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Journal of Neurology
Volumn 261, Issue 1, 2014, Pages 227-228
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
Author keywords

[No Author keywords available]
Indexed keywords

CATION TRANSPORT PROTEINS; CHELATION THERAPY; FEMALE; HUMANS; LONGITUDINAL STUDIES; METABOLIC DISEASES; MIDDLE AGED; MUTATION; PARKINSONIAN DISORDERS;
EID: 84895074352     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-013-7187-5     Document Type: Letter
Times cited : (16)
References (6)
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    • 1:CAS:528:DC%2BC38Xis1Cjtr8%3D 10.1016/j.ajhg.2012.01.017
    • Quadri M, Federico A, Zhao T et al (2012) Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. AJHG 90:467-477
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  • 2
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    • Syndrome of hepatic cirrhosis, dystonia, polycythemia and hypermanganesemia caused by mutation in SLC30A10, a manganese transporter in man
    • 1:CAS:528:DC%2BC38Xis1Cjsrc%3D 10.1016/j.ajhg.2012.01.018
    • Tuschl K, Clayton PT, Gospe SM Jr et al (2012) Syndrome of hepatic cirrhosis, dystonia, polycythemia and hypermanganesemia caused by mutation in SLC30A10, a manganese transporter in man. AJHG 90:457-466
    • (2012) AJHG , vol.90 , pp. 457-466
    • Tuschl, K.1    Clayton, P.T.2    Gospe, Jr.S.M.3
  • 3
    • 43149115142 scopus 로고    scopus 로고
    • Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia - A new metabolic disorder
    • 1:CAS:528:DC%2BD1cXltFCjsro%3D 18392750 10.1007/s10545-008-0813-1
    • Tuschl K, Mills PB, Parsons H, Malone M, Fowler D, Bitner-Glindzicz M, Clayton PT (2008) Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia - a new metabolic disorder. J Inherit Metab Dis 31(2):151-163
    • (2008) J Inherit Metab Dis , vol.31 , Issue.2 , pp. 151-163
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  • 4
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    • Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: A new treatable disorder
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    • Stamelou M, Tuschl K, Chong KW, Burroughs AK, Mills BP, Bhatia KP, Clayton PT (2012) Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder. Mov disorder 27:1317-1322
    • (2012) Mov Disorder , vol.27 , pp. 1317-1322
    • Stamelou, M.1    Tuschl, K.2    Chong, K.W.3    Burroughs, A.K.4    Mills, B.P.5    Bhatia, K.P.6    Clayton, P.T.7
  • 5
    • 0029101204 scopus 로고
    • Manganese and chronic hepatic encephalopathy
    • 1:CAS:528:DyaK2MXntlKhtL8%3D 7630246 10.1016/S0140-6736(95)92164-8
    • Krieger D, Krieger S, Jansen O, Gass P, Theilmann L, Lichtnecker H (1995) Manganese and chronic hepatic encephalopathy. Lancet 346:270-274
    • (1995) Lancet , vol.346 , pp. 270-274
    • Krieger, D.1    Krieger, S.2    Jansen, O.3    Gass, P.4    Theilmann, L.5    Lichtnecker, H.6
  • 6
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    • Chronic acquired hepatocerebral degeneration, pallidal T1 MRI hyperintensity and manganese in a series of cirrhotic patients
    • doi: 10.1007/s10072-013-1458-x
    • Maffeo E, Montuschi A, Stura G, Giordana MT (2013) Chronic acquired hepatocerebral degeneration, pallidal T1 MRI hyperintensity and manganese in a series of cirrhotic patients. Neurol Sci. doi: 10.1007/s10072-013-1458-x
    • (2013) Neurol Sci
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.