Medin M - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Case Report: Common variable immunodeficiency phenotype and granulomatous-lymphocytic interstitial lung disease with a novel SOCS1 variant.

Caldirola MS, Daiana E, Gomez Raccio AC, García AL, Bernacchia A, Medín M, Gaillard MI, Di Giovanni D. Caldirola MS, et al. Among authors: medin m. Front Pediatr. 2024 Jun 28;12:1423858. doi: 10.3389/fped.2024.1423858. eCollection 2024. Front Pediatr. 2024. PMID: 39005503 Free PMC article.

Inherited pulmonary surfactant metabolism disorders in Argentina: Differences between patients with SFTPC and ABCA3 variants.

Balinotti JE, Mallie C, Maffey A, Colom A, Epaud R, de Becdelievre A, Fanen P, Delestrain C, Medín M, Teper A. Balinotti JE, et al. Among authors: medin m. Pediatr Pulmonol. 2023 Feb;58(2):540-549. doi: 10.1002/ppul.26225. Epub 2022 Nov 11. Pediatr Pulmonol. 2023. PMID: 36324278 Free article.

Clinical, functional, and computed tomography findings in a cohort of patients with neuroendocrine cell hyperplasia of infancy.

Balinotti JE, Maffey A, Colom A, Roldán O, Díaz W, Medín M, Racimo M, Teper A. Balinotti JE, et al. Among authors: medin m. Pediatr Pulmonol. 2021 Jun;56(6):1681-1686. doi: 10.1002/ppul.25319. Epub 2021 Feb 23. Pediatr Pulmonol. 2021. PMID: 33580744

Peripheral tuberculous lymphadenitis in pediatrics: 16 years of experience in a tertiary care pediatric hospital of Buenos Aires, Argentina.

Neyro SE, Squassi IR, Medín M, Caratozzolo A, Martínez Burkett A, Cerqueiro MC. Neyro SE, et al. Among authors: medin m. Arch Argent Pediatr. 2018 Dec 1;116(6):430-436. doi: 10.5546/aap.2018.eng.430. Arch Argent Pediatr. 2018. PMID: 30457726 Free article. English, Spanish.

[Pleuropulmonary blastoma, case report].

Bosch JJ, Medín M, Garrido P, Martínez J, Teper A. Bosch JJ, et al. Among authors: medin m. Arch Argent Pediatr. 2016 Feb;114(1):e25-8. doi: 10.5546/aap.2016.e25. Arch Argent Pediatr. 2016. PMID: 26914086 Free article. Spanish.

Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN -42 C>G mutation.

Medin M, Hermida-Prieto M, Monserrat L, Laredo R, Rodriguez-Rey JC, Fernandez X, Castro-Beiras A. Medin M, et al. Eur J Heart Fail. 2007 Jan;9(1):37-43. doi: 10.1016/j.ejheart.2006.04.007. Epub 2006 Jul 7. Eur J Heart Fail. 2007. PMID: 16829191 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

6 results

Search Page

Filters