SCOPUS 정보 검색 플랫폼

Volumn 110, Issue 4, 2002, Pages 400-403

Bilateral hyperplasia of the mandibular coronoid processes in patients with nevoid basal cell carcinoma syndrome: An undescribed sign [4]

(8) Leonardi, Rosalia a Caltabiano, Mario a Lo Muzio, Lorenzo b Gorlin, Robert J c Bucci, Paolo d Pannone, Giuseppe d Canfora, Massimo d Sorge, Giuseppe a

a UNIVERSITY OF CATANIA (Italy)

b UNIVERSITÀ POLITECNICA DELLE MARCHE (Italy)

c University of Minnesota (United States)

d UNIVERSITY OF NAPLES FEDERICO II (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; BASAL CELL NEVUS SYNDROME; CHROMOSOME 9; CHROMOSOME MAP; DIAGNOSTIC ERROR; GENE EXPRESSION; GENE MUTATION; HUMAN; HYPERPLASIA; JAW MOVEMENT; LETTER; MANDIBLE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TRISMUS;

BASAL CELL NEVUS SYNDROME; FEMALE; HUMANS; HYPERPLASIA; MALE; MANDIBLE;

EID: 0037100074 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10432 Document Type: Letter

Times cited : (22)

References (27)

1
- 0031026078
- Variable expressivity of patched mutations in flies and humans
- (1997) Am J Hum Genet , vol.60 , pp. 10-12
- Bale, A.E.¹

2
- 0028219676
- Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients
- (1994) Hum Mol Genet , vol.3 , pp. 447-448
- Bonifas, J.M.¹ Bare, J.W.² Kerschmann, R.L.³ Master, S.P.⁴ Epstein E.H., Jr.⁵

3
- 0027436115
- Further localisation of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of heterozygosity
- (1993) Am J Hum Genet , vol.53 , pp. 760-767
- Chenevix-Trench, G.¹ Wicking, C.² Berkman, J.³ Sharpe, H.⁴ Hockey, A.⁵ Haan, E.⁶ Oley, C.⁷ Ravine, D.⁸ Turner, A.⁹ Goldgar, D.¹⁰ Searle, J.¹¹ Wainwright, B.¹²

4
- 0027231001
- Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study
- (1993) J Med Genet , vol.30 , pp. 460-464
- Evans, D.G.¹ Ladusans, E.J.² Rimmer, S.³ Burnell, L.D.⁴ Thakker, N.⁵ Farndon, P.A.⁶

5
- 0026602737
- Location of gene for Gorlin syndrome
- (1992) Lancet , vol.339 , pp. 581-582
- Farndon, P.A.¹ Del Mastro, R.G.² Evans, D.G.R.³ Kilpatrick, M.W.⁴

6
- 0027968936
- Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3
- (1994) Genomics , vol.23 , pp. 486-489
- Farndon, P.A.¹ Morris, D.J.² Hardy, C.³ McConville, C.M.⁴ Weissenbach, J.⁵ Kilpatrick, M.W.⁶ Reis, A.⁷

7
- 0004199106
- Normandie study group for TMJ disfunction. 7th ed. Montgomery Walker Printing Co
- (1983) A clinical outline of Temporomandibular joint diagnosis and treatment
- Farrar, W.B.¹ McCarty, W.L.²

8
- 0026627965
- Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
- (1992) Cell , vol.69 , pp. 111-117
- Gailani, M.R.¹ Bale, S.J.² Leffell, D.J.³ DiGiovanna, J.J.⁴ Peck, G.L.⁵ Poliak, S.⁶ Drum, M.A.⁷ Pastakia, B.⁸ McBride, O.W.⁹ Kase, R.¹⁰ Greene, M.¹¹ Mulvihill, J.J.¹² Bale, A.E.¹³

9
- 0009613794
- Nevoid basal cell syndrome
- (1987) Medicine , vol.66 , pp. 99-109
- Gorlin, R.J.¹

10
- 72849181879
- Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib: A syndrome
- (1960) N Engl J Med , vol.262 , pp. 908-912
- Gorlin, R.J.¹ Goltz, R.W.²

11
- 0003868876
- New York: Blakiston Division, McGraw-Hill
- (1976) Syndromes of the head and neck
- Gorlin, R.J.¹ Pindborg, J.J.² Cohen M.M., Jr.³

12
- 0006696562
- Gorlin syndrome (nevoid basal cell carcinoma syndrome)
- New York: Oxford University Press
- (1990) Syndromes of the head and neck, 3rd ed.
- Gorlin, R.J.¹ Cohen M.M., Jr.² Levin, L.S.³

13
- 15844386165
- Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
- (1996) Cell , vol.85 , pp. 841-851
- Hahn, H.¹ Wicking, C.² Zaphiropoulous, P.G.³ Gailani, M.R.⁴ Shanley, S.⁵ Chidambaram, A.⁶ Vorechovsky, I.⁷ Holmberg, E.⁸ Unden, A.B.⁹ Gillies, S.¹⁰ Negus, K.¹¹ Smyth, I.¹² Pressman, C.¹³ Leffell, D.J.¹⁴ Gerrard, B.¹⁵ Goldstein, A.M.¹⁶ Dean, M.¹⁷ Toftgard, R.¹⁸ Chenevix-Trench, G.¹⁹ Wainwright, B.²⁰ Bale, A.E.²¹ more..

14
- 0024535211
- Bilateral hyperplasia of the mandibular coronoid processes: A report of two cases
- (1989) Oral Surg Oral Med Oral Pathol , vol.67 , pp. 141-145
- Hall, R.E.¹ Orbach, S.² Landesberg, R.³

15
- 0019141133
- Bilateral coronoid hyperplasia: Review of the literature and report of case
- (1980) J Oral Surg , vol.38 , pp. 606-608
- Hecker, R.¹ Corwin, J.O.²

16
- 0028440437
- Coronoid process enlargement
- (1994) Dentomaxillofac Radiol , vol.23 , pp. 108-110
- Honig, J.F.¹ Merten, H.A.² Korth, O.E.³ Halling, F.⁴

17
- 0016434225
- Older paternal age and fresh gene mutation: Data on additional disorders
- (1975) J Pediatr , vol.86 , pp. 84-88
- Jones, K.L.¹ Smith, D.W.² Harvey, M.A.S.³ Hall, B.D.⁴ Quan, L.⁵

18
- 0032706650
- Levandoski panographic analysis in the diagnosis of hyperplasia of the coronoid process
- (1999) Br J Oral Maxillofac Surg , vol.37 , pp. 409-411
- Kubota, Y.¹ Takenoshita, Y.² Takamori, K.³ Kanamoto, M.⁴ Shirasuna, K.⁵

19
- 0035858068
- Bilateral hyperplasia of the mandibular coronoid processes associated with the nevoid basal cell carcinoma syndrome in an italian boy
- (2001) Br Dent J , vol.190 , pp. 349-350
- Leonardi, R.¹ Sorge, G.² Caltabiano, M.³

20
- 0009631332
- Limited opening of the mouth caused by enlarged coronoid process
- (1963) Br J Oral Surg , vol.67 , pp. 644-650
- Lyon, L.Z.¹ Sarnat, B.G.²

21
- 0028909537
- Hyperplasia of the mandibular coronoid process: An analysis of 31 cases and a review of the literature
- (1995) J Oral Maxillofac Surg , vol.53 , pp. 250-255
- McLoughlin, P.M.¹ Hopper, C.² Bowley, N.B.³

22
- 0029365797
- The Levandoski panoramic analysis in the diagnosis of facial and dental asymmetries
- (1995) J Clin Pediatr Dent , vol.20 , pp. 15-21
- Piedra, I.¹

23
- 0028268439
- Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin
- (1994) J Invest Dermatol , vol.102 , pp. 300-303
- Quinn, A.G.¹ Campbell, C.² Healy, E.³ Rees, J.L.⁴

24
- 0020055704
- Linkage analysis with the trismus-pseudocamptodactyly syndrome
- (1982) Am J Med Genet , vol.12 , pp. 115-120
- Robertson, R.D.¹ Spence, M.A.² Sparkes, R.S.³ Neiswanger, K.⁴ Field, L.L.⁵

25
- 0002851239
- Bilateral developmental hyperplasia of the mandibular coronoid process
- (1963) Br J Oral Surg , vol.1 , pp. 90-104
- Rowe, N.L.¹

26
- 0028271569
- Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals
- (1994) Am J Med Genet , vol.50 , pp. 282-290
- Shanley, S.¹ Ratcliffe, J.² Hockey, A.³ Haan, E.⁴ Oley, C.⁵ Ravine, D.⁶ Martin, N.⁷ Wicking, C.⁸ Chenevix-Trench, G.⁹

27
- 0021018555
- Bilateral hyperplasia of the coronoid processes in Siblings
- (1983) Oral Surg Oral Med Oral Pathol , vol.56 , pp. 584-585
- York, B.V.¹ Cockerham, S.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.