Class information for:
Level 2: CYSTINOSIS//PANTOTHENATE KINASE//PKAN

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
2859 2400 29.2 64%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)


ID, lev.
above		 Publications Label for level above
502 19766 FABRY DISEASE//GAUCHER DISEASE//MUCOPOLYSACCHARIDOSES

Classes in level below (level 1)


ID, lev. below Publications Label for level below
13328 780 CYSTINOSIS//SALLA DISEASE//NEPHROPATHIC CYSTINOSIS
14272 714 PANTETHEINASE//PANTOTHENATE SYNTHETASE//COENZYME A
16693 576 PKAN//HALLERVORDEN SPATZ SYNDROME//NBIA
22274 330 PANTETHINE//ALLITHIAMINE//ALLITHIAMIN

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 CYSTINOSIS Author keyword 330 86% 7% 171
2 PANTOTHENATE KINASE Author keyword 67 89% 1% 31
3 PKAN Author keyword 67 87% 1% 33
4 HALLERVORDEN SPATZ SYNDROME Author keyword 64 82% 2% 37
5 PANTETHEINASE Author keyword 53 95% 1% 18
6 NBIA Author keyword 50 74% 2% 37
7 HALLERVORDEN SPATZ DISEASE Author keyword 48 77% 1% 33
8 SALLA DISEASE Author keyword 45 83% 1% 25
9 PANK2 Author keyword 38 93% 1% 14
10 PLA2G6 Author keyword 35 76% 1% 25

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 CYSTINOSIS 330 86% 7% 171 Search CYSTINOSIS Search CYSTINOSIS
2 PANTOTHENATE KINASE 67 89% 1% 31 Search PANTOTHENATE+KINASE Search PANTOTHENATE+KINASE
3 PKAN 67 87% 1% 33 Search PKAN Search PKAN
4 HALLERVORDEN SPATZ SYNDROME 64 82% 2% 37 Search HALLERVORDEN+SPATZ+SYNDROME Search HALLERVORDEN+SPATZ+SYNDROME
5 PANTETHEINASE 53 95% 1% 18 Search PANTETHEINASE Search PANTETHEINASE
6 NBIA 50 74% 2% 37 Search NBIA Search NBIA
7 HALLERVORDEN SPATZ DISEASE 48 77% 1% 33 Search HALLERVORDEN+SPATZ+DISEASE Search HALLERVORDEN+SPATZ+DISEASE
8 SALLA DISEASE 45 83% 1% 25 Search SALLA+DISEASE Search SALLA+DISEASE
9 PANK2 38 93% 1% 14 Search PANK2 Search PANK2
10 PLA2G6 35 76% 1% 25 Search PLA2G6 Search PLA2G6

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 NEPHROPATHIC CYSTINOSIS 237 75% 7% 171
2 CYSTEAMINE THERAPY 197 98% 2% 50
3 HALLERVORDEN SPATZ SYNDROME 108 53% 6% 142
4 COENZYME A BIOSYNTHESIS 87 78% 2% 57
5 KINASE ASSOCIATED NEURODEGENERATION 65 60% 3% 72
6 CTNS MUTATIONS 61 88% 1% 29
7 CORNEAL CRYSTALS 57 95% 1% 19
8 PANTOTHENATE KINASE 46 70% 2% 39
9 INFANTILE CYSTINOSIS 45 94% 1% 16
10 PANK2 42 83% 1% 24

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Cystinosis 2002 205 48 96%
Clinical and genetic delineation of neurodegeneration with brain iron accumulation 2009 116 50 78%
Coenzyme A: Back in action 2005 158 166 63%
Cystinosis: the evolution of a treatable disease 2013 16 57 91%
Genetics of Neurodegeneration with Brain Iron Accumulation 2011 47 41 61%
Neuroimaging Features of Neurodegeneration with Brain Iron Accumulation 2012 43 33 55%
Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA): an Update on Clinical Presentations, Histological and Genetic Underpinnings, and Treatment Considerations 2012 34 79 63%
Nephropathic cystinosis: an international consensus document 2014 4 60 93%
Iron metabolism in the CNS: implications for neurodegenerative diseases 2013 41 128 29%
Nephropathic cystinosis: late complications of a multisystemic disease 2008 44 108 96%

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 SECT HUMAN BIOCHEM GENET 12 29% 1.5% 35
2 LEHRSTUHL MIKROBIELLE GENET 8 60% 0.4% 9
3 PIERFRANCO LUISA MARIANI STUDY MITOCHONDRIA 5 60% 0.3% 6
4 STRUCT FUNCT NUCL ACID 4 75% 0.1% 3
5 ILLING SECT CLIN MOL NEUROGENET 4 38% 0.3% 8
6 GENET FUNKT GENOMFOR 2 67% 0.1% 2
7 NEUROMUSCULAR NEUROMETAB DISORDERS 2 67% 0.1% 2
8 NEMOURS PROGRAMS 2 33% 0.2% 4
9 HUMAN GENET BRANCH HUMAN BIOCHEM GENET SECT 1 100% 0.1% 2
10 MEMBRANE PUMPS CELLS DISPUMPKIN 1 100% 0.1% 2

Related classes at same level (level 2)


Rank Relatedness score Related classes
1 0.0000012848 PEPTIDE DEFORMYLASE//ENOYL ACP REDUCTASE//PLATENSIMYCIN
2 0.0000009169 ALPHA SYNUCLEIN//PARKIN//LRRK2
3 0.0000008284 FABRY DISEASE//GAUCHER DISEASE//MUCOPOLYSACCHARIDOSES
4 0.0000007589 MAPLE SYRUP URINE DISEASE//METHYLMALONIC ACIDEMIA//JOURNAL OF INHERITED METABOLIC DISEASE
5 0.0000007069 THIAMINE DEFICIENCY//THIAMINE//WERNICKES ENCEPHALOPATHY
6 0.0000005791 CARNITINE//L CARNITINE//PROPIONYL L CARNITINE
7 0.0000005314 ADENYLATE KINASE//THYMIDYLATE KINASE//CHIM STRUCT MACROMOL
8 0.0000005195 HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA
9 0.0000005125 SOMATOSTATIN//HYPERPOLARIZED C 13//SOMATOSTATIN RECEPTORS
10 0.0000005052 TRANSHYDROGENASE//WLDS//NAD KINASE