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The Association Between Incident Nontuberculous Mycobacteria Isolation and Antibiotic Exposure in Patients with Bronchiectasis.
Marmor, Meghan; Brunton, Amanda E; Fraulino, David; Ruoss, Stephen J; Henkle, Emily; Zha, B Shoshana; Metersky, Mark; Winthrop, Kevin; Bronchiectasis and NTM Research Registry Investigators Chest 2025 Oct;
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Mycobacterium nebraskense Isolated from Patients in Connecticut and Oregon, USA.
Metersky, Mark L; Losier, Ashley J; Fraulino, David A; Warnock, Theodore A; Varley, Cara D; Le, Angela M; Winthrop, Kevin L; McArdle, John R; Shakir, Salika M; Khare, Reeti Emerging infectious diseases 2025 Mar;31(3):507-515
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Five-Year Outcomes Among U.S. Bronchiectasis and Nontuberculous Mycobacterial Registry Patients.
Aksamit, Timothy R; Locantore, Nicholas; Addrizzo-Harris, Doreen; Ali, Juzar; Barker, Alan; Basavaraj, Ashwin; Behrman, Megan; Brunton, Amanda E; Chalmers, Sarah; Choate, Radmila; Dean, Nathan C; DiMango, Angela; Fraulino, David; Johnson, Margaret M; Lapinel, Nicole C; Maselli, Diego J; McShane, Pamela J; Metersky, Mark L; Miller, Bruce E; Naureckas, Edward T; O'Donnell, Anne E; Olivier, Kenneth N; Prusinowski, Elly; Restrepo, Marcos I; Richards, Christopher J; Rhyne, Gloria; Schmid, Andreas; Solomon, George M; Tal-Singer, Ruth; Thomashow, Byron; Tino, Gregory; Tsui, Kevin; Varghese, Sumith Abraham; Warren, Heather E; Winthrop, Kevin; Zha, Beth Shoshanna American journal of respiratory and critical care medicine 2024 Apr;
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Latent tuberculosis infection in the outpatient general medicine clinic: Efficacy of a nurse-run electronic directly observed treatment program.
Levine, Susan; Fraulino, David; Krupka, Philip; Velamakanni, Sruti Preventive medicine reports 2023 Oct;35102321
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Chasing the Ghost: Hyperinflammation Does Not Cause Sepsis.
Shapiro, Leland; Scherger, Sias; Franco-Paredes, Carlos; Gharamti, Amal A; Fraulino, David; Henao-Martinez, Andrés F Frontiers in pharmacology 2022 Jan;13910516
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A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency.
Jabara, Haifa H; Boyden, Steven E; Chou, Janet; Ramesh, Narayanaswamy; Massaad, Michel J; Benson, Halli; Bainter, Wayne; Fraulino, David; Rahimov, Fedik; Sieff, Colin; Liu, Zhi-Jian; Alshemmari, Salem H; Al-Ramadi, Basel K; Al-Dhekri, Hasan; Arnaout, Rand; Abu-Shukair, Mohammad; Vatsayan, Anant; Silver, Eli; Ahuja, Sanjay; Davies, E Graham; Sola-Visner, Martha; Ohsumi, Toshiro K; Andrews, Nancy C; Notarangelo, Luigi D; Fleming, Mark D; Al-Herz, Waleed; Kunkel, Louis M; Geha, Raif S Nature genetics 2016 Jan;48(1):74-8
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A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.
Chou, Janet; Hanna-Wakim, Rima; Tirosh, Irit; Kane, Jennifer; Fraulino, David; Lee, Yu Nee; Ghanem, Soha; Mahfouz, Iman; Mégarbané, André; Lefranc, Gérard; Inati, Adlette; Dbaibo, Ghassan; Giliani, Silvia; Notarangelo, Luigi D; Geha, Raif S; Massaad, Michel J The Journal of allergy and clinical immunology 2012 Dec;130(6):1414-6
