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Year Number of Results
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Page 1
Artifacts and main lesions in fetal ocular histology.
Dubucs C, Chassaing N, Khung-Savatovsky S, Aziza J, Courtade-Saïdi M. Dubucs C, et al. Among authors: khung savatovsky s. Morphologie. 2023 Jun;107(357):207-218. doi: 10.1016/j.morpho.2022.08.002. Epub 2022 Dec 5. Morphologie. 2023. PMID: 36470718
Cytomegalovirus-induced brain malformations in fetuses.
Teissier N, Fallet-Bianco C, Delezoide AL, Laquerrière A, Marcorelles P, Khung-Savatovsky S, Nardelli J, Cipriani S, Csaba Z, Picone O, Golden JA, Van Den Abbeele T, Gressens P, Adle-Biassette H. Teissier N, et al. Among authors: khung savatovsky s. J Neuropathol Exp Neurol. 2014 Feb;73(2):143-58. doi: 10.1097/NEN.0000000000000038. J Neuropathol Exp Neurol. 2014. PMID: 24423639
Growth Restriction, Osteopenia, Placental Massive Perivillous Fibrin Deposition With (or Without) Intervillous Histiocytes and Renal Tubular Dysgenesis-An Emerging Complex.
Abdulghani S, Moretti F, Nikkels PG, Khung-Savatovsky S, Hurteau-Miller J, Grynspan D. Abdulghani S, et al. Among authors: khung savatovsky s. Pediatr Dev Pathol. 2018 Jan-Feb;21(1):91-94. doi: 10.1177/1093526617697061. Epub 2017 Mar 15. Pediatr Dev Pathol. 2018. PMID: 29187034 Review.
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders.
Abdelfattah F, Kariminejad A, Kahlert AK, Morrison PJ, Gumus E, Mathews KD, Darbro BW, Amor DJ, Walsh M, Sznajer Y, Weiß L, Weidensee S, Chitayat D, Shannon P, Bermejo-Sánchez E, Riaño-Galán I, Hayes I, Poke G, Rooryck C, Pennamen P, Khung-Savatovsky S, Toutain A, Vuillaume ML, Ghaderi-Sohi S, Kariminejad MH, Weinert S, Sticht H, Zenker M, Schanze D. Abdelfattah F, et al. Among authors: khung savatovsky s. Hum Mutat. 2020 Sep;41(9):1615-1628. doi: 10.1002/humu.24067. Epub 2020 Jul 15. Hum Mutat. 2020. PMID: 32579715
Corrigendum to: DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, Ramoz N, Imbeaud S, Loe-Mie Y, Benihoud K, Agier N, Salin PA, Cardona A, Khung-Savatovsky S, Kallunki P, Delabar JM, Puskas LG, Delacroix H, Aggerbeck L, Delezoide AL, Delattre O, Gorwood P, Moalic JM, Simonneau M. Lepagnol-Bestel AM, et al. Among authors: khung savatovsky s. Hum Mol Genet. 2022 Jun 22;31(12):2106-2107. doi: 10.1093/hmg/ddab346. Hum Mol Genet. 2022. PMID: 34918050 No abstract available.
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Grampa V, Delous M, Zaidan M, Odye G, Thomas S, Elkhartoufi N, Filhol E, Niel O, Silbermann F, Lebreton C, Collardeau-Frachon S, Rouvet I, Alessandri JL, Devisme L, Dieux-Coeslier A, Cordier MP, Capri Y, Khung-Savatovsky S, Sigaudy S, Salomon R, Antignac C, Gubler MC, Benmerah A, Terzi F, Attié-Bitach T, Jeanpierre C, Saunier S. Grampa V, et al. Among authors: khung savatovsky s. PLoS Genet. 2016 Mar 11;12(3):e1005894. doi: 10.1371/journal.pgen.1005894. eCollection 2016 Mar. PLoS Genet. 2016. PMID: 26967905 Free PMC article.
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
Delahaye A, Khung-Savatovsky S, Aboura A, Guimiot F, Drunat S, Alessandri JL, Gérard M, Bitoun P, Boumendil J, Robin S, Huel C, Guilherme R, Serero S, Gressens P, Elion J, Verloes A, Benzacken B, Delezoide AL, Pipiras E. Delahaye A, et al. Among authors: khung savatovsky s. Am J Med Genet A. 2012 Oct;158A(10):2430-8. doi: 10.1002/ajmg.a.35548. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903608
25 results