Immunology in the Clinic Review Series; focus on allergies: immunotherapy for food allergy von Mousallem, T., Burks, A. W.

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SEVERE COMBINED IMMUNODEFICIENCY MISSED BY NEWBORN SCREENING von Zhou, C., Smith, L., Sleasman, J., Tarrant, T., Mousallem, T.

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THE DIFFERENT MANIFESTATIONS OF IKAROS: INFECTION, MALIGNANCY, IMMUNE DYSREGULATION AND VARIABLE PENETRANCE von Stewart-Bates, B., Kuehn, H., Sleasman, J., Rosenzweig, S., Mousallem, T.

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TRANSIENT LOSS OF PERIPHERAL B-CELLS IN A PATIENT WITH CONGENITAL ATHYMIA AND OMENN'S SYNDROME von Stewart-Bates, B., Hall, G., Mousallem, T., Stallings, A., Sleasman, J.

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Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome von Leiding, J. W., Vogel, T. P., Santarlas, V. G. J., Mhaskar, R., Smith, M. R., Carisey, A., Vargas-Hernandez, A., Silva-Carmona, M., Heeg, M., Rensing-Ehl, A., Neven, Bénédicte, Hadjadj, Jérôme, Hambleton, S., Leahy, T. R., van Hagen, M., Cunningham-Rundles, C., Dutmer, C. M., Sharapova, S. O., Taskinen, M., Chua, I., Hague, R., Klemann, C., Kostyuchenko, L., Morio, T., Thatayatikom, A., Ozen, A., Scherbina, A., Bauer, C. S., Flanagan, S. E., Gambineri, E., Giovannini-Chami, Lisa, Heimall, J., Sullivan, K. E., Allenspach, E., Romberg, N., Deane, S. G., Prince, B. T., Rose, M., Bohnsack, J., Mousallem, T., Jesudas, R., dos Santos Vilela, M. M., O'Sullivan, M., Schmid, J. P., Průhová, Š., Rees, M., Su, H., Bahna, S., Baris, S., Bartnikas, L. M., Chang Berger, A., Briggs, T. A., Brothers, S., Bundy, V., Chan, A. Y., Chandrakasan, S., Christiansen, M., Cole, T., Cook, M. C., Desai, M. M., Fischer, U., Fulcher, D. A., Gallo, S., Gauthier, A., Gennery, A. R., Marques, J. G., Gottrand, Fréderic, Grimbacher, B., Grunebaum, E., Haapaniemi, E., Hämäläinen, S., Heiskanen, K., Heiskanen-Kosma, T., Hoffman, H. M., Gonzalez-Granado, L. I., Guerreiro, A. L., Kainulainen, L., Kumar, A., Lawrence, M. G., Levin, C., Martelius, T., Neth, O., Olbrich, P., Palma, A., Patel, N. C., Pozos, T., Preece, K., Lugo Reyes, S. O., Russell, M. A., Schejter, Y., Seroogy, C., Sinclair, J., Skevofilax, E., Suan, D., Suegeorgz, D., Szabolcs, P., Velasco, H., Warnatz, K., Walkovich, K., Worth, A.

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The CLN9 Protein, a Regulator of Dihydroceramide Synthase von Schulz, Angela, Mousallem, Talal, Venkataramani, Maya, Persaud-Sawin, Dixie-Ann, Zucker, Adam, Luberto, Chiara, Bielawska, Alicja, Bielawski, Jacek, Holthuis, Joost C.M., Jazwinski, S. Michal, Kozhaya, Lina, Dbaibo, Ghassan S., Boustany, Rose-Mary N.

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Ceramide regulates SR protein phosphorylation during adenoviral infection von Kanj, Souha S., Dandashi, Nadine, El-Hed, Aimee, Harik, Hisham, Maalouf, Maria, Kozhaya, Lina, Mousallem, Talal, Tollefson, Ann E., Wold, William S., Chalfant, Charles E., Dbaibo, Ghassan S.

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Risk of Hypospadias in Newborn Infants Exposed to Valproic Acid During the First Trimester of Pregnancy: A Case-Control Study in Spain von Rodríguez-Pinilla, Elvira, Mejías, Consuelo, Prieto-Merino, David, Fernández, Paloma, L, María

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The CLN9 protein- a regulator of dihydroceramide synthase von Schulz, A, Mousallem, T, Venkataramani, M, Persaud-Sawin, D.A, Zucker, A, Luberto, C, Bielawska, A, Bielawska, J, Holthuis, J.C.M, Jazwinski, S.M, Kozhaya, L, Dbaibo, G.S, Boustany, R.M

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Analysis of the frequencies of genotype combinations of 4 polymorphisms of genes acting on the folate cycle in the Spanish population von Martínez-Frías, María Luisa, Bermejo, Eva, Pérez, Belén, Desviat, Lourdes R, Castro, Margarita, Leal, Fátima, Mansilla, Elena, Martínez-Fernández, María Luisa, Rodríguez-Pinilla, Elvira, Rodríguez, Laura, Ugarte, Magdalena

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Single Center Oral Food Challenges: A Five Year Retrospective Review von Koutlas, Nicole, Stallings, Amy, Mousallem, Talal

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167 Differentiating IPEX- like syndrome from other causes of autoimmune enteropathy von Chen, Jenny, Hall, Geoffrey, Kim-Chang, Julie, Mousallem, Talal

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A newborn with multiple intestinal atresias found to have variants in tetratricopeptide repeat domain 7A gene von Zhou, Cynthia, Koutlas, Nicole, Kim-Chang, Julie, Mousallem, Talal

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A Single-Center Review of Severe Combined Immune Deficiency (SCID) Newborn Screening (NBS) Data in the Neonatal Intensive Care Unit (NICU) von Hall, Geoffrey, Burt, Trevor, Fisher, Kimberley, Pittman, Rick, Sleasman, John, Buckley, Rebecca, Cotten, Michael, Mousallem, Talal

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Combined immunodeficiency presenting as autoimmune hemolytic anemia von Nasir, Aman, MD, Caldwell, Jason W., DO, FAAAAI, Batt, Katharine, MD, Mousallem, Talal I., MD

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Improving Compliance with State-Recommended Guidelines for Severe Combined Immunodeficiency (SCID) Newborn Screening (NBS) in the Intensive Care Nursery (ICN) von Hall, Geoffrey, Zhou, Cynthia, Kim-Chang, Julie, DiCarlo, Camille, Bartlett, Kathleen, Sterrett, Emily, Cotten, C. Michael, Buckley, Rebecca, Mousallem, Talal

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Severe Hematologic Abnormality Associated with an Inborn Error of Immunity (IEI) von Hall, Geoffrey, Markle, Janet, Maiarana, James, Rothman, Jennifer, Martin, Paul, Sleasman, John, Mousallem, Talal

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Clinical implications of inherited chromosomally integrated HHV-6 in the setting of ADA-deficient severe combined immunodeficiency (SCID) von Purswani, Pooja, Hall, Geoffrey, Moorthy, Ganga, Mousallem, Talal

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A nonsense mutation in IKBKB causes combined immunodeficiency von Mousallem, Talal, Yang, Jialong, Urban, Thomas J., Wang, Hongxia, Adeli, Mehdi, Parrott, Roberta E., Roberts, Joseph L., Goldstein, David B., Buckley, Rebecca H., Zhong, Xiao-Ping

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Early immune reconstitution in an infant with adenosine deaminase deficient severe combined immunodeficiency started on enzyme replacement therapy von Phillips, Michael, Hall, Geoffrey, Koutlas, Nicole, Hicks, Elizabeth, Buckley, Kevin, Buckley, Rebecca, Sleasman, John, Hershfield, Michael, Tarrant, Teresa, Mousallem, Talal

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