Iron Gene Polymorphisms are Associated to Disability , Severity and Early Progression in Multiple Sclerosis
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Ajay | F. Salvi | D. Gemmati | P. Zamboni | S. D'alfonso | M. Leone | R. Asselta | C. Dall’Osso | G. Zeri | Elisa Orioli | V. Singh | Ilaria | Bartolomei | Francesca E. De Gaetano | V. Singh
[1] M. Cambron,et al. Vascular aspects of multiple sclerosis , 2011, The Lancet Neurology.
[2] Jim Mintz,et al. Gender and Iron Genes May Modify Associations Between Brain Iron and Memory in Healthy Aging , 2011, Neuropsychopharmacology.
[3] D. Mendonça,et al. HFE gene polymorphisms and severity in Portuguese patients with multiple sclerosis , 2011, European journal of neurology.
[4] F. Salvi,et al. Hypoperfusion of brain parenchyma is associated with the severity of chronic cerebrospinal venous insufficiency in patients with multiple sclerosis: a cross-sectional preliminary report , 2011, BMC medicine.
[5] J. Jankovic,et al. Iron chelation and neuroprotection in neurodegenerative diseases , 2011, Journal of Neural Transmission.
[6] C. Pozzilli,et al. Serum elements and oxidative status in clinically isolated syndromes , 2011, Neurology.
[7] G. Comi,et al. Chronic cerebro-spinal venous insufficiency (CCSVI) and multiple sclerosis , 2011, Neurological Sciences.
[8] A. González-Quintela,et al. Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant , 2010, BMC Genetics.
[9] S. J. Rensburg,et al. The controversy of CCSVI and iron in multiple sclerosis: Is ferritin the key? , 2010 .
[10] Wolfgang Vogel,et al. Ferroportin disease: A systematic meta-analysis of clinical and molecular findings☆ , 2010, Journal of hepatology.
[11] C. Férec,et al. Iron metabolism in macrophages from HFE hemochromatosis patients. , 2010, Molecular genetics and metabolism.
[12] M. Ferrari,et al. The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects , 2010, Haematologica.
[13] F. Salvi,et al. Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis , 2010, BMC Medical Genetics.
[14] P. Zamboni. Chronic cerebrospinal venous insufficiency. , 2010, International angiology : a journal of the International Union of Angiology.
[15] F. Salvi,et al. Chronic cerebrospinal venous insufficiency and iron deposition on susceptibility-weighted imaging in patients with multiple sclerosis: a pilot case-control study. , 2010, International angiology : a journal of the International Union of Angiology.
[16] D. Gemmati,et al. DNA-array of gene variants in venous leg ulcers: detection of prognostic indicators. , 2009, Journal of vascular surgery.
[17] T. Rouault,et al. Brain iron homeostasis, the choroid plexus, and localization of iron transport proteins , 2009, Metabolic Brain Disease.
[18] M. Testi,et al. Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major , 2009, Haematologica.
[19] B. Todorich,et al. Oligodendrocytes and myelination: The role of iron , 2009, Glia.
[20] M. Baiget,et al. Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes? , 2009, Annals of Hematology.
[21] J. Stankiewicz,et al. Role of iron in neurotoxicity: a cause for concern in the elderly? , 2009, Current opinion in clinical nutrition and metabolic care.
[22] C. Guttmann,et al. Deep Gray Matter Involvement on Brain MRI Scans Is Associated with Clinical Progression in Multiple Sclerosis , 2009, Journal of neuroimaging : official journal of the American Society of Neuroimaging.
[23] A. Sadovnick,et al. Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis , 2008, Journal of Neuroimmunology.
[24] Z. Rybak,et al. Hypothetical molecular mechanisms by which local iron overload facilitates the development of venous leg ulcers and multiple sclerosis lesions. , 2008, Medical hypotheses.
[25] Rohit Bakshi,et al. Iron in chronic brain disorders: Imaging and neurotherapeutic implications , 2007, Neurotherapeutics.
[26] P. Zamboni. The Big Idea: Iron-Dependent Inflammation in Venous Disease and Proposed Parallels in Multiple Sclerosis , 2006 .
[27] T. Rouault,et al. Brain iron metabolism. , 2006, Seminars in pediatric neurology.
[28] R. Bakshi,et al. Cognitive impairment is associated with subcortical magnetic resonance imaging grey matter T2 hypointensity in multiple sclerosis , 2006, Multiple sclerosis.
[29] M. Kotze,et al. Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis , 2006, Metabolic Brain Disease.
[30] S. Tognazzo,et al. The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesis. , 2006, Free radical biology & medicine.
[31] E. Frohman,et al. Multiple sclerosis--the plaque and its pathogenesis. , 2006, The New England journal of medicine.
[32] S. Reingold,et al. Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria” , 2005, Annals of neurology.
[33] C. W. Tjoa,et al. MRI T2 hypointensity of the dentate nucleus is related to ambulatory impairment in multiple sclerosis , 2005, Journal of the Neurological Sciences.
[34] F. Lublin. Clinical features and diagnosis of multiple sclerosis. , 2005, Neurologic clinics.
[35] J. Sullivan. Is stored iron safe? , 2004, The Journal of laboratory and clinical medicine.
[36] M. Barnett,et al. Relapsing and remitting multiple sclerosis: Pathology of the newly forming lesion , 2004, Annals of neurology.
[37] T. Speed,et al. Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis , 2004, Human Genetics.
[38] S. LeVine,et al. The Role of Iron in the Pathogenesis of Experimental Allergic Encephalomyelitis and Multiple Sclerosis , 2004, Annals of the New York Academy of Sciences.
[39] K. Pantopoulos. Iron Metabolism and the IRE/IRP Regulatory System: An Update , 2004, Annals of the New York Academy of Sciences.
[40] I. Biunno,et al. Transferrin C2 variant does confer a risk for Alzheimer's disease in caucasians. , 2004, Journal of Alzheimer's disease : JAD.
[41] C. Wan,et al. Association study between late-onset Alzheimer's disease and the transferrin gene polymorphisms in Chinese , 2003, Neuroscience Letters.
[42] Ya Ke,et al. Iron misregulation in the brain: a primary cause of neurodegenerative disorders , 2003, The Lancet Neurology.
[43] C. Beaumont,et al. Iron metabolism, free radicals, and oxidative injury. , 2001, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[44] J. Hillert,et al. HLA‐DR15 is associated with lower age at onset in multiple sclerosis , 2000, Annals of neurology.
[45] E. Beutler,et al. The effect of transferrin polymorphisms on iron metabolism. , 1999, Blood cells, molecules & diseases.
[46] Steven M LeVine,et al. Iron deposits in multiple sclerosis and Alzheimer's disease brains , 1997, Brain Research.
[47] M. C. Ellis,et al. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis , 1996, Nature Genetics.
[48] R. Poston,et al. Pathology, histochemistry and immunocytochemistry of lesions in acute multiple sclerosis , 1989, Journal of the Neurological Sciences.
[49] C. W. Adams,et al. Perivascular iron deposition and other vascular damage in multiple sclerosis. , 1988, Journal of neurology, neurosurgery, and psychiatry.
[50] Jim Mintz,et al. Prevalent iron metabolism gene variants associated with increased brain ferritin iron in healthy older men. , 2010, Journal of Alzheimer's disease : JAD.
[51] B. Lönnerdal,et al. Hepcidin, the recently identified peptide that appears to regulate iron absorption. , 2004, The Journal of nutrition.
[52] G. Salemi,et al. Multiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity , 2005, Neurology.
[53] P. Aisen. Transferrin, the transferrin receptor, and the uptake of iron by cells. , 1998, Metal ions in biological systems.
[54] C. Wong,et al. Effects of transferrin genetic phenotypes on total iron-binding capacity. , 1986, Acta haematologica.