Author:
Rao Chandrika,Murthy Venkata,Hegde Radhakrishna,Vishwanath Asha
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference8 articles.
1. Casteels I, Spileers W, Swinnen Tet al. Optic atrophy as presenting sign in Hallervorden Spatz syndrome.Neuropediatrics 1994; 25: 265–267.
2. Elejalde BR, Elejalde MM, San Juan R, Lopez F. Genetic and nosologic considerations in Hallervorden Spatz Disease.Clin Genet 1978; 30: 50A.
3. Zhou B, Westaway SK, Levinson B, Johnson MAet al. A novel pantothenase kinase gene (PANK 2) is defective in Hallervorden Spatz Syndrome.Nature Genet 2001; 28: 345–349.
4. Angelini L, Nardocci N, Rumi V, Zorzi C, Strdal L, Savoiardo M. Hallervorden Spatz Disease; Clinical and MRI study of 11 cases diagnosed in life.J Neuro 1992; 239: 417–425.
5. Littrup PJ, Gebarski SS. MRI Imaging of Hallervorden Spatz Disease.J Comput Assist Tomogr 1985; 9: 491–493.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The Liabilities of Iron Deficiency;Iron Physiology and Pathophysiology in Humans;2011-11-24