallo ME, et al. Among authors: hidalgo barquero eh.
An Esp Pediatr. 1989 Oct;31(4):399-400.
An Esp Pediatr. 1989.
PMID: 2627062
Spanish.
No abstract available.
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[Tuberculous peritonitis. Report of a case].
Zarallo Cortés L, Sáez Díez I, Arroyo Fernández J, Herranz Jordán B, Hidalgo Barquero E, Sanjuán Rodríguez S.
Zarallo Cortés L, et al. Among authors: hidalgo barquero e.
An Esp Pediatr. 1985 Jul;23(1):62-4.
An Esp Pediatr. 1985.
PMID: 4062077
Spanish.
No abstract available.
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