C Cheruy
Overview
Explore the profile of C Cheruy including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
6
Citations
29
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0
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Recent Articles
1.
Condorelli M, De Vos M, Lie Fong S, Autin C, Delvigne A, Vanden Meerschaut F, et al.
Hum Reprod
. 2020 Dec;
36(2):381-389.
PMID: 33289029
Study Question: What is the risk of recurrence in young breast cancer survivors who undergo ARTs following completion of anticancer treatment? Summary Answer: ART in breast cancer survivors does not...
2.
A not so harmless mass: Kaposiform hemangioendothelioma complicated by a Kasabach-Merritt phenomenon
Tribolet S, Hoyoux C, Boon L, Cheruy C, Demarche M, Jamblin P, et al.
Arch Pediatr
. 2019 Jul;
26(6):365-369.
PMID: 31353149
A vascular mass localized in the face and the neck was displayed by ultrasonography in a 38-week-old male fetus. At birth, the mass was bulky and purplish. The newborn breathed...
3.
Loumaye F, Cheruy C, Cristinelli S, Foidart J, Nisolle M
Rev Med Liege
. 2007 Sep;
62(7-8):480-3.
PMID: 17853667
Didelphys uterus with imperforated obstructed hemivagina is a rare condition. Most often, it is diagnosed a few months after the menarche. Hematocolpos, hematometria and sometimes hematosalpinx are responsible for pelvic...
4.
Chadefaux B, Allard D, Rethore M, Raoul O, POISSONNIER M, Gilgenkrantz S, et al.
Hum Genet
. 1984 Jan;
66(2-3):190-2.
PMID: 6232198
The enzymatic activity of phosphoribosylglycinamide synthetase (GARS) has been studied in several cases of partial monosomies and full and partial trisomies 21. An excess of GARS activity was found in...
5.
Boue J, Nicolas H, Cheruy C, Couillin P, BOUE A
Nouv Presse Med
. 1982 Mar;
11(13):979-83.
PMID: 7070985
The authors' experience of 155 prenatal diagnoses of inborn errors of metabolism shows that such diagnoses cannot be made without an extensive network of laboratories specialized in cell biology and...
6.
Couillin P, Boue J, Nicolas H, Cheruy C, BOUE A
Prenat Diagn
. 1981 Jan;
1(1):25-33.
PMID: 6955777
The close genetic linkage between HLA-B and congential adrenal hyperplasia due to 21-hydroxylase deficiency permits prenatal diagnosis of an affected fetus by HLA typing of amniotic fluid cells in pregnancies...