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Associate Physician (2024 - present)
Associate Physician (2024 - present)
Board Certifications: Diplomate of American Board of Allergy and Immunology (2024), American Board of Internal Medicine (2021)
Adjunct Clinical Professor of Medicine: Scripps Clinic Division of Allergy, Asthma, and Immunology (2024 - present)
Fellowship: Allergy and Clinical Immunology - Scripps Green Hospital - La Jolla, CA
Residency: Internal Medicine - Adventist Health White Memorial Medical Center - Los Angeles, CA
Publications:
Imam K, Huang J, White AA. Isotype deficiencies (IgG subclass and selective IgA, IgM, IgE deficiencies). Allergy Asthma Proc. 2024 Sep 1;45(5):317-320.
Huang J, Imam K, Criado JR, Luskin KT, Liu Y, Puglisi LH, Lyons JJ, White AA. Hereditary alpha-tryptasemia in patients with postural orthostatic tachycardia syndrome. J Allergy Clin Immunol Pract. 2024 Feb;12(2):528-529.
Imam KH, Abud EM, White AA. Systemic Contact Dermatitis to Cinnamon: A Case Report. Dermatitis. 2024 Nov-Dec;35(6):652-653.
Imam KH, Woessner KM. Nonsteroidal anti-inflammatory drug-exacerbated respiratory disease: diagnosis and current management. Pol Arch Intern Med. 2023 Sep;133(9):16544.
Sehanobish, E., Ye, K. Imam, K, et al. Elaborate biologic approval process delays care of patients with moderate-to-severe asthma. 2023 Journal of Allergy and Clinical Immunology: Global, 2(2), p. 100076.
Imam, K. and Patel, S. (2022) ‘Muscle tension dysphonia masquerading as asthma’, Annals of Allergy, Asthma & Immunology, 129(5).
Doroudchi, A., Imam, K. & Garcia Lloret, M.I. Allergen Immunotherapy in Pediatric Respiratory Allergy. Curr Treat Options Allergy 8, 147–160 (2021).
Imam, K., Cui, C. and Riedl, M. (2021) ‘M110 a novel SERPING1 mutation in a case of hereditary angioedema’, Annals of Allergy, Asthma & Immunology, 127(5).
Imam, K., Patel, S. and Cui, C. (2021) ‘M109 hereditary angioedema presenting as abdominal pain’, Annals of Allergy, Asthma & Immunology, 127(5).
Kagabo W, Imam K, Liu A. Pulvinar sign and abnormally high CSF WBC in posterior reversible encephalopathy syndrome. Clin Case Rep. 2020 Aug 19;8(12):2661-2663.
Rezkalla N, Imam K, Marti M, Ip K, Mashhadian A, Liu A. CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis. Clin Case Rep. 2020 Jul 1;8(10):1962-1964.
Imam K, Liu A. A case of Recurrent Guillain-Barre Syndrome observed by the same clinician 12 years apart. Clin Case Rep. 2020 Jun 18;8(8):1376-1378.
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