Dullinger JS - Search Results

1

CLCN2 variants in idiopathic generalized epilepsy.

Kleefuss-Lie A, Friedl W, Cichon S, Haug K, Warnstedt M, Alekov A, Sander T, Ramirez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H. Kleefuss-Lie A, et al. Among authors: dullinger js. Nat Genet. 2009 Sep;41(9):954-5. doi: 10.1038/ng0909-954. Nat Genet. 2009. PMID: 19710712 No abstract available.

2

The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Rau B, Dullinger JS, Elger CE, Propping P, Heils A. Haug K, et al. Among authors: dullinger js. Neuroreport. 2000 Aug 21;11(12):2687-9. doi: 10.1097/00001756-200008210-00016. Neuroreport. 2000. PMID: 10976944

3

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.

Haug K, Kremerskothen J, Hallmann K, Sander T, Dullinger J, Rau B, Beyenburg S, Lentze MJ, Barnekow A, Elger CE, Propping P, Heils A. Haug K, et al. Mol Cell Probes. 2000 Aug;14(4):255-60. doi: 10.1006/mcpr.2000.0314. Mol Cell Probes. 2000. PMID: 10970730

4

No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.

Haug K, Hallmann K, Horvath S, Sander T, Kubisch C, Rau B, Dullinger J, Beyenburg S, Elger CE, Propping P, Heils A. Haug K, et al. Epilepsy Res. 2000 Nov;42(1):57-62. doi: 10.1016/s0920-1211(00)00164-9. Epilepsy Res. 2000. PMID: 10996506 Clinical Trial.

5

The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy.

Haug K, Hallmann K, Rebstock J, Dullinger J, Muth S, Haverkamp F, Pfeiffer H, Rau B, Elger CE, Propping P, Heils A. Haug K, et al. Epilepsy Res. 2001 Dec;47(3):243-6. doi: 10.1016/s0920-1211(01)00312-6. Epilepsy Res. 2001. PMID: 11738931

6

Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans.

Gilling M, Dullinger JS, Gesk S, Metzke-Heidemann S, Siebert R, Meyer T, Brondum-Nielsen K, Tommerup N, Ropers HH, Tümer Z, Kalscheuer VM, Thomas NS. Gilling M, et al. Among authors: dullinger js. Am J Hum Genet. 2006 May;78(5):878-883. doi: 10.1086/503632. Epub 2006 Mar 17. Am J Hum Genet. 2006. PMID: 16642442 Free PMC article.

7

Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.

Meyer T, Jurkat-Rott K, Huebner A, Lehmann-Horn F, Linke P, Van Landeghem F, Dullinger JS, Spuler S. Meyer T, et al. Among authors: dullinger js. Muscle Nerve. 2008 Jan;37(1):120-4. doi: 10.1002/mus.20825. Muscle Nerve. 2008. PMID: 17587224

8

Early-onset ALS with long-term survival associated with spastin gene mutation.

Meyer T, Schwan A, Dullinger JS, Brocke J, Hoffmann KT, Nolte CH, Hopt A, Kopp U, Andersen P, Epplen JT, Linke P. Meyer T, et al. Among authors: dullinger js. Neurology. 2005 Jul 12;65(1):141-3. doi: 10.1212/01.wnl.0000167130.31618.0a. Neurology. 2005. PMID: 16009903

9

[Progressive muscle atrophy. A rarely diagnosed variant of amyotrophic lateral sclerosis].

Meyer T, Münch C, van Landeghem FK, Borisow N, Dullinger J, Linke P. Meyer T, et al. Nervenarzt. 2007 Dec;78(12):1383-8. doi: 10.1007/s00115-007-2288-y. Nervenarzt. 2007. PMID: 17516042 Review. German.

10

Thalidomide causes sinus bradycardia in ALS.

Meyer T, Maier A, Borisow N, Dullinger JS, Splettstösser G, Ohlraun S, Münch C, Linke P. Meyer T, et al. Among authors: dullinger js. J Neurol. 2008 Apr;255(4):587-91. doi: 10.1007/s00415-008-0756-3. Epub 2008 Apr 21. J Neurol. 2008. PMID: 18425621 Clinical Trial.

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