Pullulan: a new cytoadhesive for cell-mediated cartilage repair von Bulman, Sarah E, Coleman, Cynthia M, Murphy, J Mary, Medcalf, Nicholas, Ryan, Aideen E, Barry, Frank

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Enhancing the Mesenchymal Stem Cell Therapeutic Response: Cell Localization and Support for Cartilage Repair von Bulman, Sarah E., Barron, Valerie, Coleman, Cynthia M., Barry, Frank

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Pullulan: a new cytoadhesive for cell-mediated cartilage repair von Bulman, Sarah E, Coleman, Cynthia M, Murphy, J Mary, Medcalf, Nicholas, Ryan, Aideen E, Barry, Frank

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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 von Boycott, Kym M., Beaulieu, Chandree L., Kernohan, Kristin D., Gebril, Ola H., Mhanni, Aziz, Chudley, Albert E., Redl, David, Qin, Wen, Hampson, Sarah, Küry, Sébastien, Tetreault, Martine, Puffenberger, Erik G., Scott, James N., Bezieau, Stéphane, Reis, André, Uebe, Steffen, Schumacher, Johannes, Hegele, Robert A., McLeod, D. Ross, Gálvez-Peralta, Marina, Majewski, Jacek, Ramaekers, Vincent T., Nebert, Daniel W., Innes, A. Micheil, Parboosingh, Jillian S., Abou Jamra, Rami

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Thirty-Day Healthcare Encounters after Elective Uterine Artery Embolization for Fibroids with and without Superior Hypogastric Nerve Block von Kim, Nicole H., Sarwar, Ammar, Tahir, Muhammad Mohid, Ali, Razan, Schroeppel DeBacker, Sarah E., Faintuch, Salomao, Brook, Olga R., Bulman, Julie C.

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Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit von Daoud, Hussein, Luco, Stephanie M, Li, Rui, Bareke, Eric, Beaulieu, Chandree, Jarinova, Olga, Carson, Nancy, Nikkel, Sarah M, Graham, Gail E, Richer, Julie, Armour, Christine, Bulman, Dennis E, Chakraborty, Pranesh, Geraghty, Michael, Lines, Matthew A, Lacaze-Masmonteil, Thierry, Majewski, Jacek, Boycott, Kym M, Dyment, David A

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True Costs of Uterine Artery Embolization: Time-Driven Activity-Based Costing in Interventional Radiology Over a 3-Year Period von Bulman, Julie C., Kim, Nicole H., Kaplan, Robert S., Schroeppel DeBacker, Sarah E., Brook, Olga R., Sarwar, Ammar

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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes von Rivière, Jean-Baptiste, Mirzaa, Ghayda M, O'Roak, Brian J, Beddaoui, Margaret, Alcantara, Diana, Conway, Robert L, St-Onge, Judith, Schwartzentruber, Jeremy A, Gripp, Karen W, Nikkel, Sarah M, Worthylake, Thea, Sullivan, Christopher T, Ward, Thomas R, Butler, Hailly E, Kramer, Nancy A, Albrecht, Beate, Armour, Christine M, Armstrong, Linlea, Caluseriu, Oana, Cytrynbaum, Cheryl, Drolet, Beth A, Innes, A Micheil, Lauzon, Julie L, Lin, Angela E, Mancini, Grazia M S, Meschino, Wendy S, Reggin, James D, Saggar, Anand K, Lerman-Sagie, Tally, Uyanik, Gökhan, Weksberg, Rosanna, Zirn, Birgit, Beaulieu, Chandree L, Majewski, Jacek, Bulman, Dennis E, O'Driscoll, Mark, Shendure, Jay, Graham, John M, Boycott, Kym M, Dobyns, William B

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Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency von McMillan, Hugh J, Worthylake, Thea, Schwartzentruber, Jeremy, Gottlieb, Chloe C, Lawrence, Sarah E, Mackenzie, Alex, Beaulieu, Chandree L, Mooyer, Petra A W, Wanders, Ronald J A, Majewski, Jacek, Bulman, Dennis E, Geraghty, Michael T, Ferdinandusse, Sacha, Boycott, Kym M

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The defining DNA methylation signature of Floating-Harbor Syndrome von Hood, Rebecca L., Schenkel, Laila C., Nikkel, Sarah M., Ainsworth, Peter J., Pare, Guillaume, Boycott, Kym M., Bulman, Dennis E., Sadikovic, Bekim

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Ultrasound-guided percutaneous thrombin injection for the management of upper extremity pseudoaneurysms: 20 years of tertiary care center experience von McCarthy, Colin J, Weinstein, Jeffrey L, Bulman, Julie C, Schroeppel DeBacker, Sarah E, Berkowitz, Seth J, Dowlatshahi, Arriyan S, Ahmed, Muneeb, Faintuch, Salomao

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Wound Care for Venous Ulceration von Schroeppel DeBacker, Sarah E., Bulman, Julie C., Weinstein, Jeffrey L.

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Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia von Sawyer, Sarah L., Schwartzentruber, Jeremy, Beaulieu, Chandree L., Dyment, David, Smith, Amanda, Chardon, Jodi Warman, Yoon, Grace, Rouleau, Guy A., Suchowersky, Oksana, Siu, Victoria, Murphy, Lisa, Hegele, Robert A., Marshall, Christian R., Bulman, Dennis E., Majewski, Jacek, Tarnopolsky, Mark, Boycott, Kym M.

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Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene von Smith, Amanda, Bulman, Dennis E, Goldsmith, Claire, Bareke, Eric, Majewski, Jacek, Boycott, Kym M, Nikkel, Sarah M

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Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1 von Racacho, Lemuel, Byrnes, Ashley M, MacDonald, Heather, Dranse, Helen J, Nikkel, Sarah M, Allanson, Judith, Rosser, Elisabeth, Underhill, T Michael, Bulman, Dennis E

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A Qualitative Analysis of the Functions of Primary Care Nurses in COVID-19 Vaccination von Lyons, Rhiannon, Mathews, Maria, Ryan, Dana, Hedden, Lindsay, Lukewich, Julia, Marshall, Emily Gard, Gill, Paul S, Isenor, Jennifer E, Martin-Misener, Ruth, Wickett, Jamie, Bulman, Donna, Dufour, Emilie, Meredith, Leslie, Spencer, Sarah, Vaughan, Crystal, Brown, Judith B

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Pilot/Phase II Trial of Hypofractionated Radiation Therapy to the Whole Breast Alone Before Breast Conserving Surgery von Thorpe, Cameron S., DeWees, Todd A., Laughlin, Brady S., Vallow, Laura A., Seneviratne, Dee, Pockaj, Barbara A., Cronin, Patricia A., Halyard, Michele Y., Vern-Gross, Tamara Z., McGee, Lisa A., McLaughlin, Sarah A., Voss, Molly M., Golafshar, Michael A., Bulman, Gabriella F., Vargas, Carlos E.

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Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1 von Bhola, Priya T, Hartley, Taila, Bareke, Eric, Boycott, Kym M, Nikkel, Sarah M, Dyment, David A

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Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events von Armour, Christine M., Smith, Amanda, Hartley, Taila, Chardon, Jodi Warman, Sawyer, Sarah, Schwartzentruber, Jeremy, Hennekam, Raoul, Majewski, Jacek, Bulman, Dennis E., Suri, Mohnish, Boycott, Kym M.

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Mother‐to‐daughter transmission of Kenny–Caffey syndrome associated with the recurrent, dominant FAM111A mutation p. Arg569His von Nikkel, S.M., Ahmed, A., Smith, A., Marcadier, J., Bulman, D.E., Boycott, K.M.

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