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Expert Review of Clinical Immunology Volume 11, 2015 - Issue 3
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Drug Profile

Recombinant human C1 esterase inhibitor for the treatment of hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)

Geetika SabharwalDepartment of Pediatrics, Penn State University, 500 University Drive, 17033 Hershey, USA
&
Timothy CraigDepartment of Medicine and Pediatrics, Penn State University, Hershey, PA, USACorrespondence[email protected]
Pages 319-327 | Published online: 10 Feb 2015

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Maria Paula Henao, Jennifer L Kraschnewski, Theodore Kelbel & Timothy J Craig. (2016) Diagnosis and screening of patients with hereditary angioedema in primary care. Therapeutics and Clinical Risk Management 12, pages 701-711.
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Lise Aagaard & Anette Bygum. (2016) Adverse events reported for hereditary angioedema medications: a retrospective study of spontaneous reports submitted to the EudraVigilance database, 2007-2013. Orphan Drugs: Research and Reviews 6, pages 1-8.
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Irina Guryanova, Chiara Suffritti, Debora Parolin, Andrea Zanichelli, Nastassia Ishchanka, Ekaterina Polyakova, Mikhail Belevtsev, Francesca Perego, Marco Cicardi, Yulia Zharankova, Natalya Konoplya, Sonia Caccia & Antonio Gidaro. (2021) Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene. Clinical and Molecular Allergy 19:1.
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David J Handelsman. (2021) Androgen Misuse and Abuse. Endocrine Reviews 42:4, pages 457-501.
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I. E. Guryanova, Yu. S. Zharankova, E. A. Polyakova, V. V. Pugacheva, K. Ya. Skapavets, M. V. Belevtsev & O. V. Aleinikova. (2021) Molecular genetic diagnosis of hereditary angioedema. Proceedings of the National Academy of Sciences of Belarus, Medical series 18:1, pages 25-35.
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Maria Dolores Moya-Garzon, Jose Antonio Gomez-Vidal, Alfonso Alejo-Armijo, Joaquin Altarejos, Juan Roberto Rodriguez-Madoz, Miguel Xavier Fernandes, Eduardo Salido, Sofia Salido & Monica Diaz-Gavilan. (2021) Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias. Journal of Personalized Medicine 11:2, pages 74.
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Yasir J. Sepah, Gabriel Velez, Peter H. Tang, Jing Yang, Teja Chemudupati, Angela S. Li, Quan D. Nguyen, Alexander G. Bassuk & Vinit B. Mahajan. (2020) Proteomic analysis of intermediate uveitis suggests myeloid cell recruitment and implicates IL-23 as a therapeutic target. American Journal of Ophthalmology Case Reports 18, pages 100646.
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Prajeeda M. Nair, Matthew J. Rendo, Kristin M. Reddoch-Cardenas, Jason K. Burris, Michael A. Meledeo & Andrew P. Cap. (2020) Recent advances in use of fresh frozen plasma, cryoprecipitate, immunoglobulins, and clotting factors for transfusion support in patients with hematologic disease. Seminars in Hematology 57:2, pages 73-82.
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Ivo J.H.M. de Vos, Julia Verbist & Maurice A.M. van Steensel. 2019. Imaging Technologies and Transdermal Delivery in Skin Disorders. Imaging Technologies and Transdermal Delivery in Skin Disorders 105 146 .
Jutta Schröder-Braunstein & Michael Kirschfink. (2019) Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management. Molecular Immunology 114, pages 299-311.
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Dorit Farfara, Emily Feierman, Allison Richards, Alexey S. Revenko, Robert A. MacLeod, Erin H. Norris & Sidney Strickland. (2019) Knockdown of circulating C1 inhibitor induces neurovascular impairment, glial cell activation, neuroinflammation, and behavioral deficits. Glia 67:7, pages 1359-1373.
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Geetika Sabharwal & Timothy Craig. (2017) Pediatric hereditary angioedema: an update. F1000Research 6, pages 1205.
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David J. Handelsman. 2017. Endocrinology of the Testis and Male Reproduction. Endocrinology of the Testis and Male Reproduction 1251 1285 .
David J. Handelsman. 2017. Thyroid Diseases. Thyroid Diseases 1 35 .
Amy S. Paller & Anthony J. Mancini. 2016. Hurwitz Clinical Pediatric Dermatology. Hurwitz Clinical Pediatric Dermatology 467 494.e6 .
Yingqi Liu, Zixiang Zhu, Miaotao Zhang & Haixue Zheng. (2015) Multifunctional roles of leader protein of foot-and-mouth disease viruses in suppressing host antiviral responses. Veterinary Research 46:1.
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Dumitru Moldovan, Jonathan A Bernstein & Marco Cicardi. (2015) Recombinant replacement therapy for hereditary angioedema due to C1 inhibitor deficiency. Immunotherapy 7:7, pages 739-752.
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