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- catalog contributor b4049499.
- catalog contributor b4049500.
- catalog created "c1993.".
- catalog date "1993".
- catalog date "c1993.".
- catalog dateCopyrighted "c1993.".
- catalog description "Clinical features and classification of inherited ataxias -- Anatomy and physiology of cerebellar disease -- Neurotransmitters in the cerebellum : scientific aspects and clinical relevance -- Clinical imaging correlations in inherited ataxias -- Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) -- Early onset ataxias in Tunisia : intrafamilial heterogeneity -- Genetic aspects of Ataxia Telangiectasia -- Candidates for the molecular defect in Ataxia Telangiectasia -- Linkage studies in dominantly inherited ataxias -- Epidemiology and clinical aspects of Machado-Joseph Disease -- Inherited prion diseases -- Phosphoinositide second messenger system in human OPCA and the mouse model -- Oligodendrocyte- and Myelin-associated inhibitors of neurite growth in the adult nervous system -- Cerebellar grafting in Murine Heredodegenerative Ataxia : current limitations for a therapeutic approach -- Molecular analysis of the Friedreich's Ataxia Locus.".
- catalog description "Includes bibliographical references and index.".
- catalog extent "[xviii], 217 p. :".
- catalog identifier "0881679658".
- catalog isPartOf "Advances in neurology ; v. 61".
- catalog issued "1993".
- catalog issued "c1993.".
- catalog language "eng".
- catalog publisher "New York : Raven Press,".
- catalog subject "Ataxia.".
- catalog subject "Spinocerebellar Degenerations".
- catalog tableOfContents "Clinical features and classification of inherited ataxias -- Anatomy and physiology of cerebellar disease -- Neurotransmitters in the cerebellum : scientific aspects and clinical relevance -- Clinical imaging correlations in inherited ataxias -- Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) -- Early onset ataxias in Tunisia : intrafamilial heterogeneity -- Genetic aspects of Ataxia Telangiectasia -- Candidates for the molecular defect in Ataxia Telangiectasia -- Linkage studies in dominantly inherited ataxias -- Epidemiology and clinical aspects of Machado-Joseph Disease -- Inherited prion diseases -- Phosphoinositide second messenger system in human OPCA and the mouse model -- Oligodendrocyte- and Myelin-associated inhibitors of neurite growth in the adult nervous system -- Cerebellar grafting in Murine Heredodegenerative Ataxia : current limitations for a therapeutic approach -- Molecular analysis of the Friedreich's Ataxia Locus.".
- catalog title "Inherited ataxias / editors, A.E. Harding, Thomas Deufel.".
- catalog type "text".