Janz D - Search Results

1

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.

Sander T, Peters C, Janz D, Bianchi A, Bauer G, Wienker TF, Hildmann T, Epplen JT, Riess O. Sander T, et al. Among authors: janz d. Epilepsy Res. 1998 Jan;29(2):115-22. doi: 10.1016/s0920-1211(97)00073-9. Epilepsy Res. 1998. PMID: 9477143

2

Do idiopathic generalized epilepsies share a common susceptibility gene?

Janz D, Beck-Mannagetta G, Sander T. Janz D, et al. Neurology. 1992 Apr;42(4 Suppl 5):48-55. Neurology. 1992. PMID: 1574176

3

The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".

Sander T, Hildmann T, Janz D, Wienker TF, Neitzel H, Bianchi A, Bauer G, Sailer U, Berek K, Schmitz B, et al. Sander T, et al. Among authors: janz d. Ann Neurol. 1995 Aug;38(2):210-7. doi: 10.1002/ana.410380213. Ann Neurol. 1995. PMID: 7654068

4

Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.

Sander T, Janz D, Ramel C, Ross CA, Paschen W, Hildmann T, Wienker TF, Bianchi A, Bauer G, Sailer U, et al. Sander T, et al. Among authors: janz d. Neurology. 1995 Sep;45(9):1713-20. doi: 10.1212/wnl.45.9.1713. Neurology. 1995. PMID: 7675232

5

Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.

Sander T, Hildmann T, Wienker TF, Ramel C, Beck-Mannagetta G, Bianchi A, Sailer U, Berek K, Bauer G, Neitzel H, Schmitz B, Durner M, Johnson KJ, Janz D. Sander T, et al. Among authors: janz d. Am J Med Genet. 1996 Feb 16;67(1):31-9. doi: 10.1002/(SICI)1096-8628(19960216)67:1<31::AID-AJMG5>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8678111

6

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

Sander T, Hildmann T, Janz D, Wienker TF, Bianchi A, Bauer G, Sailer U, Scaramelli A, Neitzel H, Schmitz B, Bailey ME, Beck-Mannagetta G, Johnson KJ, Darlison MG. Sander T, et al. Among authors: janz d. Epilepsy Res. 1996 Apr;23(3):235-44. doi: 10.1016/0920-1211(95)00098-4. Epilepsy Res. 1996. PMID: 8739126

7

Lack of linkage between idiopathic generalized epilepsies and the gene encoding the neural cell adhesion molecule.

Sander T, Hildmann T, Janz D, Bianchi A, Bauer G, Scaramelli A, Beck-Mannagetta G. Sander T, et al. Among authors: janz d. Epilepsy Res. 1996 Oct;25(2):139-45. doi: 10.1016/0920-1211(96)00066-6. Epilepsy Res. 1996. PMID: 8884172

8

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.

Sander T, Hildmann T, Kretz R, Fürst R, Sailer U, Bauer G, Schmitz B, Beck-Mannagetta G, Wienker TF, Janz D. Sander T, et al. Among authors: janz d. Am J Med Genet. 1997 Jul 25;74(4):416-21. Am J Med Genet. 1997. PMID: 9259378

9

Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.

Sander T, Kretz R, Williamson MP, Elmslie FV, Rees M, Hildmann T, Bianchi A, Bauer G, Sailer U, Scaramelli A, Schmitz B, Gardiner RM, Janz D, Beck-Mannagetta G. Sander T, et al. Among authors: janz d. Acta Neurol Scand. 1997 Jul;96(1):1-7. Acta Neurol Scand. 1997. PMID: 9262125

10

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.

Sander T, Bockenkamp B, Hildmann T, Blasczyk R, Kretz R, Wienker TF, Volz A, Schmitz B, Beck-Mannagetta G, Riess O, Epplen JT, Janz D, Ziegler A. Sander T, et al. Among authors: janz d. Neurology. 1997 Sep;49(3):842-7. doi: 10.1212/wnl.49.3.842. Neurology. 1997. PMID: 9305351

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