المؤلفون: Lunny C., Veroniki A. A., Hutton B., White I., Higgins J. P. T., Wright J. M., Kim J. Y., Thirugnanasampanthar S. S., Siddiqui S., Watt J., Moja L., Taske N., Lorenz R. C., Gerrish S., Straus S., Minogue V., Hu F., Lin K., Kapani A., Nagi S., Chen L., Akbar-Nejad M., Tricco A. C.

المساهمون: C. Lunny, A.A. Veroniki, B. Hutton, I. White, J.P.T. Higgin, J.M. Wright, J.Y. Kim, S.S. Thirugnanasampanthar, S. Siddiqui, J. Watt, L. Moja, N. Taske, R.C. Lorenz, S. Gerrish, S. Strau, V. Minogue, F. Hu, K. Lin, A. Kapani, S. Nagi, L. Chen, M. Akbar-Nejad, A.C. Tricco

مصطلحات موضوعية: evidence-based practice, health care quality, access, and evaluation, health services research, methods, Settore MED/42 - Igiene Generale e Applicata

Relation: info:eu-repo/semantics/altIdentifier/pmid/35948412; info:eu-repo/semantics/altIdentifier/wos/WOS:000839606300001; volume:28; issue:1; firstpage:58; lastpage:67; numberofpages:10; journal:BMJ EVIDENCE-BASED MEDICINE; https://hdl.handle.net/2434/952620; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85136489561

الاتاحة: https://hdl.handle.net/2434/952620
https://doi.org/10.1136/bmjebm-2022-111944

المؤلفون: Everett, K, Chioza, B, Aicardi, J, Aschauer, H, Brouwer, O, Callenbach, P, Covanis, A, Dooley, J, Dulac, O, Durner, M, Eeg-Olofsson, O, Feucht, M, Friis, M, Guerrini, R, Heits, A, Kjeldsen, M, Nabbout, R, Sander, T, Wirrell, E, McKeigue, P, Robinson, R, Taske, N, Gardiner, M

المصدر: EPILEPSY RESEARCH , 75 (2-3) pp. 145-153. (2007)

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, childhood absence, epilepsy, linkage, association, mutation screening, CLCN2, IDIOPATHIC GENERALIZED EPILEPSIES, PEDIGREE DISEQUILIBRIUM TEST, GATED CHLORIDE CHANNEL, SELECTIVITY, CELLS, GENE

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/8217/1/8217.pdf; https://discovery.ucl.ac.uk/id/eprint/8217/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/8217/1/8217.pdf
https://discovery.ucl.ac.uk/id/eprint/8217/

المؤلفون: Everett, KV, Chioza, B, Aicardi, J, Aschauer, H, Brouwer, O, Callenbach, P, Covanis, A, Dulac, O, Eeg-Olofsson, O, Feucht, M, Friis, M, Goutieres, F, Guerrini, R, Heils, A, Kjeldsen, M, Lehesjoki, AE, Makoff, A, Nabbout, R, Olsson, I, Sander, T, Siren, A, McKeigue, P, Robinson, R, Taske, N, Rees, M, Gardiner, M

المصدر: EUR J HUM GENET , 15 (4) 463 - 472. (2007)

مصطلحات موضوعية: absence epilepsy, linkage, association, CACNG3, splice variants, IDIOPATHIC GENERALIZED EPILEPSY, PEDIGREE DISEQUILIBRIUM TEST, GENETIC-VARIATION, SEIZURES, CHANNEL, CACNA1H, MOUSE, MUTATIONS, RECEPTORS, VARIANTS

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/8218/1/8218.pdf; https://discovery.ucl.ac.uk/id/eprint/8218/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/8218/1/8218.pdf
https://discovery.ucl.ac.uk/id/eprint/8218/

المؤلفون: Mas, C, Taske, N, Deutsch, S, Guipponi, M, Thomas, P, Covanis, A, Friis, M, Kjeldsen, MJ, Pizzolato, GP, Villemure, JG, Buresi, C, Rees, M, Malafosse, A, Gardiner, RM, Antonarakis, SE, Meda, P

المصدر: Journal of Medical Genetics , 41 (7) , Article e93. (2004)

مصطلحات موضوعية: Connexin, Epilepsy, Gene

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/426/1/association.pdf; https://discovery.ucl.ac.uk/id/eprint/426/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/426/1/association.pdf
https://discovery.ucl.ac.uk/id/eprint/426/

المؤلفون: O'Brien, R O, Taske, N L, Hansbro, P M, Matthaei, K I, Hogan, S P, Denborough, M A, Foster, P S

المصدر: Journal of Medical Genetics ; volume 32, issue 11, page 913-914 ; ISSN 1468-6244

الاتاحة: http://dx.doi.org/10.1136/jmg.32.11.913
https://syndication.highwire.org/content/doi/10.1136/jmg.32.11.913

المؤلفون: Gabbay, M., Taylor, L., Sheppard, L., Hillage, J., Bambra, C., Ford, F., Preece, R., Taske, N., Kelly, M.P.

المصدر: British journal of general practice, 2011, Vol.61(584), pp.e118-124 [Peer Reviewed Journal]

مصطلحات موضوعية: Evidence-based medicine, Guideline, Sick leave, Sick leave cost, Work capacity evaluation

وصف الملف: application/pdf

Relation: dro:8309; http://dro.dur.ac.uk/8309/; https://doi.org/10.3399/bjgp11X561221; http://dro.dur.ac.uk/8309/1/8309.pdf

الاتاحة: http://dro.dur.ac.uk/8309/
http://dro.dur.ac.uk/8309/1/8309.pdf
https://doi.org/10.3399/bjgp11X561221

المؤلفون: Everett, K., Chioza, B., Aicardi, J., Aschauer, H., Brouwer, O., Callenbach, P., Covanis, A., Dooley, J., Dulac, O., Durner, M., Eeg-Olofsson, O., Feucht, M., Friis, M., Guerrini, R., Heils, A., Kjeldsen, M., Nabbout, R., Sander, T., Wirrell, E., McKeigue, P., Robinson, R., Taske, N., Gardiner, M.

مصطلحات موضوعية: Cardiovascular and Metabolic Diseases

Relation: Linkage and mutational analysis of CLCN2 in childhood absence epilepsy. Everett, K. and Chioza, B. and Aicardi, J. and Aschauer, H. and Brouwer, O. and Callenbach, P. and Covanis, A. and Dooley, J. and Dulac, O. and Durner, M. and Eeg-Olofsson, O. and Feucht, M. and Friis, M. and Guerrini, R. and Heils, A. and Kjeldsen, M. and Nabbout, R. and Sander, T. and Wirrell, E. and McKeigue, P. and Robinson, R. and Taske, N. and Gardiner, M. Epilepsy Research 75 (2-3): 145-153. July 2007

الاتاحة: http://edoc.mdc-berlin.de/13618/
https://edoc.mdc-berlin.de/13618/
https://doi.org/10.1016/j.eplepsyres.2007.05.004

المؤلفون: Mas, Christophe, Taske, N., Deutsch, Samuel, Guipponi, Michel, Thomas, P., Covanis, A., Friis, M., Kjeldsen, M. J., Pizzolato, G. P., Villemure, Jean-Guy, Buresi, C., Rees, M., Malafosse, Alain, Gardiner, M., Antonarakis, Stylianos, Meda, Paolo

المصدر: ISSN: 0022-2593 ; Journal of medical genetics, vol. 41, no. 7 (2004) e93.

مصطلحات موضوعية: info:eu-repo/classification/ddc/616, Case-Control Studies, Connexins/ genetics, Cytosine/metabolism, Enhancer Elements, Genetic/genetics, Exons/genetics, Genetic Testing/methods, Genotype, Haplotypes/genetics, Humans, Linkage Disequilibrium/ genetics, Myoclonic Epilepsy, Juvenile/ genetics, Nucleic Acid Conformation, Polymorphism, Single Nucleotide/genetics, RNA Splicing/genetics, RNA, Messenger/chemistry/genetics, Thymine/metabolism

Relation: info:eu-repo/semantics/altIdentifier/pmid/15235036; https://archive-ouverte.unige.ch/unige:8887; unige:8887

الاتاحة: https://archive-ouverte.unige.ch/unige:8887

المؤلفون: Mas, C., Taske, N., Deutsch, S., Guipponi, M., Thomas, P., Covanis, A., Friis, Mogens Laue, Kjeldsen, Marianne Juel, Pizzolato, G.P., Vilemure, J.G., Buresi, C., Rees, M., Malafosse, A., Gardiner, M., Antonarakis, S.E., Meda, P.

المصدر: Mas , C , Taske , N , Deutsch , S , Guipponi , M , Thomas , P , Covanis , A , Friis , M L , Kjeldsen , M J , Pizzolato , G P , Vilemure , J G , Buresi , C , Rees , M , Malafosse , A , Gardiner , M , Antonarakis , S E & Meda , P 2004 , ' Association of the connexin36 gene with juvenile myoclonic epilepsy. ' , Journal of Medical Genetics , vol. 41 , pp. e93 .

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/eb4bc700-ed9a-11db-821c-000ea68e967b

المؤلفون: Robinson, R., Taske, N., Heils, A., Sander, T., Whitehouse, W., Goutières, F., Aicardi, J., Lehesjoki, A.-E., Friis, M.L., Kjeldsen, M.J., Panayiotopoulos, C., Kennedy, C., Ferrie, C., Rees, M., Gardiner, R.M.

المصدر: Robinson , R , Taske , N , Heils , A , Sander , T , Whitehouse , W , Goutières , F , Aicardi , J , Lehesjoki , A-E , Friis , M L , Kjeldsen , M J , Panayiotopoulos , C , Kennedy , C , Ferrie , C , Rees , M & Gardiner , R M 2002 , ' Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q ' , Epilepsy Research , vol. 48 , pp. 169-179 .

Relation: https://portal.findresearcher.sdu.dk/da/publications/8ce91300-6fcf-11db-81a9-000ea68e967b

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/8ce91300-6fcf-11db-81a9-000ea68e967b

المؤلفون: Robinson, R., Taske, N., Sander, T., Heils, A., Whitehouse, W., Goutieres, F., Aicardi, J., Lehesjoki, A.E., Siren, A., Friis, M.L., Kjeldsen, M.J., Panayiotopoulos, C., Kennedy, C., Ferrie, C., Rees, M., Gardiner, R.M.

Relation: Linkage analysis between childhood absence epilepsy and genes encoding GABAAand GABA Breceptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. Robinson, R. and Taske, N. and Sander, T. and Heils, A. and Whitehouse, W. and Goutieres, F. and Aicardi, J. and Lehesjoki, A.E. and Siren, A. and Friis, M.L. and Kjeldsen, M.J. and Panayiotopoulos, C. and Kennedy, C. and Ferrie, C. and Rees, M. and Gardiner, R.M. Epilepsy Research 48 : 169-179. 1 February 2002

الاتاحة: http://edoc.mdc-berlin.de/6536/
https://edoc.mdc-berlin.de/6536/
https://doi.org/10.1016/S0920-1211(01)00335-7

المؤلفون: Taske, N L, Williamson, M P, Makoff, A, Bate, L, Curtis, D, Kerr, M, Kjeldsen, M J, Pang, K A, Sundqvist, A, Friis, M L, Chadwick, D, Richens, A, Covanis, A, Santos, M, Arzimanoglou, A, Panayiotopoulos, C P, Whitehouse, W P, Rees, M, Gardiner, R M

المصدر: Taske , N L , Williamson , M P , Makoff , A , Bate , L , Curtis , D , Kerr , M , Kjeldsen , M J , Pang , K A , Sundqvist , A , Friis , M L , Chadwick , D , Richens , A , Covanis , A , Santos , M , Arzimanoglou , A , Panayiotopoulos , C P , Whitehouse , W P , Rees , M & Gardiner , R M 2002 , ' Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus ....

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/42d9beb0-2c8c-425a-8dc2-d8f3180e4374
https://doi.org/10.1016/S0920-1211(02)00027-X
http://www.scopus.com/inward/record.url?scp=0036282139&partnerID=8YFLogxK

المؤلفون: Errington G, Athey K, Towner E, Dickinson H, Brussoni M, Hayes M, Millward L, Taske N

المصدر: 25 July 2006

Relation: https://eprints.ncl.ac.uk/12787

الاتاحة: https://eprints.ncl.ac.uk/12787

المؤلفون: Taske, N., Eyre, H., O'Brien, R., Sutherland, G., Denborough, M., Foster, P.

المصدر: http://dx.doi.org/10.1111/j.1432-1033.1995.258_1.x.

مصطلحات موضوعية: Muscle, Skeletal, Chromosomes, Human, Pair 6, Animals, Rabbits, Humans, Carrier Proteins, Muscle Proteins, DNA, Complementary, DNA Primers, In Situ Hybridization, Fluorescence, Chromosome Mapping, Cloning, Molecular, Polymerase Chain Reaction, Species Specificity, Gene Expression, Amino Acid Sequence, Base Sequence, Sequence Homology, Amino Acid, Molecular Weight, Molecular Sequence Data

Relation: The Federation of European Biochemical Societies (FEBS) Journal, 1995; 233(1):258-265; http://hdl.handle.net/2440/7213

الاتاحة: http://hdl.handle.net/2440/7213
https://doi.org/10.1111/j.1432-1033.1995.258_1.x

المؤلفون: Telgmann R, Erik Maronde, Taske N K, Gellersen B

المصدر: Europe PubMed Central

مصطلحات موضوعية: Transcription, Genetic, Cyclic AMP-Dependent Protein Kinase RIalpha Subunit, Relaxin, Cell Differentiation, Cyclic AMP-Dependent Protein Kinases, Prolactin, Enzyme Activation, Isoenzymes, Endometrium, Gene Expression Regulation, Genes, Cyclic AMP-Dependent Protein Kinase RIIbeta Subunit, Cyclic AMP-Dependent Protein Kinase RIIalpha Subunit, Cyclic AMP, Cyclic AMP-Dependent Protein Kinase RIbeta Subunit, Decidua, Humans, Female, RNA, Messenger, Stromal Cells, Promoter Regions, Genetic, Cells, Cultured

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::411b6ddb56dc252966986a51a890cee8
https://pubmed.ncbi.nlm.nih.gov/9048592