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Year | Number of Results |
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2005 | 1 |
2021 | 2 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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Page 1
Novel Germline TET2 Mutations in Two Unrelated Patients with Autoimmune Lymphoproliferative Syndrome-Like Phenotype and Hematologic Malignancy.
J Clin Immunol. 2023 Jan;43(1):165-180. doi: 10.1007/s10875-022-01361-y. Epub 2022 Sep 6.
J Clin Immunol. 2023.
PMID: 36066697
An Early Th1 Response Is a Key Factor for a Favorable COVID-19 Evolution.
Gil-Etayo FJ, Garcinuño S, Utrero-Rico A, Cabrera-Marante O, Arroyo-Sanchez D, Mancebo E, Pleguezuelo DE, Rodríguez-Frías E, Allende LM, Morales-Pérez P, Castro-Panete MJ, Lalueza A, Lumbreras C, Paz-Artal E, Serrano A.
Gil-Etayo FJ, et al. Among authors: morales perez p.
Biomedicines. 2022 Jan 27;10(2):296. doi: 10.3390/biomedicines10020296.
Biomedicines. 2022.
PMID: 35203509
Free PMC article.
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Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome.
López-Nevado M, Docampo-Cordeiro J, Ramos JT, Rodríguez-Pena R, Gil-López C, Sánchez-Ramón S, Gil-Herrera J, Díaz-Madroñero MJ, Delgado-Martín MA, Morales-Pérez P, Paz-Artal E, Magerus A, Rieux-Laucat F, Allende LM.
López-Nevado M, et al. Among authors: morales perez p.
Front Immunol. 2021 Apr 29;12:656356. doi: 10.3389/fimmu.2021.656356. eCollection 2021.
Front Immunol. 2021.
PMID: 33995372
Free PMC article.
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Towards a Change in the Diagnostic Algorithm of Autism Spectrum Disorders: Evidence Supporting Whole Exome Sequencing as a First-Tier Test.
Arteche-López A, Gómez Rodríguez MJ, Sánchez Calvin MT, Quesada-Espinosa JF, Lezana Rosales JM, Palma Milla C, Gómez-Manjón I, Hidalgo Mayoral I, Pérez de la Fuente R, Díaz de Bustamante A, Darnaude MT, Gil-Fournier B, Ramiro León S, Ramos Gómez P, Sierra Tomillo O, Juárez Rufián A, Arranz Cano MI, Villares Alonso R, Morales-Pérez P, Segura-Tudela A, Camacho A, Nuñez N, Simón R, Moreno-García M, Alvarez-Mora MI.
Arteche-López A, et al. Among authors: morales perez p.
Genes (Basel). 2021 Apr 12;12(4):560. doi: 10.3390/genes12040560.
Genes (Basel). 2021.
PMID: 33921431
Free PMC article.
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Is the IVS2+4T>C variant of the HFE gene a splicing mutation or a polymorphism? A study in the Spanish population.
de Lucas AP, Fulgencio MG, Robles JM, Sierra EM, del Rey Cerros MJ, Perez PM.
de Lucas AP, et al. Among authors: perez pm.
Genet Med. 2005 Mar;7(3):212-3. doi: 10.1097/01.gim.0000157125.89581.09.
Genet Med. 2005.
PMID: 15775762
Free article.
No abstract available.
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