Aeby A - Search Results

1

Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.

Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: aeby a. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. Mol Genet Genomic Med. 2021. PMID: 34402213 Free PMC article.

2

Facial hemangioma and cerebral corticovascular dysplasia: a syndrome associated with epilepsy.

Aeby A, Guerrini R, David P, Rodesch G, Raybaud C, Van Bogaert P. Aeby A, et al. Neurology. 2003 Mar 25;60(6):1030-2. doi: 10.1212/01.wnl.0000052688.20517.7d. Neurology. 2003. PMID: 12654977

3

Oral ketamine in paediatric non-convulsive status epilepticus.

Mewasingh LD, Sékhara T, Aeby A, Christiaens FJ, Dan B. Mewasingh LD, et al. Among authors: aeby a. Seizure. 2003 Oct;12(7):483-9. doi: 10.1016/s1059-1311(03)00028-1. Seizure. 2003. PMID: 12967577 Free article. Clinical Trial.

4

Levetiracetam efficacy in epileptic syndromes with continuous spikes and waves during slow sleep: experience in 12 cases.

Aeby A, Poznanski N, Verheulpen D, Wetzburger C, Van Bogaert P. Aeby A, et al. Epilepsia. 2005 Dec;46(12):1937-42. doi: 10.1111/j.1528-1167.2005.00337.x. Epilepsia. 2005. PMID: 16393159 Free article. Clinical Trial.

5

Posterior reversible encephalopathy syndrome revealing acute post-streptococcal glomerulonephritis.

Aeby A, David P, Fricx C, Jissendi P, Blecic S, Van Bogaert P. Aeby A, et al. J Child Neurol. 2006 Mar;21(3):250-1. doi: 10.2310/7010.2006.00057. J Child Neurol. 2006. PMID: 16901429

6

Coexistence of idiopathic rolandic epilepsy and CSWS in two families.

De Tiège X, Goldman S, Verheulpen D, Aeby A, Poznanski N, Van Bogaert P. De Tiège X, et al. Among authors: aeby a. Epilepsia. 2006 Oct;47(10):1723-7. doi: 10.1111/j.1528-1167.2006.00644.x. Epilepsia. 2006. PMID: 17054694 Free article.

7

Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.

Van Bogaert P, Azizieh R, Désir J, Aeby A, De Meirleir L, Laes JF, Christiaens F, Abramowicz MJ. Van Bogaert P, et al. Among authors: aeby a. Ann Neurol. 2007 Jun;61(6):579-86. doi: 10.1002/ana.21121. Ann Neurol. 2007. PMID: 17455289

8

Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.

Aeby A, Sznajer Y, Cavé H, Rebuffat E, Van Coster R, Rigal O, Van Bogaert P. Aeby A, et al. J Inherit Metab Dis. 2007 Oct;30(5):827. doi: 10.1007/s10545-007-0612-0. Epub 2007 Aug 20. J Inherit Metab Dis. 2007. PMID: 17703371

9

Primary angiitis of the central nervous system: neurologic deterioration despite treatment.

De Tiège X, Van Bogaert P, Aeby A, Salmon I, Parpal H, Poppe AY, Maris C, Lanthier S. De Tiège X, et al. Among authors: aeby a. Pediatrics. 2011 Apr;127(4):e1086-90. doi: 10.1542/peds.2009-2729. Epub 2011 Mar 14. Pediatrics. 2011. PMID: 21402640 Free article.

10

A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome.

Vilain C, Rens C, Aeby A, Balériaux D, Van Bogaert P, Remiche G, Smet J, Van Coster R, Abramowicz M, Pirson I. Vilain C, et al. Among authors: aeby a. Clin Genet. 2012 Sep;82(3):264-70. doi: 10.1111/j.1399-0004.2011.01743.x. Epub 2011 Jul 18. Clin Genet. 2012. PMID: 21696386

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