WISCHMEIJER, TITIA ANITA
WISCHMEIJER, TITIA ANITA
Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role
2017 Tortora, Giada; Anita, Wischmeijer; Berretta, Paolo; Alfonsi, Jacopo; Di Marco, Luca; Barbieri, Andrea; Marconi, Caterina; Isidori, Federica; Rossi, Cesare; Leone, Ornella; Di Bartolomeo, Roberto; Seri, Marco; Pacini, Davide
Diagnostic Accuracy of Aortic Root Cross-sectional Area/Height Ratio in Children and Young Adults with Marfan and Loeys-Dietz Syndrome
2016 Mariucci, E; Donti, A; Guidarini, M; Oppido, G; Angeli, E; Lovato, L; Wischmeijer, A; Finlay, M; Gargiulo, Gd; Picchio, Fm; Bonvicini, M.
Progressione della dilatazione aortica nel paziente pediatrico con sindrome di Marfan in terapia medica con losartan - Aortic root dilatation rate in pediatric patients with Marfan syndrome treated with losartan
2015 Mariucci, Elisabetta; Guidarini, Marta; Donti, Andrea; Lovato, Luigi; Wischmeijer, Anita; Angeli, Emanuela; Gargiulo, Gaetano D; Picchio, Fernando M; Bonvicini, Marco
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant.
2015 Graziano, C; Wischmeijer, TITIA ANITA; Pippucci, Tommaso; Fusco, C; Diquigiovanni, Chiara; Nõukas, M; Sauk, M; Kurg, A; Rivieri, F; Blau, N; Hoffmann, Gf; Chaubey, A; Schwartz, Ce; Romeo, Giovanni; Bonora, Elena; Garavelli, L; Seri, Marco
Thoracic Aortic Aneurysm in Infancy in Aneurysms-Osteoarthritis Syndrome Due to a Novel SMAD3 Mutation: Further Delineation of the Phenotype
2013 Wischmeijer, A.; Van Laer, L.; Tortora, G.; Bolar, N.A.; Van Camp, G.; Fransen, E.; Peeters, N.; di Bartolomeo, R.; Pacini, D.; Gargiulo, G.; Turci, S.; Bonvicini, M.; Mariucci, E.; Lovato, L.; Brusori, S.; Ritelli, M.; Colombi, M.; Garavelli, L.; Seri, M.; Loeys, B.L.
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
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Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role | Tortora, Giada; Anita, Wischmeijer; Berretta, Paolo; Alfonsi, Jacopo; Di Marco, Luca; Barbieri, A...ndrea; Marconi, Caterina; Isidori, Federica; Rossi, Cesare; Leone, Ornella; Di Bartolomeo, Roberto; Seri, Marco; Pacini, Davide | 2017-01-01 | INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY | - | 1.01 Articolo in rivista | - |
Diagnostic Accuracy of Aortic Root Cross-sectional Area/Height Ratio in Children and Young Adults with Marfan and Loeys-Dietz Syndrome | Mariucci, E; Donti, A; Guidarini, M; Oppido, G; Angeli, E; Lovato, L; Wischmeijer, A; Finlay, M; ...Gargiulo, Gd; Picchio, Fm; Bonvicini, M. | 2016-01-01 | CONGENITAL HEART DISEASE | - | 1.01 Articolo in rivista | - |
Progressione della dilatazione aortica nel paziente pediatrico con sindrome di Marfan in terapia medica con losartan - Aortic root dilatation rate in pediatric patients with Marfan syndrome treated with losartan | Mariucci, Elisabetta; Guidarini, Marta; Donti, Andrea; Lovato, Luigi; Wischmeijer, Anita; Angeli,... Emanuela; Gargiulo, Gaetano D; Picchio, Fernando M; Bonvicini, Marco | 2015-01-01 | GIORNALE ITALIANO DI CARDIOLOGIA | - | 1.01 Articolo in rivista | - |
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant. | Graziano, C; Wischmeijer, TITIA ANITA; Pippucci, Tommaso; Fusco, C; Diquigiovanni, Chiara; Nõukas..., M; Sauk, M; Kurg, A; Rivieri, F; Blau, N; Hoffmann, Gf; Chaubey, A; Schwartz, Ce; Romeo, Giovanni; Bonora, Elena; Garavelli, L; Seri, Marco | 2015-01-01 | GENE | - | 1.01 Articolo in rivista | - |
Thoracic Aortic Aneurysm in Infancy in Aneurysms-Osteoarthritis Syndrome Due to a Novel SMAD3 Mutation: Further Delineation of the Phenotype | Wischmeijer, A.; Van Laer, L.; Tortora, G.; Bolar, N.A.; Van Camp, G.; Fransen, E.; Peeters, N.; ...di Bartolomeo, R.; Pacini, D.; Gargiulo, G.; Turci, S.; Bonvicini, M.; Mariucci, E.; Lovato, L.; Brusori, S.; Ritelli, M.; Colombi, M.; Garavelli, L.; Seri, M.; Loeys, B.L. | 2013-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |