Your browser doesn't support javascript.
loading
Paroxysmal nocturnal hemoglobinuria clones are not infrequent in patients with inherited bone marrow failure syndromes.
Sreedharanunni, Sreejesh; Varma, Neelam; Sachdeva, Man Updesh Singh; Naseem, Shano; Malhotra, Pankaj; Bansal, Deepak; Sood, Anil; Bose, Parveen; Varma, Subhash.
  • Sreedharanunni S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Varma N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sachdeva MUS; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Naseem S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Malhotra P; Internal Medicine (Clinical hematology), Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Bansal D; Advance Pediatric centre (Hematology/oncology unit), Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sood A; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Bose P; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Varma S; Internal Medicine (Clinical hematology), Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Eur J Haematol ; 99(2): 194-195, 2017 08.
Article en En | MEDLINE | ID: mdl-28452421
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de la Médula Ósea / Hemoglobinuria Paroxística / Enfermedades Genéticas Congénitas / Anemia Aplásica Límite: Adult / Humans / Male Idioma: En Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de la Médula Ósea / Hemoglobinuria Paroxística / Enfermedades Genéticas Congénitas / Anemia Aplásica Límite: Adult / Humans / Male Idioma: En Año: 2017 Tipo del documento: Article