Listado de Publicaciones Científicas del año 2020

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Rey, R. A., & Grinspon, R. P. (2020). Androgen Treatment in Adolescent Males With HypogonadismAmerican Journal of Men's Health, 14(3), 155798832092244. doi: 10.1177/1557988320922443

 

Grinspon RP, Bergadá I, Rey RA. Male Hypogonadism and Disorders of Sex Development. Front Endocrinol (Lausanne). 2020 Apr 15;11:211. doi: 10.3389/fendo.2020.00211. eCollection 2020.

 

Colombero C, Cárdenas S, Venara M, Martin A, Pennisi P, Barontini M, Nowicki S. Cytochrome 450 metabolites of arachidonic acid (20-HETE, 11,12-EET and 14,15-EET) promote pheochromocytoma cell growth and tumor associated angiogenesis. Biochimie. 2020 Apr-May;171-172:147-157. doi: 10.1016/j.biochi.2020.02.014. Epub 2020 Feb 24. PMID: 32105813.

 

Ramírez L, Sanguineti N, Scaglia P, Keselman A, Ballerini MG, Karabatas L, Landi E, Castro J, Domené S, Pennisi P, Jasper H, Rey RA, Vázquez M, Domené H, Bergadá I, Gutiérrez M. A novel heterozygous STAT5B variant in a patient with short stature and partial growth hormone insensitivity (GHI). Growth Horm IGF Res. 2020 Feb;50:61-70. doi: 10.1016/j.ghir.2019.12.005. Epub 2019 Dec 27. PMID:
31902742.

 

Jaworski JP, Urrutia M, Dascal E, Jaita G, Peluffo MC. C-C motif chemokine receptor 2 as a novel intermediate in the ovulatory cascade. Mol Hum Reprod. 2020 Mar 11:gaaa020. doi: 10.1093/molehr/gaaa020. Epub ahead of print. PMID: 32159806.

 

Burgueño AL, Juarez YR, Genaro AM, Tellechea ML. Systematic review and meta- analysis on the relationship between prenatal stress and metabolic syndrome intermediate phenotypes. Int J Obes (Lond). 2020 Jan;44(1):1-12. doi: 10.1038/s41366-019-0423-z. Epub 2019 Jul 22. PMID: 31332277.

 

Oud MS, Okutman Ö, Hendricks LAJ, et al. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Hum Reprod. 2020;35(1):240‐252. doi:10.1093/humrep/dez246

 

Débora Braslavsky, Paula Scaglia, Nora Sanguineti, Miriam Aza-Carmona, Julián Nevado Blanco, Pablo D. Lapunzina Badia, María del C. Fernández, Olivia Ruiz, Alejandra Carmona, Marina Szlago, Claudia Arberase, Hamilton Cassinelli, Karen Heath, Rodolfo Rey e Ignacio Bergadá. Presentación de casos clínicos. Síndrome de osteoporosis-pseudoglioma: a propósito de un caso pediátrico de osteoporosis primaria. Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis. Arch Argent Pediatr 2020;118(x):000-000

 

Rey RA. Biomarkers of male hypogonadism in childhood and adolescence. Advances in Laboratory Medicine 2020; 20200024. doi: 10.1515/almed-2020-0024

 

Burgueño AL, Juárez YR, Genaro AM, Tellechea ML. Prenatal stress and later metabolic consequences: Systematic review and meta-analysis in rodents. Psychoneuroendocrinology. 2020 Mar;113:104560. doi: 10.1016/j.psyneuen.2019.104560. Epub 2019 Dec 20. Review. PMID: 31884321

 

Sanguineti N, Braslavsky D, Scaglia PA, Keselman A, Ballerini MG, Ropelato MG, Suco S, Vishnopolska S, Berenstein AJ, Jasper H, Domené HM, Rey RA, Pérez Millán MI, Camper SA, Bergadá I. p.R209H GH1 variant challenges short stature assessment. Growth Horm IGF Res. 2020 Feb;50:23-26. doi: 10.1016/j.ghir.2019.11.002. Epub 2019 Dec 3. PMID: 31835104

 

Cárdenas S, Colombero C, Panelo L, Dakarapu R, Falck JR, Costas MA, Nowicki S. GPR75 receptor mediates 20-HETE-signaling and metastatic features of androgen-insensitive prostate cancer cells. Biochim Biophys Acta Mol Cell Biol Lipids. 2020 Feb;1865(2):158573. doi: 10.1016/j.bbalip.2019.158573. Epub 2019 Nov 21. PMID: 31760076

 

Edelsztein NY, Kashimada K, Schteingart HF, Rey RA. CYP26B1 declines postnatally in Sertoli cells independently of androgen action in the mouse testis. Mol Reprod Dev. 2020 Jan;87(1):66-77. doi: 10.1002/mrd.23302. Epub 2019 Nov 22. PMID: 31755607

 

Gorga A, Rindone GM, Centola CL, Sobarzo C, Pellizzari EH, Camberos MDC, Cigorraga SB, Riera MF, Galardo MN, Meroni SB. In vitro effects of glyphosate and Roundup on Sertoli cell physiology. Toxicol In Vitro. 2020 Feb;62:104682. doi: 10.1016/j.tiv.2019.104682. Epub 2019 Oct 15. PMID: 31626902

 

Keselman AC, Martin A, Scaglia PA, Sanguineti NM, Armando R, Gutiérrez M, Braslavsky D, Ballerini MG, Ropelato MG, Ramirez L, Landi E, Domené S, Castro JF, Cassinelli H, Casali B, Del Rey G, Barros ÁC, Nevado Blanco J, Domené H, Jasper H, Arberas C, Rey RA, Lapunzina-Badía P, Bergadá I, Pennisi PA. A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency. Eur J Endocrinol. 2019 Nov;181(5):K43-K53. doi: 10.1530/EJE-19-0563. PMID: 31539878