LEADER 02839nam 2200661 a 450 001 9911093032003321 005 20251116141819.0 010 $a9786612355653 010 $a9780520909878 010 $a0520909879 010 $a9780585153742 010 $a0585153744 024 7 $a10.1525/9780520909878 035 $a(CKB)111004366699774 035 $a(dli)HEB08382 035 $a(OCoLC)44963401 035 $a(MdBmJHUP)muse30395 035 $a(DE-B1597)519377 035 $a(OCoLC)609850131 035 $a(DE-B1597)9780520909878 035 $a(Au-PeEL)EBL470986 035 $a(CaPaEBR)ebr10676191 035 $a(CaONFJC)MIL235565 035 $a(MiAaPQ)EBC470986 035 $a(MiU)MIU01000000000000009859161 035 $a(Perlego)551353 035 $a(EXLCZ)99111004366699774 100 $a19880809d1988 uy 0 101 0 $aeng 135 $aurmnummmmuuuu 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aGregory the Great $eperfection in imperfection /$fCarole Straw 205 $a1st ed. 210 $aBerkeley $cUniversity of California Press$dc1988 215 $a1 online resource (xiv, 295 pages) $cillustrations 225 1 $aTransformation of the classical heritage ;$v14 311 0 $a9780520068728 311 0 $a0520068726 311 0 $a9780520057678 311 0 $a0520057678 320 $aIncludes bibliographical references (p. [261]-266) and index. 327 $tFront matter --$tCONTENTS --$tLIST OF FIGURES --$tNOTE ON SOURCES AND ABBREVIATIONS --$tACKNOWLEDGMENTS --$tINTRODUCTION --$tI. MICROCOSM AND MEDIATOR --$tII. A SACRAMENTAL VISION --$tIII. THE SAINT AND THE SOCIAL MEANING OF STABILITY --$tIV. SOLIDITAS CARITATIS --$tV. LUBRICA MUTABILITAS --$tVI. THE LOGIC OF ASCETICISM --$tVII. THE MEDIATOR OF GOD AND MAN --$tVIII. THE GOD-MAN AND THE NEW DISPENSATION --$tIX. THE SACRIFICE OF A CONTRITE HEART --$tX. REFORM AND THE PREACHER --$tXI. THE JUST PENITENT --$tXII. CONSTANTIA MENTIS --$tCONCLUSION --$tBIBLIOGRAPHICAL ESSAY --$tINDEX 330 $aGregory I (590-604) is often considered the first medieval pope and the first exponent of a truly medieval spirituality. Carole Straw places Gregory in his historical context and considers the many facets of his personality-monk, preacher, and pope-in order to elucidate the structure of his thought and present a unified, thematic interpretation of his spiritual concerns. 410 0$aTransformation of the classical heritage ;$v14. 606 $aPopes$vBiography 615 0$aPopes 676 $a270.2/092/4 676 $aB 700 $aStraw$b Carole Ellen$0292862 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911093032003321 996 $aGregory the Great$91091463 997 $aUNINA LEADER 05449nam 2200625Ia 450 001 9911093555103321 005 20251116181441.0 010 $a1-61942-869-5 035 $a(CKB)2550000001040691 035 $a(EBL)3017873 035 $a(SSID)ssj0000918868 035 $a(PQKBManifestationID)12343231 035 $a(PQKBTitleCode)TC0000918868 035 $a(PQKBWorkID)10908813 035 $a(PQKB)11540774 035 $a(MiAaPQ)EBC3017873 035 $a(Au-PeEL)EBL3017873 035 $a(CaPaEBR)ebr10654844 035 $a(OCoLC)923654006 035 $a(BIP)37652814 035 $a(EXLCZ)992550000001040691 100 $a20111102d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aAtaxia $ecauses, symptoms and treatment /$fSung Hoi Hong, editor 205 $a1st ed. 210 $aNew York $cNova Science Publishers$dc2012 215 $a1 online resource (213 p.) 225 0 $aNeuroscience research progress 300 $aDescription based upon print version of record. 311 08$a1-61942-867-9 320 $aIncludes bibliographical references and index. 327 $a""ATAXIA ""; ""ATAXIA ""; ""CONTENTS ""; ""PREFACE ""; ""ROLE OF THE ATAXIA TELANGIECTASIA MUTATED PROTEIN IN STRESS-INDUCED PREMATURE SENESCENCE ""; ""ABSTRACT ""; ""INTRODUCTION ""; ""ATM ACTIVATION ""; ""ATM SUBSTRATES ""; ""P53 STRUCTURE, ACTIVATION AND FUNCTION ""; ""ROLES OF ATM AND P53 IN DNA REPAIR""; ""MULTIPLE FUNCTIONS OF P21 IN THE ATM NETWORK ""; ""SEQUENTIAL WAVES OF P53 ACTIVATION BY DNA DAMAGE ""; ""ATM-DEPENDENT SENESCENCE ""; ""ATM-INDEPENDENT SENESCENCE ""; ""ROLE OF ATM IN PREVENTING ESCAPE FROM SIPS: A NOVEL TUMOR SUPPRESSOR FUNCTION BEYOND P53? "" 327 $a""POTENTIAL THERAPEUTIC APPROACHES FOR THE TREATMENT OF AT """"CONCLUSION""; ""ACKNOWLEDGMENTS ""; ""REFERENCES""; ""ATAXIA TELANGIECTASIA: MOLECULAR BASIS, DIAGNOSIS AND TREATMENT ""; ""ABSTRACT ""; ""INTRODUCTION ""; ""CLINICAL FEATURES OF A-T ""; ""Neurological Phenotype and Cutaneous Manifestations ""; ""Immunodeficiency and Pulmonary Complications ""; ""Predisposition to Cancer and Chromosomal Instability""; ""Endocrine Dysfunction ""; ""PATHOGENESIS AND MOLECULAR DEFECT ""; ""ATM and Neurodegeneration""; ""ATM and Oxidative Stress ""; ""DIAGNOSIS AND TREATMENT ""; ""CONCLUSION "" 327 $a""REFERENCES """"THE NEUROBIOLOGY OF EPISODIC ATAXIA TYPE 1, A SHAKER-LIKE K+ CHANNEL DISORDER ""; ""ABSTRACT ""; ""INTRODUCTION ""; ""STRUCTURE AND FUNCTION OF SHAKER-LIKE K+ CHANNELS ""; ""PHYSIOLOGICAL ROLE OF KV CHANNELS ""; ""Hippocampus ""; ""Cerebellum ""; ""Sciatic Nerve ""; ""BIOTECHNOLOGY FOR STUDYING ION CHANNELS ""; ""EPISODIC ATAXIA TYPE 1: ""; ""Clinical Findings ""; ""Genetic Causes ""; ""Molecular Pathogenetic Mechanisms Underlying EA1""; ""Animal Models of EA1""; ""Treatment of EA1 ""; ""BRIEF OVERVIEW OF RELATED ATAXIA DISORDERS ""; ""CONCLUSION ""; ""ACKNOWLEDGMENTS "" 327 $a""REFERENCES """"MITOCHONDRIAL ATAXIAS ""; ""ABSTRACT ""; ""INTRODUCTION ""; ""ATAXIA IN MITOCHONDRIAL DISORDERS ""; ""MtDNA Point Mutations ""; ""MtDNA Sporadic Rearrangements ""; ""Infantile Onset Spinocerebellar Ataxia ""; ""POLG1-Related Diseases ""; ""OPA1-Related Diseases ""; ""Coenzyme Q10 Deficiency ""; ""FRIEDREICH ATAXIA ""; ""Mitochondrial Therapies for Friedreich Ataxia ""; ""MITOCHONDRIA AND OTHER GENETIC ATAXIAS ""; ""Dominant Spino-Cerebellar Ataxias ""; ""X-Linked Ataxias ""; ""CONCLUSION ""; ""REFERENCES "" 327 $a""EPIDEMIC SEASONAL ATAXIC SYNDROME: EPIDEMIOLOGY, CLINICAL PRESENTATION, ETIOLOGICAL MECHANISMS AND THERAPY """"ABSTRACT ""; ""INTRODUCTION ""; ""ETIOLOGY ""; ""Viral Hypothesis ""; ""Toxins in Food""; ""Hypothesis of Thiamine Deficiency ""; ""CLINICAL PRESENTATION OF SAS IS COMPATIBLE WITH WERNICKEa???S ENCEPHALOPATHY ""; ""MECHANISM OF THIAMINE DEFICIENCY IN SEASONAL ATAXIC SYNDROME ""; ""THERAPY AND CONTROL OF SAS ""; ""REFERENCES ""; ""CLINICAL AND GENETIC ASPECTS OF RECESSIVE ATAXIAS ""; ""ABSTRACT ""; ""INTRODUCTION ""; ""THE DEGENERATIVE ATAXIAS ""; ""Friedreicha???s Ataxia "" 327 $a""Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) "" 330 $aAtaxia is a neurological sign and symptom characterised by lack of co-ordination of muscle movement that is due to dysfunction of the parts of the nervous system, such as motor control of the cerebellum. Although the cause of the dysfunction varies from mutations in channels for potassium and/or calcium to progressive degeneration of cerebellar tissue-specific neurons, the neurological signs and symptoms of ataxia are similar. The treatment of ataxia and its effectiveness depend on the underlying cause, and it could be managed by pharmacological treatments and through physical therapy and occupational therapy. The treatment may ameliorate the signs of ataxia, but it is not likely to eliminate them entirely. In this book, the authors present current research in the study of the causes, symptoms and treatments on ataxia. 410 0$aNeuroscience Research Progress 606 $aAtaxia 606 $aMovement disorders 615 0$aAtaxia. 615 0$aMovement disorders. 701 $aHong$b Sung Hoi$01978134 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911093555103321 996 $aAtaxia$94748137 997 $aUNINA