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Items: 9

1.

Gestational trophoblastic neoplasms (GTNs) do not display epithelial-to-mesenchymal transition (EMT) features.

Dubruc E, Allias F, Morel AP, Golfier F, Puisieux A, Devouassoux-Shisheboran M.

Virchows Arch. 2019 Jul;475(1):121-125. doi: 10.1007/s00428-019-02551-7. Epub 2019 Mar 8.

PMID:
30847562
2.

Cytological features of uterine tumors resembling ovarian sex-cord tumors in liquid-based cervical cytology: a potential pitfall. Report of a unique and rare case.

Dubruc E, Alvarez Flores MT, Bernier Y, Gherasimiuc L, Ponti A, Mathevet P, Bongiovanni M.

Diagn Cytopathol. 2019 Jun;47(6):603-607. doi: 10.1002/dc.24153. Epub 2019 Feb 13.

PMID:
30761777
3.

Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis.

Dubruc E, Nadaud B, Ruchelli E, Heissat S, Baruteau J, Broué P, Debray D, Cordier MP, Miossec P, Russo P, Collardeau-Frachon S.

Pediatr Res. 2017 May;81(5):712-721. doi: 10.1038/pr.2017.8. Epub 2017 Jan 13.

PMID:
28085791
4.

Placental histological lesions in fetal and neonatal alloimmune thrombocytopenia: A retrospective cohort study of 21 cases.

Dubruc E, Lebreton F, Giannoli C, Rabilloud M, Huissoud C, Devouassoux-Shisheboran M, Allias F.

Placenta. 2016 Dec;48:104-109. doi: 10.1016/j.placenta.2016.10.009. Epub 2016 Oct 17.

PMID:
27871460
5.

Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failure.

Heissat S, Collardeau-Frachon S, Baruteau J, Dubruc E, Bouvier R, Fabre M, Cordier MP, Broué P, Guigonis V, Debray D.

J Pediatr. 2015 Jan;166(1):66-73. doi: 10.1016/j.jpeds.2014.09.030. Epub 2014 Oct 23.

PMID:
25444000
6.

Mutated and amplified NRAS in a subset of cutaneous melanocytic lesions with dermal spitzoid morphology: report of two pediatric cases located on the ear.

Dubruc E, Balme B, Dijoud F, Disant F, Thomas L, Wang Q, Pissaloux D, de la Fouchardiere A.

J Cutan Pathol. 2014 Nov;41(11):866-72. doi: 10.1111/cup.12389. Epub 2014 Oct 21.

PMID:
25263998
7.

A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.

Dubruc E, Putoux A, Labalme A, Rougeot C, Sanlaville D, Edery P.

Am J Med Genet A. 2014 Jun;164A(6):1571-5. doi: 10.1002/ajmg.a.36484. Epub 2014 Mar 25.

PMID:
24668549
8.

Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.

Schluth-Bolard C, Labalme A, Cordier MP, Till M, Nadeau G, Tevissen H, Lesca G, Boutry-Kryza N, Rossignol S, Rocas D, Dubruc E, Edery P, Sanlaville D.

J Med Genet. 2013 Mar;50(3):144-50. doi: 10.1136/jmedgenet-2012-101351. Epub 2013 Jan 12.

PMID:
23315544
9.

[Pregnancy and Ehlers-Danlos vascular syndrome: patients' care and complications].

Dubruc E, Dupuis-Girod S, Khau Van Kien P, Denis-Belicard E, Chirossel C, Fokstuen S, Touraine R, Plauchu H.

J Gynecol Obstet Biol Reprod (Paris). 2013 Apr;42(2):159-65. doi: 10.1016/j.jgyn.2012.08.003. Epub 2012 Oct 2. French.

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