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Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Clin Genet. 2021 Mar;99(3):407-417. doi: 10.1111/cge.13894. Epub 2020 Dec 15.
Clin Genet. 2021.
PMID: 33277917
Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations.
Spencer-Smith M, Knight JL, Lacaze E; Irc5 Consortium; Depienne C, Lockhart PJ, Richards LJ, Heron D, Leventer RJ, Robinson GA.
Spencer-Smith M, et al.
Dev Med Child Neurol. 2020 Jun;62(6):758-762. doi: 10.1111/dmcn.14486. Epub 2020 Feb 14.
Dev Med Child Neurol. 2020.
PMID: 32060908
Free article.
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Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.
Heide S, Argilli E, Valence S, Boutaud L, Roux N, Mignot C, Nava C, Keren B, Giraudat K, Faudet A, Gerasimenko A, Garel C, Blondiaux E, Rastetter A, Grevent D, Le C, Mackenzie L, Richards L, Attié-Bitach T, Depienne C, Sherr E, Héron D.
Heide S, et al. Among authors: giraudat k.
J Med Genet. 2024 Feb 21;61(3):244-249. doi: 10.1136/jmg-2023-109293.
J Med Genet. 2024.
PMID: 37857482
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Results and limits of posterior cranial vault expansion by osteotomy and internal distractors.
Di Rocco F, Usami K, Protzenko T, Collet C, Giraudat K, Arnaud E.
Di Rocco F, et al. Among authors: giraudat k.
Surg Neurol Int. 2018 Oct 30;9:217. doi: 10.4103/sni.sni_465_17. eCollection 2018.
Surg Neurol Int. 2018.
PMID: 30505619
Free PMC article.
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Bilambdoid and sagittal synostosis: Report of 39 cases.
Chivoret N, Arnaud E, Giraudat K, O'Brien F, Pamphile L, Meyer P, Renier D, Collet C, Di Rocco F.
Chivoret N, et al. Among authors: giraudat k.
Surg Neurol Int. 2018 Oct 11;9:206. doi: 10.4103/sni.sni_454_17. eCollection 2018.
Surg Neurol Int. 2018.
PMID: 30386676
Free PMC article.
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Factors affecting the quality of life of young neurosurgeons: a survey.
Di Rocco F, Giraudat K, Zerah M.
Di Rocco F, et al. Among authors: giraudat k.
Acta Neurochir (Wien). 2015 Mar;157(3):495-6. doi: 10.1007/s00701-014-2322-3. Epub 2015 Jan 10.
Acta Neurochir (Wien). 2015.
PMID: 25576175
No abstract available.
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