Devriendt K - Search Results

1

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kaźmierczak A, Vermeesch JR, Devriendt K, Busa T, Sigaudy S, Vigneswaran T, Simpson JM, Dungan J, Gotteiner N, Gloning KP, Digilio MC, Unolt M, Putotto C, Marino B, Repetto G, Fadic M, Garcia-Minaur S, Achón Buil A, Thomas MA, Fruitman D, Beecroft T, Hui PW, Oskarsdottir S, Bradshaw R, Criebaum A, Norton ME, Lee T, Geiger M, Dunnington L, Isaac J, Wilkins-Haug L, Hunter L, Izzi C, Toscano M, Ghi T, McGlynn J, Romana Grati F, Emanuel BS, Gaiser K, Gaynor JW, Goldmuntz E, McGinn DE, Schindewolf E, Tran O, Zackai EH, Yan Q, Bassett AS, Wapner R, McDonald-McGinn DM. Freud LR, et al. Among authors: devriendt k. Am J Obstet Gynecol. 2024 Mar;230(3):368.e1-368.e12. doi: 10.1016/j.ajog.2023.09.005. Epub 2023 Sep 16. Am J Obstet Gynecol. 2024. PMID: 37717890

2

Velocardiofacial syndrome presenting as distal arthrogryposis.

Devriendt K, Swillen A, Gewillig M, Fryns JP, Moens P, De Smet L. Devriendt K, et al. Eur J Pediatr. 2004 Jun;163(6):329-30. doi: 10.1007/s00431-004-1429-6. Eur J Pediatr. 2004. PMID: 15346917 No abstract available.

3

Chromosomal phenotypes and submicroscopic abnormalities.

Devriendt K, Vermeesch JR. Devriendt K, et al. Hum Genomics. 2004 Jan;1(2):126-33. doi: 10.1186/1479-7364-1-2-126. Hum Genomics. 2004. PMID: 15601540 Free PMC article. Review.

4

Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality: a new constellation or deletion in chromosome 22q11.2?

Devriendt K, Swillen A, Stalmans I, Casteels I. Devriendt K, et al. Am J Med Genet A. 2005 Jan 30;132A(3):340-1. doi: 10.1002/ajmg.a.30458. Am J Med Genet A. 2005. PMID: 15690382 No abstract available.

5

Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome.

Stiers P, Swillen A, De Smedt B, Lagae L, Devriendt K, D'Agostino E, Sunaert S, Fryns AP. Stiers P, et al. Among authors: devriendt k. Child Neuropsychol. 2005 Feb;11(1):87-108. doi: 10.1080/09297040590911220. Child Neuropsychol. 2005. PMID: 15823985

6

Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.

Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P, Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G. Van Esch H, et al. Among authors: devriendt k. Hum Mol Genet. 2005 Jul 1;14(13):1795-803. doi: 10.1093/hmg/ddi186. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888481

7

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect.

Swillen A, Feys H, Adriaens T, Nelissen L, Mertens L, Gewillig M, Devriendt K, Fryns JP. Swillen A, et al. Among authors: devriendt k. Dev Med Child Neurol. 2005 Dec;47(12):797-802. doi: 10.1017/S0012162205001696. Dev Med Child Neurol. 2005. PMID: 16288668 Free article.

8

Anterior cervical hypertrichosis and mental retardation.

Thienpont B, Vermeesch J, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Clin Dysmorphol. 2006 Jul;15(3):189-190. doi: 10.1097/01.mcd.0000204988.39119.9d. Clin Dysmorphol. 2006. PMID: 16760744

9

Left-ventricular non-compaction in a patient with monosomy 1p36.

Thienpont B, Mertens L, Buyse G, Vermeesch JR, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Eur J Med Genet. 2007 May-Jun;50(3):233-6. doi: 10.1016/j.ejmg.2007.01.002. Epub 2007 Jan 27. Eur J Med Genet. 2007. PMID: 17337261

10

Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome).

Van Aken K, De Smedt B, Van Roie A, Gewillig M, Devriendt K, Fryns JP, Simons J, Swillen A. Van Aken K, et al. Among authors: devriendt k. Dev Med Child Neurol. 2007 Mar;49(3):210-3. doi: 10.1111/j.1469-8749.2007.00210.x. Dev Med Child Neurol. 2007. PMID: 17355478 Free article.

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