Class information for:
Level 1: MCARDLES DISEASE//MYOPHOSPHORYLASE//GLYCOGENOSIS TYPE V

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
20822 444 28.9 61%


Bar chart of Publication_year

Last years might be incomplete

Hierarchy of classes
The table includes all classes above and classes immediately below the current class.


Cluster id Level Cluster label #P
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
584 3       POMPE DISEASE//PIN1//CYCLOPHILIN 15652
1662 2             POMPE DISEASE//GLYCOGEN STORAGE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II 6857
20822 1                   MCARDLES DISEASE//MYOPHOSPHORYLASE//GLYCOGENOSIS TYPE V 444

Terms with highest relevance score


rank Term termType Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 MCARDLES DISEASE authKW 6333956 25% 84% 109
2 MYOPHOSPHORYLASE authKW 2296319 8% 90% 37
3 GLYCOGENOSIS TYPE V authKW 1650537 5% 100% 24
4 MYOPHOSPHORYLASE DEFICIENCY authKW 1299299 5% 82% 23
5 PYGM authKW 898624 3% 93% 14
6 GLYCOGEN STORAGE DISEASE TYPE V authKW 774832 3% 87% 13
7 MYOPHOSPHORYLASE GENE authKW 412634 1% 100% 6
8 PATOL MITOCONDRIAL NEUROMUSCULAR address 298999 2% 43% 10
9 GLYCOGEN STORAGE DISEASE V authKW 275090 1% 100% 4
10 MCARDLE authKW 275090 1% 100% 4

Web of Science journal categories


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 Clinical Neurology 5742 49% 0% 219
2 Neurosciences 1272 32% 0% 143
3 Sport Sciences 374 7% 0% 32
4 Medicine, General & Internal 262 13% 0% 56
5 Genetics & Heredity 152 9% 0% 40
6 CYTOLOGY & HISTOLOGY 77 1% 0% 3
7 Medicine, Research & Experimental 71 6% 0% 26
8 Physiology 66 5% 0% 23
9 Endocrinology & Metabolism 31 5% 0% 20
10 Pediatrics 29 4% 0% 17

Address terms


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 PATOL MITOCONDRIAL NEUROMUSCULAR 298999 2% 43% 10
2 MITOCHONDRIAL PATHOL NEUROMUSCULAR DISORDERS LA 206317 1% 100% 3
3 INVEST BIOQUIM BIOL MOL CIBBIM 157191 1% 57% 4
4 NEUROMUSCULAR MITOCHONDRIAL PATHOL 137545 0% 100% 2
5 H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY 127340 2% 19% 10
6 ENFERMEDADES MITOCONDRIALES NEUROMUSCULA 123788 1% 60% 3
7 INVEST BIOQUIM BIOL MOL 95243 3% 11% 13
8 MEDEA SCI 91695 0% 67% 2
9 NEUROMUSCULAR UNITSECT 3342 91695 0% 67% 2
10 TRANSLAT NEUROMUSCULAR DIS 91695 0% 67% 2

Journals


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 NEUROMUSCULAR DISORDERS 35811 8% 1% 35
2 MUSCLE & NERVE 17144 9% 1% 42
3 NEUROLOGY 3951 8% 0% 35
4 EXERCISE AND SPORT SCIENCES REVIEWS/SERIES 2454 0% 4% 1
5 EUROPEAN JOURNAL OF BASIC AND APPLIED HISTOCHEMISTRY 2370 0% 3% 1
6 NEUROLOGIC CLINICS 1912 2% 0% 7
7 MOLECULAR GENETICS AND METABOLISM 1398 2% 0% 8
8 JOURNAL OF THE NEUROLOGICAL SCIENCES 1317 3% 0% 14
9 ARCHIVES OF NEUROLOGY 1029 2% 0% 10
10 TRANSACTIONS OF THE AMERICAN NEUROLOGICAL ASSOCIATION 927 0% 1% 1

Author Key Words


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class		 LCSH search Wikipedia search
1 MCARDLES DISEASE 6333956 25% 84% 109 Search MCARDLES+DISEASE Search MCARDLES+DISEASE
2 MYOPHOSPHORYLASE 2296319 8% 90% 37 Search MYOPHOSPHORYLASE Search MYOPHOSPHORYLASE
3 GLYCOGENOSIS TYPE V 1650537 5% 100% 24 Search GLYCOGENOSIS+TYPE+V Search GLYCOGENOSIS+TYPE+V
4 MYOPHOSPHORYLASE DEFICIENCY 1299299 5% 82% 23 Search MYOPHOSPHORYLASE+DEFICIENCY Search MYOPHOSPHORYLASE+DEFICIENCY
5 PYGM 898624 3% 93% 14 Search PYGM Search PYGM
6 GLYCOGEN STORAGE DISEASE TYPE V 774832 3% 87% 13 Search GLYCOGEN+STORAGE+DISEASE+TYPE+V Search GLYCOGEN+STORAGE+DISEASE+TYPE+V
7 MYOPHOSPHORYLASE GENE 412634 1% 100% 6 Search MYOPHOSPHORYLASE+GENE Search MYOPHOSPHORYLASE+GENE
8 GLYCOGEN STORAGE DISEASE V 275090 1% 100% 4 Search GLYCOGEN+STORAGE+DISEASE+V Search GLYCOGEN+STORAGE+DISEASE+V
9 MCARDLE 275090 1% 100% 4 Search MCARDLE Search MCARDLE
10 MUSCLE PHOSPHORYLASE 275090 1% 100% 4 Search MUSCLE+PHOSPHORYLASE Search MUSCLE+PHOSPHORYLASE

Core articles
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c:
(1) Number of references referring to publications in the class.
(2) Share of total number of active references referring to publications in the class.
(3) Age of the article. New articles get higher score than old articles.
(4) Citation rate, normalized to year.


Rank Reference # ref.
in cl.		 Shr. of ref. in
cl.		 Citations
1 NOGALES-GADEA, G , BRULL, A , SANTALLA, A , ANDREU, AL , ARENAS, J , MARTIN, MA , LUCIA, A , DE LUNA, N , PINOS, T , (2015) MCARDLE DISEASE: UPDATE OF REPORTED MUTATIONS AND POLYMORPHISMS IN THE PYGM GENE.HUMAN MUTATION. VOL. 36. ISSUE 7. P. 669 -678 76 82% 3
2 MIGOCKA-PATRZALEK, M , KOSIERADZKA, A , LEWANDOWSKI, D , POSYNIAK, E , DUBINSKA-MAGIERA, M , DACZEWSKA, M , (2015) MCARDLE DISEASE: PATHOGENESIS AND THERAPY PERSPECTIVES.POSTEPY BIOLOGII KOMORKI. VOL. 42. ISSUE 3. P. 431 -443 59 91% 0
3 NOGALES-GADEA, G , SANTALLA, A , BRULL, A , DE LUNA, N , LUCIA, A , PINOS, T , (2015) THE PATHOGENOMICS OF MCARDLE DISEASE-GENES, ENZYMES, MODELS, AND THERAPEUTIC IMPLICATIONS.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 38. ISSUE 2. P. 221 -230 52 78% 2
4 LUCIA, A , NOGALES-GADEA, G , PEREZ, M , MARTIN, MA , ANDREU, AL , ARENAS, J , (2008) MCARDLE DISEASE: WHAT DO NEUROLOGISTS NEED TO KNOW?.NATURE CLINICAL PRACTICE NEUROLOGY. VOL. 4. ISSUE 10. P. 568-577 46 90% 35
5 NOGALES-GADEA, G , ARENAS, J , ANDREU, AL , (2007) MOLECULAR GENETICS OF MCARDLE'S DISEASE.CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS. VOL. 7. ISSUE 1. P. 84-92 48 92% 8
6 SANTALLA, A , NOGALES-GADEA, G , ORTENBLAD, N , BRULL, A , DE LUNA, N , PINOS, T , LUCIA, A , (2014) MCARDLE DISEASE: A UNIQUE STUDY MODEL IN SPORTS MEDICINE.SPORTS MEDICINE. VOL. 44. ISSUE 11. P. 1531 -1544 58 51% 0
7 NOGALES-GADEA, G , SANTALLA, A , BALLESTER-LOPEZ, A , ARENAS, J , MARTIN, MA , GODFREY, R , PINOS, T , PINTOS-MORELL, G , COLL-CANTI, J , LUCIA, A , (2016) EXERCISE AND PREEXERCISE NUTRITION AS TREATMENT FOR MCARDLE DISEASE.MEDICINE AND SCIENCE IN SPORTS AND EXERCISE. VOL. 48. ISSUE 4. P. 673 -679 30 83% 1
8 QUINLIVAN, R , MARTINUZZI, A , SCHOSER, B , (2014) PHARMACOLOGICAL AND NUTRITIONAL TREATMENT FOR MCARDLE DISEASE (GLYCOGEN STORAGE DISEASE TYPE V).COCHRANE DATABASE OF SYSTEMATIC REVIEWS. VOL. . ISSUE 11. P. - 32 84% 1
9 RUBIO, JC , GARCIA-CONSUEGRA, I , NOGALES-GADEA, G , BLAZQUEZ, A , CABELLO, A , LUCIA, A , ANDREU, AL , ARENAS, J , MARTIN, MA , (2007) A PROPOSED MOLECULAR DIAGNOSTIC FLOWCHART FOR MYOPHOSPHORYLASE DEFICIENCY (MCARDLE DISEASE) IN BLOOD SAMPLES FROM SPANISH PATIENTS.HUMAN MUTATION. VOL. 28. ISSUE 2. P. - 26 96% 13
10 VIEITEZ, I , TEIJEIRA, S , FERNANDEZ, JM , SAN MILLAN, B , MIRANDA, S , ORTOLANO, S , LOUIS, S , LAFORET, P , NAVARRO, C , (2011) MOLECULAR AND CLINICAL STUDY OF MCARDLE'S DISEASE IN A COHORT OF 123 EUROPEAN PATIENTS. IDENTIFICATION OF 20 NOVEL MUTATIONS.NEUROMUSCULAR DISORDERS. VOL. 21. ISSUE 12. P. 817-823 23 92% 12

Classes with closest relation at Level 1


Rank Class id link
1 14850 AMP DEAMINASE//MYOADENYLATE DEAMINASE DEFICIENCY//PURINE NUCLEOTIDE CYCLE
2 13512 P 31 MRS//PHOSPHOCREATINE//P 31 MAGNETIC RESONANCE SPECTROSCOPY
3 35818 HYPERCKEMIA//ASYMPTOMATIC CK ELEVATION//IDIOPATHIC HYPER CK EMIA
4 21200 PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX
5 10597 POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE
6 34278 ACETYLCHOLINE RECEPTOR DEGRADATION//DIS ENVIRONM AGCY//DMPK MYOTONIC DYSTROPHY PROTEIN KINASE
7 25683 PHOSPHOGLYCERATE MUTASE//BISPHOSPHOGLYCERATE MUTASE//2 3 BISPHOSPHOGLYCERATE PHOSPHATASE
8 14988 GLYCOGEN PHOSPHORYLASE//GLYCOGEN PHOSPHORYLASE INHIBITOR//C GLUCOPYRANOSYL DERIVATIVE
9 20583 PHOSPHOGLYCERATE KINASE//PHOSPHOGLYCERATE KINASE DEFICIENCY//PGK1
10 8921 CARNITINE PALMITOYLTRANSFERASE//CARNITINE PALMITOYLTRANSFERASE I//CARNITINE PALMITOYLTRANSFERASE DEFICIENCY

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