de Meirleir L - Search Results

1

Acute pancreatitis after growth hormone treatment: disease or treatment linked?

de Beaufort C, Beck P, Seligmann R, de Meirleir L, de Schepper J. de Beaufort C, et al. Among authors: de meirleir l, de schepper j. Eur J Pediatr. 2006 Sep;165(9):652-3. doi: 10.1007/s00431-006-0126-z. Epub 2006 May 12. Eur J Pediatr. 2006. PMID: 16691411 No abstract available.

2

PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure.

Zeevaert R, Scalais E, Muino Mosquera L, De Meirleir L, De Beaufort C, Witsch M, Jaeken J, De Schepper J. Zeevaert R, et al. Among authors: de meirleir l, de beaufort c, de schepper j. Acta Clin Belg. 2016 Dec;71(6):435-437. doi: 10.1080/17843286.2016.1142043. Epub 2016 May 24. Acta Clin Belg. 2016. PMID: 27351072

3

Pearson marrow pancreas syndrome: a molecular study and clinical management.

Seneca S, De Meirleir L, De Schepper J, Balduck N, Jochmans K, Liebaers I, Lissens W. Seneca S, et al. Among authors: de meirleir l, de schepper j. Clin Genet. 1997 May;51(5):338-42. doi: 10.1111/j.1399-0004.1997.tb02484.x. Clin Genet. 1997. PMID: 9212183

4

A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Epsilon1alpha gene.

Tulinius M, Darin N, Wiklund LM, Holmberg E, Eriksson JE, Lissens W, De Meirleir L, Holme E. Tulinius M, et al. Among authors: de meirleir l. Eur J Pediatr. 2005 Feb;164(2):99-103. doi: 10.1007/s00431-004-1570-2. Epub 2004 Nov 19. Eur J Pediatr. 2005. PMID: 15558317

5

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.

Wraith JE, Scarpa M, Beck M, Bodamer OA, De Meirleir L, Guffon N, Meldgaard Lund A, Malm G, Van der Ploeg AT, Zeman J. Wraith JE, et al. Among authors: de meirleir l. Eur J Pediatr. 2008 Mar;167(3):267-77. doi: 10.1007/s00431-007-0635-4. Epub 2007 Nov 23. Eur J Pediatr. 2008. PMID: 18038146 Free PMC article. Review.

6

Early treatment of a child with NAGS deficiency using N-carbamyl glutamate results in a normal neurological outcome.

Van Leynseele A, Jansen A, Goyens P, Martens G, Peeters S, Jonckheere A, De Meirleir L. Van Leynseele A, et al. Among authors: de meirleir l. Eur J Pediatr. 2014 Dec;173(12):1635-8. doi: 10.1007/s00431-013-2205-2. Eur J Pediatr. 2014. PMID: 24233332

7

Early onset Huntington disease: a neuronal degeneration syndrome.

Seneca S, Fagnart D, Keymolen K, Lissens W, Hasaerts D, Debulpaep S, Desprechins B, Liebaers I, De Meirleir L. Seneca S, et al. Among authors: de meirleir l. Eur J Pediatr. 2004 Dec;163(12):717-21. doi: 10.1007/s00431-004-1537-3. Eur J Pediatr. 2004. PMID: 15338298

8

Revised recommendations for the management of Gaucher disease in children.

Kaplan P, Baris H, De Meirleir L, Di Rocco M, El-Beshlawy A, Huemer M, Martins AM, Nascu I, Rohrbach M, Steinbach L, Cohen IJ. Kaplan P, et al. Among authors: de meirleir l. Eur J Pediatr. 2013 Apr;172(4):447-58. doi: 10.1007/s00431-012-1771-z. Epub 2012 Jul 8. Eur J Pediatr. 2013. PMID: 22772880 Review.

9

Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy.

Scalais E, Francois B, Schlesser P, Stevens R, Nuttin C, Martin JJ, Van Coster R, Seneca S, Roels F, Van Goethem G, Löfgren A, De Meirleir L. Scalais E, et al. Among authors: de meirleir l. Eur J Paediatr Neurol. 2012 Sep;16(5):542-8. doi: 10.1016/j.ejpn.2012.01.013. Epub 2012 Feb 17. Eur J Paediatr Neurol. 2012. PMID: 22342071

10

Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: improved survival by prompt diagnosis.

Scalais E, Bottu J, Wanders RJ, Ferdinandusse S, Waterham HR, De Meirleir L. Scalais E, et al. Among authors: de meirleir l. Am J Med Genet A. 2015 Jan;167A(1):211-4. doi: 10.1002/ajmg.a.36803. Epub 2014 Oct 22. Am J Med Genet A. 2015. PMID: 25338548

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