Class information for:
Level 1: POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
10603 982 29.4 67%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1822 5688 POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//GLYCOGEN STORAGE DISEASE

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 470 83% 27% 263
2 GLYCOGEN STORAGE DISEASE TYPE II Author keyword 281 92% 11% 109
3 ACID ALPHA GLUCOSIDASE Author keyword 192 88% 9% 92
4 ACID MALTASE DEFICIENCY Author keyword 155 89% 7% 71
5 ACID MALTASE Author keyword 85 92% 3% 34
6 POMPES DISEASE Author keyword 67 87% 3% 33
7 METAB DIS GENET Address 48 77% 3% 33
8 GLYCOGENOSIS TYPE II Author keyword 45 90% 2% 19
9 LATE ONSET POMPE DISEASE Author keyword 35 89% 2% 16
10 ALGLUCOSIDASE ALFA Author keyword 34 93% 1% 13

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 470 83% 27% 263 Search POMPE+DISEASE Search POMPE+DISEASE
2 GLYCOGEN STORAGE DISEASE TYPE II 281 92% 11% 109 Search GLYCOGEN+STORAGE+DISEASE+TYPE+II Search GLYCOGEN+STORAGE+DISEASE+TYPE+II
3 ACID ALPHA GLUCOSIDASE 192 88% 9% 92 Search ACID+ALPHA+GLUCOSIDASE Search ACID+ALPHA+GLUCOSIDASE
4 ACID MALTASE DEFICIENCY 155 89% 7% 71 Search ACID+MALTASE+DEFICIENCY Search ACID+MALTASE+DEFICIENCY
5 ACID MALTASE 85 92% 3% 34 Search ACID+MALTASE Search ACID+MALTASE
6 POMPES DISEASE 67 87% 3% 33 Search POMPES+DISEASE Search POMPES+DISEASE
7 GLYCOGENOSIS TYPE II 45 90% 2% 19 Search GLYCOGENOSIS+TYPE+II Search GLYCOGENOSIS+TYPE+II
8 LATE ONSET POMPE DISEASE 35 89% 2% 16 Search LATE+ONSET+POMPE+DISEASE Search LATE+ONSET+POMPE+DISEASE
9 ALGLUCOSIDASE ALFA 34 93% 1% 13 Search ALGLUCOSIDASE+ALFA Search ALGLUCOSIDASE+ALFA
10 GLYCOGEN STORAGE DISEASE TYPE 2 34 93% 1% 13 Search GLYCOGEN+STORAGE+DISEASE+TYPE+2 Search GLYCOGEN+STORAGE+DISEASE+TYPE+2

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 232 66% 22% 213
2 RABBIT MILK 159 96% 5% 49
3 MALTASE DEFICIENCY 140 92% 6% 56
4 ACID MALTASE DEFICIENCY 128 65% 12% 122
5 GLYCOGENOSIS TYPE II 124 84% 7% 68
6 ALGLUCOSIDASE ALPHA 114 83% 7% 64
7 DISEASE TYPE II 56 60% 6% 61
8 POMPE DISEASE 45 38% 10% 95
9 HUMAN ALPHA GLUCOSIDASE 26 69% 2% 22
10 LYSOSOMAL ALPHA GLUCOSIDASE 20 58% 2% 23

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%
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature 2014 3 46 96%
Pompe disease: from pathophysiology to therapy and back again 2014 5 115 60%
The natural course of non-classic Pompe's disease; a review of 225 published cases 2005 132 77 86%
Pompe Disease: Early Diagnosis and Early Treatment Make a Difference 2013 9 69 87%
Spectrum of metabolic myopathies 2015 1 41 54%
Autopsy findings in late-onset Pompe disease: A case report and systematic review of the literature 2012 11 30 100%
Enzyme Replacement Therapy for Pompe Disease 2012 11 41 93%

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 METAB DIS GENET 48 77% 3.4% 33
2 LYSOSOMAL METAB DIS 33 55% 4.3% 42
3 GENET DIS GENOM SCI 7 67% 0.6% 6
4 LIGHT IMAGING SECT 6 42% 1.1% 11
5 CARDIOVASC SCI NEUROL 4 75% 0.3% 3
6 PEDIAT LYSOSOMAL METAB DIS 3 100% 0.3% 3
7 CELL PROT THER EUT RD 2 44% 0.4% 4
8 PATHOPHYSIOL TRANSPLANTAT NEUROL UNIT 2 67% 0.2% 2
9 PETER BELFER CARDIAC 2 67% 0.2% 2
10 REG COORDINAT RARE DIS 2 40% 0.4% 4

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000192979 MCARDLES DISEASE//MCARDLE DISEASE//MYOPHOSPHORYLASE
2 0.0000102010 DANON DISEASE//LAMP 2 DEFICIENCY//LAMP 2
3 0.0000083353 MUCOPOLYSACCHARIDOSES//HUNTER SYNDROME//MAROTEAUX LAMY SYNDROME
4 0.0000078260 RIGID SPINE SYNDROME//RIGID SPINE//EMERINOPATHY
5 0.0000077303 I CELL DISEASE//MANNOSE 6 PHOSPHATE//MUCOLIPIDOSIS TYPE III
6 0.0000075524 OLIGO 1 6 GLUCOSIDASE//ALPHA GLUCOSIDASE//DEXTRAN GLUCOSIDASE
7 0.0000061716 GLYCOGENIN//MACROGLYCOGEN//PROGLYCOGEN
8 0.0000057618 FENOVERINE//IDIOPATHIC HYPER CK EMIA//HYPERCKEMIA
9 0.0000054186 GLYCOGEN STORAGE DISEASE TYPE III//SECT CELLULAR DIFFERENTIAT//GLUCOSE 6 PHOSPHATASE
10 0.0000050631 DUCHENNE MUSCULAR DYSTROPHY//NORTH STAR AMBULATORY ASSESSMENT//REG HABILITAT