Fijalkowski I - Search Results

1

Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss.

Bayat A, Fijalkowski I, Andersen T, Abdulmunem SA, van den Ende J, Van Hul W. Bayat A, et al. Among authors: fijalkowski i. Am J Med Genet A. 2016 Jun;170(6):1479-84. doi: 10.1002/ajmg.a.37626. Epub 2016 Mar 20. Am J Med Genet A. 2016. PMID: 26994744

2

Genetic control of bone mass.

Boudin E, Fijalkowski I, Hendrickx G, Van Hul W. Boudin E, et al. Among authors: fijalkowski i. Mol Cell Endocrinol. 2016 Sep 5;432:3-13. doi: 10.1016/j.mce.2015.12.021. Epub 2015 Dec 30. Mol Cell Endocrinol. 2016. PMID: 26747728 Review.

3

Sclerosing bone dysplasias: leads toward novel osteoporosis treatments.

Fijalkowski I, Boudin E, Mortier G, Van Hul W. Fijalkowski I, et al. Curr Osteoporos Rep. 2014 Sep;12(3):243-51. doi: 10.1007/s11914-014-0220-5. Curr Osteoporos Rep. 2014. PMID: 24947952 Review.

4

Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis.

Boudin E, Piters E, Fijalkowski I, Stevenheydens G, Steenackers E, Kuismin O, Moilanen JS, Mortier G, Van Hul W. Boudin E, et al. Among authors: fijalkowski i. Bone. 2013 Jan;52(1):292-5. doi: 10.1016/j.bone.2012.09.034. Epub 2012 Oct 6. Bone. 2013. PMID: 23044044

5

The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases.

Boudin E, Fijalkowski I, Piters E, Van Hul W. Boudin E, et al. Among authors: fijalkowski i. Semin Arthritis Rheum. 2013 Oct;43(2):220-40. doi: 10.1016/j.semarthrit.2013.01.004. Epub 2013 Feb 21. Semin Arthritis Rheum. 2013. PMID: 23433961 Review.

6

A Novel Domain-Specific Mutation in a Sclerosteosis Patient Suggests a Role of LRP4 as an Anchor for Sclerostin in Human Bone.

Fijalkowski I, Geets E, Steenackers E, Van Hoof V, Ramos FJ, Mortier G, Fortuna AM, Van Hul W, Boudin E. Fijalkowski I, et al. J Bone Miner Res. 2016 Apr;31(4):874-81. doi: 10.1002/jbmr.2782. Epub 2016 Jan 24. J Bone Miner Res. 2016. PMID: 26751728 Free article.

7

Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfecta.

Hruskova L, Fijalkowski I, Van Hul W, Marik I, Mortier G, Martasek P, Mazura I. Hruskova L, et al. Among authors: fijalkowski i. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Sep;160(3):442-7. doi: 10.5507/bp.2016.022. Epub 2016 Apr 27. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016. PMID: 27132807 Free article.

8

Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters.

Hendrickx G, Boudin E, Fijałkowski I, Nielsen TL, Andersen M, Brixen K, Van Hul W. Hendrickx G, et al. Among authors: fijalkowski i. Bone. 2014 Feb;59:57-65. doi: 10.1016/j.bone.2013.10.022. Epub 2013 Nov 1. Bone. 2014. PMID: 24185276

9

The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans.

Boudin E, Yorgan T, Fijalkowski I, Sonntag S, Steenackers E, Hendrickx G, Peeters S, De Maré A, Vervaet B, Verhulst A, Mortier G, D'Haese P, Schinke T, Van Hul W. Boudin E, et al. Among authors: fijalkowski i. J Bone Miner Res. 2017 Aug;32(8):1739-1749. doi: 10.1002/jbmr.3160. J Bone Miner Res. 2017. PMID: 28477420 Free article.

10

Small Protein Enrichment Improves Proteomics Detection of sORF Encoded Polypeptides.

Fijalkowski I, Peeters MKR, Van Damme P. Fijalkowski I, et al. Front Genet. 2021 Oct 15;12:713400. doi: 10.3389/fgene.2021.713400. eCollection 2021. Front Genet. 2021. PMID: 34721520 Free PMC article.

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