Stephani U - Search Results

1

Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndrome.

Hoffmann-Riem M, Diener W, Benninger C, Rating D, Unnebrink K, Stephani U, Ernst HP, Korinthenberg R. Hoffmann-Riem M, et al. Among authors: stephani u. Neuropediatrics. 2000 Aug;31(4):169-74. doi: 10.1055/s-2000-7456. Neuropediatrics. 2000. PMID: 11071139

2

Electrolytes, amino acids and proteins in lumbar CSF during the treatment of acute leukemia in childhood.

Korinthenberg R, Ullrich K, Ritter J, Stephani U. Korinthenberg R, et al. Among authors: stephani u. Acta Paediatr Scand. 1990 Mar;79(3):335-42. doi: 10.1111/j.1651-2227.1990.tb11466.x. Acta Paediatr Scand. 1990. PMID: 2333748

3

Radiation-related disturbance of blood/brain barrier during therapy of acute lymphoblastic leukaemia.

Stephani U, Rating D, Korinthenberg R, Siemes H, Riehm H, Hanefeld F. Stephani U, et al. Lancet. 1983 Oct 29;2(8357):1036-7. doi: 10.1016/s0140-6736(83)91030-9. Lancet. 1983. PMID: 6138589 No abstract available.

4

Inheritance of photosensitivity.

Waltz S, Stephani U. Waltz S, et al. Among authors: stephani u. Neuropediatrics. 2000 Apr;31(2):82-5. doi: 10.1055/s-2000-7478. Neuropediatrics. 2000. PMID: 10832582

5

Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis.

Hahn A, Pistohl J, Neubauer BA, Stephani U. Hahn A, et al. Among authors: stephani u. Neuropediatrics. 2001 Feb;32(1):1-8. doi: 10.1055/s-2001-12216. Neuropediatrics. 2001. PMID: 11315196

6

Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family study.

Doose H, Hahn A, Neubauer BA, Pistohl J, Stephani U. Doose H, et al. Among authors: stephani u. Neuropediatrics. 2001 Feb;32(1):9-13. doi: 10.1055/s-2001-12215. Neuropediatrics. 2001. PMID: 11315204

7

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.

Weber YG, Berger A, Bebek N, Maier S, Karafyllakes S, Meyer N, Fukuyama Y, Halbach A, Hikel C, Kurlemann G, Neubauer B, Osawa M, Püst B, Rating D, Saito K, Stephani U, Tauer U, Lehmann-Horn F, Jurkat-Rott K, Lerche H. Weber YG, et al. Among authors: stephani u. Epilepsia. 2004 Jun;45(6):601-9. doi: 10.1111/j.0013-9580.2004.48203.x. Epilepsia. 2004. PMID: 15144424 Free article.

8

SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.

Ebach K, Joos H, Doose H, Stephani U, Kurlemann G, Fiedler B, Hahn A, Hauser E, Hundt K, Holthausen H, Müller U, Neubauer BA. Ebach K, et al. Among authors: stephani u. Neuropediatrics. 2005 Jun;36(3):210-3. doi: 10.1055/s-2005-865607. Neuropediatrics. 2005. PMID: 15944908 Free article.

9

The natural history of myoclonic astatic epilepsy (Doose syndrome) and Lennox-Gastaut syndrome.

Stephani U. Stephani U. Epilepsia. 2006;47 Suppl 2:53-5. doi: 10.1111/j.1528-1167.2006.00690.x. Epilepsia. 2006. PMID: 17105462 Free article. Review.

10

EEG-fMRI reveals activation of brainstem and thalamus in patients with Lennox-Gastaut syndrome.

Siniatchkin M, Coropceanu D, Moeller F, Boor R, Stephani U. Siniatchkin M, et al. Among authors: stephani u. Epilepsia. 2011 Apr;52(4):766-74. doi: 10.1111/j.1528-1167.2010.02948.x. Epub 2011 Jan 28. Epilepsia. 2011. PMID: 21275978 Free article.

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