P009 Intravenous immunoglobulin G desensitization protocol von Frith, J, Casselman, J, Tcheurekdjian, H, Hostoffer, R

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P051 Influence of winter weather on the pollen season in northeast Ohio von Michaud, C, Weaver, E, Frith, J, Peppers, B, Hostoffer, R

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P249 Common variable immunodeficiency presenting with recurrent ascending cholangitis von Johnson, J, Abraham, T, Sandhu, M, Tcheurekdjian, H, Hostoffer, R

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P072 Effectiveness of epinephrine rinse in decreasing local reactions in subcutaneous immunotherapy von Casselman, J, Kim, Y, Peppers, B, Hostoffer, R, Tcheurekdjian, H

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NOVEL NFKB1 MUTATION IN A FEMALE WITH COMMON VARIABLE IMMUNE DEFICIENCY (CVID) von Blunk, H., Kohli, E., Hostoffer, R.

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UNDEFINED AUTOINFLAMMATORY CONDITION FOLLOWING COVID-19 INFECTION von Humpel, O., Nagireddi, L., Hostoffer, R.

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NOVEL MUTATION IN BRUTON'S TYROSINE KINASE IN PATIENT WITH CUTANEOUS T CELL LYMPHOMA von Humpel, O., Kalkat, A., Hostoffer, R.

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SERUM IGM DEFICIENCY ASSOCIATED WITH CONNEXIN MUTATION IN AN 18-YEAR-OLD MALE von Sarkaria, S., Callahan, M., Hostoffer, Z., Venglarcik, J., Hostoffer, R.

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VIDEO PROCEDURAL TRAINING SERIES IMPACT ON A/I FIT COMPETENCY SELF-ASSESSMENT von Sehmi, K., Kohli, E., Wu, S., Hostoffer, R.

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LATE-ONSET GAMMA INTERFERON RECEPTOR-1 DEFICIENCY WITH NONTUBERCULOUS MYCOBACTERIAL INFECTION von Humpel, O., Shankar, A., Nagireddi, L., Kalkat, A., Hostoffer, R.

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NOVEL HETEROZYGOTE MUTATION OF LRBA ASSOCIATED WITH CVID von Sewell, C., Callahan, M., Immaneni, N., Saab, R., Hostoffer, R.

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A NOVEL MUTATION OF IL21R IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY von Huq, M., Callahan, M., Shankar, A., Hostoffer, R.

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A CASE OF PULMONARY EMBOLISM POST COVID-19 INFECTION IN A PATIENT WITH STAT3 MUTATION von Blunk, H., Birch, K., Callahan, M., Hostoffer, R.

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M152 POSNER-SCHLOSSMAN SYNDROME ASSOCIATED WITH COMMON VARIABLE IMMUNODEFICIENCY von Huq, M., Daniels, P., Sanan, N., Hostoffer, R.

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A NOVEL GENE MUTATION ASSOCIATED WITH COMMON VARIABLE IMMUNODEFICIENCY AND PYODERMA von Joseph, N., Hostoffer, R., Tcheurekdjian, H.

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M294 A HETEROZYGOUS NOVEL VARIANT OF SMARCAL1 GENE CAUSING SCHIMKE IMMUNO-OSSEOUS DYSPLASIA von Daniels, P., Valencia, R., Graven, K., Tcheurekdjian, H., Hostoffer, R.

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M295 EOSINOPHILIC FASCIITIS IN COMMON VARIABLE IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA von Daniels, P., Shilian, R., Huq, M., Hostoffer, R.

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Recurrent Facial Herpes Simplex Infections in a 4 year Old Female with a Functional Natural Killer Cell Deficiency von Marks, A, Hostoffer, R

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A Protocol for the Desensitization to Intravenous Immunoglobulin (IVIg) von Salomon, M, Hostoffer, R

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Quality of Life is Maintained in Common Variable Immunodeficiency During Long-term Immunoglobulin Replacement Therapy von Nguyen, D, Catanzaro, J, Apte, S, Palermo, T, Hostoffer, R, Tcheurekdjian, H

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