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Year Number of Results
1995 2
1996 1
1997 1
1999 1
2021 0
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Page 1
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. Ann Neurol. 1995 Aug;38(2):210-7. doi: 10.1002/ana.410380213. Ann Neurol. 1995. PMID: 7654068
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. Am J Med Genet. 1997 Jul 25;74(4):416-21. Am J Med Genet. 1997. PMID: 9259378
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. 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
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. Neurology. 1995 Sep;45(9):1713-20. doi: 10.1212/wnl.45.9.1713. Neurology. 1995. PMID: 7675232
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.
Sander T, Schulz H, Vieira-Saeker AM, Bianchi A, Sailer U, Bauer G, Scaramelli A, Wienker TF, Saar K, Reis A, Janz D, Epplen JT, Riess O. Sander T, et al. Am J Med Genet. 1999 Apr 16;88(2):182-7. Am J Med Genet. 1999. PMID: 10206240
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