Magnetic resonance of myelination and myelin disorders:
Gespeichert in:
| Format: | Elektronisch E-Book |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
Berlin [u.a.]
Springer
2005
|
| Ausgabe: | 3. ed. |
| Schlagworte: | |
| Online-Zugang: | Volltext Inhaltsverzeichnis |
| Beschreibung: | 2. Aufl. u.d.T.: Knaap, Marjo S. van der : Magnetic resonance of myelin, myelination, and myelin disorders |
| Beschreibung: | 1 Online-Ressource |
| ISBN: | 3540222863 9783540222866 9783540276609 |
| DOI: | 10.1007/3-540-27660-2 |
Internformat
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| 245 | 1 | 0 | |a Magnetic resonance of myelination and myelin disorders |c Marjo S. van der Knaap ; Jaap Valk |
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Datensatz im Suchindex
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| adam_text |
Contents
1 Myelin and White Matter 1
2 Classification of Myelin Disorders . 20
3 Selective Vulnerability 25
4 Myelination and Retarded Myelination 37
5 Lysosomes and Lysosomal Disorders . . 66
6 Metachromatic Leukodystrophy 74
7 Multiple Sulfatase Deficiency 82
8 Globoid Cell Leukodystrophy
(Krabbe Disease) 87
9 GM, Gangliosidosis 96
10 GM2 Gangliosidosis 103
11 Fabry Disease 112
12 Fucosidosis 119
13 Mucopolysaccharidoses 123
14 Free Sialic Acid Storage Disorder . 133
15 Neuronal Ceroid Lipofuscinoses . 137
16 Adult Polyglucosan Body Disease . . 147
17 Peroxisomes
and Peroxisomal Disorders 151
18 Peroxisome Biogenesis Defects 154
19 Peroxisomal D Bifunctional
Protein Deficiency 167
20 Peroxisomal Acyl CoA
Oxidase Deficiency 172
21 X linked Adrenoleukodystrophy . 176
22 Refsum Disease 191
23 Mitochondria
and Mitochondrial Disorders 195
24 Mitochondrial Encephalopathy
with Lactic Acidosis
and Stroke like Episodes 204
25 Leber Hereditary Optic Neuropathy . . 212
26 Kearns Sayre Syndrome 215
27 Mitochondrial Neurogastrointestinal
Encephalomyopathy 221
28 Leigh Syndrome and Mitochondrial
Leukoencephalopathies 224
29 Pyruvate Carboxylase Deficiency . 245
30 Multiple Carboxylase Deficiency . 248
31 Cerebrotendinous Xanthomatosis . . . 252
32 Cockayne Syndrome 259
33 Trichothiodystrophy
with Photosensitivity 268
34 Pelizaeus Merzbacher Disease
and X linked Spastic
Paraplegia Type 2 272
35 18q Syndrome 281
36 Phenylketonuria 284
37 Glutaric Aciduria Type 1 294
38 Propionic Acidemia 300
39 Nonketotic Hyperglycinemia 306
40 Maple Syrup Urine Disease 311
41 3 Hydroxy 3 Methylglutaryl CoA
Lyase Deficiency 321
42 Canavan Disease 326
43 L 2 Hydroxyglutaric Aciduria 334
44 D 2 Hydroxyglutaric Aciduria 338
45 Hyperhomocysteinemias 342
46 Urea Cycle Defects 360
47 Serine Synthesis Defect Caused
by 3 Phosphoglycerate
Dehydrogenase Deficiency 369
48 Molybdenum Cofactor
Deficiency and Isolated Sulfite
Oxidase Deficiency 372
49 Galactosemia 377
50 Sjogren Larsson Syndrome 383
51 Lowe Syndrome 387
52 Wilson Disease 392
53 Menkes Disease 400
54 Fragile X Premutation 406
55 Hypomelanosis of Ito 409
56 Incontinentia Pigmenti 412
57 Alexander Disease 416
58 Giant Axonal Neuropathy 436
59 Megalencephalic Leukoencephalo
pathy with Subcortical Cysts 442
60 Congenital Muscular Dystrophies . . 451
61 Myotonic Dystrophy Type I 469
62 Myotonic Dystrophy Type 2 473
63 X linked Charcot Marie Tooth
Disease 476
Contents
64 Oculodentodigital Dysplasia 479
65 Leukoencephalopathy
with Vanishing White Matter 481
66 Aicardi Goutieres Syndrome 496
67 Leukoencephalopathy
with Calcifications and Cysts 505
68 Leukoencephalopathy with Brain Stem
and Spinal Cord Involvement
and Elevated White Matter Lactate . 510
69 Hypomyelination with Atrophy
ofthe Basal Ganglia and Cerebellum . . 519
70 Hereditary Diffuse Leukoencephalo¬
pathy with Neuroaxonal Spheroids . . . 526
71 Dentatorubropallidoluysian Atrophy . 530
72 Cerebral Amyloid Angiopathy 535
73 Cerebral Autosomal Dominant
Arteriopathy with Subcortical Infarcts
and Leukoencephalopathy 541
74 Cerebral Autosomal Recessive
Arteriopathy with Subcortical Infarcts
and Leukoencephalopathy 549
75 Polycystic Lipomembranous
Osteodysplasia with Sclerosing
Leukoencephalopathy
(Nasu Hakola Disease) 552
76 Pigmentary Orthochromatic
Leukodystrophy 557
77 Adult Onset Autosomal Dominant
Leukoencephalopathies 559
78 Inflammatory
and Infectious Disorders 561
79 Multiple Sclerosis 566
80 Acute Disseminated Encephalomyelitis
and Acute Hemorrhagic
Encephalomyelitis 604
81 Acquired Immunodeficiency
Syndrome 616
82 Progressive Multifocal
Leukoencephalopathy 628
83 Brucellosis 635
84 Subacute Sclerosing Panencephalitis . 640
85 Congenital and Perinatal
Cytomegalovirus Infection 645
86 Whipple Disease 658
87 Toxic Encephalopathies 664
88 latrogenic Toxic Encephalopathies . . . 679
89 Central Pontine and Extrapontine
Myelinolysis 684
90 Hypernatremia 690
91 Marchiafava Bignami Syndrome . 695
92 Posterior Reversible
Encephalopathy Syndrome 699
93 Langerhans Cell Histiocytosis 709
94 Post Hypoxic lschemic Damage . 714
95 Post Hypoxic lschemic
Leukoencephalopathy of Neonates. . . 718
96 Neonatal Hypoglycemia 749
97 Delayed Posthypoxic
Leukoencephalopathy 755
98 White Matter Lesions of the Elderly. . . 759
99 Subcortical Arteriosclerotic
Encephalopathy 767
100 Vasculitis 773
101 Leukoencephalopathy
and Dural Venous Fistula 801
102 Leukoencephalopathy after Chemo¬
therapy and/or Radiotherapy 808
103 Gliomatosis Cerebri 818
104 Diffuse Axonal Injury 823
105 Wallerian Degeneration
and Myelin Loss Secondary
to Neuronal and Axonal
Degeneration 832
106 Diffusion Weighted Imaging 839
107 Magnetization Transfer Imaging . 854
108 Magnetic Resonance Spectroscopy:
Basic Principles, and Application
in White Matter Disorders 859
109 Pattern Recognition
in White Matter Disorders 881
References 905
Subject Index 1075 |
| adam_txt |
Contents
1 Myelin and White Matter 1
2 Classification of Myelin Disorders . 20
3 Selective Vulnerability 25
4 Myelination and Retarded Myelination 37
5 Lysosomes and Lysosomal Disorders . . 66
6 Metachromatic Leukodystrophy 74
7 Multiple Sulfatase Deficiency 82
8 Globoid Cell Leukodystrophy
(Krabbe Disease) 87
9 GM, Gangliosidosis 96
10 GM2 Gangliosidosis 103
11 Fabry Disease 112
12 Fucosidosis 119
13 Mucopolysaccharidoses 123
14 Free Sialic Acid Storage Disorder . 133
15 Neuronal Ceroid Lipofuscinoses . 137
16 Adult Polyglucosan Body Disease . . 147
17 Peroxisomes
and Peroxisomal Disorders 151
18 Peroxisome Biogenesis Defects 154
19 Peroxisomal D Bifunctional
Protein Deficiency 167
20 Peroxisomal Acyl CoA
Oxidase Deficiency 172
21 X linked Adrenoleukodystrophy . 176
22 Refsum Disease 191
23 Mitochondria
and Mitochondrial Disorders 195
24 Mitochondrial Encephalopathy
with Lactic Acidosis
and Stroke like Episodes 204
25 Leber Hereditary Optic Neuropathy . . 212
26 Kearns Sayre Syndrome 215
27 Mitochondrial Neurogastrointestinal
Encephalomyopathy 221
28 Leigh Syndrome and Mitochondrial
Leukoencephalopathies 224
29 Pyruvate Carboxylase Deficiency . 245
30 Multiple Carboxylase Deficiency . 248
31 Cerebrotendinous Xanthomatosis . . . 252
32 Cockayne Syndrome 259
33 Trichothiodystrophy
with Photosensitivity 268
34 Pelizaeus Merzbacher Disease
and X linked Spastic
Paraplegia Type 2 272
35 18q Syndrome 281
36 Phenylketonuria 284
37 Glutaric Aciduria Type 1 294
38 Propionic Acidemia 300
39 Nonketotic Hyperglycinemia 306
40 Maple Syrup Urine Disease 311
41 3 Hydroxy 3 Methylglutaryl CoA
Lyase Deficiency 321
42 Canavan Disease 326
43 L 2 Hydroxyglutaric Aciduria 334
44 D 2 Hydroxyglutaric Aciduria 338
45 Hyperhomocysteinemias 342
46 Urea Cycle Defects 360
47 Serine Synthesis Defect Caused
by 3 Phosphoglycerate
Dehydrogenase Deficiency 369
48 Molybdenum Cofactor
Deficiency and Isolated Sulfite
Oxidase Deficiency 372
49 Galactosemia 377
50 Sjogren Larsson Syndrome 383
51 Lowe Syndrome 387
52 Wilson Disease 392
53 Menkes Disease 400
54 Fragile X Premutation 406
55 Hypomelanosis of Ito 409
56 Incontinentia Pigmenti 412
57 Alexander Disease 416
58 Giant Axonal Neuropathy 436
59 Megalencephalic Leukoencephalo
pathy with Subcortical Cysts 442
60 Congenital Muscular Dystrophies . . 451
61 Myotonic Dystrophy Type I 469
62 Myotonic Dystrophy Type 2 473
63 X linked Charcot Marie Tooth
Disease 476
Contents
64 Oculodentodigital Dysplasia 479
65 Leukoencephalopathy
with Vanishing White Matter 481
66 Aicardi Goutieres Syndrome 496
67 Leukoencephalopathy
with Calcifications and Cysts 505
68 Leukoencephalopathy with Brain Stem
and Spinal Cord Involvement
and Elevated White Matter Lactate . 510
69 Hypomyelination with Atrophy
ofthe Basal Ganglia and Cerebellum . . 519
70 Hereditary Diffuse Leukoencephalo¬
pathy with Neuroaxonal Spheroids . . . 526
71 Dentatorubropallidoluysian Atrophy . 530
72 Cerebral Amyloid Angiopathy 535
73 Cerebral Autosomal Dominant
Arteriopathy with Subcortical Infarcts
and Leukoencephalopathy 541
74 Cerebral Autosomal Recessive
Arteriopathy with Subcortical Infarcts
and Leukoencephalopathy 549
75 Polycystic Lipomembranous
Osteodysplasia with Sclerosing
Leukoencephalopathy
(Nasu Hakola Disease) 552
76 Pigmentary Orthochromatic
Leukodystrophy 557
77 Adult Onset Autosomal Dominant
Leukoencephalopathies 559
78 Inflammatory
and Infectious Disorders 561
79 Multiple Sclerosis 566
80 Acute Disseminated Encephalomyelitis
and Acute Hemorrhagic
Encephalomyelitis 604
81 Acquired Immunodeficiency
Syndrome 616
82 Progressive Multifocal
Leukoencephalopathy 628
83 Brucellosis 635
84 Subacute Sclerosing Panencephalitis . 640
85 Congenital and Perinatal
Cytomegalovirus Infection 645
86 Whipple Disease 658
87 Toxic Encephalopathies 664
88 latrogenic Toxic Encephalopathies . . . 679
89 Central Pontine and Extrapontine
Myelinolysis 684
90 Hypernatremia 690
91 Marchiafava Bignami Syndrome . 695
92 Posterior Reversible
Encephalopathy Syndrome 699
93 Langerhans Cell Histiocytosis 709
94 Post Hypoxic lschemic Damage . 714
95 Post Hypoxic lschemic
Leukoencephalopathy of Neonates. . . 718
96 Neonatal Hypoglycemia 749
97 Delayed Posthypoxic
Leukoencephalopathy 755
98 White Matter Lesions of the Elderly. . . 759
99 Subcortical Arteriosclerotic
Encephalopathy 767
100 Vasculitis 773
101 Leukoencephalopathy
and Dural Venous Fistula 801
102 Leukoencephalopathy after Chemo¬
therapy and/or Radiotherapy 808
103 Gliomatosis Cerebri 818
104 Diffuse Axonal Injury 823
105 Wallerian Degeneration
and Myelin Loss Secondary
to Neuronal and Axonal
Degeneration 832
106 Diffusion Weighted Imaging 839
107 Magnetization Transfer Imaging . 854
108 Magnetic Resonance Spectroscopy:
Basic Principles, and Application
in White Matter Disorders 859
109 Pattern Recognition
in White Matter Disorders 881
References 905
Subject Index 1075 |
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| discipline | Medizintechnik Medizin |
| discipline_str_mv | Medizintechnik Medizin |
| doi_str_mv | 10.1007/3-540-27660-2 |
| edition | 3. ed. |
| format | Electronic eBook |
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| id | DE-604.BV022368666 |
| illustrated | Not Illustrated |
| index_date | 2024-07-02T17:06:11Z |
| indexdate | 2024-12-28T04:06:04Z |
| institution | BVB |
| isbn | 3540222863 9783540222866 9783540276609 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-015577887 |
| oclc_num | 316007676 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR DE-188 DE-12 DE-384 DE-473 DE-BY-UBG DE-703 DE-29 DE-19 DE-BY-UBM DE-91 DE-BY-TUM DE-739 DE-20 DE-706 DE-1046 DE-1047 DE-1102 DE-858 DE-1028 DE-573 DE-859 DE-860 DE-M347 DE-1049 DE-92 DE-898 DE-BY-UBR DE-863 DE-BY-FWS DE-862 DE-BY-FWS DE-128 DE-54 DE-22 DE-BY-UBG DE-150 DE-155 DE-BY-UBR DE-2070s DE-521 DE-522 DE-526 DE-11 DE-83 DE-70 DE-634 |
| owner_facet | DE-355 DE-BY-UBR DE-188 DE-12 DE-384 DE-473 DE-BY-UBG DE-703 DE-29 DE-19 DE-BY-UBM DE-91 DE-BY-TUM DE-739 DE-20 DE-706 DE-1046 DE-1047 DE-1102 DE-858 DE-1028 DE-573 DE-859 DE-860 DE-M347 DE-1049 DE-92 DE-898 DE-BY-UBR DE-863 DE-BY-FWS DE-862 DE-BY-FWS DE-128 DE-54 DE-22 DE-BY-UBG DE-150 DE-155 DE-BY-UBR DE-2070s DE-521 DE-522 DE-526 DE-11 DE-83 DE-70 DE-634 |
| physical | 1 Online-Ressource |
| psigel | ZDB-1-SMI ZDB-2-SME |
| publishDate | 2005 |
| publishDateSearch | 2005 |
| publishDateSort | 2005 |
| publisher | Springer |
| record_format | marc |
| spellingShingle | Magnetic resonance of myelination and myelin disorders Myelin (DE-588)4170920-2 gnd Entmarkungskrankheit (DE-588)4214431-0 gnd Kernspintomografie (DE-588)4120806-7 gnd Myelogenese (DE-588)4170922-6 gnd |
| subject_GND | (DE-588)4170920-2 (DE-588)4214431-0 (DE-588)4120806-7 (DE-588)4170922-6 |
| title | Magnetic resonance of myelination and myelin disorders |
| title_auth | Magnetic resonance of myelination and myelin disorders |
| title_exact_search | Magnetic resonance of myelination and myelin disorders |
| title_exact_search_txtP | Magnetic resonance of myelination and myelin disorders |
| title_full | Magnetic resonance of myelination and myelin disorders Marjo S. van der Knaap ; Jaap Valk |
| title_fullStr | Magnetic resonance of myelination and myelin disorders Marjo S. van der Knaap ; Jaap Valk |
| title_full_unstemmed | Magnetic resonance of myelination and myelin disorders Marjo S. van der Knaap ; Jaap Valk |
| title_short | Magnetic resonance of myelination and myelin disorders |
| title_sort | magnetic resonance of myelination and myelin disorders |
| topic | Myelin (DE-588)4170920-2 gnd Entmarkungskrankheit (DE-588)4214431-0 gnd Kernspintomografie (DE-588)4120806-7 gnd Myelogenese (DE-588)4170922-6 gnd |
| topic_facet | Myelin Entmarkungskrankheit Kernspintomografie Myelogenese |
| url | https://doi.org/10.1007/3-540-27660-2 http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=015577887&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT knaapmarjosvander magneticresonanceofmyelinationandmyelindisorders AT valkjaap magneticresonanceofmyelinationandmyelindisorders |