• Users Online: 321
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 

    Article Cited by others

REVIEW ARTICLE

Primary familial and congenital polycythemia; The forgotten entity

Aljabry Mansour S

Year : 2018| Volume: 9| Issue : 2 | Page no: 39-44

   This article has been cited by
 
1 Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study
Alpay Yesilaltay, Hasan Degirmenci, Turker Bilgen, Duygu Yasar Sirin, Duygu Bayir, Pelin Degirmenci, Atakan Tekinalp, Seref Alpsoy, Yildiz Okuturlar, Burhan Turgut
Medicine. 2022; 101(32): e29881
[Pubmed]  [Google Scholar]
2 Unexplained Hematocrit Increase after Therapeutic Phlebotomy in a Patient with Marked Erythrocytosis
Rushad Machhi, Ashley M. Cunningham, Kenneth Hennrick, Karen A. Schaser, Eliot C. Williams, William Nicholas Rose, Kostas Konstantopoulos
Case Reports in Hematology. 2022; 2022: 1
[Pubmed]  [Google Scholar]
3 JAK2 Variant Signaling: Genetic, Hematologic and Immune Implication in Chronic Myeloproliferative Neoplasms
Dania G. Torres, Jhemerson Paes, Allyson G. da Costa, Adriana Malheiro, George V. Silva, Lucivana P. de Souza Mourão, Andréa M. Tarragô
Biomolecules. 2022; 12(2): 291
[Pubmed]  [Google Scholar]
4 Identification of Two Novel EPOR Gene Variants in Primary Familial Polycythemia: Case Report and Literature Review
Laura Lo Riso, Gardenia Vargas-Parra, Gemma Navarro, Leonor Arenillas, Lierni Fernández-Ibarrondo, Beatriz Robredo, Carmen Ballester, Bernardo López, Albert Perez-Montaña, Antonia Sampol, Lourdes Florensa, Carles Besses, María Antonia Duran, Beatriz Bellosillo
Genes. 2022; 13(10): 1686
[Pubmed]  [Google Scholar]

 

Read this article