The natural history of Niemann–Pick disease type C in the UK

By Imrie J.   Dasgupta S.   Besley G.   Harris C.   Heptinstall L.   Knight S.   Vanier M.   Fensom A.   Ward C.   Jacklin E.   Whitehouse C.   Wraith J.  

Journal of Inherited Metabolic Disease, Vol. 30, Iss. 1, 2007-02 ,pp. : 51-59

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Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C

By Chien Y.  

Journal of Inherited Metabolic Disease, Vol. 36, Iss. 1, 2013-01 ,pp. : 129-137

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Niemann–Pick disease type C and defective peroxisomal &bgr;-oxidation of branched-chain substrates

By Sequeira J.S.S.   Vellodi A.   vanier M.T.   Clayton P.T.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 2, 1998-04 ,pp. : 149-154

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Gender dimorphism in siblings with schizophrenia-like psychosis due to Niemann-Pick disease type C

By Walterfang M.   Fietz M.   Abel L.   Bowman E.   Mocellin R.   Velakoulis D.  

Journal of Inherited Metabolic Disease, Vol. 32, Iss. 1, 2009-12 ,pp. : 221-226

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The aurora sign in a patient with type B Niemann-Pick disease

By da Costa e Silva Eduardo   Cavalcanti de Albuquerque Sílvio   de Queiroz Praxedes Eduardo   do Amaral Fernando  

Pediatric Radiology, Vol. 37, Iss. 1, 2007-01 ,pp. : 75-77

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