BRAF V600E mutation associated with papillary high-grade serous ovarian cystadenocarcinoma in a 22q11.2DS patient by Maria Antonietta Castaldi, Nadia Petrillo, Carmine Selleri, Monica Ianniello, Anna Maria Della Corte, Eloisa Evangelista, Luigia De Falco, Roberto Sirica, Marika Casillo, Alessia Caleo, Alessandro Caputo, Pio Zeppa, Salvatore Giovanni Castaldi, Pasqualina Scala, Bianca Serio, Giovanni Savarese, Valentina Giudice

Subjects: “…DiGeorge syndrome…”
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Di George syndrome: early diagnosis in pediatric practice by A. A. Pavlikov, I. M. Melnikova, T. I. Pakhomova, N. P. Myakin

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Drug-induced parkinsonism in a patient with DiGeorge syndrome: a case report by Clancy Cerejo, Nicolas De Cleene, Gerald Walser, Atbin Djamshidian, Klaus Seppi, Beatrice Heim

Subjects: “…DiGeorge syndrome…”
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A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery by T. Blaine Crowley, Ian Campbell, Abinaya Arulselvan, David Friedman, Elaine H. Zackai, Tracy R. Geoffrion, Char Witmer, J. William Gaynor, Donna M. McDonald-McGinn, Michele P. Lambert

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Severe Hypocalcemia in the Adolescent as the Only Manifestation of <i>22q11</i> Microdeletion Syndrome: Clinical Case by Anastasia O. Vechkasova, Natalia V. Buchinskaya, Mikhail M. Kostik

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Prevalence of immunological aberrations and 22q11.2 deletion in children with conotruncal anomalies: A cross-sectional study by Souvik Das, Arun Kumar Baranwal, Amit Rawat, Ashwini Nair, Sanjeev Hanumantacharya Naganur, Anupriya Kaur, Anand Kumar Mishra, Ankur Jindal, Anit Kaur

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Assessment of vascular tortuosity in 22q11.2 deletion syndrome using optical coherence tomography angiography by Luca Lucchino, Marta Armentano, Giacomo Visioli, Alessandro Beccia, Giuseppe Maria Albanese, Fabiana Mallone, Carolina Putotto, Federica Pulvirenti, Magda Gharbiya, Alessandro Lambiase, Marco Marenco

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