Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Tosolini L"'
Autor:
Canton G; gcanton@units.it., Tomic M; a:1:{s:5:'en_US';s:22:'Università di Trieste';}. tomic.marko04@gmail.com., Tosolini L; lctosolini@gmail.com., Di Lenarda L; lucadilenarda@gmail.com., Murena L; lmurena@units.it.
Publikováno v:
Acta bio-medica : Atenei Parmensis [Acta Biomed] 2023 Jun 23; Vol. 94 (S2), pp. e2023118. Date of Electronic Publication: 2023 Jun 23.
Akademický článek
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Autor:
Di Benedetto P; clinic of orthopaedics, University Hospital of Udine. dibenedetto.paolo@aoud.sanita.fvg.it., Mancuso F; Clinica Ortopedica - ASUFC - Udine, Italy. francesco.mancuso@asufc.sanita.fvg.it., Tosolini L; Orthopaedics and Traumatology Unit, Cattinara Hospital - ASUGI - Trieste, Italy. lctosolini@gmail.com., Buttironi MM; Clinica Ortopedica - ASUFC - Udine, Italy. michele.buttironi@gmail.com., Beltrame A; Clinica Ortopedica - ASUFC - Udine, Italy. alessandro.beltrame@asufc.sanita.fvg.it., Causero A; Clinica Ortopedica - ASUFC - Udine, Italy DAME - University of Udine, Italy. araldo.causero@asufc.sanita.fvg.it.
Publikováno v:
Acta bio-medica : Atenei Parmensis [Acta Biomed] 2021 Jul 26; Vol. 92 (S3), pp. e2021026. Date of Electronic Publication: 2021 Jul 26.
Autor:
Elbitar S; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Laboratory of Biochemistry and Molecular Therapeutics, Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon., Renard M; Center for Medical Genetics, Ghent University, Ghent, Belgium., Arnaud P; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Département de Génétique, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Hanna N; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Département de Génétique, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Jacob MP; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Guo DC; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA., Tsutsui K; Institute for Protein Research, Osaka University, Suita, Osaka, Japan., Gross MS; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Kessler K; Centre for Evolution and Cancer, Division of Molecular Pathology, Division of Cancer Therapeutics, The Institute of Cancer Research, London, UK., Tosolini L; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Dattilo V; IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy., Dupont S; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Jonquet J; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Langeois M; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Benarroch L; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Inserm UMRS_974, Centre de recherche en myologie, G.H. Pitié-Salpétrière, APHP, Paris, France., Aubart M; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Service de Neuropédiatrie, Hôpital Necker-Enfants-Malades, APHP, Paris, France., Ghaleb Y; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Laboratory of Biochemistry and Molecular Therapeutics, Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon., Abou Khalil Y; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Laboratory of Biochemistry and Molecular Therapeutics, Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon., Varret M; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., El Khoury P; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Laboratory of Biochemistry and Molecular Therapeutics, Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon., Ho-Tin-Noé B; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Alembik Y; Department of Clinical Genetic, Hôpitaux Universitaires de Strasbourg, Strasbourg, France., Gaertner S; Department of Hypertension, Vascular Diseases and Pharmacology, University of Strasbourg, Strasbourg, France., Isidor B; Service de Génétique Médicale, Hôpital Hôtel-Dieu, Centre Hospitalier Universitaire de Nantes, Nantes, France., Gouya L; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Milleron O; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Sekiguchi K; Institute for Protein Research, Osaka University, Suita, Osaka, Japan., Milewicz D; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA., De Backer J; Center for Medical Genetics, Ghent University, Ghent, Belgium., Le Goff C; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Michel JB; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France., Jondeau G; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France.; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France., Sakai LY; Shriners Hospital for Children, Molecular & Medical Genetics and Biochemistry & Molecular Biology, Oregon Health & Science University, Portland, OR, USA., Boileau C; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France. catherine.boileau@inserm.fr.; Département de Génétique, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France. catherine.boileau@inserm.fr.; Hospitalo-Universitaire Xavier Bichat, APHP, Centre de Référence Maladies Rares, Syndrome de Marfan et pathologies apparentées, Paris, France. catherine.boileau@inserm.fr., Abifadel M; Laboratory for Vascular Translational Science, INSERM U1148, Université de Paris, Centre Hospitalo-Universitaire Xavier Bichat, APHP, Paris, France. marianne.abi-fadel@inserm.fr.; Laboratory of Biochemistry and Molecular Therapeutics, Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon. marianne.abi-fadel@inserm.fr.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jan; Vol. 23 (1), pp. 111-122. Date of Electronic Publication: 2020 Aug 28.
Autor:
Goncharova, Irina A.1 (AUTHOR) irina.goncharova@medgenetics.ru, Shipulina, Sofia A.1 (AUTHOR) sofia.beliaeva@medgenetics.ru, Sleptcov, Aleksei A.1 (AUTHOR) alexei.sleptcov@medgenetics.ru, Zarubin, Aleksei A.1 (AUTHOR) aleksei.zarubin@medgenetics.ru, Valiakhmetov, Nail R.1 (AUTHOR) nail.valiakhmetov@medgenetics.ru, Panfilov, Dmitry S.2 (AUTHOR) pand2006@yandex.ru, Lelik, Evgeniya V.2 (AUTHOR) eva00@list.ru, Saushkin, Viktor V.2 (AUTHOR) saushkin.vv@ya.ru, Kozlov, Boris N.2 (AUTHOR) bnkozlov@yandex.ru, Nazarenko, Ludmila P.1 (AUTHOR) ludmila.nazarenko@medgenetics.ru, Nazarenko, Maria S.1 (AUTHOR) maria.nazarenko@medgenetics.ru
Publikováno v:
International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8315. 13p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Yee, Jae-Sung1 (AUTHOR) osjsyee@gmail.com, Choi, Jin-Kwan2 (AUTHOR) omydamy@naver.com, Kim, Ki-Tae2 (AUTHOR) kimkt8399@naver.com, Lee, Ho-Won3 (AUTHOR) ehw80@hallym.or.kr, Lee, Yong-Beom2 (AUTHOR) drleeyb@naver.com
Publikováno v:
Journal of Clinical Medicine. Apr2024, Vol. 13 Issue 8, p2276. 14p.
Autor:
Shin, Kyun-Ho1 (AUTHOR) kyunho.shin@gmail.com, Jang, Il-Tae2 (AUTHOR) nanoori_research@naver.com, Han, Seung-Beom3 (AUTHOR) oshan@korea.ac.kr
Publikováno v:
Journal of Clinical Medicine. Feb2024, Vol. 13 Issue 4, p1052. 17p.
Autor:
Fularski, Piotr1 (AUTHOR), Hajdys, Joanna1 (AUTHOR), Majchrowicz, Gabriela1 (AUTHOR), Stabrawa, Magdalena1 (AUTHOR), Młynarska, Ewelina1 (AUTHOR) emmlynarska@gmail.com, Rysz, Jacek2 (AUTHOR), Franczyk, Beata1 (AUTHOR)
Publikováno v:
International Journal of Molecular Sciences. Feb2024, Vol. 25 Issue 3, p1637. 25p.