Search Results - Ivan K. Chinn

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  1. 1
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    T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication by Xavier Rios, Ivan K. Chinn, Jordan S. Orange, Celine I. Hanson, Nicholas L. Rider

    Published 2017
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  2. 2
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    Treatment-Responsive Granulomatous-Lymphocytic Interstitial Lung Disease in a Pediatric Case of Common Variable Immunodeficiency by Robert Tillman, R. Paul Guillerman, Timothy Trojan, Manuel Silva-Carmona, Manuel Silva-Carmona, Ivan K. Chinn

    Published 2019
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  3. 3
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    Immune Dysregulation Mimicking Systemic Lupus Erythematosus in a Patient With Lysinuric Protein Intolerance: Case Report and Review of the Literature by Josefina Longeri Contreras, Mabel A. Ladino, Katherine Aránguiz, Gonzalo P. Mendez, Zeynep Coban-Akdemir, Zeynep Coban-Akdemir, Bo Yuan, Bo Yuan, Richard A. Gibbs, Lindsay C. Burrage, Lindsay C. Burrage, James R. Lupski, James R. Lupski, James R. Lupski, Ivan K. Chinn, Ivan K. Chinn, Tiphanie P. Vogel, Tiphanie P. Vogel, Jordan S. Orange, M. Cecilia Poli, M. Cecilia Poli, M. Cecilia Poli

    Published 2021
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  4. 4
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    Failing to Make Ends Meet: The Broad Clinical Spectrum of DNA Ligase IV Deficiency. Case Series and Review of the Literature by Aidé Tamara Staines Boone, Ivan K. Chinn, Ivan K. Chinn, Carmen Alaez-Versón, Marco A. Yamazaki-Nakashimada, Karol Carrillo-Sánchez, María de la Luz Hortensia García-Cruz, M. Cecilia Poli, M. Cecilia Poli, M. Edith González Serrano, Edgar A. Medina Torres, David Muzquiz Zermeño, Lisa R. Forbes, Lisa R. Forbes, Francisco J. Espinosa-Rosales, Francisco J. Espinosa-Rosales, Sara E. Espinosa-Padilla, Jordan S. Orange, Jordan S. Orange, Saul Oswaldo Lugo Reyes

    Published 2019
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  5. 5
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    Case Report: p40phox deficiency underlying pediatric-onset systemic lupus erythematosus by Alejandro Nieto-Patlán, Natalia S. Fernández Dávila, Yuqing Wang, Michelle Zelnick, Eyal Muscal, Martha Curry, James R. Lupski, James R. Lupski, James R. Lupski, Steven M. Holland, Bo Yuan, Douglas B. Kuhns, Tiphanie P. Vogel, Ivan K. Chinn

    Published 2024
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  6. 6
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    Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome by Alejandra Aird, Macarena Lagos, Macarena Lagos, Alexander Vargas-Hernández, Jennifer E. Posey, Zeynep Coban-Akdemir, Shalini Jhangiani, Shalini Jhangiani, Emily M. Mace, Anaid Reyes, Alejandra King, Felipe Cavagnaro, Lisa R. Forbes, Ivan K. Chinn, James R. Lupski, James R. Lupski, James R. Lupski, Jordan S. Orange, Maria Cecilia Poli, Maria Cecilia Poli

    Published 2019
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