Class information for:
Level 2: POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//GLYCOGEN STORAGE DISEASE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
1822 5688 30.3 58%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)


ID, lev.
above		 Publications Label for level above
539 16259 POMPE DISEASE//PROTEIN KINASE CK2//GLYCOGEN STORAGE DISEASE TYPE II

Classes in level below (level 1)


ID, lev. below Publications Label for level below
7164 1321 GLYCOGEN STORAGE DISEASE TYPE III//SECT CELLULAR DIFFERENTIAT//GLUCOSE 6 PHOSPHATASE
10603 982 POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE
13053 799 GLYCOGEN PHOSPHORYLASE//GLYCOGEN PHOSPHORYLASE INHIBITOR//STARCH PHOSPHORYLASE
13139 794 LAFORA DISEASE//POLYGLUCOSAN BODIES//UNVERRICHT LUNDBORG DISEASE
17347 540 AMP DEAMINASE//AMPD1 GENE//MYOADENYLATE DEAMINASE DEFICIENCY
19893 421 GLYCOGENIN//MACROGLYCOGEN//PROGLYCOGEN
19942 419 PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX
20113 412 MCARDLES DISEASE//MCARDLE DISEASE//MYOPHOSPHORYLASE

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 POMPE DISEASE Author keyword 483 84% 5% 265
2 GLYCOGEN STORAGE DISEASE TYPE II Author keyword 281 92% 2% 109
3 GLYCOGEN STORAGE DISEASE Author keyword 203 71% 3% 165
4 ACID ALPHA GLUCOSIDASE Author keyword 192 88% 2% 92
5 ACID MALTASE DEFICIENCY Author keyword 166 90% 1% 72
6 LAFORA DISEASE Author keyword 160 88% 1% 77
7 MCARDLES DISEASE Author keyword 114 83% 1% 64
8 MYOPHOSPHORYLASE Author keyword 110 95% 1% 37
9 GLYCOGEN STORAGE DISEASE TYPE III Author keyword 98 94% 1% 34
10 GLYCOGENIN Author keyword 97 85% 1% 51

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 POMPE DISEASE 483 84% 5% 265 Search POMPE+DISEASE Search POMPE+DISEASE
2 GLYCOGEN STORAGE DISEASE TYPE II 281 92% 2% 109 Search GLYCOGEN+STORAGE+DISEASE+TYPE+II Search GLYCOGEN+STORAGE+DISEASE+TYPE+II
3 GLYCOGEN STORAGE DISEASE 203 71% 3% 165 Search GLYCOGEN+STORAGE+DISEASE Search GLYCOGEN+STORAGE+DISEASE
4 ACID ALPHA GLUCOSIDASE 192 88% 2% 92 Search ACID+ALPHA+GLUCOSIDASE Search ACID+ALPHA+GLUCOSIDASE
5 ACID MALTASE DEFICIENCY 166 90% 1% 72 Search ACID+MALTASE+DEFICIENCY Search ACID+MALTASE+DEFICIENCY
6 LAFORA DISEASE 160 88% 1% 77 Search LAFORA+DISEASE Search LAFORA+DISEASE
7 MCARDLES DISEASE 114 83% 1% 64 Search MCARDLES+DISEASE Search MCARDLES+DISEASE
8 MYOPHOSPHORYLASE 110 95% 1% 37 Search MYOPHOSPHORYLASE Search MYOPHOSPHORYLASE
9 GLYCOGEN STORAGE DISEASE TYPE III 98 94% 1% 34 Search GLYCOGEN+STORAGE+DISEASE+TYPE+III Search GLYCOGEN+STORAGE+DISEASE+TYPE+III
10 GLYCOGENIN 97 85% 1% 51 Search GLYCOGENIN Search GLYCOGENIN

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 ACID ALPHA GLUCOSIDASE 251 68% 4% 219
2 ACID MALTASE DEFICIENCY 160 70% 2% 132
3 RABBIT MILK 159 96% 1% 49
4 MALTASE DEFICIENCY 140 92% 1% 56
5 PROGRESSIVE MYOCLONUS EPILEPSY 138 47% 4% 218
6 GLYCOGENOSIS TYPE II 132 85% 1% 69
7 ALGLUCOSIDASE ALPHA 121 84% 1% 65
8 DEBRANCHING ENZYME GENE 112 97% 1% 32
9 MICROSOMAL GLUCOSE 6 PHOSPHATASE 106 79% 1% 68
10 MYOPHOSPHORYLASE DEFICIENCY 105 89% 1% 48

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review 2013 34 37 100%
Lysosomal storage disease 2 - Pompe's disease 2008 140 114 80%
The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature 2003 196 40 93%
Glycogen and its metabolism: some new developments and old themes 2012 94 241 44%
The natural course of non-classic Pompe's disease; a review of 225 published cases 2005 132 77 86%
The glucose-6-phosphatase system 2002 164 215 73%
Spectrum of metabolic myopathies 2015 1 41 80%
Recent advances in the molecular basis of Lafora's progressive myoclonus epilepsy 2006 69 31 94%
Glucose-6-phosphatase deficiency 2011 24 107 89%
Regulation of glucose production by the liver 1999 219 88 52%

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 CELLULAR DIFFERENTIAT 96 88% 0.8% 45
2 GLYCOGEN STORAGE DIS PROGRAM 51 91% 0.4% 21
3 METAB DIS GENET 48 77% 0.6% 33
4 LYSOSOMAL METAB DIS 33 55% 0.7% 42
5 U855 17 51% 0.4% 24
6 HERITABLE DISORDERS BRANCH 9 19% 0.7% 42
7 GENET DIS GENOM SCI 7 67% 0.1% 6
8 CARDIOVASC METAB DIS BIOL 6 80% 0.1% 4
9 DIAG CARE EPILEPSY 6 80% 0.1% 4
10 PATOL MITOCONDRIAL NEUROMUSCULAR 6 45% 0.2% 10

Related classes at same level (level 2)


Rank Relatedness score Related classes
1 0.0000016615 CANTHARIDIN//NORCANTHARIDIN//CIP2A
2 0.0000010458 PHOSPHOFRUCTOKINASE//GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE//6 PHOSPHOFRUCTO 2 KINASE
3 0.0000008654 FABRY DISEASE//GAUCHER DISEASE//MUCOPOLYSACCHARIDOSES
4 0.0000006710 KETOGENIC DIET//CONGENITAL HYPERINSULINISM//MODIFIED ATKINS DIET
5 0.0000006700 REGUCALCIN//SMP30//ENDOCRINOL MOL METAB
6 0.0000006052 MAPLE SYRUP URINE DISEASE//METHYLMALONIC ACIDEMIA//JOURNAL OF INHERITED METABOLIC DISEASE
7 0.0000005743 CALMITINE//MOL CELLULAR BIOL PHARMACEUT SCI//HVJ SENDAI VIRUS
8 0.0000005644 STARCH SYNTHESIS//ADP GLUCOSE PYROPHOSPHORYLASE//SUCROSE SYNTHASE
9 0.0000004384 DEOXYCYTIDINE KINASE//PURINE NUCLEOSIDE PHOSPHORYLASE//NUCLEOSIDE TRANSPORT
10 0.0000004281 TRIOSEPHOSPHATE ISOMERASE//PYRUVATE KINASE DEFICIENCY//PYRUVATE KINASE