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[Care for transgender children and adolescents].
Med Sci (Paris). 2022 Nov;38(11):897-904. doi: 10.1051/medsci/2022150. Epub 2022 Nov 30.
Med Sci (Paris). 2022.
PMID: 36448896
Free article.
French.
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).
Fiot E, Alauze B, Donadille B, Samara-Boustani D, Houang M, De Filippo G, Bachelot A, Delcour C, Beyler C, Bois E, Bourrat E, Bui Quoc E, Bourcigaux N, Chaussain C, Cohen A, Cohen-Solal M, Da Costa S, Dossier C, Ederhy S, Elmaleh M, Iserin L, Lengliné H, Poujol-Robert A, Roulot D, Viala J, Albarel F, Bismuth E, Bernard V, Bouvattier C, Brac A, Bretones P, Chabbert-Buffet N, Chanson P, Coutant R, de Warren M, Demaret B, Duranteau L, Eustache F, Gautheret L, Gelwane G, Gourbesville C, Grynberg M, Gueniche K, Jorgensen C, Kerlan V, Lebrun C, Lefevre C, Lorenzini F, Manouvrier S, Pienkowski C, Reynaud R, Reznik Y, Siffroi JP, Tabet AC, Tauber M, Vautier V, Tauveron I, Wambre S, Zenaty D, Netchine I, Polak M, Touraine P, Carel JC, Christin-Maitre S, Léger J.
Fiot E, et al.
Orphanet J Rare Dis. 2022 Jul 12;17(Suppl 1):261. doi: 10.1186/s13023-022-02423-5.
Orphanet J Rare Dis. 2022.
PMID: 35821070
Free PMC article.
Item in Clipboard
SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.
Lambert S, Peycelon M, Samara-Boustani D, Hyon C, Dumeige L, Peuchmaur M, Fiot E, Léger J, Simon D, Paye-Jaouen A, Bouligand J, Siffroi JP, Carel JC, McElreavey K, El Ghoneimi A, Brachet C, Bouvattier C, Martinerie L.
Lambert S, et al. Among authors: fiot e.
Clin Endocrinol (Oxf). 2021 Apr;94(4):667-676. doi: 10.1111/cen.14389. Epub 2020 Dec 26.
Clin Endocrinol (Oxf). 2021.
PMID: 33296530
Item in Clipboard
X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome.
Fiot E, Zenaty D, Boizeau P, Haigneré J, Santos SD, Léger J; French Turner Syndrome Study Group.
Fiot E, et al.
Eur J Endocrinol. 2016 Sep;175(3):X1. doi: 10.1530/EJE-15-1000e.
Eur J Endocrinol. 2016.
PMID: 27484588
No abstract available.
Item in Clipboard
X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome.
Fiot E, Zenaty D, Boizeau P, Haigneré J, Dos Santos S, Léger J; French Turner Syndrome Study Group.
Fiot E, et al.
Eur J Endocrinol. 2016 Mar;174(3):281-8. doi: 10.1530/EJE-15-1000. Epub 2015 Dec 14.
Eur J Endocrinol. 2016.
PMID: 26744895
Item in Clipboard
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood.
Fiot E, Zénaty D, Boizeau P, Haignere J, Dos Santos S, Léger J; French Turner Syndrome Study Group.
Fiot E, et al.
Eur J Endocrinol. 2019 Jun 1;180(6):397-406. doi: 10.1530/EJE-18-0878.
Eur J Endocrinol. 2019.
PMID: 30991358
Item in Clipboard
Hormone Therapy During Infancy or Early Childhood for Patients with Hypogonadotropic Hypogonadism, Klinefelter or Turner Syndrome: Has the Time Come?
Fiot E, Léger J, Martinerie L.
Fiot E, et al.
Endocrinol Metab Clin North Am. 2024 Jun;53(2):307-320. doi: 10.1016/j.ecl.2024.02.003. Epub 2024 Mar 8.
Endocrinol Metab Clin North Am. 2024.
PMID: 38677872
Review.
Item in Clipboard
[Prognostic value of VZV PCR in cerebrospinal fluid in neurological manifestations of varicella].
Levy M, Hentgen V, Marque-Juillet S, Fiot E, Fagherazzi G, Nathanson S, Foucaud P.
Levy M, et al. Among authors: fiot e.
Arch Pediatr. 2015 May;22(5):491-7. doi: 10.1016/j.arcped.2015.02.001. Epub 2015 Mar 24.
Arch Pediatr. 2015.
PMID: 25819633
French.
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