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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1980 1
1983 1
1984 1
1986 1
1987 3
1988 3
1989 1
1990 4
1991 1
1992 1
1993 1
1995 1
1996 1
1997 1
1998 2
1999 1
2000 1
2001 4
2002 2
2005 2
2006 1
2009 5
2010 4
2011 4
2012 3
2013 4
2014 4
2015 3
2017 1
2024 0

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57 results

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Page 1
[CHARGE syndrome].
Lobete Prieto CJ, Llano Rivas I, Fernández Toral J, Madero Barrajón P. Lobete Prieto CJ, et al. Among authors: fernandez toral j. Arch Argent Pediatr. 2010 Feb;108(1):e9-e12. doi: 10.1590/S0325-00752010000100016. Arch Argent Pediatr. 2010. PMID: 20204230 Free article. Spanish.
Haploinsufficiency of BMP4 gene may be the underlying cause of Frías syndrome.
Martínez-Fernández ML, Bermejo-Sánchez E, Fernández B, MacDonald A, Fernández-Toral J, Martínez-Frías ML. Martínez-Fernández ML, et al. Among authors: fernandez toral j. Am J Med Genet A. 2014 Feb;164A(2):338-45. doi: 10.1002/ajmg.a.36224. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311462 Review.
[Tuberculous encephalopathy].
Lastra Martínez LA, Artega Manjón-Cabeza R, Madrigal Díez V, Moreno Belzue C, Fernández Toral J, Herranz Fernández JL. Lastra Martínez LA, et al. Among authors: fernandez toral j. An Esp Pediatr. 1991 Jun;34(6):468-70. An Esp Pediatr. 1991. PMID: 1929017 Review. Spanish. No abstract available.
[Prenatal diagnosis].
Hernando Acero I, Plasencia Amela A, Benavides Benavides A, Fernández Cuesta M, Fernández Toral J. Hernando Acero I, et al. Among authors: fernandez toral j. An Esp Pediatr. 1987 Sep;27(3):183-9. An Esp Pediatr. 1987. PMID: 3322120 Spanish. No abstract available.
A new overgrowth syndrome is due to mutations in RNF125.
Tenorio J, Mansilla A, Valencia M, Martínez-Glez V, Romanelli V, Arias P, Castrejón N, Poletta F, Guillén-Navarro E, Gordo G, Mansilla E, García-Santiago F, González-Casado I, Vallespín E, Palomares M, Mori MA, Santos-Simarro F, García-Miñaur S, Fernández L, Mena R, Benito-Sanz S, del Pozo Á, Silla JC, Ibañez K, López-Granados E, Martín-Trujillo A, Montaner D; SOGRI Consortium; Heath KE, Campos-Barros Á, Dopazo J, Nevado J, Monk D, Ruiz-Pérez VL, Lapunzina P. Tenorio J, et al. Hum Mutat. 2014 Dec;35(12):1436-41. doi: 10.1002/humu.22689. Hum Mutat. 2014. PMID: 25196541
[Early osteopetrosis].
Solís Sánchez G, Fernández Guinea O, Tango Bockamba C, Olay Villa-Sanjurjo E, Fernández Toral J. Solís Sánchez G, et al. Among authors: fernandez toral j. An Esp Pediatr. 1988 May;28(5):468-70. An Esp Pediatr. 1988. PMID: 3178067 Spanish. No abstract available.
Renal involvement in Down syndrome.
Málaga S, Pardo R, Málaga I, Orejas G, Fernández-Toral J. Málaga S, et al. Among authors: fernandez toral j. Pediatr Nephrol. 2005 May;20(5):614-7. doi: 10.1007/s00467-005-1825-9. Epub 2005 Mar 23. Pediatr Nephrol. 2005. PMID: 15785939
Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene.
Martín-Hernández E, García-Silva MT, Quijada-Fraile P, Rodríguez-García ME, Rivera H, Hernández-Laín A, Coca-Robinot D, Fernández-Toral J, Arenas J, Martín MA, Martínez-Azorín F. Martín-Hernández E, et al. Among authors: fernandez toral j. Pediatr Dev Pathol. 2017 Sep-Oct;20(5):416-420. doi: 10.1177/1093526616686439. Epub 2017 Jan 25. Pediatr Dev Pathol. 2017. PMID: 28812460
57 results