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Search Results - Gervasini, Gabriele
Search Results - Gervasini, Gabriele
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Linear plasma device GyM for plasma-material interaction studies
by
Uccello, Andrea
,
Bin, William
,
Bruschi, Alessandro
,
Causa, Federica
,
Cremona, Anna
,
De Angeli, Marco
,
Farina, Daniela
,
Gatto, Giuseppe
,
Gervasini, Gabriele
,
Ghezzi, Francesco
,
Gittini, Giuseppe
,
Granucci, Gustavo
,
Grosso, Giovanni
,
Laguardia, Laura
,
Lontano, Maurizio
,
Mellera, Vittoria
,
Minelli, Daniele
,
Nardone, Antonio
,
Pedroni, Matteo
,
Ripamonti, Federico
,
Rispoli, Natale
,
Vassallo, Espedito
,
Ricci, Daria
Published in
Frontiers in physics
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Comparison of dust transport modelling codes in a tokamak plasma
by
Uccello, Andrea
,
Gervasini, Gabriele
,
Ghezzi, Francesco
,
Lazzaro, Enzo
,
Bacharis, Minas
,
Flanagan, Joanne
,
Matthews, Guy
,
Järvinen, Aaro
,
Sertoli, Marco
Published in
Physics of plasmas
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Obtaining the unperturbed plasma potential in low-density, low-temperature plasmas
by
Causa, Federica
,
Gervasini, Gabriele
,
Uccello, Andrea
,
Granucci, Gustavo
,
Ricci, Daria
,
Rispoli, Natale
Published in
Plasma sources science & technology
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Physical and Numerical Model for Calculation of Ensembles of Trajectories of Dust Particles in a Tokamak
by
Gervasini, Gabriele
,
Lazzaro, Enzo
,
Uccello, Andrea
Published in
Journal of fusion energy
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An insight on beryllium dust sources in the JET ITER-like wall based on numerical simulations
by
Uccello, Andrea
,
Gervasini, Gabriele
,
Ghezzi, Francesco
,
Lazzaro, Enzo
,
Borodin, D
,
Borodkina, I
,
Douai, D
,
Huber, A
,
Jepu, I
,
Terranova, D
,
Widdowson, A
Published in
Plasma physics and controlled fusion
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Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes
by
Parenti, Ilaria
,
Teresa-Rodrigo, María E.
,
Pozojevic, Jelena
,
Ruiz Gil, Sara
,
Bader, Ingrid
,
Braunholz, Diana
,
Bramswig, Nuria C.
,
Gervasini, Cristina
,
Larizza, Lidia
,
Pfeiffer, Lutz
,
Ozkinay, Ferda
,
Ramos, Feliciano
,
Reiz, Benedikt
,
Rittinger, Olaf
,
Strom, Tim M.
,
Watrin, Erwan
,
Wendt, Kerstin
,
Wieczorek, Dagmar
,
Wollnik, Bernd
,
Baquero-Montoya, Carolina
,
Pié, Juan
,
Deardorff, Matthew A.
,
Gillessen-Kaesbach, Gabriele
,
Kaiser, Frank J.
Published in
Human genetics
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Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype
by
Parenti, I.
,
Gervasini, C.
,
Pozojevic, J.
,
Graul-Neumann, L.
,
Azzollini, J.
,
Braunholz, D.
,
Watrin, E.
,
Wendt, K.S.
,
Cereda, A.
,
Cittaro, D.
,
Gillessen-Kaesbach, G.
,
Lazarevic, D.
,
Mariani, M.
,
Russo, S.
,
Werner, R.
,
Krawitz, P.
,
Larizza, L.
,
Selicorni, A.
,
Kaiser, F.J.
Published in
Clinical epigenetics
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ANKRD11 variants: KBG syndrome and beyond
by
Parenti, Ilaria
,
Mallozzi, Mark B.
,
Hüning, Irina
,
Gervasini, Cristina
,
Kuechler, Alma
,
Agolini, Emanuele
,
Albrecht, Beate
,
Baquero‐Montoya, Carolina
,
Bohring, Axel
,
Bramswig, Nuria C.
,
Busche, Andreas
,
Dalski, Andreas
,
Guo, Yiran
,
Hanker, Britta
,
Hellenbroich, Yorck
,
Horn, Denise
,
Innes, A. Micheil
,
Leoni, Chiara
,
Li, Yun R.
,
Lynch, Sally Ann
,
Mariani, Milena
,
Medne, Livija
,
Mikat, Barbara
,
Milani, Donatella
,
Onesimo, Roberta
,
Ortiz‐Gonzalez, Xilma
,
Prott, Eva Christina
,
Reutter, Heiko
,
Rossier, Eva
,
Selicorni, Angelo
,
Wieacker, Peter
,
Wilkens, Alisha
,
Wieczorek, Dagmar
,
Zackai, Elaine H.
,
Zampino, Giuseppe
,
Zirn, Birgit
,
Hakonarson, Hakon
,
Deardorff, Matthew A.
,
Gillessen‐Kaesbach, Gabriele
,
Kaiser, Frank J.
Published in
Clinical genetics
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Development of Biochar-based Composites Electrodes from Pyrolysis of Coffee Silverskin: Microbial Fuel Cells for Wastewater Treatment
by
Stefania Marzorati
,
Mirko Magni
,
Sebastiano Campisi
,
Giorgia Ghiara
,
Gabriele Angelo Valtorta
,
Antonella Gervasini
,
Stefano P.M. Trasatti
Published in
Chemical engineering transactions
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Phenotypes and genotypes in individuals with SMC1A variants
by
Huisman, Sylvia
,
Mulder, Paul A.
,
Redeker, Egbert
,
Bader, Ingrid
,
Bisgaard, Anne‐Marie
,
Brooks, Alice
,
Cereda, Anna
,
Cinca, Constanza
,
Clark, Dinah
,
Cormier‐Daire, Valerie
,
Deardorff, Matthew A.
,
Diderich, Karin
,
Elting, Mariet
,
van Essen, Anthonie
,
FitzPatrick, David
,
Gervasini, Cristina
,
Gillessen‐Kaesbach, Gabriele
,
Girisha, Katta M.
,
Hilhorst‐Hofstee, Yvonne
,
Hopman, Saskia
,
Horn, Denise
,
Isrie, Mala
,
Jansen, Sandra
,
Jespersgaard, Cathrine
,
Kaiser, Frank J.
,
Kaur, Maninder
,
Kleefstra, Tjitske
,
Krantz, Ian D.
,
Lakeman, Phillis
,
Landlust, Annemiek
,
Lessel, Davor
,
Michot, Caroline
,
Moss, Jo
,
Noon, Sarah E.
,
Oliver, Chris
,
Parenti, Ilaria
,
Pie, Juan
,
Ramos, Feliciano J.
,
Rieubland, Claudine
,
Russo, Silvia
,
Selicorni, Angelo
,
Tümer, Zeynep
,
Vorstenbosch, Rieneke
,
Wenger, Tara L.
,
van Balkom, Ingrid
,
Piening, Sigrid
,
Wierzba, Jolanta
,
Hennekam, Raoul C.
Published in
American journal of medical genetics. Part A
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Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk prediction
by
Parenti, I.
,
Gervasini, C.
,
Pozojevic, J.
,
Wendt, K.S.
,
Watrin, E.
,
Azzollini, J.
,
Braunholz, D.
,
Buiting, K.
,
Cereda, A.
,
Engels, H.
,
Garavelli, L.
,
Glazar, R.
,
Graffmann, B.
,
Larizza, L.
,
Lüdecke, H.J.
,
Mariani, M.
,
Masciadri, M.
,
Pié, J.
,
Ramos, F.J.
,
Russo, S.
,
Selicorni, A.
,
Stefanova, M.
,
Strom, T.M.
,
Werner, R.
,
Wierzba, J.
,
Zampino, G.
,
Gillessen-Kaesbach, G.
,
Wieczorek, D.
,
Kaiser, F.J.
Published in
Clinical genetics
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Development, behaviour and autism in individuals with SMC1A variants
by
Mulder, Paul A.
,
Huisman, Sylvia
,
Landlust, Annemiek M.
,
Moss, Jo
,
Piening, Sigrid
,
Hennekam, Raoul C.
,
van Balkom, Ingrid D.C.
Published in
Journal of child psychology and psychiatry
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