Stichelbout M - Search Results

1

Is chronic histiocytic intervillositis a severe placental disease? A case-control study.

Homatter C, Stichelbout M, Devisme L, Chudzinski A, Debarge V, Garabedian C, Subtil D. Homatter C, et al. Among authors: stichelbout m. Placenta. 2020 Feb;91:31-36. doi: 10.1016/j.placenta.2019.12.020. Epub 2019 Dec 31. Placenta. 2020. PMID: 32174304

2

[Twin pregnancy with complete mole and coexisting fetus: Reach fetal viability is possible].

Arsène E, Clouqueur E, Stichelbout M, Devisme L, Vaast P, Subtil D. Arsène E, et al. Among authors: stichelbout m. J Gynecol Obstet Biol Reprod (Paris). 2015 Nov;44(9):887-90. doi: 10.1016/j.jgyn.2015.01.012. Epub 2015 Feb 24. J Gynecol Obstet Biol Reprod (Paris). 2015. PMID: 25721351 French.

3

SALL4 expression in gestational trophoblastic tumors: a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor.

Stichelbout M, Devisme L, Franquet-Ansart H, Massardier J, Vinatier D, Renaud F, Kerdraon O. Stichelbout M, et al. Hum Pathol. 2016 Aug;54:121-6. doi: 10.1016/j.humpath.2016.03.012. Epub 2016 Apr 8. Hum Pathol. 2016. PMID: 27068524

4

Perinatal outcome of placental massive perivillous fibrin deposition: a case-control study.

Devisme L, Chauvière C, Franquet-Ansart H, Chudzinski A, Stichelbout M, Houfflin-Debarge V, Subtil D. Devisme L, et al. Among authors: stichelbout m. Prenat Diagn. 2017 Apr;37(4):323-328. doi: 10.1002/pd.5013. Epub 2017 Mar 24. Prenat Diagn. 2017. PMID: 28152557

5

Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome.

Bonnard C, Shboul M, Tonekaboni SH, Ng AYJ, Tohari S, Ghosh K, Lai A, Lim JY, Tan EC, Devisme L, Stichelbout M, Alkindi A, Banu N, Yüksel Z, Ghoumid J, Elkhartoufi N, Boutaud L, Micalizzi A, Brett MS, Venkatesh B, Valente EM, Attié-Bitach T, Reversade B, Kariminejad A. Bonnard C, et al. Among authors: stichelbout m. Eur J Med Genet. 2018 Oct;61(10):585-595. doi: 10.1016/j.ejmg.2018.03.012. Epub 2018 Mar 30. Eur J Med Genet. 2018. PMID: 29605658

6

Risk factors for spontaneous hematoma of the umbilical cord: A case-control study.

Clermont-Hama Y, Thibouw K, Devisme L, Franquet-Ansart H, Stichelbout M, Subtil D. Clermont-Hama Y, et al. Among authors: stichelbout m. Placenta. 2020 Sep 15;99:152-156. doi: 10.1016/j.placenta.2020.07.020. Epub 2020 Jul 24. Placenta. 2020. PMID: 32798767

7

Associations between fetal heart rate variability and umbilical cord occlusions-induced neural injury: An experimental study in a fetal sheep model.

Ghesquière L, Perbet R, Lacan L, Hamoud Y, Stichelbout M, Sharma D, Nguyen S, Storme L, Houfflin-Debarge V, De Jonckheere J, Garabedian C. Ghesquière L, et al. Among authors: stichelbout m. Acta Obstet Gynecol Scand. 2022 Jul;101(7):758-770. doi: 10.1111/aogs.14352. Epub 2022 May 3. Acta Obstet Gynecol Scand. 2022. PMID: 35502642 Free PMC article.

8

Total alkaline phosphatase levels by gestational age in a large sample of pregnant women.

Titaux C, Ternynck C, Pauchet M, Stichelbout M, Bizet G, Maboudou P, Onraed B, Clément G, Lenne X, Potier G, Subtil D, Chudzinski A. Titaux C, et al. Among authors: stichelbout m. Placenta. 2023 Feb;132:32-37. doi: 10.1016/j.placenta.2022.12.005. Epub 2022 Dec 20. Placenta. 2023. PMID: 36623417

9

The challenging follow-up of pregnancy in women with known thrombotic thrombocytopenic purpura: a single-center experience of a preemptive management protocol.

Hamroun A, Prouteau C, Lenain R, Roger C, Bauters A, Zawadzki C, Subtil D, Gibier JB, Stichelbout M, Coppo P, Lionet A, Maanaoui M, Hazzan M, Provôt F. Hamroun A, et al. Among authors: stichelbout m. J Nephrol. 2023 Dec;36(9):2519-2529. doi: 10.1007/s40620-023-01790-x. Epub 2023 Oct 11. J Nephrol. 2023. PMID: 37816989

10

The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.

Ghesh L, Musquer MD, Devisme L, Stichelbout M, Boutaud L, Elkhartoufi N, Vaast P, Boute O, Riteau AS, Le Vaillant C, Winer N, Joubert M, Bezieau S, Thomas S, Attie-Bitach T, Beneteau C. Ghesh L, et al. Among authors: stichelbout m. Clin Genet. 2021 Oct;100(4):462-467. doi: 10.1111/cge.14021. Epub 2021 Jul 13. Clin Genet. 2021. PMID: 34212369

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