Wouters C - Search Results

1

Thoracolumbar intervertebral disc calcifications in an 8-year-old boy: case report and review of the literature.

Spapens N, Wouters C, Moens P. Spapens N, et al. Among authors: wouters c. Eur J Pediatr. 2010 May;169(5):577-80. doi: 10.1007/s00431-009-1076-z. Epub 2009 Oct 8. Eur J Pediatr. 2010. PMID: 19813021 Review.

2

Three cases of Kingella kingae infection in young children.

Costers M, Wouters C, Moens P, Verhaegen J. Costers M, et al. Among authors: wouters c. Eur J Pediatr. 2003 Jul;162(7-8):530-531. doi: 10.1007/s00431-003-1220-0. Epub 2003 May 9. Eur J Pediatr. 2003. PMID: 12739137 No abstract available.

3

Conradi-Hünermann-Happle syndrome: a novel heterozygous missense mutation, c.204G>T (p.W68C).

Lambrecht C, Wouters C, Van Esch H, Moens P, Casteels I, Morren MA. Lambrecht C, et al. Among authors: wouters c. Pediatr Dermatol. 2014 Jul-Aug;31(4):493-6. doi: 10.1111/pde.12336. Epub 2014 Jun 11. Pediatr Dermatol. 2014. PMID: 24915996

4

Overlap between linear scleroderma, progressive facial hemiatrophy and immune-inflammatory encephalitis in a paediatric cohort.

De Somer L, Morren MA, Muller PC, Despontin K, Jansen K, Lagae L, Wouters C. De Somer L, et al. Among authors: wouters c. Eur J Pediatr. 2015 Sep;174(9):1247-54. doi: 10.1007/s00431-015-2532-6. Epub 2015 Apr 8. Eur J Pediatr. 2015. PMID: 25851111

5

Fibrous Arthropathy Associated With Morphea: A New Cause of Diffuse Acquired Joint Contractures.

Merlin E, Breton S, Fraitag S, Stéphan JL, Wouters C, Bodemer C, Bader-Meunier B. Merlin E, et al. Among authors: wouters c. Pediatrics. 2017 Oct;140(4):e20161899. doi: 10.1542/peds.2016-1899. Pediatrics. 2017. PMID: 28954874

6

Reye syndrome revisited: a descriptive term covering a group of heterogeneous disorders.

Casteels-Van Daele M, Van Geet C, Wouters C, Eggermont E. Casteels-Van Daele M, et al. Among authors: wouters c. Eur J Pediatr. 2000 Sep;159(9):641-8. doi: 10.1007/pl00008399. Eur J Pediatr. 2000. PMID: 11014461 Review.

7

Tight skin and limited joint movements as early presentation of Hutchinson-Gilford progeria in a 7-week-old infant.

Sevenants L, Wouters C, De Sandre-Giovannoli A, Devlieger H, Devriendt K, van den Oord JJ, Marien K, Lévy N, Morren MA. Sevenants L, et al. Among authors: wouters c. Eur J Pediatr. 2005 May;164(5):283-6. doi: 10.1007/s00431-005-1635-x. Epub 2005 Feb 22. Eur J Pediatr. 2005. PMID: 15726408

8

Infantile onset panniculitis with uveitis and systemic granulomatosis: a new clinicopathologic entity.

Wouters CH, Martin TM, Stichweh D, Punaro M, Doyle TM, Lewis JA, Quartier P, Rose CD. Wouters CH, et al. J Pediatr. 2007 Dec;151(6):707-9. doi: 10.1016/j.jpeds.2007.08.005. J Pediatr. 2007. PMID: 18035159 Free PMC article.

9

ADA2 Deficiency Mimicking Idiopathic Multicentric Castleman Disease.

Van Nieuwenhove E, Humblet-Baron S, Van Eyck L, De Somer L, Dooley J, Tousseyn T, Hershfield M, Liston A, Wouters C. Van Nieuwenhove E, et al. Among authors: wouters c. Pediatrics. 2018 Sep;142(3):e20172266. doi: 10.1542/peds.2017-2266. Pediatrics. 2018. PMID: 30139808

10

Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy.

Van Camp S, Vande Walle S, Casteels I, Jacob J, Cassiman C, Wouters C, Schauwvlieghe PP. Van Camp S, et al. Among authors: wouters c. GMS Ophthalmol Cases. 2020 Aug 25;10:Doc37. doi: 10.3205/oc000164. eCollection 2020. GMS Ophthalmol Cases. 2020. PMID: 32884891 Free PMC article.

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