Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome von Niklasson, Lena, Rasmussen, Peder, Óskarsdóttir, Sólveig, Gillberg, Christopher

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Long-term clinical effects of early thymectomy: Associations with autoimmune diseases, cancer, infections, and atopic diseases von Gudmundsdottir, Judith, Söderling, Jonas, Berggren, Håkan, Óskarsdóttir, Sólveig, Neovius, Martin, Stephansson, Olof, Ekwall, Olov

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Approaches to studying the impact of 22q11.2 copy number variants von Bassett, Anne S., McDonald-McGinn, Donna M., Boot, Erik, Óskarsdóttir, Sólveig, Yuen, Ryan K.C.

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Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs von Framme, Jenny Lingman, Lundqvist, Christina, Lundell, Anna-Carin, van Schouwenburg, Pauline A., Lemarquis, Andri L., Thörn, Karolina, Lindgren, Susanne, Gudmundsdottir, Judith, Lundberg, Vanja, Degerman, Sofie, Zetterström, Rolf H., Borte, Stephan, Hammarström, Lennart, Telemo, Esbjörn, Hultdin, Magnus, van der Burg, Mirjam, Fasth, Anders, Oskarsdóttir, Sólveig, Ekwall, Olov

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Assessment of the outcome of ophthalmological screening for uveitis in a cohort of Swedish children with juvenile idiopathic arthritis von Papadopoulou, Maria, Zetterberg, Madeleine, Oskarsdottir, Solveig, Andersson Grönlund, Marita

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P112: Updated clinical practice guidelines for managing children and adults with 22q11.2 deletion syndrome von Bassett, Anne, Oskarsdottir, Solveig, Boot, Erik, McDonald-McGinn, Donna

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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome von Óskarsdóttir, Sólveig, Boot, Erik, Crowley, Terrence Blaine, Loo, Joanne C.Y., Arganbright, Jill M., Armando, Marco, Baylis, Adriane L., Breetvelt, Elemi J., Castelein, René M., Chadehumbe, Madeline, Cielo, Christopher M., de Reuver, Steven, Eliez, Stephan, Fiksinski, Ania M., Forbes, Brian J., Gallagher, Emily, Hopkins, Sarah E., Jackson, Oksana A., Levitz-Katz, Lorraine, Klingberg, Gunilla, Lambert, Michele P., Marino, Bruno, Mascarenhas, Maria R., Moldenhauer, Julie, Moss, Edward M., Nowakowska, Beata Anna, Orchanian-Cheff, Ani, Putotto, Carolina, Repetto, Gabriela M., Schindewolf, Erica, Schneider, Maude, Solot, Cynthia B., Sullivan, Kathleen E., Swillen, Ann, Unolt, Marta, Van Batavia, Jason P., Vingerhoets, Claudia, Vorstman, Jacob, Bassett, Anne S., McDonald-McGinn, Donna M.

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Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation von Goldmuntz, Elizabeth, Bassett, Anne S., Boot, Erik, Marino, Bruno, Moldenhauer, Julie S., Óskarsdóttir, Sólveig, Putotto, Carolina, Rychik, Jack, Schindewolf, Erica, McDonald‐McGinn, Donna M., Blagowidow, Natalie

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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome von Boot, Erik, Óskarsdóttir, Sólveig, Loo, Joanne C.Y., Crowley, Terrence Blaine, Orchanian-Cheff, Ani, Andrade, Danielle M., Arganbright, Jill M., Castelein, René M., Cserti-Gazdewich, Christine, de Reuver, Steven, Fiksinski, Ania M., Klingberg, Gunilla, Lang, Anthony E., Mascarenhas, Maria R., Moss, Edward M., Nowakowska, Beata Anna, Oechslin, Erwin, Palmer, Lisa, Repetto, Gabriela M., Reyes, Nikolai Gil D., Schneider, Maude, Silversides, Candice, Sullivan, Kathleen E., Swillen, Ann, van Amelsvoort, Therese A.M.J., Van Batavia, Jason P., Vingerhoets, Claudia, McDonald-McGinn, Donna M., Bassett, Anne S.

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T-cell receptor sequencing reveals decreased diversity 18 years after early thymectomy von Gudmundsdottir, Judith, Lundqvist, Christina, Ijspeert, Hanna, van der Slik, Eva, Óskarsdóttir, Sólveig, Lindgren, Susanne, Lundberg, Vanja, Berglund, Martin, Lingman-Framme, Jenny, Telemo, Esbjörn, van der Burg, Mirjam, Ekwall, Olov

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Retrospective Analysis of TREC Based Newborn Screening Results and Clinical Phenotypes in Infants with the 22q11 Deletion Syndrome von Lingman Framme, Jenny, Borte, Stephan, von Döbeln, Ulrika, Hammarström, Lennart, Óskarsdóttir, Sólveig

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Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions von Blagowidow, Natalie, Nowakowska, Beata, Schindewolf, Erica, Grati, Francesca Romana, Putotto, Carolina, Breckpot, Jeroen, Swillen, Ann, Crowley, Terrence Blaine, Loo, Joanne C Y, Lairson, Lauren A, Óskarsdóttir, Sólveig, Boot, Erik, Garcia-Minaur, Sixto, Cristina Digilio, Maria, Marino, Bruno, Coleman, Beverly, Moldenhauer, Julie S, Bassett, Anne S, McDonald-McGinn, Donna M

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Newborn screening for primary immunodeficiencies: beyond SCID and XLA von Borte, Stephan, Wang, Ning, Óskarsdóttir, Sólveig, von Döbeln, Ulrika, Hammarström, Lennart

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Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects von Niklasson, Lena, Rasmussen, Peder, Óskarsdóttir, Sólveig, Gillberg, Christopher

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Speech and hearing in adults with 22q11.2 deletion syndrome von Persson, Christina, Friman, Vanda, Óskarsdóttir, Sólveig, Jönsson, Radi

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Language skills in 5-8-year-old children with 22q11 deletion syndrome von Persson, Christina, Niklasson, Lena, Óskarsdóttir, Sólveig, Johansson, Susanne, Jönsson, Radi, Söderpalm, Ewa

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Antibody deficiency in adults with 22q11.2 deletion syndrome von Björk, Aron H., Óskarsdóttir, Sólveig, Andersson, Bengt A., Friman, Vanda

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22q11.2 Deletion and Duplication Syndromes and COVID-19 von Crowley, T. Blaine, McGinn, Donna McDonald, Sullivan, Kathleen E.

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Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome von Bassett, Anne S., MD, McDonald-McGinn, Donna M., MS, CGC, Devriendt, Koen, MD, Digilio, Maria Cristina, MD, Goldenberg, Paula, MD, MSW, Habel, Alex, MD, Marino, Bruno, MD, Oskarsdottir, Solveig, MD, PhD, Philip, Nicole, MD, Sullivan, Kathleen, MD, PhD, Swillen, Ann, PhD, Vorstman, Jacob, MD, PhD

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A prospective cross-sectional study of speech in patients with the 22q11 deletion syndrome von Persson, Christina, Lohmander, Anette, Jönsson, Radi, Óskarsdóttir, Sólveig, Söderpalm, Ewa

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