Digital indicators for red cell disorder

Autor: Dasgupta, Anjan Kr., Lahiri, Prabir

Publikováno v: Current Science, 2000 May . 78(10), 1250-1255.

Externí odkaz: https://www.jstor.org/stable/24103927

The intriguing contribution of white blood cells to sickle cell disease – a red cell disorder

Autor: Okpala, Iheanyi

Publikováno v: In Blood Reviews 2004 18(1):65-73

The intriguing contribution of white blood cells to sickle cell disease - a red cell disorder

Autor: Iheanyi Okpala

Publikováno v: Blood reviews. 18(1)

Sickle cell disease (SCD) is characterized by a point mutation that replaces adenine with thymidine in the sixth codon of the beta-globin gene, a unique morphological abnormality of red blood cells, vaso-occlusion with ischaemic tissue injury, and su

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1214de23c551edccc2e4d04ef6d95066
https://pubmed.ncbi.nlm.nih.gov/14684149

UPAYA MENURUNKAN ANGKA KEJADIAN TALASEMIA MAYOR MELALUI EDUKASI DAN PEMERIKSAAN DARAH PADA ACARA DONOR DARAH: MENUJU ZERO GROWTH TALASEMIA MAYOR DI INDONESIA.

Autor: Panigoro, Ramdan^1,2, Prihatni, Delita^2,3, Sribudiani, Yunia^1,2, Ghozali, Mohammad^1,2, Maskoen, Ani Melani^1,4, Susanah, Susi, Turbawati, Dewi Kartika³, Lismayanti, Leni³, Purwanti, Ratu³, Sahiratmadja, Edhyana^1,2 e.sahiratmadja@unpad.ac.id

Publikováno v: Dharmakarya: Jurnal Aplikasi Ipteks Untuk Masyarakat. jun2023, Vol. 12 Issue 2, p182-188. 7p.

Novel mutations associated with pyruvate kinase deficiency in Brazil

Autor: Paulo Augusto Achucarro Silveira, Fernando Ferreira Costa, Jhonathan Angel Araujo Fernandez, Silvia Regina Brandalise, Ana Paula Hitomi Yokoyama, Sara Teresinha Olalla Saad, Maria Carolina Costa Melo Svidnicki, Andrey Santos, Isis Q. Magalhães, Vitória Régia Pereira Pinheiro

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 40, Iss 1, Pp 5-11 (2018)
Hematology, Transfusion and Cell Therapy, Volume: 40, Issue: 1, Pages: 11-5, Published: MAR 2018

Background: Pyruvate kinase deficiency is a hereditary disease that affects the glycolytic pathway of the red blood cell, causing nonspherocytic hemolytic anemia. The disease is transmitted as an autosomal recessive trait and shows a marked variabili

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a957079edc35789245d40a437c032856
http://www.sciencedirect.com/science/article/pii/S1516848417301305