Cargando…

Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema

Detalles Bibliográficos
Autores principales:	Magerl, Markus, Gothe, Holger, Krupka, Simon, Lachmann, Anja, Ohlmeier, Christoph
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901175/ https://www.ncbi.nlm.nih.gov/pubmed/33618747 http://dx.doi.org/10.1186/s13023-021-01714-7

Ejemplares similares

A Germany-wide survey study on the patient journey of patients with hereditary angioedema
por: Magerl, Markus, et al.
Publicado: (2020)

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey
por: Mengel, Eugen, et al.
Publicado: (2020)

Management of patients with hereditary angioedema in Germany: comparison with other countries in the Icatibant Outcome Survey
por: Maurer, M., et al.
Publicado: (2018)

Expert perspectives on hereditary angioedema: Key areas for advancements in care across the patient journey
por: Banerji, Aleena, et al.
Publicado: (2016)

Correction to: The International/Canadian Hereditary Angioedema Guideline
por: Betschel, Stephen, et al.
Publicado: (2020)

Correction to: Content validation and psychometric evaluation of the Angioedema Quality of Life Questionnaire for hereditary angioedema
por: Vanya, Magdalena, et al.
Publicado: (2023)

Epidemiology and health care utilization of patients suffering from Huntington’s disease in Germany: real world evidence based on German claims data
por: Ohlmeier, Christoph, et al.
Publicado: (2019)

Correction to: Mitigating Disparity in Healthcare Resources Between Countries for Management of Hereditary Angioedema
por: Jindal, Ankur Kumar, et al.
Publicado: (2021)

Improvement in diagnostic delays over time in patients with hereditary angioedema: findings from the Icatibant Outcome Survey
por: Zanichelli, Andrea, et al.
Publicado: (2018)

WAO Guideline for the Management of Hereditary Angioedema
por: Craig, Timothy, et al.
Publicado: (2012)

Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
por: Zanichelli, Andrea, et al.
Publicado: (2013)

Could it be hereditary angioedema?—Perspectives from different medical specialties
por: Magerl, Markus, et al.
Publicado: (2023)

Patient‐physician interactions in hereditary angioedema—Key learnings from the coronavirus disease 2019 pandemic
por: Maurer, Marcus, et al.
Publicado: (2023)

Epidemiology and treatment of children with hereditary angioedema in Germany: A retrospective database study
por: Prenzel, Freerk, et al.
Publicado: (2023)

Hereditary angioedema
por: Lesser, Helen, et al.
Publicado: (2021)

Hereditary Angioedema
por: Banerjee, Anjali, et al.
Publicado: (2023)

Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series
por: Maurer, Marcus, et al.
Publicado: (2022)

On demand treatment and home therapy of hereditary angioedema in Germany - the Frankfurt experience
por: Aygören-Pürsün, Emel, et al.
Publicado: (2010)

Correction: Considerations in the management of hereditary angioedema due to C1-INH deficiency in women of childbearing age
por: Hsu, Florence Ida, et al.
Publicado: (2022)

Perioperative management for patients with hereditary angioedema
por: Williams, Anesu H., et al.
Publicado: (2015)

Anaesthetic Approach for Patient with Hereditary Angioedema
por: Melo, Maize Cordeiro, et al.
Publicado: (2020)

Microbiota dysbiosis in hereditary angioedema patients
por: Özdemir, Öner
Publicado: (2023)

Correction to: Long-term health-related quality of life in patients treated with subcutaneous C1-inhibitor replacement therapy for the prevention of hereditary angioedema attacks: findings from the COMPACT open-label extension study
por: Lumry, William R., et al.
Publicado: (2021)

Food as a trigger for abdominal angioedema attacks in patients with hereditary angioedema
por: Steiner, Urs C., et al.
Publicado: (2018)

Impact of lanadelumab on health‐related quality of life in patients with hereditary angioedema in the HELP study
por: Lumry, William R., et al.
Publicado: (2020)

National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia
por: Kanepa, Adine, et al.
Publicado: (2023)

Clinical Utility Gene Card for hereditary angioedema with normal C1 inhibitor (HAEnC1)
por: Stieber, Christiane, et al.
Publicado: (2017)

Hereditary angioedema in women
por: Bouillet, Laurence
Publicado: (2010)

Hereditary Angioedema: Not An Allergy
por: Bhivgade, Sanjay, et al.
Publicado: (2012)

The Pathophysiology of Hereditary Angioedema
por: Zuraw, Bruce L
Publicado: (2010)

Pediatric hereditary angioedema
por: MacGinnitie, Andrew J
Publicado: (2014)

Hereditary angioedema in childhood
por: Ahn, Young Min
Publicado: (2020)

Lanadelumab for hereditary angioedema
Publicado: (2022)

Biomarkers in Hereditary Angioedema
por: Porebski, Grzegorz, et al.
Publicado: (2021)

Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
por: Johnsrud, Irene, et al.
Publicado: (2015)

Efficacy of Omalizumab in a Patient with Angioedema Clinically Resembling a Hereditary Angioedema
por: Kutlu, Ali, et al.
Publicado: (2016)

Hereditary angioedema: quality of life in Brazilian patients
por: Gomide, Maria Abadia Consuelo M S, et al.
Publicado: (2013)

Ongoing Contact Activation in Patients with Hereditary Angioedema
por: Konings, Joke, et al.
Publicado: (2013)

Oxidative stress markers in patients with hereditary angioedema
por: Del Giacco, Stefano R., et al.
Publicado: (2017)

Screening for Plasminogen Mutations in Hereditary Angioedema Patients
por: Farkas, Henriette, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_igdfkt5hjo4u93m0k7qtodmmif