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Gaillez Stephanie

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Main Referenced Co-authors
Bours, Vincent  (4)
Caberg, Jean-Hubert  (4)
Debray, François-Guillaume  (4)
Pierquin, Geneviève  (3)
Bulk, Saskia  (2)
Main Referenced Keywords
Humans (6); Female (5); Adult (4); Male (4); Pregnancy (4);
Main Referenced Disciplines
Genetics & genetic processes (11)
Pediatrics (3)
Endocrinology, metabolism & nutrition (1)
Neurology (1)
Reproductive medicine (gynecology, andrology, obstetrics) (1)

Publications (total 16)

The most downloaded
1636 downloads
Salmon, C., Gaillez, S., Pieltain, C., Sacre, F., Misson, J.-P., Rocour-Brumioul, D., Bourguignon, J.-P., & LEBRETHON, M.-C. (2006). Le syndrome de Prader Willi: intérêt d'une prise en charge pluridisciplinaire. Revue Médicale de Liège, 61 (7-8, Jul-Aug), 593-599. https://hdl.handle.net/2268/71726

The most cited

195 citations (Scopus®)

Young, J., Bouligand, J., Francou, B., Raffin-Sanson, M.-L., Gaillez, S., Jeanpierre, M., Grynberg, M., Kamenicky, P., Chanson, P., Brailly-Tabard, S., & Guiochon-Mantel, A. (2010). TAC3 and TACR3 defects cause hypothalamic congenital hypogonadotropic hypogonadism in humans. Journal of Clinical Endocrinology and Metabolism, 95 (5), 2287-95. doi:10.1210/jc.2009-2600 https://hdl.handle.net/2268/82471

Potorac, I., FUDVOYE, J., GAILLEZ, S., Beckers, A., & Parent, A.-S. (2016). Novel composite heterozygous mutation of the receptor for hCG and LH leading to male disorder of sexual development. In Abstract book - 17th World Congress of Gynecological Endocrinology.

BOEMER, F., DEBERG, M., SCHOOS, R., CABERG, J.-H., GAILLEZ, S., Dugauquier, C., Delbecque, K., François, A., Maton, P., Demonceau, N., Senterre, G., Ferdinandusse, S., & DEBRAY, F.-G. (2016). Diagnostic pitfall in antenatal manifestations of CPT II deficiency. Clinical Genetics. doi:10.1111/cge.12593
Peer Reviewed verified by ORBi

BULK, S., PIERQUIN, G., GAILLEZ, S., GATOT, J.-S., CABERG, J.-H., & Bours, V. (07 February 2014). Evaluation of the distal 22q11 deletion syndrome. A highly variable phenotype [Poster presentation]. 14th Belgium Society of Human Genetics Meeting.

DELCOMINETTE, S., CHANTRAINE, F., GAILLEZ, S., DELBECQUE, K., & NISOLLE, M. (2014). Prenatal management of an intrauterine fetal growth restriction caused by trisomy 2 confined placental mosaicism [Poster presentation]. Internationnal Society of Gynecology and Endocrinology, Italy.

Vanakker, O., Vilain, C., Janssens, K., Van der Aa, N., Smits, G., Bandelier, C., Blaumeiser, B., BULK, S., CABERG, J.-H., De Leener, A., De Rademaeker, M., de Ravel, T., Desir, J., Destree, A., Dheedene, A., GAILLEZ, S., Grisart, B., Hellin, A.-C., Janssens, S., ... Devriendt, K. (2014). Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. European Journal of Medical Genetics, 57 (4), 151-6. doi:10.1016/j.ejmg.2014.02.002
Peer Reviewed verified by ORBi

SEGERS, K., PIERQUIN, G., GAILLEZ, S., Delbecque, K., Retz, M., Tebache, M., Waterham, H., Wanders, R., Ferdinandusse, S., & DEBRAY, F.-G. (2013). Rapid prenatal diagnosis of fetal Zellweger syndrome by biochemical tests, complementation studies, and molecular analyses. Prenatal Diagnosis, 33 (2), 201-3. doi:10.1002/pd.4038
Peer Reviewed verified by ORBi

CASTERMANS, E., GAILLEZ, S., & BOURS, V. (2013). Existe-t-il une predisposition genetique aux addictions ? Revue Médicale de Liège, 68 (5-6), 226-32.
Peer reviewed

Uwineza, A., PIERQUIN, G., GAILLEZ, S., JAMAR, M., CABERG, J.-H., & BOURS, V. (2013). Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. Genetic Counseling, 24 (2), 193-200.
Peer Reviewed verified by ORBi

DEBRAY, F.-G., de Halleux, V., GUIDI, O., DETREMBLEUR, N., GAILLEZ, S., Rausin, L., Goyens, P., Pan, X., & Whitington, P. F. (2012). Neonatal liver cirrhosis without iron overload caused by gestational alloimmune liver disease. Pediatrics, 129 (4), 1076-9. doi:10.1542/peds.2011-0568
Peer Reviewed verified by ORBi

HARVENGT, J., de HALLEUX, V., GUIDI, O., Rausin, L., DETREMBLEUR, N., Goyens, P., GAILLEZ, S., & Debray, F.-G. (19 March 2011). Neonatal cirrhosis without iron overload: congenital alloimmune hepatitis [Paper presentation]. Société belge de pédiatrie, Bruxelles, Belgium.

Syrios, K., Delbecoue, K., GAILLEZ, S., Schaaps, J.-P., & CHANTRAINE, F. (2011). Le cas clinique du mois. Hydrocephalie liee a i'X: a spropos d'un cas en medecine foetale. Revue Médicale de Liège, 66 (3), 126-9.
Peer reviewed

Young, J., Bouligand, J., Francou, B., Raffin-Sanson, M.-L., Gaillez, S., Jeanpierre, M., Grynberg, M., Kamenicky, P., Chanson, P., Brailly-Tabard, S., & Guiochon-Mantel, A. (2010). TAC3 and TACR3 defects cause hypothalamic congenital hypogonadotropic hypogonadism in humans. Journal of Clinical Endocrinology and Metabolism, 95 (5), 2287-95. doi:10.1210/jc.2009-2600
Peer Reviewed verified by ORBi

Delbecque, K., Gaillez, S., & Schaaps, J.-P. (2009). Histopathological diagnosis of a type vii mucopolysaccharidosis after pregnancy termination. Fetal and Pediatric Pathology, 28 (1), 1-8. doi:10.1080/15513810802547943
Peer Reviewed verified by ORBi

SEGERS, K., MATHIAS, V., GAILLEZ, S., & Bours, V. (23 October 2007). Identification of a point mutation associated with SMA by direct sequencing of genomic DNA [Poster presentation]. 57° American Society of Human Genetics Meeting, San Diego, United States - California.

Mathot, M., Maton, P., Henrion, E., Francois-Adant, A., Marguglio, A., Gaillez, S., Robberechts, L., & Langhendries, J. P. (July 2006). Pseudo-Bartter syndrome in a pregnant mother and her fetus. Pediatric Nephrology, 21 (7), 1037-1040. doi:10.1007/s00467-006-0123-5
Peer Reviewed verified by ORBi

Salmon, C., Gaillez, S., Pieltain, C., Sacre, F., Misson, J.-P., Rocour-Brumioul, D., Bourguignon, J.-P., & LEBRETHON, M.-C. (2006). Le syndrome de Prader Willi: intérêt d'une prise en charge pluridisciplinaire. Revue Médicale de Liège, 61 (7-8, Jul-Aug), 593-599.
Peer reviewed

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