Zobrazeno 1 - 10
of 120
pro vyhledávání: '"F. Ida"'
Autor:
Douglas H. Jones, MD, Priya Bansal, MD, Jonathan A. Bernstein, MD, Shahnaz Fatteh, MD, Joseph Harper, PharmD, F. Ida Hsu, MD, Maeve O’Connor, MD, Nami Park, PharmD, Daniel Suez, MD
Publikováno v:
World Allergy Organization Journal, Vol 15, Iss 1, Pp 100621- (2022)
Background: Hereditary angioedema (HAE) is often caused by low serum levels or functional deficiency in C1 inhibitor (C1-INH); however, in some cases, C1-INH serum level and function are measured as normal (HAE-nl-C1INH). Management of HAE-nl-C1INH i
Externí odkaz:
https://doaj.org/article/532c5bdec9a240c88b9e8106405ecd30
Autor:
Jones, Douglas H., Bansal, Priya, Bernstein, Jonathan A., Fatteh, Shahnaz, Harper, Joseph, Hsu, F. Ida, O’Connor, Maeve, Park, Nami, Suez, Daniel
Publikováno v:
In World Allergy Organization Journal January 2022 15(1)
Autor:
Brooks, Joel P., Radojicic, Cristine, Riedl, Marc A., Newcomer, Scott D., Banerji, Aleena, Hsu, F. Ida
Publikováno v:
In The Journal of Allergy and Clinical Immunology: In Practice June 2020 8(6):1875-1880
Autor:
Romberg, Neil, Le Coz, Carole, Glauzy, Salomé, Schickel, Jean-Nicolas, Trofa, Melissa, Nolan, Brian E., Paessler, Michele, Xu, Mina L., Lambert, Michele P., Lakhani, Saquib A., Khokha, Mustafa K., Jyonouchi, Soma, Heimall, Jennifer, Takach, Patricia, Maglione, Paul J., Catanzaro, Jason, Hsu, F. Ida, Sullivan, Kathleen E., Cunningham-Rundles, Charlotte, Meffre, Eric
Publikováno v:
In The Journal of Allergy and Clinical Immunology January 2019 143(1):258-265
Autor:
Tobias M. Suiter, Radana Zachova, Sladjana Andrejevic, Anna Valerieva, Ralph Shapiro, Katarina Hrubiskova, Ljerka Karadza-Lapic, Roman Hakl, Vesna Grivcheva-Panovska, Maria Staevska, D. Soteres, Vinay Mehta, Milos Jesenak, Marta Sobotkova, F. Ida Hsu, Jeffrey Rumbyrt, Andrea Zanichelli, Raffi Tachdjian
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 8:799-802
Hereditary angioedema (HAE), an inherited deficiency offunctional C1 esterase inhibitor (C1-INH), is characterized byrecurrent episodes of disabling and often painful swelling insubcutaneous and/or submucosal tissues.1HAE attacks aregenerally unpredi
Autor:
Valerieva, Anna, Staevska, Maria, Jesenak, Milos, Hrubiskova, Katarina, Sobotkova, Marta, Zachova, Radana, Hakl, Roman, Andrejevic, Sladjana, Suiter, Tobias, Grivcheva-Panovska, Vesna, Karadza-Lapic, Ljerka, Soteres, Daniel, Shapiro, Ralph, Rumbyrt, Jeffrey, Tachdjian, Raffi, Mehta, Vinay, Hsu, F. Ida, Zanichelli, Andrea
Publikováno v:
In The Journal of Allergy and Clinical Immunology: In Practice February 2020 8(2):799-802
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Joel P Brooks, Marc A. Riedl, Cristine Radojicic, Scott D. Newcomer, F. Ida Hsu, Aleena Banerji
Publikováno v:
The journal of allergy and clinical immunology. In practice. 8(6)
Consensus guidelines recommend plasma-derived C1 inhibitor (C1-INH) as first-line treatment in pregnant women with hereditary angioedema (HAE). We conducted a systematic review of the literature that describes experience with plasma-derived C1-INH du
Autor:
Joel P Brooks, Veronica Azmy, Stephanie Prozora, Christina Price, Alison Thompson, F. Ida Hsu, Darren Luon
Publikováno v:
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners. 26(1)
Background Hypersensitivity reactions to etoposide have been reported and patients have been safely transitioned to etoposide phosphate for continued therapy. However, the safety and efficacy of substituting etoposide phosphate for etoposide has not