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Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation.
Le Rouzic MA, Fouquet C, Leblanc T, Touati M, Fouyssac F, Vermylen C, Jäkel N, Guichard JF, Maloum K, Toutain F, Lutz P, Perel Y, Manceau H, Kannengiesser C, Vannier JP. Le Rouzic MA, et al. Among authors: fouquet c. Blood Cells Mol Dis. 2017 Jul;66:11-18. doi: 10.1016/j.bcmd.2017.07.003. Epub 2017 Jul 26. Blood Cells Mol Dis. 2017. PMID: 28772256
Genotype/phenotype correlations of childhood-onset congenital sideroblastic anaemia in a European cohort.
Fouquet C, Le Rouzic MA, Leblanc T, Fouyssac F, Leverger G, Hessissen L, Marlin S, Bourrat E, Fahd M, Raffoux E, Vannier JP, Jäkel N, Knoefler R, Triolo V, Pasquet M, Bayart S, Thuret I, Lutz P, Vermylen C, Touati M, Rose C, Matthes T, Isidor B, Kannengiesser C, Ducassou S. Fouquet C, et al. Br J Haematol. 2019 Nov;187(4):530-542. doi: 10.1111/bjh.16100. Epub 2019 Jul 23. Br J Haematol. 2019. PMID: 31338833 Free article.
Pheochromocytoma and Paraganglioma in Children and Adolescents: Experience of the French Society of Pediatric Oncology (SFCE).
de Tersant M, Généré L, Freyçon C, Villebasse S, Abbas R, Barlier A, Bodet D, Corradini N, Defachelles AS, Entz-Werle N, Fouquet C, Galmiche L, Gandemer V, Lacour B, Mansuy L, Orbach D, Pluchart C, Réguerre Y, Rigaud C, Sarnacki S, Sirvent N, Stephan JL, Thebaud E, Gimenez-Roqueplo AP, Brugières L. de Tersant M, et al. Among authors: fouquet c. J Endocr Soc. 2020 Apr 3;4(5):bvaa039. doi: 10.1210/jendso/bvaa039. eCollection 2020 May 1. J Endocr Soc. 2020. PMID: 32432211 Free PMC article.
Pediatric Tumors and Developmental Anomalies: A French Nationwide Cohort Study.
Semeraro M, Fouquet C, Vial Y, Amiel J, Galmiche L, Cretolle C, Blanc T, Jolaine V, Garcelon N, Entz-Werle N, Pellier I, Vérité C, Sophie Taque, Coulomb A, Petit A, Corradini N, Bouazza N, Lacour B, Clavel J, Brugières L, Bourdeaut F, Sarnacki S; members of the TED Consortium. Semeraro M, et al. Among authors: fouquet c. J Pediatr. 2023 Aug;259:113451. doi: 10.1016/j.jpeds.2023.113451. Epub 2023 May 9. J Pediatr. 2023. PMID: 37169337
[Defense mechanisms in trypanosomiasis].
Daulouede PS, Okomo-Assoumou MC, Labassa M, Fouquet C, Vincendeau P. Daulouede PS, et al. Among authors: fouquet c. Bull Soc Pathol Exot. 1994;87(5):330-2. Bull Soc Pathol Exot. 1994. PMID: 7496195 French.
FMRP regulates postnatal neuronal migration via MAP1B.
Messaoudi S, Allam A, Stoufflet J, Paillard T, Le Ven A, Fouquet C, Doulazmi M, Trembleau A, Caille I. Messaoudi S, et al. Among authors: fouquet c. Elife. 2024 May 17;12:RP88782. doi: 10.7554/eLife.88782. Elife. 2024. PMID: 38757694 Free PMC article.
Congenital mirror movements are associated with defective polymerisation of RAD51.
Trouillard O, Dupaigne P, Dunoyer M, Doulazmi M, Herlin MK, Frismand S, Riou A, Legros V, Chevreux G, Veaute X, Busso D, Fouquet C, Saint-Martin C, Méneret A, Trembleau A, Dusart I, Dubacq C, Roze E. Trouillard O, et al. Among authors: fouquet c. J Med Genet. 2023 Nov;60(11):1116-1126. doi: 10.1136/jmg-2023-109189. Epub 2023 Jun 12. J Med Genet. 2023. PMID: 37308287
VEGF Mediates Commissural Axon Chemoattraction through Its Receptor Flk1.
Ruiz de Almodovar C, Fabre PJ, Knevels E, Coulon C, Segura I, Haddick PCG, Aerts L, Delattin N, Strasser G, Oh WJ, Lange C, Vinckier S, Haigh J, Fouquet C, Gu C, Alitalo K, Castellani V, Tessier-Lavigne M, Chedotal A, Charron F, Carmeliet P. Ruiz de Almodovar C, et al. Among authors: fouquet c. Neuron. 2023 Apr 19;111(8):1348. doi: 10.1016/j.neuron.2023.03.029. Neuron. 2023. PMID: 37080170 Free article. No abstract available.
FMRP regulates tangential neuronal migration via MAP1B.
Messaoudi S, Allam A, Stoufflet J, Paillard T, Fouquet C, Doulazmi M, Le Ven A, Trembleau A, Caillé I. Messaoudi S, et al. Among authors: fouquet c. bioRxiv [Preprint]. 2023 Dec 28:2023.03.06.530447. doi: 10.1101/2023.03.06.530447. bioRxiv. 2023. PMID: 36945472 Free PMC article. Updated. Preprint.
72 results