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1C Verny Key Opinion Leader In [C Verny is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]Keywords (12) [keywords assigned to C Verny articles by PubMed, the leading number and the color conveys importance]- 1Humans | 1Middle Aged | 1Magnetic Resonance Imaging | 1Leukodystrophy, Metachromatic | 1Adult | 1Male | 1Genes, Dominant | 1Age of Onset | 1Female | 1Phenotype | 1Pedigree | 1Brain
Other [context-specific ads]C Verny Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; C Verny might be a good expert witness on these terms]- 5leucodystrophy | 5orthochromatic | 3features | 3clinicopathological | 3onset | 3cases | 2dominantly | 2adult | 2mri | 2case | 2inherited | 2aged | 2epilepsy | 2dementia | 2years | 1frontal | 1heterogeneous | 1suggest | 1radiological | 1type | 1histopathological | 1age | 1characteristics | 1inheritance | 1enzyme | 1phenotypes | 1motor | 1white | 1mostly | 1based | 1subtype | 1leucodystrophies
- 3orthochromatic leucodystrophy | 2cases dominantly | 2onset orthochromatic | 2dominantly inherited | 2clinicopathological cases | 2inherited adult | 2adult onset | 2aged years | 2dementia epilepsy | 1mri mostly | 1mri findings | 1histopathological features | 1sequences case | 1main characteristics | 1flair sequences | 1clinicopathological features | 1suggest leucodystrophy | 1leucodystrophy leucodystrophies | 1orthochromatic type | 1report clinicopathological | 1orthochromatic subtype | 1years frontal | 1abnormalities white | 1leucodystrophy clinicopathological | 1matter mri | 1features mri | 1probably autosomal | 1findings case | 1histopathological | 1dominant inheritance | 1occur mainly | 1case suggest
- 2clinicopathological cases dominantly | 2onset orthochromatic leucodystrophy | 2inherited adult onset | 2cases dominantly inherited | 2dominantly inherited adult | 2adult onset orthochromatic | 1heterogeneous group occur | 1histopathological features | 1characteristics probably autosomal | 1dementia epilepsy aged | 1patient aged years | 1matter mri findings | 1mainly childhood known | 1radiological features mri | 1type heterogeneous group | 1report clinicopathological | 1flair sequences case | 1known enzyme deficiency | 1features family orthochromatic | 1dementia epilepsy radiological | 1motor signs dementia | 1features cases leucodystrophy | 1mri mostly flair | 1histopathological | 1report clinicopathological features | 1histopathological features cases | 1main characteristics probably | 1onset abnormalities white | 1subtype clinicopathological cases | 1frontal dementia epilepsy | 1years motor signs | 1patient aged
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