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

Year Number of Results
1981 1
1984 1
1989 1
1991 1
1992 2
1993 2
1995 1
1996 2
1997 1
1998 5
1999 1
2000 1
2001 1
2002 1
2003 2
2005 1
2006 1
2007 2
2009 1
2010 1
2011 4
2012 3
2013 2
2015 1
2016 1
2024 0

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36 results

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Page 1
Bilateral striatal lesions in childhood.
Roig M, Calopa M, Rovira A, Macaya A, Riudor E, Losada M. Roig M, et al. Among authors: riudor e. Pediatr Neurol. 1993 Sep-Oct;9(5):349-58. doi: 10.1016/0887-8994(93)90103-j. Pediatr Neurol. 1993. PMID: 8292209 Review.
Medium-chain acyl-CoA dehydrogenase deficiency in Spain.
Martínez G, Ribes A, Briones P, Rodés M, Baldellou A, Pineda M, Rodrigo C, Lorente I, García-Silva MT, Riudor E, Jaraba P, Lopez-Casas J, Nuñez-Roldan A. Martínez G, et al. Among authors: riudor e. J Inherit Metab Dis. 1998 Aug;21(6):693-4. doi: 10.1023/a:1005461407231. J Inherit Metab Dis. 1998. PMID: 9762615 No abstract available.
Partial ornithine transcarbamylase deficiency.
Riudor E, Arranz JA, Rodés M. Riudor E, et al. Pediatrics. 2003 May;111(5 Pt 1):1123-4; author reply 1123-4. doi: 10.1542/peds.111.5.1123-a. Pediatrics. 2003. PMID: 12728104 No abstract available.
Glycogen storage disease type III with hypoketosis.
Clemente M, Gussinyer M, Arranz JA, Riudor E, Yeste D, Albisu M, Carrascosa A. Clemente M, et al. Among authors: riudor e. J Pediatr Endocrinol Metab. 2010 Aug;23(8):833-6. doi: 10.1515/jpem.2010.134. J Pediatr Endocrinol Metab. 2010. PMID: 21073127
Protein expression profiles in patients carrying NFU1 mutations. Contribution to the pathophysiology of the disease.
Ferrer-Cortès X, Font A, Bujan N, Navarro-Sastre A, Matalonga L, Arranz JA, Riudor E, del Toro M, Garcia-Cazorla A, Campistol J, Briones P, Ribes A, Tort F. Ferrer-Cortès X, et al. Among authors: riudor e. J Inherit Metab Dis. 2013 Sep;36(5):841-7. doi: 10.1007/s10545-012-9565-z. Epub 2012 Nov 22. J Inherit Metab Dis. 2013. PMID: 23179554
A leaky splicing mutation in NFU1 is associated with a particular biochemical phenotype. Consequences for the diagnosis.
Ferrer-Cortès X, Narbona J, Bujan N, Matalonga L, Del Toro M, Arranz JA, Riudor E, Garcia-Cazorla A, Jou C, O'Callaghan M, Pineda M, Montero R, Arias A, García-Villoria J, Alston CL, Taylor RW, Briones P, Ribes A, Tort F. Ferrer-Cortès X, et al. Among authors: riudor e. Mitochondrion. 2016 Jan;26:72-80. doi: 10.1016/j.mito.2015.12.004. Epub 2015 Dec 11. Mitochondrion. 2016. PMID: 26688339
36 results