| P2093 | author name string | B Ludwig | |
| | T Kishikawa | |
| | M Rochel | |
| | S Wende | |
| | J Gehler | |
| P2860 | cites work | CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase | Q72650614 |
| | Adrenoleukodystrophy. Report of two cases with relapsing and remitting courses | Q72854889 |
| | The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism | Q28610244 |
| | Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients | Q34216813 |
| | Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritance. | Q34697284 |
| | Computed tomography in white-matter disease | Q38525337 |
| | Sudanophil leucodystrophy in a pachygyric brain | Q39412932 |
| | The systemic mucopolysaccharidoses. | Q39885962 |
| | Alexander's disease: A report and reappraisal | Q39997784 |
| | Computed tomographic evaluation of the early phase of adrenoleukodystrophy | Q40721890 |
| | Computed tomography in neurodegenerative disorders in childhood | Q41936597 |
| | Computerized cranial tomography in cerebral diseases of white matter | Q43673243 |
| | Adrenoleukodystrophy. A correlative analysis of computed tomography and radionuclide studies | Q44012005 |
| | Computerized axial tomography and cerebral scintigraphy in leukodystrophy. A study of two boys presumably suffering from lysosomal disease | Q44358658 |
| | A dominant form of neuronal ceroid-lipofuscinosis | Q45075142 |
| | Mucopolysaccharidosis. VII. Beta-glucuronidase deficiency | Q45083643 |
| | CT scanning and diagnosis of adrenoleukodystrophy | Q45803524 |
| | CT scans in Menkes disease | Q48097825 |
| | Computerized tomography in demyelinating disease of the young | Q48269546 |
| | Computer Assisted Tomography in Adrenoleukodystrophy | Q48281914 |
| | Presidential address: Studies in the neuronal ceroid-lipofuscinoses | Q48590270 |
| | Noninvasive CT diagnosis of infantile Alexander disease: pathologic correlation. | Q48800643 |
| | Computed tomography in Krabbe's disease: comparison with neuropathology | Q48823098 |
| | Case report. An additional case of adrenoleukodystrophy with both type I and type II CT features. | Q48958678 |
| | Case report. Atypical findings in adrenoleukodystrophy. | Q49142121 |
| | Computerized tomography in neurodegenerative diseases in childhood (author's transl) | Q66878829 |
| | Prenatal diagnosis of mucolipidosis II (I-cell disease) | Q67522517 |
| | Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome | Q67524410 |
| | Cranial computed tomography in disorders of complex carbohydrate metabolism and related storage diseases | Q70443513 |
| | Computed tomography in Pelizaeus-Merzbacher disease | Q70669562 |
| | Alexander disease: clinical, electrodiagnostic and radiographic studies | Q70838076 |
| | Demyelinating and neuro-degenerative disease in childhood. CT appearances and their differential diagnosis | Q71046244 |
| | Computed tomography in neuronal ceroid lipofuscinosis | Q71134406 |
| | Computed tomography in Alexander's disease | Q71339295 |
| | A new CT pattern in adrenoleukodystrophy | Q71414987 |
| | Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistry | Q71444552 |
| | Genetic heterogeneity and allelic variation in the mucopolysaccharidoses. Introduction | Q71493628 |
| | Computed tomography studies on patients with mucopolysaccharidoses | Q71543334 |
| | Cranial CT in fucosidosis | Q71580291 |
| | Sanfilippo B syndrome (MPS III B): case report with analysis of CSF mucopolysaccharides and conjunctival biopsy | Q72634280 |
| P433 | issue | 2 | |
| P304 | page(s) | 57-70 | |
| P577 | publication date | 1984-01-01 | |
| P1433 | published in | Journal of Neurology | Q6295649 |
| P1476 | title | The value of CT in diagnosis and prognosis of different inborn neurodegenerative disorders in childhood | |
| P478 | volume | 231 | |