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Treatment of juvenile recurrent respiratory papillomatosis in a lung transplantation recipient pediatric patient.
Gómez-Ganda L, Iglesias-Serrano I, Parramón-Teixidó CJ, Batlle-Masó L, Peña-Zarza JA, Díez-Izquierdo A. Gómez-Ganda L, et al. Among authors: batlle maso l. Farm Hosp. 2024 Mar 11:S1130-6343(24)00029-1. doi: 10.1016/j.farma.2024.02.008. Online ahead of print. Farm Hosp. 2024. PMID: 38472063 Free article. English, Spanish. No abstract available.
Role of Skewed X-Chromosome Inactivation in Common Variable Immunodeficiency.
Garcia-Prat M, Batlle-Masó L, Parra-Martínez A, Franco-Jarava C, Martinez-Gallo M, Aguiló-Cucurull A, Perurena-Prieto J, Castells N, Urban B, Dieli-Crimi R, Soler-Palacín P, Colobran R. Garcia-Prat M, et al. Among authors: batlle maso l. J Clin Immunol. 2024 Jan 24;44(2):54. doi: 10.1007/s10875-024-01659-z. J Clin Immunol. 2024. PMID: 38265673
Molecular Challenges in the Diagnosis of X-Linked Chronic Granulomatous Disease: CNVs, Intronic Variants, Skewed X-Chromosome Inactivation, and Gonosomal Mosaicism.
Batlle-Masó L, Rivière JG, Franco-Jarava C, Martín-Nalda A, Garcia-Prat M, Parra-Martínez A, Aguiló-Cucurull A, Castells N, Martinez-Gallo M, Soler-Palacín P, Colobran R. Batlle-Masó L, et al. J Clin Immunol. 2023 Nov;43(8):1953-1963. doi: 10.1007/s10875-023-01556-x. Epub 2023 Aug 19. J Clin Immunol. 2023. PMID: 37597073
Detection and evolutionary dynamics of somatic FAS variants in autoimmune lymphoproliferative syndrome: Diagnostic implications.
Batlle-Masó L, Garcia-Prat M, Parra-Martínez A, Franco-Jarava C, Aguiló-Cucurull A, Velasco P, Antolín M, Rivière JG, Martín-Nalda A, Soler-Palacín P, Martínez-Gallo M, Colobran R. Batlle-Masó L, et al. Front Immunol. 2022 Nov 18;13:1014984. doi: 10.3389/fimmu.2022.1014984. eCollection 2022. Front Immunol. 2022. PMID: 36466883 Free PMC article.
Somatic genetic variation in healthy tissue and non-cancer diseases.
Solís-Moruno M, Batlle-Masó L, Bonet N, Aróstegui JI, Casals F. Solís-Moruno M, et al. Among authors: batlle maso l. Eur J Hum Genet. 2023 Jan;31(1):48-54. doi: 10.1038/s41431-022-01213-8. Epub 2022 Oct 27. Eur J Hum Genet. 2023. PMID: 36289407 Free PMC article. Review.
Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report.
Franco-Jarava C, Valenzuela I, Riviere JG, Garcia-Prat M, Martínez-Gallo M, Dieli-Crimi R, Castells N, Batlle-Masó L, Soler-Palacin P, Colobran R. Franco-Jarava C, et al. Among authors: batlle maso l. Front Immunol. 2022 Jun 17;13:897975. doi: 10.3389/fimmu.2022.897975. eCollection 2022. Front Immunol. 2022. PMID: 35784294 Free PMC article.
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