Devriendt K - Search Results

1

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.

Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L. Ivanovski I, et al. Among authors: devriendt k. Genet Med. 2018 Sep;20(9):965-975. doi: 10.1038/gim.2017.221. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300384 Free article.

2

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

3

Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities.

Devriendt K, van den Oord J, De Vos R, Van den Berghe H, Fryns JP. Devriendt K, et al. Am J Med Genet. 1996 Jan 11;61(2):127-30. doi: 10.1002/(SICI)1096-8628(19960111)61:2<127::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8669437

4

Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.

Devriendt K, D'Espallier L, Fryns JP. Devriendt K, et al. J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224. J Med Genet. 1996. PMID: 8728696 Free PMC article.

5

Cohen syndrome: the clinical symptoms and stigmata at a young age.

Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, Van den Berghe H. Fryns JP, et al. Among authors: devriendt k. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131

6

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Swillen A, Devriendt K, Legius E, Eyskens B, Dumoulin M, Gewillig M, Fryns JP. Swillen A, et al. Among authors: devriendt k. J Med Genet. 1997 Jun;34(6):453-8. doi: 10.1136/jmg.34.6.453. J Med Genet. 1997. PMID: 9192263 Free PMC article.

7

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.

Claeys I, Holvoet M, Eyskens B, Adriaensens P, Gewillig M, Fryns JP, Devriendt K. Claeys I, et al. Among authors: devriendt k. Am J Med Genet. 1997 Sep 19;74(5):515-20. doi: 10.1002/(sici)1096-8628(19970919)74:5<515::aid-ajmg12>3.0.co;2-f. Am J Med Genet. 1997. PMID: 9342203

8

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: devriendt k. Am J Med Genet. 1997 Dec 31;73(4):474-9. Am J Med Genet. 1997. PMID: 9415477

9

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.

Devriendt K, Standaert L, Van Hole C, Devlieger H, Fryns JP. Devriendt K, et al. J Med Genet. 1998 Jan;35(1):70-1. doi: 10.1136/jmg.35.1.70. J Med Genet. 1998. PMID: 9475100 Free PMC article.

10

Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophy.

Fryns JP, Van Lingen C, Devriendt K, Legius E, Raus P. Fryns JP, et al. Among authors: devriendt k. J Med Genet. 1998 Apr;35(4):333-5. doi: 10.1136/jmg.35.4.333. J Med Genet. 1998. PMID: 9598731 Free PMC article.

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