Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
12686 | 826 | 28.2 | 81% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
330 | 17366 | FABRY DISEASE//GAUCHER DISEASE//MUCOPOLYSACCHARIDOSES |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | ALEXANDER DISEASE | Author keyword | 155 | 86% | 10% | 79 |
2 | LEUKODYSTROPHY | Author keyword | 47 | 36% | 13% | 105 |
3 | VANISHING WHITE MATTER DISEASE | Author keyword | 42 | 94% | 2% | 15 |
4 | MLC1 | Author keyword | 36 | 83% | 2% | 20 |
5 | ALEXANDERS DISEASE | Author keyword | 32 | 78% | 3% | 21 |
6 | VANISHING WHITE MATTER | Author keyword | 24 | 82% | 2% | 14 |
7 | NEUROAXONAL SPHEROIDS | Author keyword | 24 | 91% | 1% | 10 |
8 | MEGALENCEPHALIC LEUKOENCEPHALOPATHY | Author keyword | 21 | 90% | 1% | 9 |
9 | HEPACAM | Author keyword | 19 | 80% | 1% | 12 |
10 | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH SPHEROIDS | Author keyword | 18 | 89% | 1% | 8 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | ALEXANDER DISEASE | 155 | 86% | 10% | 79 | Search ALEXANDER+DISEASE | Search ALEXANDER+DISEASE |
2 | LEUKODYSTROPHY | 47 | 36% | 13% | 105 | Search LEUKODYSTROPHY | Search LEUKODYSTROPHY |
3 | VANISHING WHITE MATTER DISEASE | 42 | 94% | 2% | 15 | Search VANISHING+WHITE+MATTER+DISEASE | Search VANISHING+WHITE+MATTER+DISEASE |
4 | MLC1 | 36 | 83% | 2% | 20 | Search MLC1 | Search MLC1 |
5 | ALEXANDERS DISEASE | 32 | 78% | 3% | 21 | Search ALEXANDERS+DISEASE | Search ALEXANDERS+DISEASE |
6 | VANISHING WHITE MATTER | 24 | 82% | 2% | 14 | Search VANISHING+WHITE+MATTER | Search VANISHING+WHITE+MATTER |
7 | NEUROAXONAL SPHEROIDS | 24 | 91% | 1% | 10 | Search NEUROAXONAL+SPHEROIDS | Search NEUROAXONAL+SPHEROIDS |
8 | MEGALENCEPHALIC LEUKOENCEPHALOPATHY | 21 | 90% | 1% | 9 | Search MEGALENCEPHALIC+LEUKOENCEPHALOPATHY | Search MEGALENCEPHALIC+LEUKOENCEPHALOPATHY |
9 | HEPACAM | 19 | 80% | 1% | 12 | Search HEPACAM | Search HEPACAM |
10 | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH SPHEROIDS | 18 | 89% | 1% | 8 | Search HEREDITARY+DIFFUSE+LEUKOENCEPHALOPATHY+WITH+SPHEROIDS | Search HEREDITARY+DIFFUSE+LEUKOENCEPHALOPATHY+WITH+SPHEROIDS |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MILD CLINICAL COURSE | 161 | 88% | 9% | 75 |
2 | CHILDHOOD ATAXIA | 122 | 86% | 8% | 62 |
3 | NERVOUS SYSTEM HYPOMYELINATION | 106 | 91% | 5% | 43 |
4 | NEUROAXONAL SPHEROIDS | 86 | 90% | 4% | 37 |
5 | ROSENTHAL FIBER FORMATION | 68 | 100% | 3% | 22 |
6 | SUBCORTICAL CYSTS | 63 | 78% | 5% | 42 |
7 | PIGMENTED GLIA | 61 | 95% | 2% | 20 |
8 | VANISHING WHITE MATTER | 58 | 54% | 9% | 76 |
9 | AXONAL SPHEROIDS | 58 | 92% | 3% | 23 |
10 | INITIATION FACTOR EIF2B | 50 | 61% | 6% | 53 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Vanishing white matter disease | 2006 | 116 | 53 | 62% |
Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD) A single entity? | 2009 | 36 | 29 | 97% |
Leukoencephalopathy With Vanishing White Matter: A Review | 2010 | 37 | 88 | 75% |
The clinical spectrum of late-onset Alexander disease: a systematic literature review | 2010 | 23 | 26 | 92% |
Megalencephalic leukoencephalopathy with subcortical cysts: chronic white matter oedema due to a defect in brain ion and water homoeostasis | 2012 | 16 | 88 | 66% |
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Can Present as Frontotemporal Dementia Syndrome | 2011 | 14 | 43 | 79% |
Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation | 2012 | 7 | 37 | 95% |
Vanishing white matter disease: A review with focus on its genetics | 2006 | 25 | 32 | 94% |
GFAP and its role in Alexander disease | 2007 | 77 | 75 | 37% |
Alexander disease | 2003 | 20 | 35 | 91% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | REFERENCE LEUCODYSTROPHIES | 8 | 70% | 0.8% | 7 |
2 | UMR 384 | 4 | 36% | 1.2% | 10 |
3 | REFERENCE MALAD RA LEUCODYSTROPHIES | 4 | 75% | 0.4% | 3 |
4 | PEDIAT CHILD NEUROL | 3 | 19% | 1.9% | 16 |
5 | INVEST RED ENFERMEDADES RARAS CIBERER | 3 | 43% | 0.7% | 6 |
6 | NEUROGENET MOT | 3 | 38% | 0.7% | 6 |
7 | CNRS 6247 | 2 | 67% | 0.2% | 2 |
8 | SCDU NEURORADIOL | 2 | 67% | 0.2% | 2 |
9 | SERV GENET NEUROVASC | 2 | 67% | 0.2% | 2 |
10 | UNIT NEURODEGENERAT DISORDERS | 2 | 67% | 0.2% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000161731 | GLOBOID CELL LEUKODYSTROPHY//KRABBE DISEASE//PSYCHOSINE |
2 | 0.0000098845 | METACHROMATIC LEUKODYSTROPHY//ARYLSULFATASE A//MULTIPLE SULFATASE DEFICIENCY |
3 | 0.0000096168 | ADRENOLEUKODYSTROPHY//ADRENOMYELONEUROPATHY//X LINKED ADRENOLEUKODYSTROPHY |
4 | 0.0000087607 | PELIZAEUS MERZBACHER DISEASE//PROTEOLIPID PROTEIN//PL NEUROBIOL GRP |
5 | 0.0000078159 | DAP3//ICT1//MITOCHONDRIAL RIBOSOMAL PROTEINS |
6 | 0.0000076387 | GIANT AXONAL NEUROPATHY//GIGAXONIN//GAN MUTATIONS |
7 | 0.0000069430 | TRANSALDOLASE DEFICIENCY//ESA 8080//NEONATAL HAEMORRHAGIC DIATHESIS |
8 | 0.0000062367 | L 2 HYDROXYGLUTARIC ACIDURIA//GLUTARIC ACIDURIA TYPE I//GLUTARIC ACIDURIA TYPE 1 |
9 | 0.0000058974 | GFAP//STELLATION//ASTROCYTE DEVELOPMENT |
10 | 0.0000054810 | CADASIL//NOTCH3//NOTCH3 GENE |