Naeyaert JM - Search Results

1

Multiple myofibromas and an epidermal verrucous nevus in a child with neurofibromatosis type 1.

De Schepper S, Janssens S, Messiaen L, Van den Broecke C, Naeyaert JM. De Schepper S, et al. Among authors: naeyaert jm. Dermatology. 2004;209(3):223-7. doi: 10.1159/000079894. Dermatology. 2004. PMID: 15459537

2

Pigment cell-related manifestations in neurofibromatosis type 1: an overview.

De Schepper S, Boucneau J, Lambert J, Messiaen L, Naeyaert JM. De Schepper S, et al. Among authors: naeyaert jm. Pigment Cell Res. 2005 Feb;18(1):13-24. doi: 10.1111/j.1600-0749.2004.00206.x. Pigment Cell Res. 2005. PMID: 15649148 Review.

3

Gene expression profiling of cultured human NF1 heterozygous (NF1+/-) melanocytes reveals downregulation of a transcriptional cis-regulatory network mediating activation of the melanocyte-specific dopachrome tautomerase (DCT) gene.

Boucneau J, De Schepper S, Vuylsteke M, Van Hummelen P, Naeyaert JM, Lambert J. Boucneau J, et al. Among authors: naeyaert jm. Pigment Cell Res. 2005 Aug;18(4):285-99. doi: 10.1111/j.1600-0749.2005.00237.x. Pigment Cell Res. 2005. PMID: 16033338

4

Café-au-lait spots in neurofibromatosis type 1 and in healthy control individuals: hyperpigmentation of a different kind?

De Schepper S, Boucneau J, Vander Haeghen Y, Messiaen L, Naeyaert JM, Lambert J. De Schepper S, et al. Among authors: naeyaert jm. Arch Dermatol Res. 2006 Apr;297(10):439-49. doi: 10.1007/s00403-006-0644-6. Epub 2006 Feb 15. Arch Dermatol Res. 2006. PMID: 16479403

5

Cutis laxa of the autosomal recessive type in a consanguineous family.

de Schepper S, Loeys B, de Paepe A, Lambert J, Naeyaert JM. de Schepper S, et al. Among authors: naeyaert jm. Eur J Dermatol. 2003 Nov-Dec;13(6):529-33. Eur J Dermatol. 2003. PMID: 14721770

6

Management of vitiligo patients and attitude of dermatologists towards vitiligo.

Ongenae K, Van Geel N, De Schepper S, Vander Haeghen Y, Naeyaert JM. Ongenae K, et al. Among authors: naeyaert jm. Eur J Dermatol. 2004 May-Jun;14(3):177-81. Eur J Dermatol. 2004. PMID: 15246945

7

Rab27b is up-regulated in human Griscelli syndrome type II melanocytes and linked to the actin cytoskeleton via exon F-Myosin Va transcripts.

Westbroek W, Lambert J, De Schepper S, Kleta R, Van Den Bossche K, Seabra MC, Huizing M, Mommaas M, Naeyaert JM. Westbroek W, et al. Among authors: naeyaert jm. Pigment Cell Res. 2004 Oct;17(5):498-505. doi: 10.1111/j.1600-0749.2004.00173.x. Pigment Cell Res. 2004. PMID: 15357836

8

Somatic mutation analysis in NF1 café au lait spots reveals two NF1 hits in the melanocytes.

De Schepper S, Maertens O, Callens T, Naeyaert JM, Lambert J, Messiaen L. De Schepper S, et al. Among authors: naeyaert jm. J Invest Dermatol. 2008 Apr;128(4):1050-3. doi: 10.1038/sj.jid.5701095. Epub 2007 Oct 4. J Invest Dermatol. 2008. PMID: 17914445 Free article. No abstract available.

9

Bowen's disease of the nail.

Ongenae K, Van De Kerckhove M, Naeyaert JM. Ongenae K, et al. Among authors: naeyaert jm. Dermatology. 2002;204(4):348-50. doi: 10.1159/000063383. Dermatology. 2002. PMID: 12077545

10

Diffuse plane normolipaemic xanthomatosis in a patient with chronic lymphatic leukaemia and monoclonal gammopathy.

Stockman A, Delanghe J, Geerts ML, Naeyaert JM. Stockman A, et al. Among authors: naeyaert jm. Dermatology. 2002;204(4):351-4. doi: 10.1159/000063384. Dermatology. 2002. PMID: 12077546

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