278 related articles for article (PubMed ID: 26315463)
1. Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.
Mañú-Pereira Mdel M; Gonzalez-Roca E; van Solinge WW; Llaudet-Planas E; Sevilla J; Montllor L; Mensa-Vilaro A; Ploos van Amstel HK; van Wijk R; Vives-Corrons J
Am J Hematol; 2015 Dec; 90(12):E217-9. PubMed ID: 26315463
[No Abstract] [Full Text] [Related]
2. [Chronic non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency in a Costa Rican family carrying hemoglobin C disease].
Chaves M; Vives-Corrons JL; Sáenz GF; Pujades MA; Briceño J; Colomer D
Sangre (Barc); 1990 Apr; 35(2):128-33. PubMed ID: 2363093
[TBL] [Abstract][Full Text] [Related]
3. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
[TBL] [Abstract][Full Text] [Related]
4. Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan).
Karadsheh NS; Gelbart T; Naffa RG
Int J Lab Hematol; 2014 Aug; 36(4):e66-8. PubMed ID: 24330591
[No Abstract] [Full Text] [Related]
5. A novel and a previously described compound heterozygous PKLR gene mutations causing pyruvate kinase deficiency in a Chinese child.
Li H; Gu P; Yao RE; Wang J; Fu Q; Wang J
Fetal Pediatr Pathol; 2014 Jun; 33(3):182-90. PubMed ID: 24601847
[TBL] [Abstract][Full Text] [Related]
6. Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
Manco L; Vagace JM; Relvas L; Rebelo U; Bento C; Villegas A; Letícia Ribeiro M
Eur J Haematol; 2010 Jan; 84(1):89-90. PubMed ID: 19758413
[No Abstract] [Full Text] [Related]
7. Novel PLKR mutations in four families with pyruvate kinase deficiency.
Qin L; Nie Y; Chen L; Zhang D; Lin Y; Ru K
Int J Lab Hematol; 2020 Apr; 42(2):e84-e87. PubMed ID: 31747117
[No Abstract] [Full Text] [Related]
8. Coexistence of congenital red cell pyruvate kinase and band 3 deficiency.
Branca R; Costa E; Rocha S; Coelho H; Quintanilha A; Cabeda JM; Santos-Silva A; Barbot J
Clin Lab Haematol; 2004 Aug; 26(4):297-300. PubMed ID: 15279669
[TBL] [Abstract][Full Text] [Related]
9. Tanaka KR, Valentine WN, Miwa S. Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia. Blood. 1962;19(3):267-295.
Blood; 2016 May; 127(21):2505. PubMed ID: 27231390
[No Abstract] [Full Text] [Related]
10. Dyserythropoiesis in a child with pyruvate kinase deficiency and coexistent unilateral multicystic dysplastic kidney.
Haija MA; Qian YW; Muthukumar A
Pediatr Blood Cancer; 2014 Aug; 61(8):1463-5. PubMed ID: 24481986
[TBL] [Abstract][Full Text] [Related]
11. The mouse Char10 locus regulates severity of pyruvate kinase deficiency and susceptibility to malaria.
Laroque A; Min-Oo G; Tam M; Ponka P; Stevenson MM; Gros P
PLoS One; 2017; 12(5):e0177818. PubMed ID: 28542307
[TBL] [Abstract][Full Text] [Related]
12. Pyruvate kinase deficiency.
Miwa S
Nihon Ketsueki Gakkai Zasshi; 1987 Dec; 50(8):1445-52. PubMed ID: 3328943
[No Abstract] [Full Text] [Related]
13. RLS with PLMS in a child with hemolytic anemia caused by pyruvate kinase deficiency.
Peraita-Adrados R; Medrano-Martinez P; Peirano P; Algarín C; Lillo-Triguero L
Sleep Med; 2020 May; 69():100-102. PubMed ID: 32062035
[No Abstract] [Full Text] [Related]
14. A previously unknown mutation in the pyruvate kinase gene (PKLR) identified from a neonate with severe jaundice.
Yaish HM; Nussenzveig RH; Agarwal AM; Siddiqui AH; Christensen RD
Neonatology; 2014; 106(2):140-2. PubMed ID: 24969675
[TBL] [Abstract][Full Text] [Related]
15. Safe and Efficient Gene Therapy for Pyruvate Kinase Deficiency.
Garcia-Gomez M; Calabria A; Garcia-Bravo M; Benedicenti F; Kosinski P; López-Manzaneda S; Hill C; Del Mar Mañu-Pereira M; Martín MA; Orman I; Vives-Corrons JL; Kung C; Schambach A; Jin S; Bueren JA; Montini E; Navarro S; Segovia JC
Mol Ther; 2016 Aug; 24(7):1187-98. PubMed ID: 27138040
[TBL] [Abstract][Full Text] [Related]
16. Compound heterozygosity in
Bagla S; Bhambhani K; Gadgeel M; Buck S; Jin JP; Ravindranath Y
Haematologica; 2019 Sep; 104(9):e428-e431. PubMed ID: 30948487
[No Abstract] [Full Text] [Related]
17. Pyruvate kinase "Göttingen 1,2": congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity.
Schröter W; Lakomek M; Scharnetzky M; Tillmann W; Winkler H
Hum Genet; 1982; 60(4):381-6. PubMed ID: 7106777
[No Abstract] [Full Text] [Related]
18. A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat.
Aksu T; Yarali N; Fermo E; Marcello A; Hacisalihoğlu Ş; Bianchi P; Özbek NY
J Pediatr Hematol Oncol; 2018 Oct; 40(7):e458-e460. PubMed ID: 29309376
[TBL] [Abstract][Full Text] [Related]
19. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
Warang P; Kedar P; Ghosh K; Colah R
Blood Cells Mol Dis; 2013 Oct; 51(3):133-7. PubMed ID: 23770304
[TBL] [Abstract][Full Text] [Related]
20. Red blood cell PK deficiency: An update of PK-LR gene mutation database.
Canu G; De Bonis M; Minucci A; Capoluongo E
Blood Cells Mol Dis; 2016 Mar; 57():100-9. PubMed ID: 26832193
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]