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Items: 15

1.

Cranial ultrasound and neurophysiological testing to predict neurological outcome in infants born very preterm.

Franckx H, Hasaerts D, Huysentruyt K, Cools F.

Dev Med Child Neurol. 2018 Dec;60(12):1232-1238. doi: 10.1111/dmcn.13961. Epub 2018 Jul 7.

2.

Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 gene.

de Filette J, Hasaerts D, Seneca S, Gheldof A, Stouffs K, Keymolen K, Velkeniers B.

Neurol Genet. 2016 Jan 7;2(1):e42. doi: 10.1212/NXG.0000000000000042. eCollection 2016 Feb.

3.

Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.

Weckhuysen S, Holmgren P, Hendrickx R, Jansen AC, Hasaerts D, Dielman C, de Bellescize J, Boutry-Kryza N, Lesca G, Von Spiczak S, Helbig I, Gill D, Yendle S, Møller RS, Klitten L, Korff C, Godfraind C, Van Rijckevorsel K, De Jonghe P, Hjalgrim H, Scheffer IE, Suls A.

Epilepsia. 2013 May;54(5):e74-80. doi: 10.1111/epi.12124. Epub 2013 Feb 14.

4.

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P.

Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644.

PMID:
22275249
5.

Identification of two de novo mutations responsible for type I antithrombin deficiency.

Orlando C, Lissens W, Hasaerts D, Jochmans K.

Thromb Haemost. 2012 Jan;107(1):187-9. doi: 10.1160/TH11-08-0526. Epub 2011 Nov 24. No abstract available.

PMID:
22116592
6.

Outcome at 3 years of age in a population-based cohort of extremely preterm infants.

De Groote I, Vanhaesebrouck P, Bruneel E, Dom L, Durein I, Hasaerts D, Laroche S, Oostra A, Ortibus E, Roeyers H, van Mol C; Extremely Preterm Infants in Belgium (EPIBEL) Study Group.

Obstet Gynecol. 2007 Oct;110(4):855-64.

PMID:
17906020
7.

Steroids in intractable childhood epilepsy: clinical experience and review of the literature.

Verhelst H, Boon P, Buyse G, Ceulemans B, D'Hooghe M, Meirleir LD, Hasaerts D, Jansen A, Lagae L, Meurs A, Coster RV, Vonck K.

Seizure. 2005 Sep;14(6):412-21.

8.

De novo KCNQ2 mutations in patients with benign neonatal seizures.

Claes LR, Ceulemans B, Audenaert D, Deprez L, Jansen A, Hasaerts D, Weckx S, Claeys KG, Del-Favero J, Van Broeckhoven C, De Jonghe P.

Neurology. 2004 Dec 14;63(11):2155-8.

PMID:
15596769
9.

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.

Eur J Pediatr. 2004 Dec;163(12):717-21.

PMID:
15338298
10.

Dancing eye syndrome and hyperphosphatasemia.

Hasaerts DE, Gorus FK, De Meirleir LJ.

Pediatr Neurol. 1998 May;18(5):432-4.

PMID:
9650686
11.

Anterior fontanelle pressure variations during sleep in healthy infants.

Wayenberg JL, Hasaerts D, Franco P, Valente F, Massager N.

Sleep. 1995 May;18(4):223-8.

PMID:
7618018
12.

Early MR detection of cortical and subcortical hypoxic-ischemic encephalopathy in full-term-infants.

Christophe C, Clercx A, Blum D, Hasaerts D, Segebarth C, Perlmutter N.

Pediatr Radiol. 1994;24(8):581-4.

PMID:
7724281
13.

[Hydrocortisone therapy of secondary generalized epilepsy in children].

Hasaerts D, Dulac O.

Arch Fr Pediatr. 1989 Nov;46(9):635-9. French.

PMID:
2604521
14.

Phenothiazine-induced sleep apneas in normal infants.

Kahn A, Hasaerts D, Blum D.

Pediatrics. 1985 May;75(5):844-7.

PMID:
3991270
15.

[Low blood zinc levels in children with nephrotic syndrome (author's transl)].

Bensman A, Morgant G, Hasaerts D, Lasfargues G.

Nouv Presse Med. 1981 Dec 19;10(46):3779-81. French.

PMID:
7322912

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