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

Year Number of Results
2005 2
2006 1
2008 1
2015 1
2016 1
2017 3
2018 1
2020 2
2021 9
2022 8
2023 6
2024 2

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33 results

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Page 1
Recommendations for the Diagnosis and Therapeutic Management of Hyperammonaemia in Paediatric and Adult Patients.
Bélanger-Quintana A, Arrieta Blanco F, Barrio-Carreras D, Bergua Martínez A, Cañedo Villarroya E, García-Silva MT, Lama More R, Martín-Hernández E, López AM, Morales-Conejo M, Pedrón-Giner C, Quijada-Fraile P, Stanescu S, Casanova MM. Bélanger-Quintana A, et al. Among authors: morales conejo m. Nutrients. 2022 Jul 2;14(13):2755. doi: 10.3390/nu14132755. Nutrients. 2022. PMID: 35807935 Free PMC article. Review.
Acute intermittent porphyria, givosiran, and homocysteine.
Fontanellas A, Ávila MA, Arranz E, Enríquez de Salamanca R, Morales-Conejo M. Fontanellas A, et al. Among authors: morales conejo m. J Inherit Metab Dis. 2021 Jul;44(4):790-791. doi: 10.1002/jimd.12411. Epub 2021 Jun 22. J Inherit Metab Dis. 2021. PMID: 34145602 Free PMC article. No abstract available.
Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review.
Gómez-Rodríguez MJ, Morales-Conejo M, Arteche-López A, Sánchez-Calvín MT, Quesada-Espinosa JF, Gómez-Manjón I, Palma-Milla C, Lezana-Rosales JM, Pérez de la Fuente R, Martin-Ramos ML, Fernández-Guijarro M, Moreno-García M, Alvarez-Mora MI. Gómez-Rodríguez MJ, et al. Among authors: morales conejo m. Genes (Basel). 2022 Sep 8;13(9):1609. doi: 10.3390/genes13091609. Genes (Basel). 2022. PMID: 36140775 Free PMC article. Review.
Diagnosis, evaluation and monitoring of acute hepatic porphyria.
Solares I, Castelbón FJ, Enríquez de Salamanca R, Morales-Conejo M. Solares I, et al. Among authors: morales conejo m. Med Clin (Barc). 2023 Sep;159 Suppl 1:S19-S24. doi: 10.1016/j.medcli.2023.07.005. Epub 2023 Oct 10. Med Clin (Barc). 2023. PMID: 37827888 English, Spanish. No abstract available.
[Transition process from paediatric to adult care in patients with inborn errors of metabolism. Consensus statement].
Pérez-López J, Ceberio-Hualde L, García Morillo JS, Grau-Junyent JM, Hermida Ameijeiras Á, López-Rodríguez M, Morales-Conejo M, Nava Mateos JJ, Aldámiz Echevarri Azuara LJ, Campistol J, Couce ML, García-Silva MT, González Gutiérrez-Solana L, Del Toro M; Sociedad Española de Medicina Interna (SEMI); Sociedad Española de Neurología Pediátrica (SENEP). Pérez-López J, et al. Among authors: morales conejo m. Med Clin (Barc). 2016 Dec 2;147(11):506.e1-506.e7. doi: 10.1016/j.medcli.2016.09.018. Epub 2016 Nov 3. Med Clin (Barc). 2016. PMID: 27816186 Spanish.
Efficacy of laronidase therapy in patients with mucopolysaccharidosis type I who initiated enzyme replacement therapy in adult age. A systematic review and meta-analysis.
Pérez-López J, Morales-Conejo M, López-Rodríguez M, Hermida-Ameijeiras Á, Moltó-Abad M. Pérez-López J, et al. Among authors: morales conejo m. Mol Genet Metab. 2017 Jun;121(2):138-149. doi: 10.1016/j.ymgme.2017.04.004. Epub 2017 Apr 9. Mol Genet Metab. 2017. PMID: 28410878 Review.
33 results