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      Developmental neuropathology

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      https://www.riss.kr/link?id=M14970957

      • 저자
      • 발행사항

        Hoboken, NJ : Wiley, 2018

      • 발행연도

        2018

      • 작성언어

        영어

      • 주제어
      • ISBN

        9781119013082 (cloth)

      • 자료형태

        일반단행본

      • 발행국(도시)

        미국

      • 서명/저자사항

        Developmental neuropathology / [edited by] Homa Adle-Biassette, Brian Harding, Jeffrey Golden.

      • 판사항

        2nd ed

      • 형태사항

        xiii, 546 p. : ill. (some col.) ; 29 cm.

      • 일반주기명

        Includes bibliographical references and index.

      • 소장기관
        • 한림대학교 도서관 소장기관정보
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      부가정보

      목차 (Table of Contents)

      • 자료제공 : aladin
      • List of contributors Introduction Chapter 1: CNS Manifestations of Chromosomal Change Chapter 2: Neural tube defects Chapter 3: MIDLINE  PATTERNING  DEFECTS Chapter 4: MICROCEPHALY Chapter 5: Hemimegalencephaly and Dysplastic Megalencephaly Chapter 6: Lissencephaly, Type I Chapter 7: Lissencephaly, Type II (Cobblestone Lissencephaly) Chapter 8: Polymicrogyria Chapter 9: Cerebral Heterotopia Chapter 10: Hippocampal sclerosis and granule cell dysplasia, and cortical dysplasia Chapter 11: Tuberous Sclerosis Complex Chapter 12: Chiari Malformations Chapter 13: Dandy-Walker Malformation, Mega-Cisterna Magna, and Blake's Pouch Cyst Chapter 14: Joubert Syndrome Chapter 15: Cerebellar Heterotopia and Dysplasia Chapter 16: Brainstem Malformations Chapter 17: SPINAL CORD LESIONS Chapter 18: HYDROCEPHALUS Chapter 19: Antenatal Disruptive Lesions Chapter 20: Hemorrhagic Lesions Chapter 21: White Matter Lesions in the Perinatal Period Chapter 22: Gray Matter Lesions Chapter 23: Pediatric Head Injury Chapter 24: Pediatric Vascular Malformations Chapter 25: Sudden Infant Death Syndrome Chapter 26: Kernicterus Chapter 27: Lesions Induced by Toxins Chapter 28: Disorders of Carbohydrate Metabolism Chapter 29: Sphingolipidoses and related disorders  Chapter 30: The Neuronal Ceroid-Lipofuscinoses Chapter 31: Peroxisomal Disorders Chapter 32: Mitochondrial Disorders Chapter 33: DISORDERS OF AMINO ACID METABOLISM AND CANAVAN DISEASE Chapter 34: Pelizaeus-Merzbacher Disease Chapter 35: Cockayne Syndrome Chapter 36: VANISHING WHITE MATTER DISEASE Chapter 37: Alexander Disease Chapter 38: Pathology and Genetics of Neuroaxonal Dystrophy/ Neurodegeneration with Brain Iron Accumulation Chapter 39: Spinal Muscular Atrophy Chapter 40: Autism Spectrum Disorders Chapter 41: Intrauterine Infections Chapter 42: Perinatal and Postnatal Infections Chapter 43: Rasmussen Encephalitis
      • 자료제공 : aladin
      • List of contributors Introduction Chapter 1: CNS Manifestations of Chromosomal Change Chapter 2: Neural tube defects Chapter 3: MIDLINE  PATTERNING  DEFECTS Chapter 4: MICROCEPHALY Chapter 5: Hemimegalencephaly and Dysplastic Megalencephaly Chapter 6: Lissencephaly, Type I Chapter 7: Lissencephaly, Type II (Cobblestone Lissencephaly) Chapter 8: Polymicrogyria Chapter 9: Cerebral Heterotopia Chapter 10: Hippocampal sclerosis and granule cell dysplasia, and cortical dysplasia Chapter 11: Tuberous Sclerosis Complex Chapter 12: Chiari Malformations Chapter 13: Dandy-Walker Malformation, Mega-Cisterna Magna, and Blake's Pouch Cyst Chapter 14: Joubert Syndrome Chapter 15: Cerebellar Heterotopia and Dysplasia Chapter 16: Brainstem Malformations Chapter 17: SPINAL CORD LESIONS Chapter 18: HYDROCEPHALUS Chapter 19: Antenatal Disruptive Lesions Chapter 20: Hemorrhagic Lesions Chapter 21: White Matter Lesions in the Perinatal Period Chapter 22: Gray Matter Lesions Chapter 23: Pediatric Head Injury Chapter 24: Pediatric Vascular Malformations Chapter 25: Sudden Infant Death Syndrome Chapter 26: Kernicterus Chapter 27: Lesions Induced by Toxins Chapter 28: Disorders of Carbohydrate Metabolism Chapter 29: Sphingolipidoses and related disorders  Chapter 30: The Neuronal Ceroid-Lipofuscinoses Chapter 31: Peroxisomal Disorders Chapter 32: Mitochondrial Disorders Chapter 33: DISORDERS OF AMINO ACID METABOLISM AND CANAVAN DISEASE Chapter 34: Pelizaeus-Merzbacher Disease Chapter 35: Cockayne Syndrome Chapter 36: VANISHING WHITE MATTER DISEASE Chapter 37: Alexander Disease Chapter 38: Pathology and Genetics of Neuroaxonal Dystrophy/ Neurodegeneration with Brain Iron Accumulation Chapter 39: Spinal Muscular Atrophy Chapter 40: Autism Spectrum Disorders Chapter 41: Intrauterine Infections Chapter 42: Perinatal and Postnatal Infections Chapter 43: Rasmussen Encephalitis
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