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Year | Number of Results |
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2018 | 1 |
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Page 1
Clinical and Genetic Analysis of Multiple Osteochondromas in A Cohort of Argentine Patients.
Genes (Basel). 2022 Nov 7;13(11):2063. doi: 10.3390/genes13112063.
Genes (Basel). 2022.
PMID: 36360300
Free PMC article.
Mass spectrometry glycophenotype characterization of ALG2-CDG in Argentinean patients with a new genetic variant in homozygosis.
Papazoglu GM, Cubilla M, Pereyra M, de Kremer RD, Pérez B, Sturiale L, Asteggiano CG.
Papazoglu GM, et al. Among authors: asteggiano cg.
Glycoconj J. 2021 Apr;38(2):191-200. doi: 10.1007/s10719-021-09976-w. Epub 2021 Mar 1.
Glycoconj J. 2021.
PMID: 33644825
Free article.
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Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls.
Asteggiano CG, Papazoglu M, Bistué Millón MB, Peralta MF, Azar NB, Spécola NS, Guelbert N, Suldrup NS, Pereyra M, Dodelson de Kremer R.
Asteggiano CG, et al.
Pediatr Res. 2018 Dec;84(6):837-841. doi: 10.1038/s41390-018-0206-6. Epub 2018 Oct 18.
Pediatr Res. 2018.
PMID: 30397276
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A novel nonsense mutation of the EXT1 gene in an Argentinian patient with multiple hereditary exostoses: a case report.
Delgado MA, Sarrión P, Azar N, Zecchini L, Robledo HH, Segura F, Balcells S, Grinberg D, Dodelson de Kremer R, Asteggiano CG.
Delgado MA, et al. Among authors: asteggiano cg.
J Bone Joint Surg Am. 2012 Jun 6;94(11):e76. doi: 10.2106/JBJS.J.01920.
J Bone Joint Surg Am. 2012.
PMID: 22637216
No abstract available.
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