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Salivary and serum cortisol levels in newborn infants.
Arch Argent Pediatr. 2017 Jun 1;115(3):262-266. doi: 10.5546/aap.2017.eng.262.
Arch Argent Pediatr. 2017.
PMID: 28504492
Free article.
English, Spanish.
Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrum.
da Silva TE, Gomes NL, Lerário AM, Keegan CE, Nishi MY, Carvalho FM, Vilain E, Barseghyan H, Martinez-Aguayo A, Forclaz MV, Papazian R, Pedroso de Paula LC, Costa EC, Carvalho LR, Jorge AAL, Elias FM, Mitchell R, Costa EMF, Mendonca BB, Domenice S.
da Silva TE, et al. Among authors: forclaz mv.
J Clin Endocrinol Metab. 2019 Dec 1;104(12):5923-5934. doi: 10.1210/jc.2019-00984.
J Clin Endocrinol Metab. 2019.
PMID: 31287541
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Knockout mice with pituitary malformations help identify human cases of hypopituitarism.
Martinez-Mayer J, Brinkmeier ML, O'Connell SP, Ukagwu A, Marti MA, Miras M, Forclaz MV, Benzrihen MG, Cheung LYM, Camper SA, Ellsworth BS, Raetzman LT, Pérez-Millán MI, Davis SW.
Martinez-Mayer J, et al. Among authors: forclaz mv.
Genome Med. 2024 May 31;16(1):75. doi: 10.1186/s13073-024-01347-y.
Genome Med. 2024.
PMID: 38822427
Free PMC article.
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Exome Sequencing has a high diagnostic rate in sporadic congenital hypopituitarism and reveals novel candidate genes.
Martinez-Mayer J, Vishnopolska S, Perticarari C, Garcia LI, Hackbartt M, Martinez M, Zaiat J, Jacome-Alvarado A, Braslavsky D, Keselman A, Bergadá I, Marino R, Ramírez P, Garrido NP, Ciaccio M, Di Palma MI, Belgorosky A, Forclaz MV, Benzrihen G, D'Amato S, Cirigliano ML, Miras M, Nuñez AP, Castro L, Mallea-Gil MS, Ballarino C, Latorre-Villacorta L, Casiello AC, Hernandez C, Figueroa V, Alonso G, Morin A, Guntsche Z, Lee H, Lee E, Song Y, Marti MA, Perez-Millan MI.
Martinez-Mayer J, et al. Among authors: forclaz mv.
J Clin Endocrinol Metab. 2024 May 8:dgae320. doi: 10.1210/clinem/dgae320. Online ahead of print.
J Clin Endocrinol Metab. 2024.
PMID: 38717911
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