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CLINICAL STUDY

ACE Gene Polymorphism in Turkish Children with Nephrotic Syndrome

, M.D., , M.D., , M.D., , M.D., , M.D., , M.D., , M.D. & , M.D. show all
Pages 401-403 | Published online: 07 Jul 2009

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Read on this site (2)

Belgin Alasehirli, Ayşe Balat & Mithat Büyükçelik. (2012) DD Genotype of ACE Gene in Boys: May it be a Risk Factor for Minimal Change Nephrotic Syndrome?. Renal Failure 34:1, pages 19-23.
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Tian-Biao Zhou, Yuan-Han Qin, Li-Na Su, Feng-Ying Lei, Wei-Fang Huang, Yan-Jun Zhao & Yu-Sheng Pang. (2011) Insertion/Deletion (I/D) Polymorphism of Angiotensin-Converting Enzyme Gene in Steroid-Resistant Nephrotic Syndrome for Children: A Genetic Association Study and Meta-analysis. Renal Failure 33:7, pages 741-748.
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Articles from other publishers (12)

Jiwon M. Lee, Yo Han Ahn, Seon Hee Lim & Hee Gyung Kang. (2021) Biomarkers Predicting Treatment-Response in Nephrotic Syndrome of Children: A Systematic Review. Childhood Kidney Diseases 25:2, pages 92-111.
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Aravind Selvin Kumar Ramanathan, Balakrishnan Karuppiah, Murali Vijayan, Kamaraj Raju, Dhivakar Mani, Rathika Chinniah, Manikandan Thirunavukkarasu, Padma Malini Ravi, Jeyaram Illiayaraja Krishnan & Prabha Senguttuvan. (2019) Effect of angiotensin converting enzyme gene I/D polymorphism in South Indian children with nephrotic syndrome. The Journal of Biomedical Research 33:3, pages 201.
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Danko Batinić, Jadranka Sertić, Marijana Ćorić, Paško Konjevoda, Danica Batinić & Danko Milošević. (2015) Angiotensin-Converting Enzyme Genotype Is Not a Significant Genetic Risk Factor for Idiopathic Nephrotic Syndrome in Croatian Children. Nephron 130:1, pages 29-34.
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Wali Unnisa, Asra Tabassum, Umme N. Mahwish, G. Suman Latha, D. Sree Bhushan Raju & Parveen Jahan. (2012) Des Disease Status and Steroid Responsivenoess in Idiopathic Nephrotic Syndrome Depend on ACE I/D Gene Polymorphism? A Study from South India. Asian Journal of Biological Sciences 5:3, pages 148-156.
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Tian-Biao Zhou, Yuan-Han Qin, Chao Ou, Li-Na Su, Feng-Ying Lei, Wei-Fang Huang, Yan-Jun Zhao & Yu-Sheng Pang. (2011) A meta-analysis of the association between angiotensin-converting enzyme insertion/deletion gene polymorphism and steroid-sensitive nephrotic syndrome in children. Journal of the Renin-Angiotensin-Aldosterone System 13:1, pages 175-183.
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Tian-Biao Zhou, Chao Ou, Yuan-Han Qin, Li-Na Su, Feng-Ying Lei, Wei-Fang Huang, Yan-Jun Zhao, Yu-Sheng Pang & Kun-Peng Yang. (2011) Association of angiotensin converting enzyme insertion/deletion gene polymorphism with idiopathic nephrotic syndrome susceptibility in children: a meta-analysis. Journal of the Renin-Angiotensin-Aldosterone System 12:4, pages 601-610.
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Tian-Biao Zhou, Yuan-Han Qin, Li-Na Su, Feng-Ying Lei, Wei-Fang Huang, Yan-Jun Zhao, Yu-Sheng Pang & Kun-Peng Yang. (2011) The association between angiotensin-converting enzyme insertion/deletion gene variant and risk of focal segmental glomerulosclerosis: a systematic review and meta-analysis. Journal of the Renin-Angiotensin-Aldosterone System 12:4, pages 624-633.
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Hyun Jin Choi, Hee Yeon Cho, Han Ro, So Hee Lee, Kyung Hee Han, HyunKyung Lee, Hee Gyung Kang, Il Soo Ha, Yong Choi & Hae Il Cheong. (2011) Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome. Pediatric Nephrology 26:11, pages 1981-1988.
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Tian-Biao Zhou, Yuan-Han Qin, Li-Na Su, Feng-Ying Lei, Wei-Fang Huang & Yan-Jun Zhao. (2011) ACE I/D Gene Polymorphism Can't Predict the Steroid Responsiveness in Asian Children with Idiopathic Nephrotic Syndrome: A Meta-Analysis. PLoS ONE 6:5, pages e19599.
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Hee Yeon ChoHyun Jin ChoiSo Hee LeeHyun Kyung LeeHee Kyung KangIl Soo HaYong ChoiHae Il Cheong. (2009) Polymorphisms of the NR3C1 gene in Korean children with nephrotic syndrome. Korean Journal of Pediatrics 52:11, pages 1260.
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E Kasap, M Akyıldız & U Akarca. (2009) Cholangitis of Pancreatitis? Does the Angiotensin-Converting Enzyme Genotype Favor Either?. Balkan Journal of Medical Genetics 12:2, pages 53-57.
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E Kasap, M Akyıldız, F Tekin & U Akarca. (2009) Angiotensin-Converting Enzyme Genotype and Acute Pancreatitis in Turkey. Balkan Journal of Medical Genetics 12:2, pages 39-44.
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