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Results: 11

1.

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.

Eur J Paediatr Neurol. 2014 May;18(3):439-43. doi: 10.1016/j.ejpn.2014.01.001. Epub 2014 Jan 15.

PMID:
24461257
[PubMed - in process]
2.

Hypocretin-1 deficiency in a girl with ROHHAD syndrome.

Dhondt K, Verloo P, Verhelst H, Van Coster R, Overeem S.

Pediatrics. 2013 Sep;132(3):e788-92. doi: 10.1542/peds.2012-3225. Epub 2013 Aug 12.

PMID:
23940246
[PubMed - indexed for MEDLINE]
3.

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.

Neurology. 2011 Mar 15;76(11):988-92. doi: 10.1212/WNL.0b013e31821043f5.

PMID:
21403111
[PubMed - indexed for MEDLINE]
4.

Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster.

Verhelst H, Verloo P, Dhondt K, De Paepe B, Menten B, Dalmau J, Van Coster R.

Eur J Paediatr Neurol. 2011 Mar;15(2):163-6. doi: 10.1016/j.ejpn.2010.07.004. Epub 2010 Aug 6.

PMID:
20692195
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

Acta Gastroenterol Belg. 2009 Jul-Sep;72(3):365-8.

PMID:
19902874
[PubMed - indexed for MEDLINE]
6.

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.

BMC Clin Pathol. 2009 Jun 5;9:4. doi: 10.1186/1472-6890-9-4.

PMID:
19500334
[PubMed]
Free PMC Article
7.

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.

Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney VK, Crolla JA, Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, Bongers EM, de Leeuw N, Reardon W, Gimelli S, Bena F, Hennekam RC, Male A, Gaunt L, Clayton-Smith J, Simonic I, Park SM, Mehta SG, Nik-Zainal S, Woods CG, Firth HV, Parkin G, Fichera M, Reitano S, Lo Giudice M, Li KE, Casuga I, Broomer A, Conrad B, Schwerzmann M, Räber L, Gallati S, Striano P, Coppola A, Tolmie JL, Tobias ES, Lilley C, Armengol L, Spysschaert Y, Verloo P, De Coene A, Goossens L, Mortier G, Speleman F, van Binsbergen E, Nelen MR, Hochstenbach R, Poot M, Gallagher L, Gill M, McClellan J, King MC, Regan R, Skinner C, Stevenson RE, Antonarakis SE, Chen C, Estivill X, Menten B, Gimelli G, Gribble S, Schwartz S, Sutcliffe JS, Walsh T, Knight SJ, Sebat J, Romano C, Schwartz CE, Veltman JA, de Vries BB, Vermeesch JR, Barber JC, Willatt L, Tassabehji M, Eichler EE.

N Engl J Med. 2008 Oct 16;359(16):1685-99. doi: 10.1056/NEJMoa0805384. Epub 2008 Sep 10.

PMID:
18784092
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Electrophysiological studies of malaria parasite-infected erythrocytes: current status.

Staines HM, Alkhalil A, Allen RJ, De Jonge HR, Derbyshire E, Egée S, Ginsburg H, Hill DA, Huber SM, Kirk K, Lang F, Lisk G, Oteng E, Pillai AD, Rayavara K, Rouhani S, Saliba KJ, Shen C, Solomon T, Thomas SL, Verloo P, Desai SA.

Int J Parasitol. 2007 Apr;37(5):475-82. Epub 2007 Jan 9. Review.

PMID:
17292372
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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

vande Velde S, Verloo P, Van Biervliet S, Robberecht E.

Eur J Pediatr. 2007 Jan;166(1):75-6. Epub 2006 Aug 8. No abstract available.

PMID:
16896643
[PubMed - indexed for MEDLINE]
10.

Plasmodium falciparum-activated chloride channels are defective in erythrocytes from cystic fibrosis patients.

Verloo P, Kocken CH, Van der Wel A, Tilly BC, Hogema BM, Sinaasappel M, Thomas AW, De Jonge HR.

J Biol Chem. 2004 Mar 12;279(11):10316-22. Epub 2003 Dec 16.

PMID:
14679190
[PubMed - indexed for MEDLINE]
Free Article
11.

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.

Pediatr Res. 2001 Nov;50(5):658-65.

PMID:
11641463
[PubMed - indexed for MEDLINE]

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