Red cell pyruvate kinase deficiency in neonatal jaundice cases in India

Author:

Kedar Prabhakar S.,Warang Prashant,Colah Roshan B.,Mohanty Dipika

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Valentine WN, Tanaka KK, Miwa S. A specific erythrocyte glycolytic enzyme defect (Pyruvate Kinase) in three subjects with congenital non-spherocytic hemolytic anemia.Trans Assoc Am Phys 1961; 74: 100–110.

2. Lilleyman J, Hann I, Blanchette V eds.Pediatric Hematology, 2nd edn. New York, Churchill Livingstone, 1999; pp. 191–192.

3. Carey PJ, Chandler J, Hendrick A, Reid MM, Saunders PWG, Tinegate H, Taylor PR, West N. Prevalence of pyruvate kinase deficiency in a northern European population in the north of England. (Letter)Blood 2000; 96: 4005.

4. Lenzner, C., Nurnberg P, Jacobasch G, Gerth, C, Thiele, BJ. Molecular analysis of 29 pyruvate kinase-deficient patients from Central Europe with hereditary hemolytic anemia.Blood 1997; 89: 1793–1799.

5. Miwa S, Nishina T. Studies on pyruvate kinase (PK) deficiency Clinical, hematological and erythrocyte enzyme studies.Acta Hematologica Japonica 1974; 37: 1–16.

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