“I’m Doing My Part, I Just Need Help From the Community”: Intervention Implications of Foster and Adoptive Parents’ Experiences Raising Children and Young Adults With FASD by Petrenko, Christie L. M., Alto, Michelle E., Hart, Andrea R., Freeze, Sarah M., Cole, Lynn L.

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Autosomal recessive phosphoglucomutase 3 ( PGM3 ) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment by Zhang, Yu, PhD, Yu, Xiaomin, PhD, Ichikawa, Mie, BSc, Lyons, Jonathan J., MD, Datta, Shrimati, PhD, Lamborn, Ian T., BSc, Jing, Huie, PhD, Kim, Emily S., BSc, Biancalana, Matthew, BSc, Wolfe, Lynne A., CRNP, DiMaggio, Thomas, ADN, Matthews, Helen F., BSN, Kranick, Sarah M., MD, Stone, Kelly D., MD, PhD, Holland, Steven M., MD, Reich, Daniel S., MD, PhD, Hughes, Jason D., PhD, Mehmet, Huseyin, PhD, McElwee, Joshua, PhD, Freeman, Alexandra F., MD, Freeze, Hudson H., PhD, Su, Helen C., MD, PhD, Milner, Joshua D., MD

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Asymptomatic Erythematous and Tan, Shiny, Well-Defined Plaques by Freeze, Megan E., Miles, J. Alex, Miedema, Jayson R., Corley, Sarah

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International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1‐CDG): Diagnosis, follow‐up, and management by Altassan, Ruqaiah, Radenkovic, Silvia, Edmondson, Andrew C., Barone, Rita, Brasil, Sandra, Cechova, Anna, Coman, David, Donoghue, Sarah, Falkenstein, Kristina, Ferreira, Vanessa, Ferreira, Carlos, Fiumara, Agata, Francisco, Rita, Freeze, Hudson, Grunewald, Stephanie, Honzik, Tomas, Jaeken, Jaak, Krasnewich, Donna, Lam, Christina, Lee, Joy, Lefeber, Dirk, Marques‐da‐Silva, Dorinda, Pascoal, Carlota, Quelhas, Dulce, Raymond, Kimiyo M., Rymen, Daisy, Seroczynska, Malgorzata, Serrano, Mercedes, Sykut‐Cegielska, Jolanta, Thiel, Christian, Tort, Frederic, Vals, Mari‐Anne, Videira, Paula, Voermans, Nicol, Witters, Peter, Morava, Eva

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MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature by Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.

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Impaired Glycosylation Due To Autosomal Recessive PGM3 Mutations Results In Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment by Milner, Joshua D., Dr, Lyons, Jonathan J., Dr, Zhang, Yu, Dr, Yu, Xiaomin, Dr, Datta, Shrimati, Dr, Lamborn, Ian T., BSc, Biancalana, Matthew R., BSc, Wolfe, Lynne A., CRNP, DiMaggio, Thomas, BSN, Matthews, Helen F., BSN, Kranick, Sarah M., Dr, Stone, Kelly D., Dr, Holland, Steven M., Dr, Reich, Daniel S., Dr, Hughes, Jason D., Dr, Mehmet, Huseyin, Dr, McElwee, Joshua, Dr, Freeze, Hudson H., Dr, Freeman, Alexandra F.F., Dr, Su, Helen C., Dr

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Autosomal recessive PGM3 mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment by Zhang, Yu, Yu, Xiaomin, Ichikawa, Mie, Lyons, Jonathan J., Datta, Shrimati, Lamborn, Ian T., Jing, Huie, Kim, Emily S., Biancalana, Matthew, Wolfe, Lynne A., DiMaggio, Thomas, Matthews, Helen F., Kranick, Sarah M., Stone, Kelly D., Holland, Steven M., Reich, Daniel S., Hughes, Jason D., Mehmet, Huseyin, McElwee, Joshua, Freeman, Alexandra F., Freeze, Hudson H., Su, Helen C., Milner, Joshua D.

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MPI-CDG from a hepatic perspective: Report of two Egyptian cases and review of literature by Abdel Ghaffar, Tawhida Y, Ng, Bobby G, Elsayed, Solaf M, El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H

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Airships: A New Horizon for Science by Miller, Sarah H, Fesen, Robert, Hillenbrand, Lynne, Rhodes, Jason, Baird, Gil, Blake, Geoffrey, Booth, Jeff, Carlile, David E, Riley Duren, Edworthy, Frederick G, Freeze, Brent, Friedl, Randall R, Goldsmith, Paul F, Hall, Jeffery L, Hoffman, Scott E, Hovarter, Scott E, Jensen-Clem, Rebecca M, Jones, Ross M, Kauffmann, Jens, Kiessling, Alina, King, Oliver G, Konidaris, Nick, Lachenmeier, Timothy L, Lord, Steven D, Neu, Jessica, Quetin, Gregory R, Ram, Alan, Sander, Stanley, Simard, Marc, Smith, Mike, Smith, Steve, Smoot, Sara, Susca, Sara, Swann, Abigail, Young, Eliot F, Zambrano, Thomas

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