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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
10597 1050 30.4 69%


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
10597 1                   POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE 1050

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 POMPE DISEASE authKW 8628772 31% 90% 330
2 GLYCOGEN STORAGE DISEASE TYPE II authKW 3120318 11% 95% 113
3 ACID ALPHA GLUCOSIDASE authKW 2414378 9% 86% 96
4 ACID MALTASE DEFICIENCY authKW 1990497 7% 93% 74
5 ACID MALTASE authKW 890558 3% 88% 35
6 METAB DIS GENET address 774389 3% 76% 35
7 LYSOSOMAL METAB DIS address 654557 4% 49% 46
8 LATE ONSET POMPE DISEASE authKW 615324 2% 92% 23
9 POMPE authKW 549391 2% 82% 23
10 GLYCOGENOSIS TYPE II authKW 499891 2% 90% 19

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 Genetics & Heredity 6327 33% 0% 343
2 Medicine, Research & Experimental 3385 22% 0% 229
3 Clinical Neurology 2673 23% 0% 240
4 Endocrinology & Metabolism 1011 13% 0% 136
5 Pediatrics 468 8% 0% 86
6 Neurosciences 442 14% 0% 149
7 Biochemistry & Molecular Biology 156 15% 0% 153
8 Medical Laboratory Technology 143 2% 0% 23
9 Biotechnology & Applied Microbiology 119 6% 0% 63
10 Pathology 91 3% 0% 35

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 METAB DIS GENET 774389 3% 76% 35
2 LYSOSOMAL METAB DIS 654557 4% 49% 46
3 LIGHT IMAGING SECT 125653 1% 39% 11
4 GENET DIS GENOM SCI 116315 1% 67% 6
5 PEDIAT LYSOSOMAL METAB DIS 87239 0% 100% 3
6 POWELL GENE THER Y 70533 3% 9% 28
7 CARDIOVASC SCI NEUROL 65428 0% 75% 3
8 CHINESE FDN 58159 0% 100% 2
9 FONDS ERASME RECH MED 58159 0% 100% 2
10 METAB DIS GENET LYSOSOMAL METAB DIS 58159 0% 100% 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 MOLECULAR GENETICS AND METABOLISM 58146 8% 3% 79
2 NEUROMUSCULAR DISORDERS 24991 4% 2% 45
3 JOURNAL OF INHERITED METABOLIC DISEASE 15378 5% 1% 49
4 ORPHANET JOURNAL OF RARE DISEASES 7538 2% 2% 17
5 GENETICS IN MEDICINE 6483 2% 1% 19
6 MOLECULAR THERAPY 5942 3% 1% 27
7 MUSCLE & NERVE 5888 4% 1% 38
8 AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS 4859 1% 2% 9
9 MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT 3985 0% 3% 5
10 CRC CRITICAL REVIEWS IN CLINICAL NEUROBIOLOGY 1614 0% 6% 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 POMPE DISEASE 8628772 31% 90% 330 Search POMPE+DISEASE Search POMPE+DISEASE
2 GLYCOGEN STORAGE DISEASE TYPE II 3120318 11% 95% 113 Search GLYCOGEN+STORAGE+DISEASE+TYPE+II Search GLYCOGEN+STORAGE+DISEASE+TYPE+II
3 ACID ALPHA GLUCOSIDASE 2414378 9% 86% 96 Search ACID+ALPHA+GLUCOSIDASE Search ACID+ALPHA+GLUCOSIDASE
4 ACID MALTASE DEFICIENCY 1990497 7% 93% 74 Search ACID+MALTASE+DEFICIENCY Search ACID+MALTASE+DEFICIENCY
5 ACID MALTASE 890558 3% 88% 35 Search ACID+MALTASE Search ACID+MALTASE
6 LATE ONSET POMPE DISEASE 615324 2% 92% 23 Search LATE+ONSET+POMPE+DISEASE Search LATE+ONSET+POMPE+DISEASE
7 POMPE 549391 2% 82% 23 Search POMPE Search POMPE
8 GLYCOGENOSIS TYPE II 499891 2% 90% 19 Search GLYCOGENOSIS+TYPE+II Search GLYCOGENOSIS+TYPE+II
9 ENZYME REPLACEMENT THERAPY 491678 12% 14% 124 Search ENZYME+REPLACEMENT+THERAPY Search ENZYME+REPLACEMENT+THERAPY
10 ALGLUCOSIDASE ALFA 466889 2% 94% 17 Search ALGLUCOSIDASE+ALFA Search ALGLUCOSIDASE+ALFA

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 VAN DER PLOEG, AT , REUSER, AJJ , (2008) LYSOSOMAL STORAGE DISEASE 2 - POMPE'S DISEASE.LANCET. VOL. 372. ISSUE 9646. P. 1342-1353 92 81% 171
2 KISHNANI, PS , BECKEMEYER, AA , (2014) NEW THERAPEUTIC APPROACHES FOR POMPE DISEASE: ENZYME REPLACEMENT THERAPY AND BEYOND.PEDIATRIC ENDOCRINOLOGY REVIEWS PER. VOL. 12. ISSUE . P. 114 -124 83 94% 9
3 TARNOPOLSKY, M , KATZBERG, H , PETROF, BJ , SIRRS, S , SARNAT, HB , MYERS, K , DUPRE, N , DODIG, D , GENGE, A , VENANCE, SL , ET AL (2016) POMPE DISEASE: DIAGNOSIS AND MANAGEMENT. EVIDENCE-BASED GUIDELINES FROM A CANADIAN EXPERT PANEL.CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES. VOL. 43. ISSUE 4. P. 472 -485 98 75% 0
4 SCHULLER, A , WENNINGER, S , STRIGL-PILL, N , SCHOSER, B , (2012) TOWARD DECONSTRUCTING THE PHENOTYPE OF LATE-ONSET POMPE DISEASE.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 160C. ISSUE 1. P. 80 -88 67 94% 28
5 KROOS, M , HOOGEVEEN-WESTERVELD, M , VAN DER PLOEG, A , REUSER, AJJ , (2012) THE GENOTYPE-PHENOTYPE CORRELATION IN POMPE DISEASE.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 160C. ISSUE 1. P. 59-68 62 98% 31
6 AL JASMI, F , AL JUMAH, M , ALQARNI, F , AL-SANNA'A, N , AL-SHARIF, F , BOHLEGA, S , CUPLER, EJ , FATHALLA, W , HAMDAN, MA , MAKHSEED, N , ET AL (2015) DIAGNOSIS AND TREATMENT OF LATE-ONSET POMPE DISEASE IN THE MIDDLE EAST AND NORTH AFRICA REGION: CONSENSUS RECOMMENDATIONS FROM AN EXPERT GROUP.BMC NEUROLOGY. VOL. 15. ISSUE . P. - 70 91% 0
7 BEMBI, B , CERINI, E , DANESINO, C , DONATI, MA , GASPERINI, S , MORANDI, L , MUSUMECI, O , PARENTI, G , RAVAGLIA, S , SEIDITA, F , ET AL (2008) MANAGEMENT AND TREATMENT OF GLYCOGENOSIS TYPE II.NEUROLOGY. VOL. 71. ISSUE 23. P. S12-S36 85 75% 25
8 TURACA, LT , DE FARIA, DOS , KYOSEN, SO , TEIXEIRA, VD , MOTTA, FL , PESSOA, JG , SILVA, MRE , ALMEIDA, SS , D'ALMEIDA, V , ROJAS, MVM , ET AL (2015) NOVEL GAA MUTATIONS IN PATIENTS WITH POMPE DISEASE.GENE. VOL. 561. ISSUE 1. P. 124 -131 60 92% 0
9 RICHARD, E , DOUILLARD-GUILLOUX, G , CAILLAUD, C , (2011) NEW INSIGHTS INTO THERAPEUTIC OPTIONS FOR POMPE DISEASE.IUBMB LIFE. VOL. 63. ISSUE 11. P. 979 -986 62 95% 7
10 CHIEN, YH , HWU, WL , LEE, NC , (2013) POMPE DISEASE: EARLY DIAGNOSIS AND EARLY TREATMENT MAKE A DIFFERENCE.PEDIATRICS AND NEONATOLOGY. VOL. 54. ISSUE 4. P. 219-227 60 87% 16

Classes with closest relation at Level 1


Rank Class id link
1 20822 MCARDLES DISEASE//MYOPHOSPHORYLASE//GLYCOGENOSIS TYPE V
2 1052 MUCOPOLYSACCHARIDOSIS//MUCOPOLYSACCHARIDOSES//HUNTER SYNDROME
3 7726 MANNOSE 6 PHOSPHATE//MANNOSE 6 PHOSPHATE RECEPTOR//I CELL DISEASE
4 19319 DANON DISEASE//LAMP 2//LAMP 2 DEFICIENCY
5 21661 ALPHA GLUCOSIDASE//OLIGO 1 6 GLUCOSIDASE//GLYCOSIDE HYDROLASE FAMILY 31
6 35818 HYPERCKEMIA//ASYMPTOMATIC CK ELEVATION//IDIOPATHIC HYPER CK EMIA
7 36499 RIGID SPINE SYNDROME//RIGID SPINE//1ST AFFILIATED HOSP NEUROL
8 21054 ALPHA MANNOSIDOSIS//BETA MANNOSIDOSIS//MANNOSIDOSIS
9 21317 GLYCOGENIN//MACROGLYCOGEN//PROGLYCOGEN
10 7488 GLUCOSE 6 PHOSPHATASE//SECT CELLULAR DIFFERENTIAT//GLYCOGEN STORAGE DISEASE

Go to start page