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2017 | 1 |
2022 | 1 |
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YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse.
Genet Med. 2023 Jul;25(7):100835. doi: 10.1016/j.gim.2023.100835. Epub 2023 Mar 28.
Genet Med. 2023.
PMID: 36999555
Free article.
Review.
Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency Syndrome.
Mochel F, Gras D, Luton MP, Nizou M, Giovannini D, Delattre C, Aubart M, Barth M, De Saint-Martin A, Doummar D, Essid N, Garros A, Le Camus CH, Hoebeke C, The Tich SN, Perivier M, Rivera S, Rolland A, Roubertie A, Sarret C, Sevin C, Ville D, Sitbon M, Costa JM, Pons R, Garcia-Cazorla A, Vuillaumier S, Petit V, Boespflug-Tanguy O, De Vivo DC; MetaGlut1 Study Group.
Mochel F, et al.
Neurology. 2023 Jun 6;100(23):e2360-e2373. doi: 10.1212/WNL.0000000000207296. Epub 2023 Apr 19.
Neurology. 2023.
PMID: 37076312
Free PMC article.
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Glucocorticoid induced adrenal insufficiency in children: Morning cortisol values to avoid LDSST.
Laulhé M, Dumaine C, Chevenne D, Leye F, Faye A, Dozières B, Strullu M, Viala J, Hogan J, Houdouin V, Léger J, Simon D, Carel JC, Storey C, Guilmin-Crépon S, Martinerie L.
Laulhé M, et al. Among authors: dozieres b.
Front Pediatr. 2022 Dec 15;10:981765. doi: 10.3389/fped.2022.981765. eCollection 2022.
Front Pediatr. 2022.
PMID: 36589156
Free PMC article.
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Use of perampanel in children and adolescents with Lennox-Gastaut Syndrome.
Auvin S, Dozieres B, Ilea A, Delanoë C.
Auvin S, et al. Among authors: dozieres b.
Epilepsy Behav. 2017 Sep;74:59-63. doi: 10.1016/j.yebeh.2017.05.036. Epub 2017 Jul 14.
Epilepsy Behav. 2017.
PMID: 28715780
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