Verloo P - Search Results

1

Abdominal pain and vomiting as first sign of mitochondrial disease.

Van Biervliet S, Verloo P, Vande Veldel S, Van Winckel M, Smet J, Seneca S, De Meirleir L, Van Coster R. Van Biervliet S, et al. Among authors: verloo p. Acta Gastroenterol Belg. 2009 Jul-Sep;72(3):365-8. Acta Gastroenterol Belg. 2009. PMID: 19902874

2

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects.

Roels F, Verloo P, Eyskens F, François B, Seneca S, De Paepe B, Martin JJ, Meersschaut V, Praet M, Scalais E, Espeel M, Smet J, Van Goethem G, Van Coster R. Roels F, et al. Among authors: verloo p. BMC Clin Pathol. 2009 Jun 5;9:4. doi: 10.1186/1472-6890-9-4. BMC Clin Pathol. 2009. PMID: 19500334 Free PMC article.

3

Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects.

Van Coster R, Smet J, George E, De Meirleir L, Seneca S, Van Hove J, Sebire G, Verhelst H, De Bleecker J, Van Vlem B, Verloo P, Leroy J. Van Coster R, et al. Among authors: verloo p. Pediatr Res. 2001 Nov;50(5):658-65. doi: 10.1203/00006450-200111000-00020. Pediatr Res. 2001. PMID: 11641463

4

Heroin withdrawal leads to metabolic alkalosis in an infant with cystic fibrosis.

vande Velde S, Verloo P, Van Biervliet S, Robberecht E. vande Velde S, et al. Among authors: verloo p. Eur J Pediatr. 2007 Jan;166(1):75-6. doi: 10.1007/s00431-006-0215-z. Epub 2006 Aug 8. Eur J Pediatr. 2007. PMID: 16896643 No abstract available.

5

Successful liver transplantation in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: Case report.

De Bruyne P, Verloo P, Van Hove JLK, de Hemptinne B, Vande Velde S, Van Winckel M, Van Biervliet S, De Bruyne R. De Bruyne P, et al. Among authors: verloo p. Pediatr Transplant. 2021 Sep;25(6):e13943. doi: 10.1111/petr.13943. Epub 2020 Dec 14. Pediatr Transplant. 2021. PMID: 33314525

6

Hypocretin-1 deficiency in a girl with ROHHAD syndrome.

Dhondt K, Verloo P, Verhelst H, Van Coster R, Overeem S. Dhondt K, et al. Among authors: verloo p. Pediatrics. 2013 Sep;132(3):e788-92. doi: 10.1542/peds.2012-3225. Epub 2013 Aug 12. Pediatrics. 2013. PMID: 23940246

7

Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication.

Verbeek S, Vanakker O, Mercelis R, Lipka AF, Haerynck F, Dullaers M, Verloo P, Van Coster R, Verhelst H. Verbeek S, et al. Among authors: verloo p. Eur J Paediatr Neurol. 2014 May;18(3):439-43. doi: 10.1016/j.ejpn.2014.01.001. Epub 2014 Jan 15. Eur J Paediatr Neurol. 2014. PMID: 24461257

8

TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism.

Jennions E, Hedberg-Oldfors C, Berglund AK, Kollberg G, Törnhage CJ, Eklund EA, Oldfors A, Verloo P, Vanlander AV, De Meirleir L, Seneca S, Sterky FH, Darin N. Jennions E, et al. Among authors: verloo p. J Inherit Metab Dis. 2019 Sep;42(5):898-908. doi: 10.1002/jimd.12149. Epub 2019 Jul 24. J Inherit Metab Dis. 2019. PMID: 31276219

9

Two cases of DCDC2-related neonatal sclerosing cholangitis with developmental delay and literature review.

Syryn H, Hoorens A, Grammatikopoulos T, Deheragoda M, Symoens S, Vande Velde S, Van Biervliet S, Van Winckel M, Verloo P, Callewaert B, De Bruyne R. Syryn H, et al. Among authors: verloo p. Clin Genet. 2021 Oct;100(4):447-452. doi: 10.1111/cge.14012. Epub 2021 Jun 30. Clin Genet. 2021. PMID: 34155636 Review.

10

TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria.

Jansen AC, Oostra A, Desprechins B, De Vlaeminck Y, Verhelst H, Régal L, Verloo P, Bockaert N, Keymolen K, Seneca S, De Meirleir L, Lissens W. Jansen AC, et al. Among authors: verloo p. Neurology. 2011 Mar 15;76(11):988-92. doi: 10.1212/WNL.0b013e31821043f5. Neurology. 2011. PMID: 21403111

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