المؤلفون: Rice G. I., Park S., Gavazzi F., Adang L. A., Ayuk L. A., Van Eyck L., Seabra L., Barrea C., Battini R., Belot A., Berg S., Billette de Villemeur T., Bley A. E., Blumkin L., Boespflug-Tanguy O., Briggs T. A., Brimble E., Dale R. C., Darin N., Debray F. -G., De Giorgis V., Denecke J., Doummar D., Drake af Hagelsrum G., Eleftheriou D., Estienne M., Fazzi E., Feillet F., Galli J., Hartog N., Harvengt J., Heron B., Heron D., Kelly D. A., Lev D., Levrat V., Livingston J. H., Marti I., Mignot C., Mochel F., Nougues M. -C., Oppermann I., Perez-Duenas B., Popp B., Rodero M. P., Rodriguez D., Saletti V., Sharpe C., Tonduti D., Vadlamani G., Van Haren K., Tomas Vila M., Vogt J., Wassmer E., Wiedemann A., Wilson C. J., Zerem A., Zweier C., Zuberi S. M., Orcesi S., Vanderver A. L., Hur S., Crow Y. J.

المساهمون: Rice, G. I., Park, S., Gavazzi, F., Adang, L. A., Ayuk, L. A., Van Eyck, L., Seabra, L., Barrea, C., Battini, R., Belot, A., Berg, S., Billette de Villemeur, T., Bley, A. E., Blumkin, L., Boespflug-Tanguy, O., Briggs, T. A., Brimble, E., Dale, R. C., Darin, N., Debray, F. -G., De Giorgis, V., Denecke, J., Doummar, D., Drake af Hagelsrum, G., Eleftheriou, D., Estienne, M., Fazzi, E., Feillet, F., Galli, J., Hartog, N., Harvengt, J., Heron, B., Heron, D., Kelly, D. A., Lev, D., Levrat, V., Livingston, J. H., Marti, I., Mignot, C., Mochel, F., Nougues, M. -C., Oppermann, I., Perez-Duenas, B., Popp, B., Rodero, M. P., Rodriguez, D., Saletti, V., Sharpe, C., Tonduti, D., Vadlamani, G., Van Haren, K., Tomas Vila, M., Vogt, J., Wassmer, E., Wiedemann, A., Wilson, C. J., Zerem, A., Zweier, C., Zuberi, S. M., Orcesi, S., Vanderver, A. L., Hur, S., Crow, Y. J.

مصطلحات موضوعية: Aicardi–Goutières syndrome, IFIH1, MDA5, Singleton Merten syndrome, Type I interferonopathy

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31898846; info:eu-repo/semantics/altIdentifier/wos/WOS:000506940000001; volume:41; issue:4; firstpage:837; lastpage:849; numberofpages:13; journal:HUMAN MUTATION; http://hdl.handle.net/11568/1071295Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85078038174

الإتاحة: https://doi.org/10.1002/humu.23975Test
http://hdl.handle.net/11568/1071295Test

المؤلفون: Ho, PP, Kanter, JL, Johnson, AM, Srinagesh, HK, Chang, EJ, Purdy, TM, van Haren, K, Wikoff, WR, Kind, T, Khademi, M, Matloff, LY, Narayana, S, Hur, EM, Lindstrom, TM, He, ZG, Fiehn, O, Olsson, T, Han, XL, Han, MH, Steinman, L, Robinson, WH

المصدر: Science translational medicine. 4(137)

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:124778329Test

المؤلفون: Rice, G, Park, S, Gavazzi, F, Adang, LA, Ayuk, LA, Van Eyck, L, Seabra, L, Barrea, C, Battini, R, Belot, A, Berg, S, de Villemeur, TB, Bley, AE, Blumkin, L, Boespflug-Tanguy, O, Briggs, TA, Brimble, E, Dale, RC, Darin, N, Debray, F-G, De Giorgis, V, Denecke, J, Doummar, D, af Hagelsrum, GD, Eleftheriou, D, Estienne, M, Fazzi, E, Feillet, F, Galli, J, Hartog, N, Harvengt, J, Heron, B, Heron, D, Kelly, DA, Lev, D, Levrat, V, Livingston, JH, Marti, I, Mignot, C, Mochel, F, Nougues, M-C, Oppermann, I, Perez-Duenas, B, Popp, B, Rodero, MP, Rodriguez, D, Saletti, V, Sharpe, C, Tonduti, D, Vadlamani, G, Van Haren, K, Vila, MT, Vogt, J, Wassmer, E, Wiedemann, A, Wilson, CJ, Zerem, A, Zweier, C, Zuberi, SM, Orcesi, S, Vanderver, AL, Hur, S, Crow, YJ

المصدر: Human Mutation (2020) (In press).

مصطلحات موضوعية: Aicardi–Goutières syndrome, IFIH1, MDA5, Singleton Merten syndrome, Type I interferonopathy

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10090388/1/Rice_et_al-2020-Human_Mutation.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10090388Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10090388/1/Rice_et_al-2020-Human_Mutation.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10090388Test/

المؤلفون: Armangue T, Orsini JJ, Takanohashi A, Gavazzi F, Conant A, Ulrick N, Morrissey MA, Nahhas N, Helman G, Gordish-Dressman H, Orcesi S, Tonduti D, Stutterd C, van Haren K, Toro C, Iglesias AD, van der Knaap MS, Goldbach Mansky R, Moser AB, Jones RO, Vanderver A.

المساهمون: Armangue, T, Orsini, Jj, Takanohashi, A, Gavazzi, F, Conant, A, Ulrick, N, Morrissey, Ma, Nahhas, N, Helman, G, Gordish-Dressman, H, Orcesi, S, Tonduti, D, Stutterd, C, van Haren, K, Toro, C, Iglesias, Ad, van der Knaap, M, Goldbach Mansky, R, Moser, Ab, Jones, Ro, Vanderver, A.

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28739201; info:eu-repo/semantics/altIdentifier/wos/WOS:000418395100018; volume:122; issue:3; firstpage:134; lastpage:139; numberofpages:6; journal:MOLECULAR GENETICS AND METABOLISM; http://hdl.handle.net/11571/1359772Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85025116578; https://www.sciencedirect.com/science/article/pii/S1096719217303694?via=ihubTest

الإتاحة: https://doi.org/10.1016/j.ymgme.2017.07.006Test
http://hdl.handle.net/11571/1359772Test
https://www.sciencedirect.com/science/article/pii/S1096719217303694?via=ihubTest

المؤلفون: Helman, G., van Haren, K., Bonkowsky, J.L., Bernard, G., Pizzino, A., Braverman, N., Suhr, D., Patterson, M.C., Fatemi, S.A., Leonard, J., van der Knaap, M.S., Back, S.A., Damiani, S., Goldman, S.A., Takanohashi, A., Petryniak, M., Rowitch, D., Messing, A., Wrabetz, L., Schiffmann, R., Eichler, F., Escolar, M.L., Vanderver, A.

المصدر: Helman , G , van Haren , K , Bonkowsky , J L , Bernard , G , Pizzino , A , Braverman , N , Suhr , D , Patterson , M C , Fatemi , S A , Leonard , J , van der Knaap , M S , Back , S A , Damiani , S , Goldman , S A , Takanohashi , A , Petryniak , M , Rowitch , D , Messing , A , Wrabetz , L , Schiffmann , R , Eichler , F , Escolar , M L & Vanderver ....

العلاقة: https://research.vumc.nl/en/publications/24cd9494-76eb-43f4-8b72-95bd62ca3a8fTest

الإتاحة: https://doi.org/10.1016/j.ymgme.2015.01.014Test
https://research.vumc.nl/en/publications/24cd9494-76eb-43f4-8b72-95bd62ca3a8fTest

المؤلفون: Singhal, N., Van Haren, K., Wu, Y.

المصدر: Neurology ; volume 78, issue Meeting Abstracts 1, page P01.236-P01.236 ; ISSN 0028-3878 1526-632X

الإتاحة: https://doi.org/10.1212/wnl.78.1_meetingabstracts.p01.236Test

المؤلفون: Singhal, N., Van Haren, K., Wu, Y.

المصدر: Neurology ; volume 78, issue Meeting Abstracts 1, page IN10-1.008-IN10-1.008 ; ISSN 0028-3878 1526-632X

الإتاحة: https://doi.org/10.1212/wnl.78.1_meetingabstracts.in10-1.008Test

المؤلفون: Vlahovic, L., Lock, C.B., Han, M.H., Van Haren, K., Sampson, J.B.

المصدر: Multiple Sclerosis & Related Disorders; Sep2021, Vol. 54, pN.PAG-N.PAG, 1p

المؤلفون: Van Haren K

المصدر: Alive: Canada's Natural Health & Wellness Magazine; Sep2009, Issue 323, p83-85, 3p

المؤلفون: Van Haren K

المصدر: Alive: Canada's Natural Health & Wellness Magazine; Jul2009, Issue 321, p45-45, 1p

مصطلحات موضوعية: MUSCLE contraction, MUSCLES, PAIN, PELVIC floor, SEXUAL excitement, SEXUAL intercourse