Cargando…
Guidelines for screening, diagnosis and management of hemoglobinopathies
The β-thalassemias and sickle cell disorders are a major health burden in India. Diagnosis and management of these disorders both in adults and in newborns using appropriate approaches and uniform technology are important in different regions of a vast and diverse country as India. In view of a Nati...
Autores principales: | Ghosh, Kanjaksha, Colah, Roshan, Manglani, Mamta, Choudhry, Ved Prakash, Verma, Ishwar, Madan, Nishi, Saxena, Renu, Jain, Dipty, Marwaha, Neelam, Das, Reena, Mohanty, Dipika, Choudhary, Rajendra, Agarwal, Sarita, Ghosh, Malay, Ross, Cecil |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228561/ https://www.ncbi.nlm.nih.gov/pubmed/25400338 http://dx.doi.org/10.4103/0971-6866.142841 |
Ejemplares similares
-
Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in Hemoglobinopathies
por: Italia, Khushnooma, et al.
Publicado: (2013) -
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India
por: Madan, Nishi, et al.
Publicado: (2010) -
Haemoglobinopathies in tribal populations of India
por: Ghosh, Kanjaksha, et al.
Publicado: (2015) -
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India
por: Mukherjee, Malay B., et al.
Publicado: (2010) -
Sickle cell disease in tribal populations in India
por: Colah, Roshan B., et al.
Publicado: (2015)