DNA ligase III promotes alternative nonhomologous end-joining during chromosomal translocation formation von Simsek, Deniz, Brunet, Erika, Wong, Sunnie Yan-Wai, Katyal, Sachin, Gao, Yankun, McKinnon, Peter J, Lou, Jacqueline, Zhang, Lei, Li, James, Rebar, Edward J, Gregory, Philip D, Holmes, Michael C, Jasin, Maria

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Expanding the clinical and metabolic phenotype of DPM2 deficient congenital disorders of glycosylation von Radenkovic, Silvia, Fitzpatrick-Schmidt, Taylor, Byeon, Seul Kee, Madugundu, Anil K., Saraswat, Mayank, Lichty, Angie, Wong, Sunnie Y.W., McGee, Stephen, Kubiak, Katharine, Ligezka, Anna, Ranatunga, Wasantha, Zhang, Yuebo, Wood, Tim, Friez, Michael J., Clarkson, Katie, Pandey, Akhilesh, Jones, Julie R., Morava, Eva

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Robust ZFN-mediated genome editing in adult hemophilic mice von Anguela, Xavier M., Sharma, Rajiv, Doyon, Yannick, Miller, Jeffrey C., Li, Hojun, Haurigot, Virginia, Rohde, Michelle E., Wong, Sunnie Y., Davidson, Robert J., Zhou, Shangzhen, Gregory, Philip D., Holmes, Michael C., High, Katherine A.

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Oral D-galactose supplementation in PGM1-CDG von Wong, Sunnie Yan-Wai, Gadomski, Therese, van Scherpenzeel, Monique, Honzik, Tomas, Hansikova, Hana, Holmefjord, Katja S Brocke, Mork, Marit, Bowling, Francis, Sykut-Cegielska, Jolanta, Koch, Dieter, Hertecant, Jozef, Preston, Graeme, Jaeken, Jaak, Peeters, Nicole, Perez, Stefanie, Nguyen, David Do, Crivelly, Kea, Emmerzaal, Tim, Gibson, K Michael, Raymond, Kimiyo, Abu Bakar, Nurulamin, Foulquier, Francois, Poschet, Gernot, Ackermann, Amanda M, He, Miao, Lefeber, Dirk J, Thiel, Christian, Kozicz, Tamas, Morava, Eva

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The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG von Radenkovic, Silvia, Bird, Matthew J., Emmerzaal, Tim L., Wong, Sunnie Y., Felgueira, Catarina, Stiers, Kyle M., Sabbagh, Leila, Himmelreich, Nastassja, Poschet, Gernot, Windmolders, Petra, Verheijen, Jan, Witters, Peter, Altassan, Ruqaiah, Honzik, Tomas, Eminoglu, Tuba F., James, Phillip M., Edmondson, Andrew C., Hertecant, Jozef, Kozicz, Tamas, Thiel, Christian, Vermeersch, Pieter, Cassiman, David, Beamer, Lesa, Morava, Eva, Ghesquière, Bart

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J., Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y., van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y., Mak, Christopher C.Y., Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M., Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E., Leung, Peter K.C., Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B., Malfait, Fransiska, Morava, Eva, Callewaert, Bert, Wevers, Ron A.

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In vivo genome editing restores haemostasis in a mouse model of haemophilia von Li, Hojun, Haurigot, Virginia, Doyon, Yannick, Li, Tianjian, Wong, Sunnie Y., Bhagwat, Anand S., Malani, Nirav, Anguela, Xavier M., Sharma, Rajiv, Ivanciu, Lacramiora, Murphy, Samuel L., Finn, Jonathan D., Khazi, Fayaz R., Zhou, Shangzhen, Paschon, David E., Rebar, Edward J., Bushman, Frederic D., Gregory, Philip D., Holmes, Michael C., High, Katherine A.

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Severe intracranial and intra-abdominal hemorrhage: timing is everything von Farooqi, Najiha B, Wong, Sunnie Y W, Wang, Simeng, Knowlton, Lisa Marie

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Large uterine fibroids causing a closed loop small bowel obstruction following uterine fibroid embolization von Antono, Amanda C, Najar, Julie, Wong, Sunnie Y W, Junn, Justin, Knowlton, Lisa Marie

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Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots von Conte, Federica, Morava, Eva, Bakar, Nurulamin Abu, Wortmann, Saskia B., Poerink, Anne Jonge, Grunewald, Stephanie, Crushell, Ellen, Al-Gazali, Lihadh, de Vries, Maaike C., Mørkrid, Lars, Hertecant, Jozef, Brocke Holmefjord, Katja S., Kronn, David, Feigenbaum, Annette, Fingerhut, Ralph, Wong, Sunnie Y., van Scherpenzeel, Monique, Voermans, Nicol C., Lefeber, Dirk J.

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Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency von Wong, Sunnie Yan-Wai, BA, Beamer, Lesa J., PhD, Gadomski, Therese, BS, Honzik, Tomas, MD, PhD, Mohamed, Miski, MD, PhD, Wortmann, Saskia B., MD, PhD, Brocke Holmefjord, Katja S., MD, Mork, Marit, MD, Bowling, Francis, MD, PhD, Sykut-Cegielska, Jolanta, MD, PhD, Koch, Dieter, MD, Ackermann, Amanda, MD, PhD, Stanley, Charles A., MD, Rymen, Daisy, MD, PhD, Zeharia, Avraham, MD, Al-Sayed, Moeen, MD, Marquardt, Thomas, MD, Jaeken, Jaak, MD, PhD, Lefeber, Dirk, PhD, Conrad, Donald F., PhD, Kozicz, Tamas, MD, PhD, Morava, Eva, MD, PhD

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Late presentation of type-I jejunal atresia in an infant: A case report von Wong, Sunnie, Landisch, Rachel, Ruiz, Rachel, Datta, Sumit, Fuchs, Julie

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Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies von Gardeitchik, Thatjana, Mohamed, Miski, Ruzzenente, Benedetta, Karall, Daniela, Guerrero-Castillo, Sergio, Dalloyaux, Daisy, van den Brand, Mariël, van Kraaij, Sanne, van Asbeck, Ellyze, Assouline, Zahra, Rio, Marlene, de Lonlay, Pascale, Scholl-Buergi, Sabine, Wolthuis, David F.G.J., Hoischen, Alexander, Rodenburg, Richard J., Sperl, Wolfgang, Urban, Zsolt, Brandt, Ulrich, Mayr, Johannes A., Wong, Sunnie, de Brouwer, Arjan P.M., Nijtmans, Leo, Munnich, Arnold, Rötig, Agnès, Wevers, Ron A., Metodiev, Metodi D., Morava, Eva

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An unknown (and unexpected) cause of septic shock von Kang, Augustine, Gupta, Pranjal, Wong, Sunnie, Tung, Jamie, Gallegos, Moises

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What solid organ transplant healthcare providers should know about renin‐angiotensin‐aldosterone system inhibitors and COVID‐19 von Wong, Sunnie Y., Brubaker, Aleah L., Wang, Aileen X., Taiwo, Adetokunbo A., Melcher, Marc L.

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J., Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y., van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y., Mak, Christopher C.Y., Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M., Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E., Leung, Kai Ching Peter, Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B., Malfait, Fransiska, Morava, Eva, Callewaert, Bert, Wevers, Ron A.

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Defining a new immune deficiency syndrome: MAN2B2-CDG von Verheijen, Jan, Wong, Sunnie Y., Rowe, Jared H., Raymond, Kimiyo, Stoddard, Jennifer, Delmonte, Ottavia M., Bosticardo, Marita, Dobbs, Kerry, Niemela, Julie, Calzoni, Enrica, Pai, Sung-Yun, Choi, Uimook, Yamazaki, Yasuhiro, Comeau, Anne Marie, Janssen, Erin, Henderson, Lauren, Hazen, Melissa, Berry, Gerard, Rosenzweig, Sergio D., Aldhekri, Hasan Hamdan, He, Miao, Notarangelo, Luigi D., Morava, Eva

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Etonogestrel Subdermal Implant–Associated Regression of Endometrial Intraepithelial Neoplasia von Wong, Sunnie, Naresh, Amber

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Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects von Morelle, Willy, Potelle, Sven, Witters, Peter, Wong, Sunnie, Climer, Leslie, Lupashin, Vladimir, Matthijs, Gert, Gadomski, Therese, Jaeken, Jaak, Cassiman, David, Morava, Eva, Foulquier, François

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Disease severity and clinical outcome in phosphosglucomutase deficiency von Morava, Eva, Wong, Sunnie, Lefeber, Dirk

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