Zobrazeno 1 - 10
of 149
pro vyhledávání: '"M Demarche"'
Autor:
T, Vereecken, A S, Parent, C, Van Linthout, M, Laterre, J, Fudvoye, V, Nechifor, M, Demarche, A, Pintiaux
Publikováno v:
Revue medicale de Liege. 77(12)
Complete androgen insensitivity syndrome is the most frequent cause of disorder of sexual development in 46 XY patients. It is caused by mutations of the AR gene coding for the androgen receptor. Transmission is X-linked and mutations are most of the
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-9 (2020)
BMC Pediatrics
BMC Pediatrics
Background Unusual clinical presentation of acute appendicitis in preschool children leads to misdiagnosis and complications. We aimed to analyze the influence of age on clinical presentation, laboratory findings and complications in preschool childr
Publikováno v:
Revue medicale de Liege. 76(9)
We report the case of a child suffering from a neonatal cervicomediastinal neuroblastoma encasing the left subclavian artery and the left vertebral artery. There is only a few pediatric tumors extending from the neck to the upper part of the thorax.
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Autor:
M F, Dresse, B A, David, M, Demarche, B, Florkin, P, Forget, S, Gatineau, J, Longton, C, Piette, M C, Seghaye
Publikováno v:
Revue medicale de Liege. 76(5-6)
Cancers are rare pathologies in children. Improvement in survival rates has been obtained thanks to new therapeutic strategies based on the identification of risk factors. Targeted therapies in paediatric oncology are new treatments providing hope th
Autor:
M Demarche, Pierre-Arnaud Wuidar, Laurent Kohnen, Maud Neuberg, Nikos Kotzampassakis, Arnaud De Roover, Jenny Deflines
Publikováno v:
Obesity Surgery. 29:3212-3219
The Magenstrasse and Mill gastroplasty (M&M) is a gastric restrictive procedure without band or stomach resection. Short-term evaluation of the laparoscopic procedure showed low morbidity and satisfactory results on weight loss. Evidence of the valid
Publikováno v:
Archives de Pédiatrie, Vol. 24, no.7, p. 600-606 (2017)
Vascular anomalies (VAs) result from the defective development of the embryonic vascular system and feature dysplastic malformed vessels, which are not always apparent at birth. They do not regress over the patient's lifetime; they usually have comme
Autor:
P Leyman, A De Backer, R Tambucci, M. Demarche, S Van Cauwenberge, Lucas Matthyssens, C Vercauteren, Dirk Vervloessem, M Ruppert, H Reusens
Publikováno v:
Diseases of the Esophagus. 32
Introduction No data are available on surgical management and outcomes of oesophageal atresia (OA) in Belgium. In collaboration with the Belgian Association of Paediatric Surgery (BELAPS) a retrospective study was organized to analyze data from child
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Publikováno v:
Revue medicale de Liege. 73(9)
The persistence of the embryonic vitelline duct can lead to omphalomesenteric duct anomalies. A wide variety of anomalies, depending on the remnant segment and its degree of involution, may occur as a result of the omphalomesenteric duct failing to o