Standaert L - Search Results

1

Selecting neonates with congenital cytomegalovirus infection for ganciclovir therapy.

Smets K, De Coen K, Dhooge I, Standaert L, Laroche S, Mahieu L, Logghe N, Cossey V, Boudewyns A. Smets K, et al. Among authors: standaert l. Eur J Pediatr. 2006 Dec;165(12):885-90. doi: 10.1007/s00431-006-0192-2. Epub 2006 Jun 20. Eur J Pediatr. 2006. PMID: 16786362 Review.

2

Otological manifestations of CHARGE association.

Dhooge I, Lemmerling M, Lagache M, Standaert L, Govaert P, Mortier G. Dhooge I, et al. Among authors: standaert l. Ann Otol Rhinol Laryngol. 1998 Nov;107(11 Pt 1):935-41. doi: 10.1177/000348949810701106. Ann Otol Rhinol Laryngol. 1998. PMID: 9823842

3

Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.

Stinckens C, Kremer H, van Wijk E, Hoefsloot LH, Huygen PL, Standaert L, Fryns JP, Cremers CW. Stinckens C, et al. Among authors: standaert l. Ann Otol Rhinol Laryngol. 2004 Jul;113(7):587-93. doi: 10.1177/000348940411300714. Ann Otol Rhinol Laryngol. 2004. PMID: 15274422

4

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. Among authors: standaert l. 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.

5

Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes.

Coppieters F, Casteels I, Meire F, De Jaegere S, Hooghe S, van Regemorter N, Van Esch H, Matuleviciene A, Nunes L, Meersschaut V, Walraedt S, Standaert L, Coucke P, Hoeben H, Kroes HY, Vande Walle J, de Ravel T, Leroy BP, De Baere E. Coppieters F, et al. Among authors: standaert l. Hum Mutat. 2010 Oct;31(10):E1709-66. doi: 10.1002/humu.21336. Hum Mutat. 2010. PMID: 20683928 Free PMC article.

6

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.

Stinckens C, Standaert L, Casselman JW, Huygen PL, Kumar S, Van de Wallen J, Cremers CW. Stinckens C, et al. Among authors: standaert l. Int J Pediatr Otorhinolaryngol. 2001 Jul 2;59(3):163-72. doi: 10.1016/s0165-5876(01)00473-6. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11397497

7

De novo Robertsonian D/D type translocations: the Leuven experience.

Kleczkowska A, Fryns JP, Standaert L, van den Berghe H. Kleczkowska A, et al. Among authors: standaert l. Clin Genet. 1989 Jul;36(1):65-8. doi: 10.1111/j.1399-0004.1989.tb03368.x. Clin Genet. 1989. PMID: 2766564

8

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: standaert l. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131

9

De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).

Jaeken J, Fryns JP, Standaert L, De Cock P, Van den Berghe H. Jaeken J, et al. Among authors: standaert l. Ann Genet. 1980;23(2):105-7. Ann Genet. 1980. PMID: 6967281

10

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis.

Meire F, Standaert L, De Laey JJ, Zeng LH. Meire F, et al. Among authors: standaert l. Am J Med Genet. 1987 Jul;27(3):683-6. doi: 10.1002/ajmg.1320270322. Am J Med Genet. 1987. PMID: 3631139

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

57 results

Search Page