Cargando…
Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations
Glanzmann thrombasthenia (GT) is an inherited genetic disorder affecting platelets, which is characterized by spontaneous mucocutaneous bleeding and abnormally prolonged bleeding in response to injury or trauma. The underlying defect is failure of platelet aggregation due to qualitative and/or quant...
Autores principales: | Haghighi, A., Borhany, M., Ghazi, A., Edwards, N., Tabaksert, A., Fatima, N., Shamsi, T.S., Sayer, J.A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737203/ https://www.ncbi.nlm.nih.gov/pubmed/26096001 http://dx.doi.org/10.1111/cge.12622 |
Ejemplares similares
-
Glanzmann thrombasthenia
por: Nurden, Alan T
Publicado: (2006) -
Glanzmann’s thrombasthenia and molecular mimicry
por: Wiwanitkit, Viroj
Publicado: (2010) -
Dental Considerations in the Management of Glanzmann’s Thrombasthenia
por: Mehta, Diana N, et al.
Publicado: (2010) -
Disease Burden in Patients with Glanzmann’s Thrombasthenia: Perspectives from the Glanzmann’s Thrombasthenia Patient/Caregiver Questionnaire
por: Duncan, Alexander, et al.
Publicado: (2020) -
The Glanzmann Thrombasthenia Registry: safety of platelet therapy in patients with Glanzmann thrombasthenia and changes in alloimmunization status
por: Poon, Man-Chiu, et al.
Publicado: (2023)