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

Year Number of Results
1997 2
1998 2
2012 1
2013 1
2014 2
2015 1
2018 2
2019 1
2021 1
2024 0

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11 results

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Page 1
[Infrequent mutation in renal-coloboma syndrome: case report and review].
Ruiz Del Olmo Izuzquiza I, Romero Salas Y, Rodríguez Valle A, González Viejo I, Justa Roldán ML. Ruiz Del Olmo Izuzquiza I, et al. Among authors: justa roldan ml. Arch Argent Pediatr. 2018 Feb 1;116(1):e106-e109. doi: 10.5546/aap.2018.e106. Arch Argent Pediatr. 2018. PMID: 29333833 Free article. Review. Spanish.
[Postinfectious rapidly progressive glomerulonephritis in a pediatric patient].
Serrano Viñuales I, Ruiz Del Olmo Izuzquiza I, Romero Salas Y, Montaner Ramón A, Justa Roldán ML. Serrano Viñuales I, et al. Among authors: justa roldan ml. Arch Argent Pediatr. 2019 Aug 1;117(4):e363-e367. doi: 10.5546/aap.2019.e363. Arch Argent Pediatr. 2019. PMID: 31339276 Free article. Spanish.
URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia.
Claverie-Martin F, Trujillo-Suarez J, Gonzalez-Acosta H, Aparicio C, Justa Roldan ML, Stiburkova B, Ichida K, Martín-Gomez MA, Herrero Goñi M, Carrasco Hidalgo-Barquero M, Iñigo V, Enriquez R, Cordoba-Lanus E, Garcia-Nieto VM; RenalTube Group. Claverie-Martin F, et al. Among authors: justa roldan ml. Clin Chim Acta. 2018 Jun;481:83-89. doi: 10.1016/j.cca.2018.02.030. Epub 2018 Feb 24. Clin Chim Acta. 2018. PMID: 29486147
Encephalopathy, kidney failure and retinopathy. CoQ10 deficiency due to COQ8B mutation.
Adán Lanceta V, Romero Salas Y, Justa Roldán ML, García Jiménez MC, Ariceta Iraola G. Adán Lanceta V, et al. Among authors: justa roldan ml. An Pediatr (Engl Ed). 2021 Jun;94(6):415-417. doi: 10.1016/j.anpede.2020.05.008. Epub 2021 Apr 27. An Pediatr (Engl Ed). 2021. PMID: 34090639 Free article. No abstract available.
Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome.
Sánchez Chinchilla D, Pinto S, Hoppe B, Adragna M, Lopez L, Justa Roldan ML, Peña A, Lopez Trascasa M, Sánchez-Corral P, Rodríguez de Córdoba S. Sánchez Chinchilla D, et al. Among authors: justa roldan ml. Clin J Am Soc Nephrol. 2014 Sep 5;9(9):1611-9. doi: 10.2215/CJN.01640214. Epub 2014 Aug 18. Clin J Am Soc Nephrol. 2014. PMID: 25135762 Free PMC article.
[Type 1 polyglandular autoimmune syndrome associated with C322fsx372 mutation].
Roncalés-Samanes P, de Arriba Muñoz A, Lou Francés GM, Ferrer Lozano M, Justa Roldán ML, Labarta Aizpun JI. Roncalés-Samanes P, et al. Among authors: justa roldan ml. An Pediatr (Barc). 2015 Jan;82(1):e60-3. doi: 10.1016/j.anpedi.2014.01.012. Epub 2014 Feb 26. An Pediatr (Barc). 2015. PMID: 24582129 Free article. Spanish.
[Postkala-azar dermal leishmaniasis].
de Juan Martín F, Justa Roldán ML, Sáez de Adana Pérez E, Navarro Serrano E, Bouthelier Moreno M, Gilaberte Calzada Y, Fortuño Cebamanos B. de Juan Martín F, et al. Among authors: justa roldan ml. An Esp Pediatr. 1997 Jan;46(1):63-4. An Esp Pediatr. 1997. PMID: 9082890 Spanish. No abstract available.
[Pulmonary thromboembolism in a child with lupus nephropathy].
Cabrejas Lalmolda A, Orden Rueda C, García Iñiguez JP, Madurga Revilla P, Janer Subías E, Justa Roldán ML. Cabrejas Lalmolda A, et al. Among authors: justa roldan ml. An Pediatr (Barc). 2013 May;78(5):348-9. doi: 10.1016/j.anpedi.2012.11.012. Epub 2012 Dec 30. An Pediatr (Barc). 2013. PMID: 23280238 Free article. Spanish. No abstract available.
[Pseudoachondroplasia: a case report].
Justa Roldán ML, Baldellou Vázquez A, Oteiza Orradre C, Carranza Ferrer M, Ros Mar L, García Asensio S. Justa Roldán ML, et al. An Esp Pediatr. 1997 May;46(5):490-2. An Esp Pediatr. 1997. PMID: 9297405 Spanish. No abstract available.
[Microscopic polyangiitis: a case report].
Justa Roldán ML, Heras Gironella M, Loris Pablo C, Plaza Más L, Alonso Tomás L. Justa Roldán ML, et al. An Esp Pediatr. 1998 Aug;49(2):165-7. An Esp Pediatr. 1998. PMID: 9773553 Spanish. No abstract available.
11 results