Zobrazeno 1 - 10
of 993
pro vyhledávání: '"GLUCOSE PHOSPHATE"'
Publikováno v:
International Journal of General Medicine, Vol Volume 17, Pp 5825-5836 (2024)
Jie Li,1,* Wenyang Ma,1,* Wuzhuang Tang,1 Kaixuan Yang,2 Hongqiu Gu,2 Junfeng Shi,1 Feng Chen,1 Chenhan Xu,1 Shiyuan Gu,1 Yongjun Wang2,3 1Department of Neurology, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People’s Repub
Externí odkaz:
https://doaj.org/article/29efee18071345209d642e814cb977f6
Autor:
Abhilasha Sampagar, Abhishek Chandira, Swapnil Pattanshetti, Santosh Kurbet, Ashwini Doddannavar, Krishna Prasanna
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp 274-278 (2024)
Background: There is a lack of literature on the role of splenectomy in hemolytic anemias due to glucose-6-phosphate isomerase (GPI) deficiency. GPI deficiency is a rare red blood cell (RBC) enzymopathy of the glycolytic pathway. Most present with se
Externí odkaz:
https://doaj.org/article/09eca44e65a1468cb10fecea7f47269a
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp 283-286 (2024)
Introduction: Glucose phosphate isomerase (GPI) deficiency is a rare autosomal recessive disorder that causes hereditary nonspherocytic hemolytic anemia (HNSHA). It is caused by homozygous or compound heterozygous mutation of the GPI gene on chromoso
Externí odkaz:
https://doaj.org/article/296de1d999e9481588f125ddd94a07c3
Autor:
Zaidi, Ahmar U.1 (AUTHOR) azaidi@dmc.org, Kedar, Prabhakar2 (AUTHOR), Koduri, Prasad Rao3 (AUTHOR), Goyette, Gerard W.1 (AUTHOR), Buck, Steven1 (AUTHOR), Paglia, Donald E.4 (AUTHOR), Ravindranath, Yaddanapudi1 (AUTHOR)
Publikováno v:
Pediatric Hematology & Oncology. Nov2017, Vol. 34 Issue 8, p449-454. 6p.
Publikováno v:
Hereditas. 5/18/2017, Vol. 154, p1-10. 10p.
Autor:
Niitepõld, Kristjan1, Saastamoinen, Marjo1
Publikováno v:
Annales Zoologici Fennici. May2017, Vol. 54 Issue 1-4, p259-273. 15p.
Autor:
Yang Wang, Tao Liu, Jiaqi Liu, Yan Xiang, Lan Huang, Jiacheng Li, Xizhou An, Shengyan Cui, Zishuai Feng, Jie Yu
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Background and Aims: Glucose phosphate isomerase (GPI) deficiency is an extremely rare autosomal recessive disorder caused by mutations in the GPI gene. In this research, the proband displaying typical manifestations of haemolytic anaemia an
Externí odkaz:
https://doaj.org/article/b54b4b5c35c14e958b5863628a1661a4
Autor:
Tine, Mbaye1,2 mbtine@hotmail.fr
Publikováno v:
BMC Research Notes. 12/18/2015, Vol. 8, p1-16. 16p. 3 Diagrams, 2 Charts, 2 Graphs.
Autor:
Li, Yuan1 Yuan.Li@biol.lu.se, Canbäck, Björn1, Johansson, Tomas1, Tunlid, Anders1, Prentice, Honor C.1
Publikováno v:
PLoS ONE. May2015, Vol. 10 Issue 5, p1-18. 18p.
Autor:
Bahaji, Abdellatif1, Sánchez-López, Ángela M.1, De Diego, Nuria2, Muñoz, Francisco J.1, Baroja-Fernández, Edurne1, Li, Jun1, Ricarte-Bermejo, Adriana1, Baslam, Marouane1, Aranjuelo, Iker3, Almagro, Goizeder1, Humplík, Jan F.2, Novák, Ondřej4, Spíchal, Lukáš3, Doležal, Karel3, Pozueta-Romero, Javier1 javier.pozueta@unavarra.es
Publikováno v:
PLoS ONE. Mar2015, Vol. 10 Issue 3, p1-35. 35p.