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2. A case of complete adenylate kinase deficiency due to a nonsense mutation in AK-1 gene (Arg 107 --> Stop, CGA --> TGA) associated with chronic haemolytic anaemia. Bianchi P; Zappa M; Bredi E; Vercellati C; Pelissero G; Barraco F; Zanella A Br J Haematol; 1999 Apr; 105(1):75-9. PubMed ID: 10233365 [TBL] [Abstract][Full Text] [Related]
3. [Familial multinuclear erythroblasts with macrocytic anemia caused by ineffective erythropoiesis and increased hemolysis]. Minssen M; Klaus D Med Welt; 1968 Oct; 42():2280-3. PubMed ID: 5730695 [No Abstract] [Full Text] [Related]
4. Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase. Matsuura S; Igarashi M; Tanizawa Y; Yamada M; Kishi F; Kajii T; Fujii H; Miwa S; Sakurai M; Nakazawa A J Biol Chem; 1989 Jun; 264(17):10148-55. PubMed ID: 2542324 [TBL] [Abstract][Full Text] [Related]
5. A new variant of adenylate kinase (delG138) associated with severe hemolytic anemia. Fermo E; Bianchi P; Vercellati C; Micheli S; Marcello AP; Portaleone D; Zanella A Blood Cells Mol Dis; 2004; 33(2):146-9. PubMed ID: 15315793 [TBL] [Abstract][Full Text] [Related]
6. Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemia. Abrusci P; Chiarelli LR; Galizzi A; Fermo E; Bianchi P; Zanella A; Valentini G Exp Hematol; 2007 Aug; 35(8):1182-9. PubMed ID: 17662886 [TBL] [Abstract][Full Text] [Related]
7. Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia. Qualtieri A; Pedace V; Bisconte MG; Bria M; Gulino B; Andreoli V; Brancati C Br J Haematol; 1997 Dec; 99(4):770-6. PubMed ID: 9432020 [TBL] [Abstract][Full Text] [Related]
8. Hemolytic anemia with null PKLR mutations identified using whole exome sequencing and cured by hematopoietic stem cell transplantation combined with splenectomy. Kim M; Park J; Lee J; Jang W; Chae H; Choi H; Kim J; Kwon A; Lee JW; Cho B; Kim Y; Chung NG Bone Marrow Transplant; 2016 Dec; 51(12):1605-1608. PubMed ID: 27595284 [No Abstract] [Full Text] [Related]
9. Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia. Beutler E; Carson D; Dannawi H; Forman L; Kuhl W; West C; Westwood B J Clin Invest; 1983 Aug; 72(2):648-55. PubMed ID: 6308059 [TBL] [Abstract][Full Text] [Related]
10. [Value of splenectomy in hemolytic anemias]. Juvara I; Prişcu A; Rădulescu D; Dragomirescu C Chirurgia (1951); 1971 Jul; 20(7):577-88. PubMed ID: 5153617 [No Abstract] [Full Text] [Related]
13. [Blood changes following splenectomy in systemic hemolytic anemia]. ALEKSEEW G Pol Arch Med Wewn; 1956; 26(11):1677-82. PubMed ID: 13419725 [No Abstract] [Full Text] [Related]
15. [Effectiveness of splenectomy in various diseases of the hematopoietic system. Part I. Splenectomy in hemolytic anemias]. EFENDIEV FA; AKHUNDOVA AM Probl Gematol Pereliv Krovi; 1960 Jan; 5():21-4. PubMed ID: 13819463 [No Abstract] [Full Text] [Related]
16. [Effect of splenectomy on serological reactions in hemolytic and aplastic syndromes]. MIRKOWSKA-STELMACHOWSKA A; PELCZARSKA E; JASSER S Pol Arch Med Wewn; 1959; 29(3):367-70. PubMed ID: 13667695 [No Abstract] [Full Text] [Related]
17. A simple screening procedure for adenylate kinase, hexokinase and glucose-6-phosphate dehydrogenase deficiencies. Vaca G; Sanchez-Corona J; Olivares N; Medina C; Cantu JM Ann Genet; 1980; 23(3):190-2. PubMed ID: 6252822 [TBL] [Abstract][Full Text] [Related]