171 results on '"Heils, Armin"'
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2. Malignes Neuroleptisches Syndrom vs. Akute lebensbedrohliche Katatonie
3. Linkage and mutational analysis of CLCN2 in childhood absence epilepsy
4. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy
5. Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy
6. Effect of 1-Trichloromethyl-l,2,3,4-Tetrahydro-β-Carboline (TaClo) on Human Serotonergic Cells
7. Molecular manipulations as tools for enhancing our understanding of 5-HT neurotransmission
8. Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia
9. Susceptibility for schizophrenia is not influenced by a functional insertion/deletion variant in the promoter of the serotonin transporter gene
10. A new EF-hand containing gene EFHC2 on Xp11.4: Tentative evidence for association with juvenile myoclonic epilepsy
11. Association analysis of the Arg220His variation of the human gene encoding the GABA δ subunit with idiopathic generalized epilepsy
12. A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy
13. Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies
14. Association Analysis of Malic Enzyme 2 Gene Polymorphisms with Idiopathic Generalized Epilepsy
15. Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
16. Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
17. A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions
18. Functional Characterization of the Murine Serotonin Transporter Gene Promoter in Serotonergic Raphe Neurons
19. Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy
20. Linkage analysis between childhood absence epilepsy and genes encoding GABA A and GABA B receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q
21. Allelic Variation of Human Serotonin Transporter Gene Expression
22. The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy
23. A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy
24. No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy
25. Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy
26. Serotonin transporter function is modulated by brain-derived neurotrophic factor (BDNF) but not nerve growth factor (NGF)
27. Linkage and association analysis of CACNG3 in childhood absence epilepsy (vol 15, pg 463, 2007)
28. Linkage and association analysis of CACNG3 in childhood absence epilepsy
29. A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.
30. Evaluation of CACNA1H in European patients with childhood absence epilepsy.
31. Retraction Note: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
32. Erratum: Linkage and association analysis of CACNG3 in childhood absence epilepsy
33. Linkage and association analysis of CACNG3 in childhood absence epilepsy
34. Genetik und Krankheitsmechanismen erblicher Epilepsien
35. Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy
36. A mutation in the GABAAreceptor α1-subunit is associated with absence epilepsy
37. Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity
38. Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy
39. Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy
40. Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
41. Prodynorphin gene promoter polymorphism and temporal lobe epilepsy
42. Association analysis between the human interleukin 1β (−511) gene polymorphism and susceptibility to febrile convulsions
43. Allelic Variation of Human Serotonin Transporter Gene Expression
44. Functional Characterization of the Murine Serotonin Transporter Gene Promoter in Serotonergic Raphe Neurons
45. Linkage Analysis between Childhood Absence Epilepsy and Genes Encoding GABAA and GABAB Receptors
46. Failure to replicate an allelic association between an exon 8 polymorphism of the human α1A calcium channel gene and common syndromes of idiopathic generalized epilepsy
47. Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q
48. Interleukin-1? gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis
49. Reduction in the Density and Expression, But Not G-Protein Coupling, of Serotonin Receptors (5-HT1A) in 5-HT Transporter Knock-Out Mice: Gender and Brain Region Differences
50. The voltage-gated sodium channel β2-subunit gene and idiopathic generalized epilepsy
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