Cargando…

Systemic therapy for hereditary cancer

Detalles Bibliográficos
Autor principal:	Imyanitov, Evgeny N
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Meeting Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518234/ http://dx.doi.org/10.1186/1897-4287-10-S4-A16

Ejemplares similares

Drug therapy for hereditary cancers
por: Imyanitov, Evgeny N, et al.
Publicado: (2011)

Cytotoxic and targeted therapy for hereditary cancers
por: Iyevleva, Aglaya G., et al.
Publicado: (2016)

Systemic treatment for hereditary cancers: a 2012 update
por: Imyanitov, Evgeny N, et al.
Publicado: (2013)

Hereditary cerebellar degeneration and stem-cell based therapy
por: Ostasov, Pavel, et al.
Publicado: (2014)

Overview of genetic markers for hereditary colorectal cancer
por: Scott, Rodney J
Publicado: (2012)

Hereditary angioedema without deficiency of C1 inhibitor: response to therapy
por: Pimenta, Fabiane Milena Castro Araújo, et al.
Publicado: (2015)

Hereditary cancer syndromes
por: Imyanitov, Evgeny N, et al.
Publicado: (2023)

Retrospective analysis of patients with hereditary nonpolyposis colorectal cancer (HNPCC)
por: Zbigniew, Banaszkiewicz, et al.
Publicado: (2015)

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016
por: Cybulski, C., et al.
Publicado: (2017)

Role of oncology/genetics nurse in management of individuals with hereditary diffuse gastric cancer
por: Shanahan, M, et al.
Publicado: (2012)

Clinical features of diabetes mellitus in hereditary pancreatitis
por: Dytz, Marcio Garrison, et al.
Publicado: (2015)

Type-III hereditary angioedema resolved by surgery
por: Fu, Lisa W, et al.
Publicado: (2014)

Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC)
por: Kaszuba, M, et al.
Publicado: (2012)

Therapeutic trial in hereditary angioedema type III: Icatibant
por: Garro, Laila Sabino, et al.
Publicado: (2015)

Early presentation of clinical hereditary angioedema symptoms in an infant
por: Pham, Hoang, et al.
Publicado: (2014)

P01-026 – A case of FMF and hereditary coproporphyria
por: Ganesha, A, et al.
Publicado: (2013)

Selected abstracts submitted to the Third International Symposium on Hereditary Breast and Ovarian Cancer: BRCA: Fifteen Years of Progress, Third International Symposium on Hereditary Breast and Ovarian Cancer; October 14–16, 2009; Centre Mont-Royal, Montreal, Quebec, Canada
Publicado: (2009)

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland
por: Plawski, Andrzej, et al.
Publicado: (2012)

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015
por: Thompson, Ella R., et al.
Publicado: (2017)

Spectrum of tumors in the families with Hereditary Breast Ovarian Cancer syndrome carrying germline mutations in BRCA1 and 2 genes
por: Budryk, M, et al.
Publicado: (2012)

Analysis of icatibant for the treatment of laryngeal hereditary angioedema attacks in the FAST-3 study
por: Yang, William, et al.
Publicado: (2014)

A new mutation in the SERPING1 gene in a Brazilian family with hereditary angioedema
por: Da Silva, Jane, et al.
Publicado: (2015)

Hereditary angioedema with C1 inhibitor deficiency: experience of a new reference center
por: Palma, Sandra Mitie Ueda, et al.
Publicado: (2015)

A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
por: Zanichelli, Andrea, et al.
Publicado: (2015)

Cytotoxic and targeted therapy for BRCA1/2-driven cancers
por: Imyanitov, Evgeny N.
Publicado: (2021)

Home treatment with conestat alfa in attacks of hereditary angioedema due to C1-inhibitor deficiency
por: Farkas, Henriette, et al.
Publicado: (2015)

Case report: follow-up of long term prophylaxis of hereditary angioedema with an alternative attenuated androgenic drug
por: Tebyrica, João
Publicado: (2015)

Breast cancer therapy for BRCA1 carriers: moving towards platinum standard?
por: Imyanitov, Evgeny N
Publicado: (2009)

Clinical and epidemiological profile of patients with hereditary angioedema treated in a referral outpatient clinic in Vitória, Espírito Santo - Brazil
por: Arantes, Rafael Cicconi, et al.
Publicado: (2015)

Treatment of hereditary angioedema with recombinant human C1 Inhibitor in a real-life setting: the experience of the HAE Centre in Milan
por: Zanichelli, Andrea, et al.
Publicado: (2015)

Self-administration of intravenous C1 esterase inhibitor (Berinertâ) in patients with Hereditary Angioedema decreases number of days spent in an emergency room
por: Rizk, Caroline, et al.
Publicado: (2011)

Self-administration of a novel subcutaneous bradykinin b(2) receptor antagonist, icatibant, as an effective treatment option in patients with hereditary angioedema
por: Santucci, Stephanie, et al.
Publicado: (2014)

Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
por: Gnoli, Maria, et al.
Publicado: (2014)

Selected Abstracts from the 3rd European Hereditary Tumour Group Meeting (EHTG 2018): Nice, France. 23-25 September 2018
Publicado: (2019)

Cancer Therapy Guided by Mutation Tests: Current Status and Perspectives
por: Aleksakhina, Svetlana N., et al.
Publicado: (2021)

Genome-proteome system for prostate cancer
por: Peshkov, Maxim N
Publicado: (2014)

Early breast cancer in elderly women: surgery or primary endocrine therapy?
por: Rocco, N, et al.
Publicado: (2010)

Baseline audit of manipulation and management of intravenous therapy delivery systems
por: Martinsen, C, et al.
Publicado: (2000)

Targeted therapy in head/neck and gastric cancers
por: Hsueh, Chung-Tsen
Publicado: (2012)

Treatment of advanced thyroid cancer refractory to therapy
por: Jarząb, Barbara
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_ucd4nrpgolh4urude7ug3kn76v