Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Ph. Moerman"'
Autor:
Ignace Vergote, Patrick Neven, Patrick Berteloot, Ph. Moerman, Ingrid Vandenput, Frédéric Amant, B. Van Calster, Karin Leunen, An Capoen
Publikováno v:
British Journal of Cancer
British journal of cancer, 101(2), 244-249. Nature Publishing Group
British journal of cancer, 101(2), 244-249. Nature Publishing Group
BACKGROUND: To investigate the value of neoadjuvant chemotherapy (NACT), followed by interval debulking surgery (IDS), in endometrial cancer with transperitoneal spread (stage IV). METHODS: Patients with endometrial cancer with transperitoneal spread
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1849ea31845c612a448d9da48abfca4
https://doi.org/10.1038/sj.bjc.6605157
https://doi.org/10.1038/sj.bjc.6605157
Autor:
Ph. Moerman, Hugo Devlieger, Marc Gewillig, K Devriendt, R. Van Hoestenberghe, J. P. Fryns, H. Van den Berghe, C. Van Hole
Publikováno v:
Clinical Genetics. 51:246-249
A submicroscopic deletion of chromosome 22q11 was demonstrated in three triplets and in their father. Two children had the typical DiGeorge sequence with at least three of the four cardinal features: conotruncal heart disease, hypoplastic thymus and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed71b58ee7a446be83864372322b4d42
https://doi.org/10.1111/j.1399-0004.1997.tb02463.x
https://doi.org/10.1111/j.1399-0004.1997.tb02463.x
Publikováno v:
Clinical Genetics. 32:49-56
In this paper we report detailed autopsy data of a malformed male newborn with 5p trisomy due to a de novo inverted 5p duplication, inv dup (5)(p13.1----p15.3), and we compare these data with the findings in previous reports on 5p trisomy. Cerebral m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dca334f3f612a8ef355be2d811ea49a
https://doi.org/10.1111/j.1399-0004.1987.tb03323.x
https://doi.org/10.1111/j.1399-0004.1987.tb03323.x
Publikováno v:
Clinical Genetics. 24:252-256
A case of Monocephalus diprosopus, associated with craniorachischisis and duplication of most of the foregut derivates is presented. The major part of the cardiovascular system remained single but the heart exhibited severe defects, including a compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c91736c836cc3576809832e51364d6c
https://doi.org/10.1111/j.1399-0004.1983.tb00079.x
https://doi.org/10.1111/j.1399-0004.1983.tb00079.x
Publikováno v:
Clinical Genetics. 54:86-89
In this report we present evidence that Marden-Walker syndrome and isolated distal arthrogryposis may be variable manifestations of the same entity. We describe the clinical and pathological findings in two affected siblings, the first two children o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9329d92b35cca1911dc88fe6f4618db2
https://doi.org/10.1111/j.1399-0004.1998.tb03701.x
https://doi.org/10.1111/j.1399-0004.1998.tb03701.x
Autor:
Ph. Moerman, Patrick Berteloot, Patrick Neven, Ignace Vergote, Isabelle Cadron, Frédéric Amant
Publikováno v:
Gynecologic oncology, 90(1), 37-43. Academic Press Inc.
Objective The objective was to look for the incidence and clinicopathologic findings of women in whom the diagnosis of endometrial stromal sarcoma was initially missed. Methods We carried out a retrospective analysis of cases treated at our instituti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4168c11d7eedc60f515b70bb2a71d513
https://doi.org/10.1016/s0090-8258(03)00207-5
https://doi.org/10.1016/s0090-8258(03)00207-5
Autor:
W. Foulon, R. Vanheste, Mieke Cannie, J. De Mey, C. Votino, Jacques Jani, K. Van Berkel, Luisa Divano, Valérie Segers, L. Balepa, M. Kir, Myriam Hanssens, Ph. Moerman, Theresa Cos, Xin Kang
Publikováno v:
Obstetrical & Gynecological Survey. 67:615-617
Objectives To compare prospectively maternal acceptance of fetal and neonatal virtuopsy with that of conventional autopsy and to determine the confidence with which magnetic resonance (MR) virtuopsy can be used to diagnose normality/abnormality of va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a703453757fc646b06ba35cd122fab
https://doi.org/10.1097/ogx.0b013e31826f78bd
https://doi.org/10.1097/ogx.0b013e31826f78bd
Autor:
D. Van Schoubroeck, P. Braet, J. P. Fryns, F.A. Van Assche, Koenraad Devriendt, Ph. Moerman, Ingrid Witters
Publikováno v:
American Journal of Medical Genetics. 108:41-44
We report a 13-week-old female fetus with early onset fetal akinesia deformation sequence (FADS) and hydranencephaly. In a previous pregnancy, the same ultrasonographic findings were noted at 13 weeks. Fetopathological examination of both female fetu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::033179a9e6535491d5ad3ec48b75957d
https://doi.org/10.1002/ajmg.10208
https://doi.org/10.1002/ajmg.10208
Publikováno v:
American Journal of Medical Genetics. 107:233-236
We report the second trimester prenatal diagnosis of severe symmetrical limb deficiencies with posterior fossa cyst and cardiac anomaly in a female fetus. Fetopathological examination revealed additional anomalies: renal-hepatic-pancreatic dysplasia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::710289bba0ad831011a387655e5aadc1
https://doi.org/10.1002/ajmg.10131
https://doi.org/10.1002/ajmg.10131
Autor:
Ingrid Witters, Ph. Moerman, F.A. Van Assche, D. Timmerman, D. Van Schoubroeck, J. P. Fryns, Eric Legius, Jan Deprest
Publikováno v:
American Journal of Medical Genetics. 103:278-282
We present a retrospective study of the frequency and type of associated malformations and chromosomal anomalies in 42 consecutive cases of congenital diaphragmatic hernia (CDH) diagnosed in utero during the period from 1985 to 1999. In 26% (11/42) o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db06385dd9f7b86e11144d98447feaf2
https://doi.org/10.1002/ajmg.1564
https://doi.org/10.1002/ajmg.1564