Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Bertola, Débora R.
Castro, Matheus A. A.
Yamamoto, Guilherme L.
Honjo, Rachel S.
Ceroni, José Ricardo
Buscarilli, Michele M.
Freitas, Amanda B.
Malaquias, Alexsandra C.
Pereira, Alexandre C.
Jorge, Alexander A. L.
Passos‐Bueno, Maria Rita
and
Kim, Chong A.
2020.
Phenotype–genotype analysis of 242 individuals with RASopathies: 18‐year experience of a tertiary center in Brazil.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics,
Vol. 184,
Issue. 4,
p.
896.
Linglart, Léa
and
Gelb, Bruce D.
2020.
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics,
Vol. 184,
Issue. 1,
p.
73.
Ovaert, Caroline
and
Leobon, Bertrand
2021.
Cardiologie du Foetus et de L'enfant.
p.
342.
Lioncino, Michele
Monda, Emanuele
Verrillo, Federica
Moscarella, Elisabetta
Calcagni, Giulio
Drago, Fabrizio
Marino, Bruno
Digilio, Maria Cristina
Putotto, Carolina
Calabrò, Paolo
Russo, Maria Giovanna
Roberts, Amy E.
Gelb, Bruce D.
Tartaglia, Marco
and
Limongelli, Giuseppe
2022.
Hypertrophic Cardiomyopathy in RASopathies.
Heart Failure Clinics,
Vol. 18,
Issue. 1,
p.
19.
Delogu, Angelica Bibiana
Limongelli, Giuseppe
Versacci, Paolo
Adorisio, Rachele
Kaski, Juan Pablo
Blandino, Rita
Maiolo, Stella
Monda, Emanuele
Putotto, Carolina
De Rosa, Gabriella
Chatfield, Kathryn C.
Gelb, Bruce D.
and
Calcagni, Giulio
2022.
The heart in RASopathies.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics,
Vol. 190,
Issue. 4,
p.
440.
Abumehdi, Mohammad
Mehta, Chetan
Afifi, Ahmed Reda Sanad Arafa
Yong, San‐Fui
Chaudhari, Milind
Bhole, Vinay
Dhillon, Rami
and
Stumper, Oliver
2022.
Supravalvular pulmonary stenosis: A risk factor for reintervention in Noonan syndrome with pulmonary valve stenosis.
Catheterization and Cardiovascular Interventions,
Vol. 99,
Issue. 5,
p.
1538.
Wolf, Cordula M.
Zenker, Martin
Burkitt-Wright, Emma
Edouard, Thomas
García-Miñaúr, Sixto
Lebl, Jan
Shaikh, Guftar
Tartaglia, Marco
Verloes, Alain
and
Östman-Smith, Ingegerd
2022.
Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists.
European Journal of Medical Genetics,
Vol. 65,
Issue. 1,
p.
104372.
Sun, Ling
Xie, Yu-mei
Wang, Shu-shui
and
Zhang, Zhi-wei
2022.
Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome.
Frontiers in Genetics,
Vol. 13,
Issue. ,
Arbelo, Elena
Protonotarios, Alexandros
Gimeno, Juan R
Arbustini, Eloisa
Barriales-Villa, Roberto
Basso, Cristina
Bezzina, Connie R
Biagini, Elena
Blom, Nico A
de Boer, Rudolf A
De Winter, Tim
Elliott, Perry M
Flather, Marcus
Garcia-Pavia, Pablo
Haugaa, Kristina H
Ingles, Jodie
Jurcut, Ruxandra Oana
Klaassen, Sabine
Limongelli, Giuseppe
Loeys, Bart
Mogensen, Jens
Olivotto, Iacopo
Pantazis, Antonis
Sharma, Sanjay
Van Tintelen, J Peter
Ware, James S
Kaski, Juan Pablo
Charron, Philippe
Imazio, Massimo
Abdelhamid, Magdy
Aboyans, Victor
Arad, Michael
Asselbergs, Folkert W
Asteggiano, Riccardo
Bilinska, Zofia
Bonnet, Damien
Bundgaard, Henning
Cardim, Nuno Miguel
Čelutkienė, Jelena
Cikes, Maja
De Ferrari, Gaetano Maria
Dusi, Veronica
Falk, Volkmar
Fauchier, Laurent
Gandjbakhch, Estelle
Heliö, Tiina
Koskinas, Konstantinos
Kotecha, Dipak
Landmesser, Ulf
Lazaros, George
Lewis, Basil S
Linhart, Ales
Løchen, Maja-Lisa
Meder, Benjamin
Mindham, Richard
Moon, James
Nielsen, Jens Cosedis
Petersen, Steffen
Prescott, Eva
Sheppard, Mary N
Sinagra, Gianfranco
Sitges, Marta
Tfelt-Hansen, Jacob
Touyz, Rhian
Veltrop, Rogier
Veselka, Josef
Wahbi, Karim
Wilde, Arthur
Zeppenfeld, Katja
Kichou, Brahim
Sisakian, Hamayak
Scherr, Daniel
Gerber, Bernhard
Džubur, Alen
Gospodinova, Mariana
Planinc, Ivo
Moustra, Hera Heracleous
Zemánek, David
Jensen, Morten Steen Kvistholm
Samir, Ahmad
Palm, Kairit
Heliö, Tiina
Wahbi, Karim
Schulze-Bahr, Eric
Haralambos, Vlachopoulos
Sepp, Róbert
Aðalsteinsdóttir, Berglind
Ward, Deirdre
Blich, Miry
Sinagra, Gianfranco
Poniku, Afrim
Lunegova, Olga
Rudzitis, Ainars
Kassab, Roland
Barysienė, Jūratė
Huijnen, Steve
Felice, Tiziana
Vataman, Eleonora
Pavlovic, Nikola
Doghmi, Nawal
Asselbergs, Folkert W
Kostovska, Elizabeta Srbinovska
Almaas, Vibeke Marie
Biernacka, Elżbieta Katarzyna
Brito, Dulce
Rosca, Monica
Zavatta, Marco
Ristic, Arsen
Goncalvesová, Eva
Šinkovec, Matjaž
Cañadas-Godoy, Victoria
Platonov, Pyotr G
Saguner, Ardan M
Saadi, Ahmad Rasheed Al
Kammoun, Ikram
Celik, Ahmet
Nesukay, Elena
Abdullaev, Timur
Prescott, Eva
James, Stefan
Arbelo, Elena
Baigent, Colin
Borger, Michael A
Buccheri, Sergio
Ibanez, Borja
Køber, Lars
Koskinas, Konstantinos C
McEvoy, John William
Mihaylova, Borislava
Mindham, Richard
Neubeck, Lis
Nielsen, Jens Cosedis
Pasquet, Agnes
Rakisheva, Amina
Rocca, Bianca
Rossello, Xavier
Vaartjes, Ilonca
Vrints, Christiaan
Witkowski, Adam
and
Zeppenfeld, Katja
2023.
2023 ESC Guidelines for the management of cardiomyopathies.
European Heart Journal,
Vol. 44,
Issue. 37,
p.
3503.
Ichikawa, Yasuhiro
Kuroda, Hiroyuki
Ikegawa, Takeshi
Kawai, Shun
Ono, Shin
Kim, Ki-Sung
Yanagi, Sadamitsu
Kurosawa, Kenji
Aoki, Yoko
and
Ueda, Hideaki
2023.
Cardiac features of Noonan syndrome in Japanese patients.
Cardiology in the Young,
Vol. 33,
Issue. 4,
p.
564.
Faienza, Maria Felicia
Meliota, Giovanni
Mentino, Donatella
Ficarella, Romina
Gentile, Mattia
Vairo, Ugo
and
D’amato, Gabriele
2024.
Cardiac Phenotype and Gene Mutations in RASopathies.
Genes,
Vol. 15,
Issue. 8,
p.
1015.