203 related articles for article (PubMed ID: 8650134)
21. Inherited erythrocyte pyruvate kinase deficiency: Studies on 15 members of two related families.
Dachà M; Canestrari F; Bossù M; Ferrini PL; Fornaini G
Acta Haematol; 1977; 57(1):37-46. PubMed ID: 190844
[TBL] [Abstract][Full Text] [Related]
22. [Identification of pyruvate kinase variants from red blood cells using trypsinization and electrophoresis].
Tzanev D; Schulz J; Jacobasch G; Richter A; Gerth C
Acta Biol Med Ger; 1980; 39(7):745-61. PubMed ID: 7211063
[TBL] [Abstract][Full Text] [Related]
23. Biochemical characterization of four new erythrocyte pyruvate kinase variants.
Tegos C; Anagnostoulis G
Acta Haematol; 1994; 92(2):91-6. PubMed ID: 7817710
[TBL] [Abstract][Full Text] [Related]
24. Molecular characterization of the PK-LR gene in pyruvate kinase deficient Spanish patients. Red Cell Pathology Group of the Spanish Society of Haematology (AEHH).
Zarza R; Alvarez R; Pujades A; Nomdedeu B; Carrera A; Estella J; Remacha A; Sánchez JM; Morey M; Cortes T; Pérez Lungmus G; Bureo E; Vives Corrons JL
Br J Haematol; 1998 Nov; 103(2):377-82. PubMed ID: 9827908
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. PK Aarau: first homozygous nonsense mutation causing pyruvate kinase deficiency.
Sedano IB; Röthlisberger B; Délèze G; Ottiger C; Panchard MA; Spahr A; Hergersberg M; Bürgi W; Huber A
Br J Haematol; 2004 Nov; 127(3):364-6. PubMed ID: 15491302
[No Abstract] [Full Text] [Related]
27. Congenital non-spherocytic haemolytic anaemias.
Zanella A; Colombo MB; Rossi F; Merati G; Sirchia G
Haematologica; 1989; 74(4):387-96. PubMed ID: 2551797
[TBL] [Abstract][Full Text] [Related]
28. Frame shift mutation, exon skipping, and a two-codon deletion caused by splice site mutations account for pyruvate kinase deficiency.
Kanno H; Fujii H; Wei DC; Chan LC; Hirono A; Tsukimoto I; Miwa S
Blood; 1997 Jun; 89(11):4213-8. PubMed ID: 9166866
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [Hereditary haemolytic anaemia due to pyruvate kinase deficiency. Prognosis of neonatal forms (author's transl)].
Boivin P; Ottenwaelter T
Nouv Presse Med; 1982 Mar; 11(12):917-9. PubMed ID: 7063368
[TBL] [Abstract][Full Text] [Related]
31. Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes.
Kedar P; Hamada T; Warang P; Nadkarni A; Shimizu K; Fujji H; Ghosh K; Kanno H; Colah R
Clin Genet; 2009 Feb; 75(2):157-62. PubMed ID: 18759866
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. [Diagnosis of pyruvate kinase deficiency].
Illum NO
Ugeskr Laeger; 1995 Apr; 157(15):2160-1. PubMed ID: 7652957
[TBL] [Abstract][Full Text] [Related]
34. Hematologically important mutations: red cell pyruvate kinase (Third update).
Bianchi P; Zanella A
Blood Cells Mol Dis; 2000 Feb; 26(1):47-53. PubMed ID: 10772876
[No Abstract] [Full Text] [Related]
35. Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.
Dongerdiye R; Bokde M; More TA; Saptarshi A; Devendra R; Chiddarwar A; Warang P; Kedar P
Ann Hematol; 2023 May; 102(5):1029-1036. PubMed ID: 36892591
[TBL] [Abstract][Full Text] [Related]
36. Red cell pyruvate kinase deficiency: adverse effect of oral contraceptives.
Kendall AG; Charlow GF
Acta Haematol; 1977; 57(2):116-20. PubMed ID: 402766
[TBL] [Abstract][Full Text] [Related]
37. [Analysis and prenatal diagnosis of PKLR gene mutations in a family with pyruvate kinase deficiency].
Li D; Zhang J; Jiao B; Liu Y; Wang Y; Wang Z; Li W; Hou L; Sun Y; Guo H; Guo X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):53-6. PubMed ID: 26829734
[TBL] [Abstract][Full Text] [Related]
38. Molecular characterization of the PK-LR gene in sixteen pyruvate kinase-deficient patients.
Zanella A; Bianchi P; Fermo E; Iurlo A; Zappa M; Vercellati C; Boschetti C; Baronciani L; Cotton F
Br J Haematol; 2001 Apr; 113(1):43-8. PubMed ID: 11328279
[TBL] [Abstract][Full Text] [Related]
39. Life-threatening nonspherocytic hemolytic anemia in a patient with a null mutation in the PKLR gene and no compensatory PKM gene expression.
Diez A; Gilsanz F; Martinez J; Pérez-Benavente S; Meza NW; Bautista JM
Blood; 2005 Sep; 106(5):1851-6. PubMed ID: 15870173
[TBL] [Abstract][Full Text] [Related]
40. First reported case of prenatal diagnosis for pyruvate kinase deficiency in a Chinese family.
So CC; Tang M; Li CH; Ha SY; Pissard S; Chan LC
Hematology; 2011 Nov; 16(6):377-9. PubMed ID: 22183074
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
