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Items: 1 to 20 of 29

1.

LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs.

Herbst SM, Proepper CR, Geis T, Borggraefe I, Hahn A, Debus O, Haeussler M, von Gersdorff G, Kurlemann G, Ensslen M, Beaud N, Budde J, Gilbert M, Heiming R, Morgner R, Philippi H, Ross S, Strobl-Wildemann G, Muelleder K, Vosschulte P, Morris-Rosendahl DJ, Schuierer G, Hehr U.

Brain Dev. 2016 Apr;38(4):399-406. doi: 10.1016/j.braindev.2015.10.001.

PMID:
26494205
2.

[The earlier, the better].

Batenhorst B, Hidding H, Debus O.

Kinderkrankenschwester. 2015 Apr;34(4):138-9. German. No abstract available.

PMID:
26309975
3.

Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.

Banka S, de Goede C, Yue WW, Morris AA, von Bremen B, Chandler KE, Feichtinger RG, Hart C, Khan N, Lunzer V, Mataković L, Marquardt T, Makowski C, Prokisch H, Debus O, Nosaka K, Sonwalkar H, Zimmermann FA, Sperl W, Mayr JA.

Mol Genet Metab. 2014 Dec;113(4):301-6. doi: 10.1016/j.ymgme.2014.09.010.

PMID:
25458521
4.

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium., Dobyns WB, Baas F, Poll-The BT.

Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287.

PMID:
20952379
5.

Treatment of childhood migraine attacks with oral zolmitriptan and ibuprofen.

Evers S, Rahmann A, Kraemer C, Kurlemann G, Debus O, Husstedt IW, Frese A.

Neurology. 2006 Aug 8;67(3):497-9.

PMID:
16775229
6.

P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG.

Fiedler BJ, Debus OM, Neubauer BA, Kienle M, Kurlemann G.

Neurosci Lett. 2006 Jan 30;393(2-3):206-10.

PMID:
16246492
7.

Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins.

Denecke J, Kranz C, von Kleist-Retzow JCh, Bosse K, Herkenrath P, Debus O, Harms E, Marquardt T.

Pediatr Res. 2005 Aug;58(2):248-53.

PMID:
16006436
8.

The factor V G1691A mutation is a risk for porencephaly: A case-control study.

Debus OM, Kosch A, Sträter R, Rossi R, Nowak-Göttl U.

Ann Neurol. 2004 Aug;56(2):287-90.

PMID:
15293282
9.

Acute and subacute intracerebral hemorrhages: comparison of MR imaging at 1.5 and 3.0 T--initial experience.

Allkemper T, Tombach B, Schwindt W, Kugel H, Schilling M, Debus O, Möllmann F, Heindel W.

Radiology. 2004 Sep;232(3):874-81.

PMID:
15284437
10.

Familial occurrence of dysembryoplastic neuroepithelial tumor.

Hasselblatt M, Kurlemann G, Rickert CH, Debus OM, Brentrup A, Schachenmayr W, Paulus W.

Neurology. 2004 Mar 23;62(6):1020-1. No abstract available.

PMID:
15037719
12.

[Life-threatening theophylline intoxication: a variant of Munchhausen syndrome by proxy].

Föll D, Debus O, Schmitt GM, Harms E, Zimmer KP.

Klin Padiatr. 2003 Mar-Apr;215(2):86-9. German.

PMID:
12677549
13.

Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF study.

Debus OM, Lerchl A, Bothe HW, Bremer J, Fiedler B, Franssen M, Koehring J, Steils M, Kurlemann G.

J Pineal Res. 2002 Nov;33(4):213-7.

PMID:
12390503
14.

Add-on treatment with pyridoxine and sulthiame in 12 infants with West syndrome: an open clinical study.

Debus OM, Köhring J, Fiedler B, Franssen M, Kurlemann G.

Seizure. 2002 Sep;11(6):381-3.

15.

Moyamoya syndrome: impaired hemodynamics on ECD SPECT after EEG controlled hyperventilation.

Matheja P, Weckesser M, Debus O, Franzius Ch, Löttgen J, Schober O, Kurlemann G.

Nuklearmedizin. 2002 Feb;41(1):42-6.

PMID:
11917348
16.

Periventricular cystic lesions in a preterm infant after a car accident during pregnancy.

Rabe H, Debus O, Frosch M, Stüssel J, Louwen F, Kurlemann G, Harms E.

Eur J Ultrasound. 2001 Dec;14(2-3):171-8. Review.

PMID:
11704435
17.

Dextromethorphan in pregnancy.

Debus O, Kurlemann G, Gehrmann J, Krasemann T.

Chest. 2001 Sep;120(3):1038-40. No abstract available.

PMID:
11555552
18.

Early infantile epileptic encephalopathy (Ohtahara syndrome) after maternal electric injury during pregnancy: etiological considerations.

Krasemann T, Hoovey S, Uekoetter J, Bosse H, Kurlemann G, Debus OM.

Brain Dev. 2001 Aug;23(5):359-62.

PMID:
11504609
19.

Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity.

Young P, Grote K, Kuhlenbäumer G, Debus O, Kurlemann H, Halfter H, Funke H, Ringelstein EB, Stögbauer F.

J Neurol. 2001 May;248(5):410-5.

PMID:
11437164
20.

[Cockayne syndrome with marked cerebral symptoms].

Menges-Wenzel EM, Debus O, Sträter R, Schuierer G, Kurlemann G.

Klin Padiatr. 2001 May-Jun;213(3):134-8. German.

PMID:
11417366

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