E-LIB Suche - Ergebnisse für: Karle, Kathrin

1

Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutat..:

Altmann, Judith ; Büchner, Boriana ; Nadaj-Pakleza, Aleksandra...
Journal of Neurology. 263 (2016) 5 - p. 961-972 , 2016

Link: https://doi.org/10.1007/..

2

A Hereditary Spastic Paraplegia Mouse Model Supports a Role..:

Khundadze, Mukhran ; Kollmann, Katrin ; Koch, Nicole...
PLoS Genetics. 9 (2013) 12 - p. e1003988 , 2013

Link: https://doi.org/10.1371/..

3

Netzwerk mitochondrialer Erkrankungen (mitoNET), Teilprojek..

Schlussbericht

Karle, Kathrin ; Rapaport, Doron ; Schöls, Ludger , 2012

Link: http://edok01.tib.uni-ha..

4

Soziotherapie bei psychisch kranken Eltern - Grundlagen und..:

Karle, Kathrin , 2009

Link: http://nbn-resolving.de/..

5

Identification of a heterozygous genomic deletion in the sp..:

Bauer, Peter ; Winner, Beate ; Schüle, Rebecca...
neurogenetics. 10 (2008) 1 - p. 43-48 , 2008

Link: https://doi.org/10.1007/..

6

Distinct and overlapping alterations in motor and sensory n..:

Jablonka, Sibylle ; Karle, Kathrin ; Sandner, Beatrice...
Human Molecular Genetics. 15 (2006) 3 - p. 511-518 , 2006

Link: https://doi.org/10.1093/..

7

DNA METHYLATION SIGNATURES OF CHRONIC ALCOHOL DEPENDENCE IN..:

Thomas, Mara ; Brueckmann, Christof ; Islam, Sumaiya A....
European Neuropsychopharmacology. 29 (2019) - p. S852-S853 , 2019

Link: https://doi.org/10.1016/..

8

Neurobiological correlates of emotional intelligence in voi..:

Karle, Kathrin N ; Ethofer, Thomas ; Jacob, Heike...
Social Cognitive and Affective Neuroscience. 13 (2018) 2 - p. 233-244 , 2018

Link: https://doi.org/10.1093/..

9

DNA methylation signatures of chronic alcohol dependence in..:

Brückmann, Christof ; Islam, Sumaiya A. ; MacIsaac, Julia L....
Scientific Reports. 7 (2017) 1 - p. , 2017

Link: https://doi.org/10.1038/..

10

Validation of differential GDAP1 DNA methylation in alcohol..:

Brückmann, Christof ; Di Santo, Adriana ; Karle, Kathrin Nora..
Epigenetics. 11 (2016) 6 - p. 456-463 , 2016

Link: https://doi.org/10.1080/..

11

Hereditary spastic paraplegia: Clinicogenetic lessons from ..:

Schüle, Rebecca ; Wiethoff, Sarah ; Martus, Peter...
Annals of Neurology. 79 (2016) 4 - p. 646-658 , 2016

Link: https://doi.org/10.1002/..

12

A recurrent mutation in KCNA2 as a novel cause of hereditar..:

Helbig, Katherine L. ; Hedrich, Ulrike B.S. ; Shinde, Deepali N....
Annals of Neurology. 80 (2016) 4 - p. , 2016

Link: https://doi.org/10.1002/..

13

Gray and white matter alterations in hereditary spastic par..:

Lindig, Tobias ; Bender, Benjamin ; Hauser, Till-Karsten...
Journal of Neurology. 262 (2015) 8 - p. 1961-1971 , 2015

Link: https://doi.org/10.1007/..

14

AP5Z1/SPG48 frequency in autosomal recessive and sporadic s..:

Schlipf, Nina A. ; Schüle, Rebecca ; Klimpe, Sven...
Molecular Genetics & Genomic Medicine. 2 (2014) 5 - p. 379-382 , 2014

Link: https://doi.org/10.1002/..

15

Clozapine serum concentrations in dopamimetic psychosis in ..:

Lutz, Ulrich C. ; Sirfy, Ahmad ; Wiatr, Gerlinde...
European Journal of Clinical Pharmacology. 70 (2014) 12 - p. 1471-1476 , 2014

Link: https://doi.org/10.1007/..