المؤلفون: Coste, T., Aloui, C., Petit, F., Moutton, S., Devisme, L., Wells, C., Leboucq, N., Verpillat, P., Yvert, M., Rivier, Francois, Tournier-Lasserve, E.

المساهمون: Physiologie & médecine expérimentale du Cœur et des Muscles U 1046 (PhyMedExp), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier)

المصدر: ISSN: 0960-7692.

مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

الاتاحة: https://hal.science/hal-03750977
https://hal.science/hal-03750977v1/document
https://hal.science/hal-03750977v1/file/2022%20%20Coste%20%20%20et%20al.,%20Rare%20metabolic.pdf
https://doi.org/10.1002/uog.26046

المؤلفون: Tinelli F., Nava S., Arioli F., Bedini G., Scelzo E., Lisini D., Faragò G., Gioppo A., Ciceri E. F., Acerbi F., Ferroli P., Vetrano I. G., Esposito S., Saletti V., Pantaleoni C., Zibordi F., Nardocci N., Zedde M. L., Pezzini A., Lazzaro V. D., Capone F., Dell'acqua M. L., Vajkoczy P., Tournier-Lasserve E., Parati E. A., Bersano A., Gatti L.

المساهمون: Tinelli, F, Nava, S, Arioli, F, Bedini, G, Scelzo, E, Lisini, D, Faragò, G, Gioppo, A, Ciceri, E, Acerbi, F, Ferroli, P, Vetrano, I, Esposito, S, Saletti, V, Pantaleoni, C, Zibordi, F, Nardocci, N, Zedde, M, Pezzini, A, Lazzaro, V, Capone, F, Dell'Acqua, M, Vajkoczy, P, Tournier-Lasserve, E, Parati, E, Bersano, A, Gatti, L

مصطلحات موضوعية: Endothelial progenitor cell, Moyamoya angiopathy, Neovascularization, RNF213

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/32796702; info:eu-repo/semantics/altIdentifier/wos/WOS:000565157000001; volume:21; issue:16; firstpage:1; lastpage:22; numberofpages:22; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/10281/510659; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089486186

الاتاحة: https://hdl.handle.net/10281/510659
https://doi.org/10.3390/ijms21165763

المؤلفون: Mertens, R., Graupera, M., Gerhardt, H., Bersano, A., Tournier-Lasserve, E., Mensah, M. A., Mundlos, S., Vajkoczy, Peter

المصدر: http://lobid.org/resources/99370675589506441#!, 13(1):25-45.

مصطلحات موضوعية: Stroke, Adenosine Triphosphatases/genetics [MeSH], Genetics, Humans [MeSH], RNF 213, Review Article, Moyamoya Disease/genetics [MeSH], Moyamoya disease, Ubiquitin-Protein Ligases/genetics [MeSH], 17q25, Genetic Predisposition to Disease/genetics [MeSH], Moyamoya Disease/diagnostic imaging [MeSH]

Relation: https://repository.publisso.de/resource/frl:6444154; https://doi.org/10.1007/s12975-021-00940-2; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766392/

الاتاحة: https://repository.publisso.de/resource/frl:6444154
https://doi.org/10.1007/s12975-021-00940-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766392/

المؤلفون: MANCUSO, M., ARNOLD, M., BERSANO, A., BURLINA, A., CHABRIAT, H., DEBETTE, Stephanie, ENZINGER, C., FEDERICO, A., FILLA, A., FINSTERER, J., HUNT, D., LESNIK OBERSTEIN, S., TOURNIER-LASSERVE, E., MARKUS, H. S.

مصطلحات موضوعية: VINTAGE, Sciences du Vivant [q-bio]/Santé publique et épidémiologie

Relation: 1468-1331 (Electronic) 1351-5101 (Linking); https://oskar-bordeaux.fr/handle/20.500.12278/26137

الاتاحة: https://oskar-bordeaux.fr/handle/20.500.12278/26137
https://hdl.handle.net/20.500.12278/26137
https://doi.org/10.1111/ene.14183

المؤلفون: Grangeon, L., Charbonnier, C., Zarea, A., Rousseau, S., Rovelet-Lecrux, A., Bendetowicz, D., Lemaitre, M., Malrain, C., Quillard-Muraine, M., Cassinari, K., Maltete, D., Pariente, J., Moreaud, O., Magnin, E., Cretin, B., Mackowiak, Marie-Anne, Sillaire, A. R., Vercelletto, M., Dionet, E., Felician, O., Rod-Olivieri, P., Thomas-Antérion, C., Godeneche, G., Sauvée, M., Cartz-Piver, L., Le Ber, I., Chauvire, V., Jonveaux, T., Balageas, A. C., Laquerriere, A., Duyckaerts, C., Vital, A., De Paula, A. M., Meyronet, D., Guyant-Marechal, L., Hannequin, D., Tournier-Lasserve, E., Campion, D., Nicolas, G., Wallon, D.

المساهمون: Université de Lille, Inserm, CHU Lille, Lille Neurosciences & Cognition (LilNCog) - U 1172

مصطلحات موضوعية: Cerebral amyloid angiopathy, Alzheimer disease, APP duplication, Cerebral MRI, Autosomal dominant

Relation: Alzheimers Res Ther; http://hdl.handle.net/20.500.12210/110865

الاتاحة: https://hdl.handle.net/20.500.12210/110865

المؤلفون: Lecca, M., Pehlivan, D., Suñer, D.H., Weiss, K., Coste, T., Zweier, M., Oktay, Y., Danial-Farran, N., Rosti, V., Bonasoni, M.P., Malara, A., Contrò, G., Zuntini, R., Pollazzon, M., Pascarella, R., Neri, A., Fusco, C., Marafi, D., Mitani, T., Posey, J.E., Bayramoglu, S.E., Gezdirici, A., Hernandez-Rodriguez, J., Cladera, E.A., Miravet, E., Roldan-Busto, J., Ruiz, M.A., Bauzá, C.V., Ben-Sira, L., Sigaudy, S., Begemann, A., Unger, S., Güngör, S., Hiz, S., Sonmezler, E., Zehavi, Y., Jerdev, M., Balduini, A., Zuffardi, O., Horvath, R., Lochmüller, H., Rauch, A., Garavelli, L., Tournier-Lasserve, E., Spiegel, R., Lupski, J.R., Errichiello, E.

المصدر: American journal of human genetics, vol. 110, no. 4, pp. 681-690

مصطلحات موضوعية: Animals, Mice, Alleles, Brain Diseases/genetics, Cell Adhesion Molecules/genetics, Endothelial Cells/metabolism, Intracranial Hemorrhages/genetics, Nervous System Malformations/genetics, Neurodevelopmental Disorders/genetics, Tight Junctions/genetics, Humans, ESAM, blood-brain barrier, epilepsy, exome sequencing, global developmental delay, intellectual disability, intracranial hemorrhage, neurodevelopmental disorders, pregnancy loss, retinopathy, tight junctions

Relation: info:eu-repo/semantics/altIdentifier/pmid/36996813; info:eu-repo/semantics/altIdentifier/eissn/1537-6605; https://serval.unil.ch/notice/serval:BIB_261A60E3FC55

الاتاحة: https://serval.unil.ch/notice/serval:BIB_261A60E3FC55
https://doi.org/10.1016/j.ajhg.2023.03.005

المؤلفون: Coste, T., Aloui, C., Petit, F., Moutton, S., Devisme, L., Wells, C. F., Leboucq, N., Verpillat, P., Yvert, M., Rivier, F., Tournier‐Lasserve, E., Tournier-Lasserve, E

المصدر: Ultrasound in Obstetrics & Gynecology; Dec2022, Vol. 60 Issue 6, p805-811, 7p

مصطلحات موضوعية: FETAL brain, METABOLIC disorders, CEREBRAL hemorrhage, ABORTION, AGENESIS of corpus callosum, FETAL death, POSTMORTEM changes

المؤلفون: Otten, C., Knox, J., Boulday, G., Eymery, M., Haniszewski, M., Neuenschwander, M., Radetzki, S., Vogt, I., Hähn, K., De Luca, C., Cardoso, C., Hamad, S., Igual Gil, C., Roy, P., Albiges‐Rizo, C., Faurobert, E., von Kries, J.P., Campillos, M., Tournier‐Lasserve, E., Derry, W.B., Abdelilah-Seyfried, S.

مصطلحات موضوعية: Technology Platforms

وصف الملف: application/pdf; other

Relation: http://edoc.mdc-berlin.de/17761/1/17761oa.pdf; http://edoc.mdc-berlin.de/17761/2/17761suppl.zip; Systematic pharmacological screens uncover novel pathways involved in cerebral cavernous malformations. Otten, C. and Knox, J. and Boulday, G. and Eymery, M. and Haniszewski, M. and Neuenschwander, M. and Radetzki, S. and Vogt, I. and Hähn, K. and De Luca, C. and Cardoso, C. and Hamad, S. and Igual Gil, C. and Roy, P. and Albiges‐Rizo, C. and Faurobert, E. and von Kries, J.P. and Campillos, M. and Tournier‐Lasserve, E. and Derry, W.B. and Abdelilah-Seyfried, S. EMBO Molecular Medicine 10 (10): e9155. 1 October 2018

الاتاحة: http://edoc.mdc-berlin.de/17761/
https://edoc.mdc-berlin.de/17761/
http://edoc.mdc-berlin.de/17761/1/17761oa.pdf
http://edoc.mdc-berlin.de/17761/2/17761suppl.zip
https://doi.org/10.15252/emmm.201809155

المؤلفون: Debette, S., Strbian, D., Wardlaw, J. M., van der Worp, H. B., Rinkel, G. J.E., Caso, V., Dichgans, M., Tournier-Lasserve, E., Grefkes, C., Kelly, P. J., Muir, K., Berge, E., Trégouët, D. A., Roffe, C., Brainin, M., Beck, J., Steiner, T., de Lau, L. M., Jouvent, E., Veltkamp, R., Baron, J. C., Nedeltchev, K., Bath, P. M., Quinn, T. J., Richard, E., Ziemann, U., Liesz, A., Ntaios, G., Iadecola, C., Lees, K. R., Christensen, H. Krarup, van Veluw, S. J., Endres, M., Anderson, C. S., Molina, C. A., Düring, M., Dufouil, C., Ostergaard, L., Samani, N. J., Fischer, U., de Leeuw, F. E., Norrving, B., Biessels, G. J., Cordonnier, C., Mas, J. L., Mattle, H.

المصدر: Debette , S , Strbian , D , Wardlaw , J M , van der Worp , H B , Rinkel , G J E , Caso , V , Dichgans , M , Tournier-Lasserve , E , Grefkes , C , Kelly , P J , Muir , K , Berge , E , Trégouët , D A , Roffe , C , Brainin , M , Beck , J , Steiner , T , de Lau , L M , Jouvent , E , Veltkamp , R , Baron , J C , Nedeltchev , K , ....

مصطلحات موضوعية: genomics, intracerebral hemorrhage, small vessel disease, Stroke, stroke recovery, stroke therapy, thrombectomy, vascular cognitive impairment

الاتاحة: https://curis.ku.dk/portal/da/publications/fourth-european-stroke-science-workshop(992d3715-cf1e-4ab9-84f2-e9839661d29c).html
https://doi.org/10.1177/2396987318774443
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453207/pdf/10.1177_2396987318774443.pdf

المؤلفون: Guey S, Tournier-Lasserve E, Hervé D, Kossorotoff M

المصدر: The Application of Clinical Genetics, Vol 2015, Iss default, Pp 49-68 (2015)

مصطلحات موضوعية: Medicine (General), R5-920, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.dovepress.com/moyamoya-disease-and-syndromes-from-genetics-to-clinical-management-peer-reviewed-article-TACG; https://doaj.org/toc/1178-704X

URL الوصول: https://doaj.org/article/80b9dcaa300c4756afde99b5c7109bf3

المؤلفون: GARACI, FRANCESCO, MARZIALI, SIMONE, PASQUARELLI, ROBERTO, SANGIUOLO, FEDERICA CARLA, FLORIS, ROBERTO, NOVELLI, GIUSEPPE, Marsili, L, Riant, F, Cécillon, M, Tournier Lasserve, E, Brancati, F.

المساهمون: Garaci, F, Marsili, L, Riant, F, Marziali, S, Cécillon, M, Pasquarelli, R, Sangiuolo, Fc, Floris, R, Novelli, G, Tournier Lasserve, E, Brancati, F

مصطلحات موضوعية: Magnetic resonance imaging, PDCD10, cerebral cavernous malformation, multiple meningioma, Settore MED/03 - GENETICA MEDICA, Settore MED/37 - NEURORADIOLOGIA, Settore MED/36 - DIAGNOSTICA PER IMMAGINI E RADIOTERAPIA

Relation: info:eu-repo/semantics/altIdentifier/pmid/26246098; info:eu-repo/semantics/altIdentifier/wos/WOS:000359430200010; volume:28; issue:3; firstpage:289; lastpage:293; numberofpages:5; journal:THE NEURORADIOLOGY JOURNAL; http://hdl.handle.net/2108/119706; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84945352521

الاتاحة: http://hdl.handle.net/2108/119706
https://doi.org/10.1177/1971400915591688

المؤلفون: Coste, T., Vincent, Catherine, Stichelbout, M., Devisme, Louise, Gelot, A., Deryabin, I., Pelluard, F., Aloui, C., Leutenegger, A. L., Jouannic, J. M., Héron, D., Gould, D. B., Tournier-Lasserve, E.

المساهمون: Université de Lille, CHU Lille, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364

Relation: Prenat Diagn; http://hdl.handle.net/20.500.12210/115580

الاتاحة: https://hdl.handle.net/20.500.12210/115580

المؤلفون: Li, A., Cordoliani, F., Charvet, E., Jachiet, M., Vignon-Pennamen, M.D., Bouaziz, J.D., Bagot, M., Chasset, F., Ghitu, A., Derache, N., Buffon-Porcher, F., Tournier-Lasserve, E., Guey, S., Mahévas, T.

المصدر: Annales de Dermatologie et de Vénéréologie - FMC ; volume 2, issue 8, page A272 ; ISSN 2667-0623

الاتاحة: http://dx.doi.org/10.1016/j.fander.2022.09.441
https://api.elsevier.com/content/article/PII:S2667062322007176?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2667062322007176?httpAccept=text/plain

المؤلفون: Debette, S, Goeggel Simonetti, B, Schilling, S, Martin, Jj, Kloss, M, Sarikaya, H, Hausser, I, Engelter, S, Metso, Tm, Thijs, V, Touzé, E, Paolucci, S, Costa, P, Sessa, M, Samson, Y, Béjot, Y, Altintas, A, Metso, Aj, Hervé, D, Lichy, C, Jung, S, Fischer, U, Lamy, C, Grau, A, Chabriat, H, Caso, V, Lyrer, Pa, Stapf, C, Tatlisumak, T, Brandt, T, Tournier Lasserve, E, Germain, Dp, Frank, M, Baumgartner, Rw, Grond Ginsbach, C, Bousser, Mg, Leys, D, Dallongeville, J, Bersano, A, Arnold, M., PEZZINI, Alessandro

المساهمون: Debette S, Goeggel Simonetti B, Schilling S, Martin Jj, Kloss M, Sarikaya H, Hausser I, Engelter S, Metso Tm, Pezzini Alessandro, Thijs V, Touzé, E, Paolucci S, Costa P, Sessa M, Samson Y, Béjot Y, Altintas A, Metso Aj, Hervé, D, Lichy C, Jung S, Fischer U, Lamy C, Grau A, Chabriat H, Caso V, Lyrer Pa, Stapf C, Tatlisumak T, Brandt T, Tournier Lasserve E, Germain Dp, Frank M, Baumgartner Rw, Grond Ginsbach C, Bousser Mg, Leys D, Dallongeville J, Bersano A, Arnold M.

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000345535700011; volume:83; issue:22; firstpage:2023; lastpage:2031; numberofpages:9; journal:NEUROLOGY; http://hdl.handle.net/11379/389710; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84961288150

الاتاحة: http://hdl.handle.net/11379/389710

المؤلفون: Bersano, Anna, Guey, Stephanie, Bedini, Gloria, Nava, Sara, Hervé, Dominique, Vajkoczy, Peter, Tatlisumak, Turgut, Sareela, Marika, van der Zwan, Albert, Klijn, Catharina J M, Braun, Kees P J, Kronenburg, Annick, Acerbi, Francesco, Brown, Martin M, Calviere, Lionel, Cordonnier, Charlotte, Henon, Hilde, Thines, Laurent, Khan, Nadia, Czabanka, M, Kraemer, Markus, Simister, Robert, Prontera, Paolo, Tournier-Lasserve, E, Parati, Eugenio

المصدر: Bersano, Anna; Guey, Stephanie; Bedini, Gloria; Nava, Sara; Hervé, Dominique; Vajkoczy, Peter; Tatlisumak, Turgut; Sareela, Marika; van der Zwan, Albert; Klijn, Catharina J M; Braun, Kees P J; Kronenburg, Annick; Acerbi, Francesco; Brown, Martin M; Calviere, Lionel; Cordonnier, Charlotte; Henon, Hilde; Thines, Laurent; Khan, Nadia; Czabanka, M; Kraemer, Markus; Simister, Robert; Prontera, Paolo; Tournier-Lasserve, E; Parati, Eugenio (2016). Research progresses in understanding the pathophysiology of moyamoya disease. Cerebrovascular Diseases, 41(3-4):105-118.

مصطلحات موضوعية: Clinic for Surgery, 610 Medicine & health

وصف الملف: application/pdf

Relation: https://www.zora.uzh.ch/id/eprint/134389/1/ZORA134389.pdf; info:pmid/26756907; urn:issn:1015-9770

الاتاحة: https://www.zora.uzh.ch/id/eprint/134389/
https://www.zora.uzh.ch/id/eprint/134389/1/ZORA134389.pdf
https://doi.org/10.1159/000442298

المؤلفون: Tinelli, F, Nava, S, Arioli, F, Bedini, G, Scelzo, E, Lisini, D, Faragò, G, Gioppo, A, Ciceri, E, Acerbi, F, Ferroli, P, Vetrano, I, Esposito, S, Saletti, V, Pantaleoni, C, Zibordi, F, Nardocci, N, Zedde, M, Pezzini, A, Lazzaro, V, Capone, F, Dell'Acqua, M, Vajkoczy, P, Tournier-Lasserve, E, Parati, E, Bersano, A, Gatti, L, Tinelli F., Nava S., Arioli F., Bedini G., Scelzo E., Lisini D., Faragò G., Gioppo A., Ciceri E. F., Acerbi F., Ferroli P., Vetrano I. G., Esposito S., Saletti V., Pantaleoni C., Zibordi F., Nardocci N., Zedde M. L., Pezzini A., Lazzaro V. D., Capone F., Dell'acqua M. L., Vajkoczy P., Tournier-Lasserve E., Parati E. A., Bersano A., Gatti L.

مصطلحات الفهرس: Endothelial progenitor cell, Moyamoya angiopathy, Neovascularization, RNF213, info:eu-repo/semantics/article

URL: https://hdl.handle.net/10281/510659
info:eu-repo/semantics/altIdentifier/pmid/32796702
info:eu-repo/semantics/altIdentifier/wos/WOS:000565157000001
volume:21
issue:16
firstpage:1
lastpage:22
numberofpages:22
journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

المؤلفون: Guey, S., Oberstein, S.A.J.L., Tournier-Lasserve, E., Chabriat, H.

المصدر: Stroke

مصطلحات موضوعية: CADASIL, cerebral small vessel diseases, hemorrhagic stroke, ischemic stroke, medical genetics

Relation: lumc-id: 122461072; https://hdl.handle.net/1887/3256859

الاتاحة: https://hdl.handle.net/1887/3256859
https://doi.org/10.1161/STROKEAHA.121.032620

المؤلفون: Maurice, P., Guilbaud, L., Garel, J., Mine, M., Dugas, A., Friszer, S., Maisonneuve, E., Moutard, M.‐L., Coste, T., Héron, D., Tournier‐Lasserve, E., Garel, C., Jouannic, J.‐M.

المصدر: Ultrasound in Obstetrics & Gynecology ; volume 57, issue 5, page 783-789 ; ISSN 0960-7692 1469-0705

الاتاحة: http://dx.doi.org/10.1002/uog.22106
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fuog.22106
https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.22106
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/uog.22106
https://obgyn.onlinelibrary.wiley.com/doi/pdf/10.1002/uog.22106

المؤلفون: Feldmeyer, L, Baumann-Vogel, H, Tournier-Lasserve, E, Riant, F, Jung, H H, French, L E, Kamarashev, J

المصدر: Feldmeyer, L; Baumann-Vogel, H; Tournier-Lasserve, E; Riant, F; Jung, H H; French, L E; Kamarashev, J (2014). Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation. European Journal of Dermatology, 24(2):255-257.

مصطلحات موضوعية: Clinic for Neurology, Dermatology Clinic, 610 Medicine & health

وصف الملف: application/pdf

Relation: https://www.zora.uzh.ch/id/eprint/100460/1/KRIT1_mutation120427.pdf; info:pmid/24721395; urn:issn:1167-1122

الاتاحة: https://www.zora.uzh.ch/id/eprint/100460/
https://www.zora.uzh.ch/id/eprint/100460/1/KRIT1_mutation120427.pdf
https://doi.org/10.1684/ejd.2014.2280

المؤلفون: Riant, F., Bergametti, F., Fournier, H.-D., Chapon, F., Michalak-Provost, S., Cecillon, M., Lejeune, P., Hosseini, H., Choe, C., Orth, M., Bernreuther, C., Boulday, G., Denier, C., Labauge, P., Tournier-Lasserve, E.

المصدر: Molecular Syndromology ; volume 4, issue 4, page 165-172 ; ISSN 1661-8769 1661-8777

الاتاحة: http://dx.doi.org/10.1159/000350042
https://www.karger.com/Article/Pdf/350042