Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Valerie Meersschaut"'
Autor:
R. De Bruyne, Helene Verhelst, Laurence Pratte, M. Van Winckel, S. Vande Velde, S. Van Biervliet, Valerie Meersschaut, Koenraad Verstraete
Publikováno v:
Archives de Pédiatrie. 20:831-836
Resume Introduction Les sujets atteints de dysraphisme ouvert (DO) souffrent frequemment de constipation et d’incontinence, necessitant une prise en charge adaptee. Objectif Evaluation du temps de transit colique (TTC) chez des enfants avec DO en r
Autor:
Johan Vande Walle, Paul Coucke, Sophie Walraedt, Frauke Coppieters, Elfride De Baere, Hester Y. Kroes, Luis Nunes, Françoise Meire, Valerie Meersschaut, Nicole Van Regemorter, Thomy de Ravel, Ingele Casteels, Hilde Van Esch, Heidi Hoeben, Bart P. Leroy, Lieve Standaert, Sally Hooghe, Sarah De Jaegere, Aušra Matulevičienė
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2010, 31 (10), ⟨10.1002/humu.21336⟩
Human mutation, 31 (10
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Human Mutation, Wiley, 2010, 31 (10), ⟨10.1002/humu.21336⟩
Human mutation, 31 (10
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Leber Congenital Amaurosis (LCA), the most severe inherited retinal dystrophy, is genetically heterogeneous, with 14 genes accounting for 70% of patients. Here, 91 LCA probands underwent LCA chip analysis and subsequent sequencing of 6 genes (CEP290,
Autor:
Philip Vlummens, Karel Deblaere, Koenraad Verstraete, Eric Achten, Lennart Jans, Valerie Meersschaut, Laurence Abernethy, Anna Tietze
Publikováno v:
Pediatric Radiology. 38:570-618
Autor:
Björn Menten, Bee Ling Ng, Jo Vandesompele, Valerie Meersschaut, Karen Buysse, Nigel P. Carter, Geert Mortier, Stefan Vermeulen, Frank Speleman
Publikováno v:
European Journal of Medical Genetics. 50:446-454
We report on a patient with mental retardation, seizures and tall stature with advanced bone age in whom a de novo apparently balanced chromosomal rearrangement 46,XX,t(X;9)(q12;p13.3) was identified. Using array CGH on flow-sorted derivative chromos
Publikováno v:
Tijdschrift voor Geneeskunde. 63:574-577
Autor:
Karel Deblaere, Eric Achten, Sofie Dekeyser, Thomas De Groote, Valerie Meersschaut, Lennart Jans
Publikováno v:
European Radiology Supplements
Autor:
Valerie Meersschaut, Hilde Peeters, Linde Goossens, Sandra Janssens, Koenraad Devriendt, Hugo Devlieger
Publikováno v:
Clinical Dysmorphology. 15:71-74
We present two siblings from unrelated parents presenting with intrauterine growth retardation, a congenital heart defect, postaxial polydactyly, a brain malformation (ectopic neuropituitary gland associated with a hypoplastic adenopituitary in one o
Autor:
Frederik Berrevoet, Sofie Van Damme, Valerie Meersschaut, Eddy Robberecht, Marleen Praet, Luc Defreyne
Publikováno v:
European Radiology. 13:L138-L141
A case of lower gastrointestinal hemorrhage in a child caused by an arteriovenous malformation (AVM) of the colon is presented. On diagnostic angiography, the lesion was misinterpretated as an idiopathic colonic varicosis because none of the characte
Autor:
Nele Herregods, S. Vande Velde, M. Van Winckel, Anneleen Notebaert, Valerie Meersschaut, S. Van Biervliet
Publikováno v:
International journal of colorectal disease. 28(12)
The aims of this study are to describe normal colon transit time (CTT) in healthy children, correlate results with age, the Bristol stool scale, and stool frequency, and to evaluate intra- and interobserver variability. Inclusion criteria were as fol
Autor:
S. Vande Velde, Valerie Meersschaut, Nele Herregods, Helene Verhelst, M. Van Winckel, S. Van Biervliet, Laurence Pratte
Publikováno v:
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
This study evaluates colon transit time (CTT) and anorectal manometry (ARM) in spina bifida (SB) patients in relation to the level of lesion, mobility, constipation, and continence status. SB patients between 6 and 19 years, who are not using antegra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b389c62426fb6a5cd3452bd84739d8c
https://hdl.handle.net/1854/LU-4116025
https://hdl.handle.net/1854/LU-4116025