Class information for:
Level 1: MCARDLES DISEASE//MCARDLE DISEASE//MYOPHOSPHORYLASE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
20113 412 28.1 59%


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 MCARDLES DISEASE Author keyword 101 81% 15% 62
2 MCARDLE DISEASE Author keyword 70 86% 9% 36
3 MYOPHOSPHORYLASE Author keyword 62 85% 8% 33
4 GLYCOGENOSIS TYPE V Author keyword 61 95% 5% 20
5 MYOPHOSPHORYLASE DEFICIENCY Author keyword 40 82% 6% 23
6 PYGM Author keyword 31 92% 3% 12
7 GLYCOGEN STORAGE DISEASE TYPE V Author keyword 17 79% 3% 11
8 MYOPHOSPHORYLASE GENE Author keyword 11 100% 1% 6
9 MUSCLE PHOSPHORYLASE Author keyword 6 100% 1% 4
10 PATOL MITOCONDRIAL NEUROMUSCULAR Address 5 41% 2% 9

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 MCARDLES DISEASE 101 81% 15% 62 Search MCARDLES+DISEASE Search MCARDLES+DISEASE
2 MCARDLE DISEASE 70 86% 9% 36 Search MCARDLE+DISEASE Search MCARDLE+DISEASE
3 MYOPHOSPHORYLASE 62 85% 8% 33 Search MYOPHOSPHORYLASE Search MYOPHOSPHORYLASE
4 GLYCOGENOSIS TYPE V 61 95% 5% 20 Search GLYCOGENOSIS+TYPE+V Search GLYCOGENOSIS+TYPE+V
5 MYOPHOSPHORYLASE DEFICIENCY 40 82% 6% 23 Search MYOPHOSPHORYLASE+DEFICIENCY Search MYOPHOSPHORYLASE+DEFICIENCY
6 PYGM 31 92% 3% 12 Search PYGM Search PYGM
7 GLYCOGEN STORAGE DISEASE TYPE V 17 79% 3% 11 Search GLYCOGEN+STORAGE+DISEASE+TYPE+V Search GLYCOGEN+STORAGE+DISEASE+TYPE+V
8 MYOPHOSPHORYLASE GENE 11 100% 1% 6 Search MYOPHOSPHORYLASE+GENE Search MYOPHOSPHORYLASE+GENE
9 MUSCLE PHOSPHORYLASE 6 100% 1% 4 Search MUSCLE+PHOSPHORYLASE Search MUSCLE+PHOSPHORYLASE
10 MCARDLE 3 100% 1% 3 Search MCARDLE Search MCARDLE

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 MYOPHOSPHORYLASE DEFICIENCY 63 78% 10% 42
2 GLYCOGEN PHOSPHORYLASE GENE 33 100% 3% 13
3 2ND WIND 27 92% 3% 11
4 MCARDLES DISEASE 15 33% 9% 37
5 MYOPHOSPHORYLASE GENE 14 100% 2% 7
6 SPANISH PATIENT 14 100% 2% 7
7 MUSCLE PHOSPHORYLASE DEFICIENCY 10 73% 2% 8
8 CREATINE THERAPY 9 64% 2% 9
9 ISCHEMIC EXERCISE 7 67% 1% 6
10 IMPROVED EXERCISE CAPACITY 6 80% 1% 4

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
McArdle disease: a clinical review 2010 29 33 76%
McArdle disease: what do neurologists need to know? 2008 26 51 88%
Molecular genetics of McArdle's disease 2007 7 51 90%
Physical training for McArdle disease 2011 2 20 95%
Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V) 2010 2 33 79%
Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V) 2008 5 29 69%
McArdle's disease (glycogen storage disease type V) and anesthesia - a case report and review of the literature 2013 2 24 46%
Muscle glycogenoses 2001 69 118 21%
RHABDOMYOLYSIS IN CHILDHOOD - A PRIMER ON NORMAL MUSCLE FUNCTION AND SELECTED METABOLIC MYOPATHIES CHARACTERIZED BY DISORDERED ENERGY-PRODUCTION 1992 50 120 43%
McArdle's disease and anaesthesia: Case reports. Review of potential problems and association with malignant hyperthermia 2005 7 20 45%

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 PATOL MITOCONDRIAL NEUROMUSCULAR 5 41% 2.2% 9
2 INVEST BIOQUIM BIOL MOL CIBBIM 3 57% 1.0% 4
3 NEUROMUSCULAR UNITSECT 3342 2 67% 0.5% 2
4 H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY 2 19% 2.4% 10
5 MOL GENET METAB DIS 2 43% 0.7% 3
6 INVEST BIOQUIM BIOL MOL 1 11% 3.2% 13
7 ENFERMEDADES MITOCONDRIALES NEUROMUSCULA 1 50% 0.5% 2
8 MITOCHONDRIAL PATHOL NEUROMUSCULAR DISORDERS LA 1 100% 0.5% 2
9 SPANISH NETWORK RARE DIS CIBERER 1 50% 0.5% 2
10 EQUIPE ERI 25 1 50% 0.2% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000286041 AMP DEAMINASE//AMPD1 GENE//MYOADENYLATE DEAMINASE DEFICIENCY
2 0.0000193785 P 31 MRS//P 31 MAGNETIC RESONANCE SPECTROSCOPY//PCR RECOVERY
3 0.0000193329 FENOVERINE//IDIOPATHIC HYPER CK EMIA//HYPERCKEMIA
4 0.0000192979 POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE
5 0.0000168651 PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX
6 0.0000161727 PURINE NUCLEOTIDE CYCLE//TRICARBOXYLIC ACID CYCLE INTERMEDIATES//GLYCOGEN SYNTHASE PHOSPHATASE
7 0.0000136723 HUMAN MUSCLE DEVELOPMENT//UNITE PEDAG RECH MED//HUMAN MUSCLE CULTURE
8 0.0000110894 GLYCOGEN PHOSPHORYLASE//GLYCOGEN PHOSPHORYLASE INHIBITOR//STARCH PHOSPHORYLASE
9 0.0000106605 PHOSPHOGLYCERATE MUTASE//BISPHOSPHOGLYCERATE MUTASE//2 3 BISPHOSPHOGLYCERATE MUTASE
10 0.0000093488 CARNITINE PALMITOYLTRANSFERASE//CARNITINE PALMITOYLTRANSFERASE DEFICIENCY//MITOCHONDRIAL HMG COA SYNTHASE