Childhood Hypertrophic Cardiomyopathy: A Disease of the Cardiac Sarcomere

di Norrish, Gabrielle, Field, Ella, Kaski, Juan P.
Pubblicato in Front Pediatr (2021)

Increased Left Ventricular Posterior Wall End-Diastolic Thickness in Adolescents With Delayed Diagnosis of Vertically Acquired HIV Infection

di Miller, Robert F., Meghji, Jamilah, Kaski, Juan P., Matenga, Jonathan, Ferrand, Rashida A.
Pubblicazione 2014

Cardiac Disease in Adolescents With Delayed Diagnosis of Vertically Acquired HIV Infection

di Miller, Robert F., Kaski, Juan P., Hakim, James, Matenga, Jonathan, Nathoo, Kusum, Munyati, Shungu, Desai, Sujal R., Corbett, Elizabeth L., Ferrand, Rashida A.
Pubblicazione 2013

Racial Variation in Echocardiographic Reference Ranges for Left Chamber Dimensions in Children and Adolescents: A Systematic Review

di Majonga, Edith D., Norrish, Gabrielle, Rehman, Andrea M., Kranzer, Katharina, Mujuru, Hilda A., Nathoo, Kusum, Odland, Jon O., Kaski, Juan P., Ferrand, Rashida A.
Pubblicato in Pediatr Cardiol (2018)

High prevalence of echocardiographic abnormalities in older HIV-infected children taking antiretroviral therapy

di Majonga, Edith D., Rehman, Andrea M., Simms, Victoria, Mchugh, Grace, Mujuru, Hilda A., Nathoo, Kusum, Odland, Jon O., Patel, Mohammad S., Kaski, Juan P., Ferrand, Rashida A.
Pubblicato in AIDS (2018)

Proinflammatory and cardiovascular biomarkers are associated with echocardiographic abnormalities in children with HIV taking antiretroviral therapy

di Majonga, Edith D, Yindom, Louis-Marie, Hameiri-Bowen, Dan, Mayini, Justin, Rehman, Andrea M, Kaski, Juan P, Mujuru, Hilda A, Rowland-Jones, Sarah L, Ferrand, Rashida A
Pubblicato in AIDS (2022)

Echocardiographic reference ranges in older children and adolescents in sub-Saharan Africa

di Majonga, Edith D., Rehman, Andrea M., McHugh, Grace, Mujuru, Hilda A., Nathoo, Kusum, Patel, Mohammad S., Munyati, Shungu, Odland, Jon O., Kranzer, Katharina, Kaski, Juan P., Ferrand, Rashida A.
Pubblicato in Int J Cardiol (2017)

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

di Prasad, Rathi, Chan, Li F., Hughes, Claire R., Kaski, Juan P., Kowalczyk, Julia C., Savage, Martin O., Peters, Catherine J., Nathwani, Nisha, Clark, Adrian J. L., Storr, Helen L., Metherell, Louise A.
Pubblicazione 2014

Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry

di Gimeno, Juan R, Elliott, Perry M, Tavazzi, Luigi, Tendera, Michal, Kaski, Juan P, Laroche, Cecile, Barriales-Villa, Roberto, Seferovic, Petar, Biagini, Elena, Arbustini, Eloisa, Lopes, Luis R, Linhart, Ales, Mogensen, Jens, Hagege, Albert, Espinosa, Maria A, Saad, Aly, Maggioni, Aldo P, Caforio, Alida L P, Charron, Philippe H
Pubblicato in Eur Heart J Qual Care Clin Outcomes (2020)

Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

di Calcagni, Giulio, Limongelli, Giuseppe, D'Ambrosio, Angelo, Gesualdo, Francesco, Digilio, Maria Cristina, Baban, Anwar, Albanese, Sonia B., Versacci, Paolo, De Luca, Enrica, Ferrero, Giovanni B., Baldassarre, Giuseppina, Agnoletti, Gabriella, Banaudi, Elena, Marek, Jan, Kaski, Juan P., Tuo, Giulia, Russo, Maria Giovanna, Pacileo, Giuseppe, Milanesi, Ornella, Messina, Daniela, Marasini, Maurizio, Cairello, Francesca, Formigari, Roberto, Brighenti, Maurizio, Dallapiccola, Bruno, Tartaglia, Marco, Marino, Bruno
Pubblicato in Data Brief (2017)

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

di Jaffer, Fatima, Avbersek, Andreja, Vavassori, Rosaria, Fons, Carmen, Campistol, Jaume, Stagnaro, Michela, De Grandis, Elisa, Veneselli, Edvige, Rosewich, Hendrik, Gianotta, Melania, Zucca, Claudio, Ragona, Francesca, Granata, Tiziana, Nardocci, Nardo, Mikati, Mohamed, Helseth, Ashley R., Boelman, Cyrus, Minassian, Berge A., Johns, Sophia, Garry, Sarah I., Scheffer, Ingrid E., Gourfinkel-An, Isabelle, Carrilho, Ines, Aylett, Sarah E., Parton, Matthew, Hanna, Michael G., Houlden, Henry, Neville, Brian, Kurian, Manju A., Novy, Jan, Sander, Josemir W., Lambiase, Pier D., Behr, Elijah R., Schyns, Tsveta, Arzimanoglou, Alexis, Cross, J. Helen, Kaski, Juan P., Sisodiya, Sanjay M.
Pubblicato in Brain (2015)

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

di Crotti, Lia, Spazzolini, Carla, Tester, David J, Ghidoni, Alice, Baruteau, Alban-Elouen, Beckmann, Britt-Maria, Behr, Elijah R, Bennett, Jeffrey S, Bezzina, Connie R, Bhuiyan, Zahurul A, Celiker, Alpay, Cerrone, Marina, Dagradi, Federica, De Ferrari, Gaetano M, Etheridge, Susan P, Fatah, Meena, Garcia-Pavia, Pablo, Al-Ghamdi, Saleh, Hamilton, Robert M, Al-Hassnan, Zuhair N, Horie, Minoru, Jimenez-Jaimez, Juan, Kanter, Ronald J, Kaski, Juan P, Kotta, Maria-Christina, Lahrouchi, Najim, Makita, Naomasa, Norrish, Gabrielle, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Parati, Gianfranco, Sekarski, Nicole, Tveten, Kristian, Vatta, Matteo, Webster, Gregory, Wilde, Arthur A M, Wojciak, Julianne, George, Alfred L, Ackerman, Michael J, Schwartz, Peter J
Pubblicato in Eur Heart J (2019)

Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

di Norrish, Gabrielle, Ding, Tao, Field, Ella, Ziółkowska, Lidia, Olivotto, Iacopo, Limongelli, Giuseppe, Anastasakis, Aristides, Weintraub, Robert, Biagini, Elena, Ragni, Luca, Prendiville, Terence, Duignan, Sophie, McLeod, Karen, Ilina, Maria, Fernández, Adrián, Bökenkamp, Regina, Baban, Anwar, Kubuš, Peter, Daubeney, Piers E. F., Sarquella-Brugada, Georgia, Cesar, Sergi, Marrone, Chiara, Bhole, Vinay, Medrano, Constancio, Uzun, Orhan, Brown, Elspeth, Gran, Ferran, Castro, Francisco J., Stuart, Graham, Vignati, Gabriele, Barriales-Villa, Roberto, Guereta, Luis G., Adwani, Satish, Linter, Katie, Bharucha, Tara, Garcia-Pavia, Pablo, Rasmussen, Torsten B., Calcagnino, Margherita M., Jones, Caroline B., De Wilde, Hans, Toru-Kubo, J., Felice, Tiziana, Mogensen, Jens, Mathur, Sujeev, Reinhardt, Zdenka, O’Mahony, Constantinos, Elliott, Perry M., Omar, Rumana Z., Kaski, Juan P.
Pubblicato in JAMA Cardiol (2019)

Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study

di Balestrini, Simona, Mikati, Mohamad A., Álvarez-García-Rovés, Reyes, Carboni, Michael, Hunanyan, Arsen S., Kherallah, Bassil, McLean, Melissa, Prange, Lyndsey, De Grandis, Elisa, Gagliardi, Alessandra, Pisciotta, Livia, Stagnaro, Michela, Veneselli, Edvige, Campistol, Jaume, Fons, Carmen, Pias-Peleteiro, Leticia, Brashear, Allison, Miller, Charlotte, Samões, Raquel, Brankovic, Vesna, Padiath, Quasar S., Potic, Ana, Pilch, Jacek, Vezyroglou, Aikaterini, Bye, Ann M.E., Davis, Andrew M., Ryan, Monique M., Semsarian, Christopher, Hollingsworth, Georgina, Scheffer, Ingrid E., Granata, Tiziana, Nardocci, Nardo, Ragona, Francesca, Arzimanoglou, Alexis, Panagiotakaki, Eleni, Carrilho, Inês, Zucca, Claudio, Novy, Jan, Dzieżyc, Karolina, Parowicz, Marek, Mazurkiewicz-Bełdzińska, Maria, Weckhuysen, Sarah, Pons, Roser, Groppa, Sergiu, Sinden, Daniel S., Pitt, Geoffrey S., Tinker, Andrew, Ashworth, Michael, Michalak, Zuzanna, Thom, Maria, Cross, J. Helen, Vavassori, Rosaria, Kaski, Juan P., Sisodiya, Sanjay M.
Pubblicato in Neurology (2020)