Verloo P - Search Results

1

Towards an Algorithm-Based Tailored Treatment of Acute Neonatal Hyperammonemia.

Eloot S, De Rudder J, Verloo P, Dhont E, Raes A, Van Biesen W, Snauwaert E. Eloot S, et al. Among authors: verloo p. Toxins (Basel). 2021 Jul 13;13(7):484. doi: 10.3390/toxins13070484. Toxins (Basel). 2021. PMID: 34357956 Free PMC article.

2

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

3

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.

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

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

6

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

7

A child presenting with severe hypertension and circulatory failure, a diagnostic conundrum: Questions.

Keenswijk W, Verloo P, Walle JV. Keenswijk W, et al. Among authors: verloo p. Pediatr Nephrol. 2017 Nov;32(11):2057-2058. doi: 10.1007/s00467-017-3589-4. Epub 2017 Feb 2. Pediatr Nephrol. 2017. PMID: 28154940 No abstract available.

8

A child presenting with severe hypertension and circulatory failure-a diagnostic conundrum: Answers.

Keenswijk W, Verloo P, Walle JV. Keenswijk W, et al. Among authors: verloo p. Pediatr Nephrol. 2017 Nov;32(11):2059-2062. doi: 10.1007/s00467-017-3600-0. Epub 2017 Feb 8. Pediatr Nephrol. 2017. PMID: 28175987 Free PMC article. No abstract available.

9

Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

Schuermans N, Hemelsoet D, Terryn W, Steyaert S, Van Coster R, Coucke PJ, Steyaert W, Callewaert B, Bogaert E, Verloo P, Vanlander AV, Debackere E, Ghijsels J, LeBlanc P, Verdin H, Naesens L, Haerynck F, Callens S, Dermaut B, Poppe B; for UD-PrOZA. Schuermans N, et al. Among authors: verloo p. Orphanet J Rare Dis. 2022 May 23;17(1):210. doi: 10.1186/s13023-022-02365-y. Orphanet J Rare Dis. 2022. PMID: 35606766 Free PMC article.

10

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.

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