Anaemia — Impact of Vitamin B12 Supplementation With Iron and Folic Acid on Adolescent Girls
Citation(s)
Agarwal KN, Gomber S, Bisht H, Som M Anemia prophylaxis in adolescent school girls by weekly or daily iron-folate supplementation. Indian Pediatr. 2003 Apr;40(4):296-301.
Deshmukh PR, Garg BS, Bharambe MS Effectiveness of weekly supplementation of iron to control anaemia among adolescent girls of Nashik, Maharashtra, India. J Health Popul Nutr. 2008 Mar;26(1):74-8.
Hettiarachchi M, Liyanage C, Wickremasinghe R, Hilmers DC, Abrams SA The efficacy of micronutrient supplementation in reducing the prevalence of anaemia and deficiencies of zinc and iron among adolescents in Sri Lanka. Eur J Clin Nutr. 2008 Jul;62(7):856-65. Epub 2007 May 16.
Kotecha PV, Nirupam S, Karkar PD Adolescent girls' Anaemia Control Programme, Gujarat, India. Indian J Med Res. 2009 Nov;130(5):584-9.
Mozaffari-Khosravi H, Noori-Shadkam M, Fatehi F, Naghiaee Y Once weekly low-dose iron supplementation effectively improved iron status in adolescent girls. Biol Trace Elem Res. 2010 Jun;135(1-3):22-30. doi: 10.1007/s12011-009-8480-0. Epub 2009 Aug 4.
Sen A, Kanani SJ Impact of iron-folic acid supplementation on cognitive abilities of school girls in Vadodara. Indian Pediatr. 2009 Feb;46(2):137-43.
Shobha S, Sharada D Efficacy of twice weekly iron supplementation in anemic adolescent girls. Indian Pediatr. 2003 Dec;40(12):1186-90.
Worthington-White DA, Behnke M, Gross S Premature infants require additional folate and vitamin B-12 to reduce the severity of the anemia of prematurity. Am J Clin Nutr. 1994 Dec;60(6):930-5.
Impact of Vitamin B12 Supplementation With Iron and Folic Acid on Adolescent Girls
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