de Klein A - Search Results

1

A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies.

van de Putte R, Dworschak GC, Brosens E, Reutter HM, Marcelis CLM, Acuna-Hidalgo R, Kurtas NE, Steehouwer M, Dunwoodie SL, Schmiedeke E, Märzheuser S, Schwarzer N, Brooks AS, de Klein A, Sloots CEJ, Tibboel D, Brisighelli G, Morandi A, Bedeschi MF, Bates MD, Levitt MA, Peña A, de Blaauw I, Roeleveld N, Brunner HG, van Rooij IALM, Hoischen A. van de Putte R, et al. Among authors: de blaauw i, de klein a. Front Pediatr. 2020 Jun 23;8:310. doi: 10.3389/fped.2020.00310. eCollection 2020. Front Pediatr. 2020. PMID: 32656166 Free PMC article.

2

Postmortem findings and clinicopathological correlation in congenital diaphragmatic hernia.

van Dooren MF, Goemaere NN, de Klein A, Tibboel D, de Krijger RR. van Dooren MF, et al. Among authors: de klein a, de krijger rr. Pediatr Dev Pathol. 2004 Sep-Oct;7(5):459-67. doi: 10.1007/s10024-004-1118-2. Epub 2004 Oct 6. Pediatr Dev Pathol. 2004. PMID: 15547770

3

Agenesis of the trachea: phenotypic expression of a rare cause of fatal neonatal respiratory insufficiency in six patients.

Felix JF, van Looij MA, Pruijsten RV, de Krijger RR, de Klein A, Tibboel D, Hoeve HL. Felix JF, et al. Among authors: de klein a, de krijger rr. Int J Pediatr Otorhinolaryngol. 2006 Feb;70(2):365-70. doi: 10.1016/j.ijporl.2005.07.009. Epub 2005 Aug 25. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16125794

4

Chromosomal anomalies in the aetiology of oesophageal atresia and tracheo-oesophageal fistula.

Felix JF, Tibboel D, de Klein A. Felix JF, et al. Among authors: de klein a. Eur J Med Genet. 2007 May-Jun;50(3):163-75. doi: 10.1016/j.ejmg.2006.12.004. Epub 2007 Jan 21. Eur J Med Genet. 2007. PMID: 17336605 Review.

5

Genetic factors in congenital diaphragmatic hernia.

Holder AM, Klaassens M, Tibboel D, de Klein A, Lee B, Scott DA. Holder AM, et al. Among authors: de klein a. Am J Hum Genet. 2007 May;80(5):825-45. doi: 10.1086/513442. Epub 2007 Apr 4. Am J Hum Genet. 2007. PMID: 17436238 Free PMC article. Review.

6

Linking animal models to human congenital diaphragmatic hernia.

Beurskens N, Klaassens M, Rottier R, de Klein A, Tibboel D. Beurskens N, et al. Among authors: de klein a. Birth Defects Res A Clin Mol Teratol. 2007 Aug;79(8):565-72. doi: 10.1002/bdra.20370. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17469205 Review.

7

Esophageal atresia and tracheoesophageal fistula in children of women exposed to diethylstilbestrol in utero.

Felix JF, Steegers-Theunissen RP, de Walle HE, de Klein A, Torfs CP, Tibboel D. Felix JF, et al. Among authors: de walle he, de klein a. Am J Obstet Gynecol. 2007 Jul;197(1):38.e1-5. doi: 10.1016/j.ajog.2007.02.036. Am J Obstet Gynecol. 2007. PMID: 17618749

8

Genetic and environmental factors in the etiology of esophageal atresia and/or tracheoesophageal fistula: an overview of the current concepts.

Felix JF, de Jong EM, Torfs CP, de Klein A, Rottier RJ, Tibboel D. Felix JF, et al. Among authors: de klein a, de jong em. Birth Defects Res A Clin Mol Teratol. 2009 Sep;85(9):747-54. doi: 10.1002/bdra.20592. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19452513 Review.

9

The etiology of congenital diaphragmatic hernia: still largely unknown?

Klaassens M, de Klein A, Tibboel D. Klaassens M, et al. Among authors: de klein a. Eur J Med Genet. 2009 Sep-Oct;52(5):281-6. doi: 10.1016/j.ejmg.2009.05.005. Epub 2009 May 21. Eur J Med Genet. 2009. PMID: 19464395 Review.

10

The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformations.

Goemaere N, Douben H, Van Opstal D, Wouters C, Tibboel D, de Krijger R, de Klein A. Goemaere N, et al. Among authors: de krijger r, de klein a. Pediatr Dev Pathol. 2010 Mar-Apr;13(2):85-94. doi: 10.2350/09-02-0612-OA.1. Pediatr Dev Pathol. 2010. PMID: 19594201

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