Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
31123 | 127 | 19.4 | 45% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
2846 | 2447 | ORAL MUCOSITIS//MUCOSITIS//WIEDEMANN RAUTENSTRAUCH SYNDROME |
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 | WIEDEMANN RAUTENSTRAUCH SYNDROME | Author keyword | 52 | 100% | 14% | 18 |
2 | NEONATAL PROGEROID SYNDROME | Author keyword | 21 | 85% | 9% | 11 |
3 | HALLERMANN STREIFF SYNDROME | Author keyword | 19 | 70% | 13% | 16 |
4 | NEONATAL PROGERIA | Author keyword | 8 | 75% | 5% | 6 |
5 | OCULOMANDIBULODYSCEPHALY | Author keyword | 3 | 100% | 2% | 3 |
6 | FRANCOIS SYNDROME | Author keyword | 2 | 67% | 2% | 2 |
7 | PROGRAMA MAESTRIA NEUROCIENCIAS | Address | 1 | 100% | 2% | 2 |
8 | BENEFITS OF QUALITY MANAGEMENT | Author keyword | 1 | 50% | 1% | 1 |
9 | CHRONIC OBSTRUCTIVE SLEEP APNEA | Author keyword | 1 | 50% | 1% | 1 |
10 | CONGENITAL SYNDROMES | Author keyword | 1 | 50% | 1% | 1 |
Web of Science journal categories |
Author Key Words |
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 | NEONATAL PROGEROID SYNDROME | 10 | 61% | 9% | 11 |
2 | WIEDEMANN RAUTENSTRAUCH SYNDROME | 8 | 100% | 4% | 5 |
3 | FRANCOIS DYSCEPHALIC SYNDROME | 3 | 100% | 2% | 3 |
4 | WIEDEMANN RAUTENSTRAUCH | 3 | 50% | 3% | 4 |
5 | FRANCOIS SYNDROME | 1 | 100% | 2% | 2 |
6 | KUGELKERN | 1 | 100% | 2% | 2 |
7 | RAUTENSTRAUCH SYNDROME | 1 | 100% | 2% | 2 |
8 | SKIN DIMPLES | 1 | 100% | 2% | 2 |
9 | SYNDROME WIEDEMANN RAUTENSTRAUCH | 1 | 50% | 1% | 1 |
10 | HEREDITARY RETINOCHOROIDAL DYSTROPHIES | 0 | 33% | 1% | 1 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Hallermann-Streiff syndrome: Experience with 15 patients and review of the literature | 1999 | 12 | 17 | 88% |
Hallermann-Streiff syndrome: A case review | 2004 | 5 | 4 | 100% |
The neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): Case report and review of the literature | 2000 | 4 | 15 | 93% |
THE NEONATAL PSEUDO-HYDROCEPHALIC PROGEROID SYNDROME (WIEDEMANN-RAUTENSTRAUCH) - REPORT OF A NEW PATIENT AND REVIEW OF THE LITERATURE | 1988 | 26 | 3 | 67% |
Classification of biomedical research reports as a reference for evidence-based medicine in ophthalmology. A survey considering as example the journal Der Ophthalmologe | 2005 | 1 | 301 | 4% |
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 | PROGRAMA MAESTRIA NEUROCIENCIAS | 1 | 100% | 1.6% | 2 |
2 | KLIN POLIKLIN IELBEHANDLUNG NEUROOPHTHALMO | 1 | 50% | 0.8% | 1 |
3 | GRP PATOL MOL | 0 | 33% | 0.8% | 1 |
4 | PEDIAT DIABETOL BIRTH DEFECTS | 0 | 25% | 0.8% | 1 |
5 | SEZIONE DERMATOL | 0 | 20% | 0.8% | 1 |
6 | MED GENET SERV WALES | 0 | 17% | 0.8% | 1 |
7 | HOSP PESQUISA REABILITACAO LESOES IO PALATAI | 0 | 11% | 0.8% | 1 |
8 | POLIKLIN RECHTS ISAR | 0 | 100% | 0.8% | 1 |
9 | REFERENCE CONGENITAL ANOMALIES DEV | 0 | 100% | 0.8% | 1 |
10 | REFERENCE CONGENITAL HEREDITARY DEAFNE | 0 | 100% | 0.8% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000246359 | REGIONAL ODONTODYSPLASIA//ENAMEL PEARLS//GHOST TEETH |
2 | 0.0000100753 | ARTHROGRYPOSIS//NEU LAXOVA SYNDROME//AMYOPLASIA |
3 | 0.0000096837 | NANOPHTHALMOS//ANOPHTHALMIA//MICROPHTHALMIA |
4 | 0.0000073723 | BASALOID FOLLICULAR HAMARTOMA//MILIA EN PLAQUE//INFUNDIBULOCYSTIC BASAL CELL CARCINOMA |
5 | 0.0000073715 | NUCLEAR LAMINA//EMERIN//NUCLEAR ENVELOPE |
6 | 0.0000070657 | AXENFELD RIEGER SYNDROME//PETERS ANOMALY//FOXC1 |
7 | 0.0000068629 | INVOLUTIONAL ENTROPION//MEDIAL CANTHAL TENDON//LATERAL TARSAL STRIP |
8 | 0.0000066452 | SECKEL SYNDROME//FLOATING HARBOR SYNDROME//MOPD II |
9 | 0.0000065411 | CONGENITAL GENERALIZED LIPODYSTROPHY//SEIPIN//BSCL2 |
10 | 0.0000063077 | EOSINOPHILIC ULCER//RIGA FEDE DISEASE//NEONATAL TEETH |