Falix FA - Search Results

1

Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature.

Hoogenboom A, Falix FA, van der Laan L, Kerkhof J, Alders M, Sadikovic B, van Haelst MM. Hoogenboom A, et al. Among authors: falix fa. Eur J Hum Genet. 2024 Apr;32(4):435-439. doi: 10.1038/s41431-023-01527-1. Epub 2024 Jan 25. Eur J Hum Genet. 2024. PMID: 38273166 Free PMC article. Review.

2

Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean.

Verberne EA, Westermann JM, de Vries TI, Ecury-Goossen GM, Lo-A-Njoe SM, Manshande ME, Faries S, Veenhuis HD, Philippi P, Falix FA, Rosina-Angelista I, Ponson-Wever M, Rafael-Croes L, Thorsen P, Arends E, de Vroomen M, Nagelkerke SQ, Tilanus M, van der Veken LT, Huijsdens-van Amsterdam K, van der Kevie-Kersemaekers AM, Alders M, Mannens MMAM, van Haelst MM. Verberne EA, et al. Among authors: falix fa. Am J Med Genet A. 2022 Jun;188(6):1777-1791. doi: 10.1002/ajmg.a.62708. Epub 2022 Mar 7. Am J Med Genet A. 2022. PMID: 35253369 Free PMC article.

3

A novel mutation of laminin β2 (LAMB2) in two siblings with renal failure.

Falix FA, Bennebroek CA, van der Zwaag B, Lapid-Gortzak R, Florquin S, Oosterveld MJ. Falix FA, et al. Eur J Pediatr. 2017 Apr;176(4):515-519. doi: 10.1007/s00431-017-2871-6. Epub 2017 Feb 10. Eur J Pediatr. 2017. PMID: 28188379 Free PMC article.

4

Mommers EC, Leonhart AM, Falix F, Michalides R, Meijer CJ, Baak JP, Diest PJ. Mommers EC, et al. J Pathol. 2001 Jul;194(3):327-33. doi: 10.1002/path.910. J Pathol. 2001. PMID: 11439365

5

Diagnostic dilemmas in a girl with acute glomerulonephritis: Answers.

Falix FA, Oosterveld MJS, Florquin S, Groothoff JW, Bouts AHM. Falix FA, et al. Pediatr Nephrol. 2018 Jan;33(1):65-69. doi: 10.1007/s00467-017-3626-3. Epub 2017 Mar 9. Pediatr Nephrol. 2018. PMID: 28280937 Free PMC article. No abstract available.

6

Diagnostic dilemmas in a girl with acute glomerulonephritis: Questions.

Falix FA, Oosterveld MJS, Florquin S, Groothoff JW, Bouts AHM. Falix FA, et al. Pediatr Nephrol. 2018 Jan;33(1):63-64. doi: 10.1007/s00467-017-3625-4. Epub 2017 Mar 20. Pediatr Nephrol. 2018. PMID: 28321509 Free PMC article. No abstract available.

7

DLK1, a serum marker for hepatoblastoma in young infants.

Falix FA, Aronson DC, Lamers WH, Hiralall JK, Seppen J. Falix FA, et al. Pediatr Blood Cancer. 2012 Oct;59(4):743-5. doi: 10.1002/pbc.24024. Epub 2011 Dec 16. Pediatr Blood Cancer. 2012. PMID: 22180200

8

Hepatic Notch2 deficiency leads to bile duct agenesis perinatally and secondary bile duct formation after weaning.

Falix FA, Weeda VB, Labruyere WT, Poncy A, de Waart DR, Hakvoort TB, Lemaigre F, Gaemers IC, Aronson DC, Lamers WH. Falix FA, et al. Dev Biol. 2014 Dec 15;396(2):201-13. doi: 10.1016/j.ydbio.2014.10.002. Epub 2014 Oct 18. Dev Biol. 2014. PMID: 25446530 Free article.

9

Possible roles of DLK1 in the Notch pathway during development and disease.

Falix FA, Aronson DC, Lamers WH, Gaemers IC. Falix FA, et al. Biochim Biophys Acta. 2012 Jun;1822(6):988-95. doi: 10.1016/j.bbadis.2012.02.003. Epub 2012 Feb 12. Biochim Biophys Acta. 2012. PMID: 22353464 Free article. Review.

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