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

Year Number of Results
2013 1
2014 5
2015 7
2016 2
2017 3
2018 4
2019 10
2020 6
2021 7
2022 5
2023 3
2024 0

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46 results

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Page 1
Early prediction of phenotypic severity in Citrullinemia Type 1.
Zielonka M, Kölker S, Gleich F, Stützenberger N, Nagamani SCS, Gropman AL, Hoffmann GF, Garbade SF, Posset R; Urea Cycle Disorders Consortium (UCDC) and the European Registry and Network for Intoxication type Metabolic Diseases (E-IMD) Consortia Study Group. Zielonka M, et al. Ann Clin Transl Neurol. 2019 Sep;6(9):1858-1871. doi: 10.1002/acn3.50886. Epub 2019 Aug 30. Ann Clin Transl Neurol. 2019. PMID: 31469252 Free PMC article.
Metabolic Serendipities of Expanded Newborn Screening.
Yahyaoui R, Blasco-Alonso J, Gonzalo-Marín M, Benito C, Serrano-Nieto J, González-Gallego I, Ruiz-Sala P, Pérez B, González-Lamuño D. Yahyaoui R, et al. Among authors: blasco alonso j. Genes (Basel). 2020 Aug 29;11(9):1018. doi: 10.3390/genes11091018. Genes (Basel). 2020. PMID: 32872442 Free PMC article.
Influence of early identification and therapy on long-term outcomes in early-onset MTHFR deficiency.
Yverneau M, Leroux S, Imbard A, Gleich F, Arion A, Moreau C, Nassogne MC, Szymanowski M, Tardieu M, Touati G, Bueno M, Chapman KA, Chien YH, Huemer M, Ješina P, Janssen MCH, Kölker S, Kožich V, Lavigne C, Lund AM, Mochel F, Morris A, Pons MR, Porras-Hurtado GL, Benoist JF, Damaj L, Schiff M; E-HOD Consortium. Yverneau M, et al. J Inherit Metab Dis. 2022 Jul;45(4):848-861. doi: 10.1002/jimd.12504. Epub 2022 May 9. J Inherit Metab Dis. 2022. PMID: 35460084 Free article.
Non-alcoholic fatty liver in hereditary fructose intolerance.
Aldámiz-Echevarría L, de Las Heras J, Couce ML, Alcalde C, Vitoria I, Bueno M, Blasco-Alonso J, Concepción García M, Ruiz M, Suárez R, Andrade F, Villate O. Aldámiz-Echevarría L, et al. Among authors: blasco alonso j. Clin Nutr. 2020 Feb;39(2):455-459. doi: 10.1016/j.clnu.2019.02.019. Epub 2019 Feb 15. Clin Nutr. 2020. PMID: 30833214 Free article.
Metastatic Crohn's disease in pediatrics.
Blasco Alonso J, Girón Fernández-Crehuet F, Lendínez Ramírez MA, Gallego Gutiérrez S, Luque Pérez S, Serrano Nieto J, Navas López VM, Sierra Salinas C. Blasco Alonso J, et al. Rev Esp Enferm Dig. 2016 Sep;108(9):598-603. doi: 10.17235/reed.2016.3948/2015. Rev Esp Enferm Dig. 2016. PMID: 26856545 Free article.
Dual latent tuberculosis screening with tuberculin skin tests and QuantiFERON-TB assays before TNF-α inhibitor initiation in children in Spain.
Calzada-Hernández J, Anton J, Martín de Carpi J, López-Montesinos B, Calvo I, Donat E, Núñez E, Blasco Alonso J, Mellado MJ, Baquero-Artigao F, Leis R, Vegas-Álvarez AM, Medrano San Ildefonso M, Pinedo-Gago MDC, Eizaguirre FJ, Tagarro A, Camacho-Lovillo M, Pérez-Gorricho B, Gavilán-Martín C, Guillén S, Sevilla-Pérez B, Peña-Quintana L, Mesa-Del-Castillo P, Fortuny C, Tebruegge M, Noguera-Julian A. Calzada-Hernández J, et al. Among authors: blasco alonso j. Eur J Pediatr. 2023 Jan;182(1):307-317. doi: 10.1007/s00431-022-04640-3. Epub 2022 Nov 5. Eur J Pediatr. 2023. PMID: 36335186 Free PMC article.
Sirolimus for the Treatment of Juvenile Polyposis in Childhood.
Martín-Masot R, Cardelo Autero N, Ortiz Pérez P, Torcuato Rubio E, Vázquez Pedreño L, Gallego Fernández C, Blasco-Alonso J, Navas-López VM. Martín-Masot R, et al. Among authors: blasco alonso j. ACG Case Rep J. 2021 Aug 25;8(8):e00646. doi: 10.14309/crj.0000000000000646. eCollection 2021 Aug. ACG Case Rep J. 2021. PMID: 34476273 Free PMC article.
Cardiometabolic and Nutritional Morbidities of a Large, Adult, PKU Cohort from Andalusia.
Dios-Fuentes E, Gonzalo Marin M, Remón-Ruiz P, Benitez Avila R, Bueno Delgado MA, Blasco Alonso J, Doulatram Gamgaram VK, Olveira G, Soto-Moreno A, Venegas-Moreno E. Dios-Fuentes E, et al. Among authors: blasco alonso j. Nutrients. 2022 Mar 21;14(6):1311. doi: 10.3390/nu14061311. Nutrients. 2022. PMID: 35334968 Free PMC article.
Newborn screening for homocystinurias: Recent recommendations versus current practice.
Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M; individual contributors of the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD); Barić I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla S, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH, Zeyda M. Keller R, et al. Among authors: blasco alonso j. J Inherit Metab Dis. 2019 Jan;42(1):128-139. doi: 10.1002/jimd.12034. J Inherit Metab Dis. 2019. PMID: 30740731 Free article.
46 results