메뉴 건너뛰기




Volumn 15, Issue 1, 2014, Pages

Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ANTINUCLEAR ANTIBODY; AUTOANTIBODY; A\DRENAL CORTEX AUTOANTIBODY; ENDOMYSIUM ANTIBODY; GLIADIN ANTIBODY; GLUTAMATE DECARBOXYLASE ANTIBODY; HETERODIMER; HLA DQ2 ANTIGEN; HLA DQ8 ANTIGEN; HLA DQA1 ANTIGEN; HLA DQB1 ANTIGEN; IMMUNOGLOBULIN A ANTIBODY; IMMUNOGLOBULIN G ANTIBODY; INSULIN ANTIBODY; PANCREAS ISLET CELL ANTIBODY; PARIETAL CELL ANTIBODY; PHOSPHOLIPID ANTIBODY; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE ANTIBODY; SMOOTH MUSCLE ANTIBODY; THYROGLOBULIN ANTIBODY; THYROID ANTIBODY; THYROID PEROXIDASE ANTIBODY; THYROTROPIN RECEPTOR ANTIBODY; TYROSINE PHOSPHATASE 2 AUTOANTIBODY; UNCLASSIFIED DRUG;

EID: 84901605382     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-15-61     Document Type: Article
Times cited : (15)

References (32)
  • 1
    • 0018865534 scopus 로고
    • The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families
    • Grimm T, Wesselhoeft H. The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families. Z Kardiol 1980, 69:168-172.
    • (1980) Z Kardiol , vol.69 , pp. 168-172
    • Grimm, T.1    Wesselhoeft, H.2
  • 2
    • 0028905182 scopus 로고
    • Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome
    • 1801441, 7726172
    • Nickerson E, Greenberg F, Keating MT, McCaskill C, Shaffer LG. Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome. Am J Hum Genet 1995, 56:1156-1161. 1801441, 7726172.
    • (1995) Am J Hum Genet , vol.56 , pp. 1156-1161
    • Nickerson, E.1    Greenberg, F.2    Keating, M.T.3    McCaskill, C.4    Shaffer, L.G.5
  • 3
    • 0037265835 scopus 로고    scopus 로고
    • Williams-Beuren syndrome: a model of recurrent genomic mutation
    • Pérez Jurado AL. Williams-Beuren syndrome: a model of recurrent genomic mutation. Horm Res 2003, 59(Suppl 1):106-113.
    • (2003) Horm Res , vol.59 , Issue.SUPPL. 1 , pp. 106-113
    • Pérez Jurado, A.L.1
  • 4
    • 33646592342 scopus 로고    scopus 로고
    • Clinical practice in Turner syndrome
    • 10.1038/ncpendmet0024, 16929365
    • Gravholt CH. Clinical practice in Turner syndrome. Nat Clin Pract Endocrinol Metab 2005, 1:41-52. 10.1038/ncpendmet0024, 16929365.
    • (2005) Nat Clin Pract Endocrinol Metab , vol.1 , pp. 41-52
    • Gravholt, C.H.1
  • 5
    • 34247630020 scopus 로고    scopus 로고
    • Tissue transglutaminase antibodies are a useful serological marker for the diagnosis of celiac disease in patients with Down syndrome
    • 10.1097/MPG.0b013e3180320679, 17460490
    • Shamaly H, Hartman C, Pollack S, Hujerat M, Katz R, Gideoni O, Shamir R. Tissue transglutaminase antibodies are a useful serological marker for the diagnosis of celiac disease in patients with Down syndrome. J Pediatr Gastroenterol Nutr 2007, 44:583-586. 10.1097/MPG.0b013e3180320679, 17460490.
    • (2007) J Pediatr Gastroenterol Nutr , vol.44 , pp. 583-586
    • Shamaly, H.1    Hartman, C.2    Pollack, S.3    Hujerat, M.4    Katz, R.5    Gideoni, O.6    Shamir, R.7
  • 6
    • 0027364232 scopus 로고
    • Williams syndrome and coeliac disease
    • 10.1111/j.1651-2227.1993.tb12596.x, 8111167
    • Pittschieler K, Morini G, Crepaz R. Williams syndrome and coeliac disease. Acta Paediatr 1993, 82:iv. 10.1111/j.1651-2227.1993.tb12596.x, 8111167.
    • (1993) Acta Paediatr , vol.82
    • Pittschieler, K.1    Morini, G.2    Crepaz, R.3
  • 9
    • 0029840422 scopus 로고    scopus 로고
    • Williams-Beuren syndrome and celiac disease
    • 10.1097/00005176-199610000-00029, 8890095
    • Santer R, Pankau R, Schaub J, Bürgin-Wolff A. Williams-Beuren syndrome and celiac disease. J Pediatr Gastroenterol Nutr 1996, 23:339-340. 10.1097/00005176-199610000-00029, 8890095.
    • (1996) J Pediatr Gastroenterol Nutr , vol.23 , pp. 339-340
    • Santer, R.1    Pankau, R.2    Schaub, J.3    Bürgin-Wolff, A.4
  • 12
    • 26644446903 scopus 로고    scopus 로고
    • Thyroid function and morphology in patients affected by Williams syndrome
    • 10.1111/j.1365-2265.2005.02365.x, 16181239
    • Stagi S, Bindi G, Neri AS, Lapi E, Losi S, Jenuso R, Salti R, Chiarelli F. Thyroid function and morphology in patients affected by Williams syndrome. Clin Endocrinol (Oxf) 2005, 63:456-460. 10.1111/j.1365-2265.2005.02365.x, 16181239.
    • (2005) Clin Endocrinol (Oxf) , vol.63 , pp. 456-460
    • Stagi, S.1    Bindi, G.2    Neri, A.S.3    Lapi, E.4    Losi, S.5    Jenuso, R.6    Salti, R.7    Chiarelli, F.8
  • 13
    • 18744412378 scopus 로고    scopus 로고
    • Thyroid function, autoimmune thyroiditis and coeliac disease in juvenile idiopathic arthritis
    • 10.1093/rheumatology/keh531, 15695302
    • Stagi S, Giani T, Simonini G, Falcini F. Thyroid function, autoimmune thyroiditis and coeliac disease in juvenile idiopathic arthritis. Rheumatology (Oxford) 2005, 44:517-520. 10.1093/rheumatology/keh531, 15695302.
    • (2005) Rheumatology (Oxford) , vol.44 , pp. 517-520
    • Stagi, S.1    Giani, T.2    Simonini, G.3    Falcini, F.4
  • 15
    • 19944433266 scopus 로고    scopus 로고
    • Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
    • 10.1097/00005176-200501000-00001, 15625418, North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
    • Hill ID, Dirks MH, Liptak GS, Colletti RB, Fasano A, Guandalini S, Hoffenberg EJ, Horvath K, Murray JA, Pivor M, Seidman EG, . North American Society for Pediatric Gastroenterology, Hepatology and Nutrition Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr 2005, 40:1-19. 10.1097/00005176-200501000-00001, 15625418, North American Society for Pediatric Gastroenterology, Hepatology and Nutrition.
    • (2005) J Pediatr Gastroenterol Nutr , vol.40 , pp. 1-19
    • Hill, I.D.1    Dirks, M.H.2    Liptak, G.S.3    Colletti, R.B.4    Fasano, A.5    Guandalini, S.6    Hoffenberg, E.J.7    Horvath, K.8    Murray, J.A.9    Pivor, M.10    Seidman, E.G.11
  • 19
    • 33845603619 scopus 로고    scopus 로고
    • Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome
    • 10.1016/j.jpeds.2006.10.060, 17188616
    • Cambiaso P, Orazi C, Digilio MC, Loche S, Capolino R, Tozzi A, Faedda A, Cappa M. Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome. J Pediatr 2007, 150:62-65. 10.1016/j.jpeds.2006.10.060, 17188616.
    • (2007) J Pediatr , vol.150 , pp. 62-65
    • Cambiaso, P.1    Orazi, C.2    Digilio, M.C.3    Loche, S.4    Capolino, R.5    Tozzi, A.6    Faedda, A.7    Cappa, M.8
  • 20
    • 79953215645 scopus 로고    scopus 로고
    • Coeliac disease: the histology report
    • Gruppo Italiano Patologi Apparato Digerente (GIPAD)
    • Villanacci V, Ceppa P, Tavani E, Vindigni C, Volta U, . Gruppo Italiano Patologi Apparato Digerente (GIPAD) Coeliac disease: the histology report. Dig Liver Dis 2011, 43(Suppl 4):S385-395. Gruppo Italiano Patologi Apparato Digerente (GIPAD).
    • (2011) Dig Liver Dis , vol.43 , Issue.SUPPL. 4
    • Villanacci, V.1    Ceppa, P.2    Tavani, E.3    Vindigni, C.4    Volta, U.5
  • 21
    • 0025921769 scopus 로고
    • Chromosome abnormalities found among 34 910 newborn children: results from a 13-year incidence study in Århus, Denmark
    • 10.1007/BF01213097, 2037286
    • Nielsen J, Wohlert M. Chromosome abnormalities found among 34 910 newborn children: results from a 13-year incidence study in Århus, Denmark. Hum Genet 1991, 87:81-83. 10.1007/BF01213097, 2037286.
    • (1991) Hum Genet , vol.87 , pp. 81-83
    • Nielsen, J.1    Wohlert, M.2
  • 23
    • 0029154026 scopus 로고
    • Frequency, clinical and laboratory features of thyroiditis in girls with Turner's syndrome
    • 10.1111/j.1651-2227.1995.tb13791.x, 7488816
    • Radetti G, Mazzanti L, Paganini C, Bernasconi S, Russo G, Rigon F, Cacciari E. Frequency, clinical and laboratory features of thyroiditis in girls with Turner's syndrome. Acta Paediatr 1995, 84:909-912. 10.1111/j.1651-2227.1995.tb13791.x, 7488816.
    • (1995) Acta Paediatr , vol.84 , pp. 909-912
    • Radetti, G.1    Mazzanti, L.2    Paganini, C.3    Bernasconi, S.4    Russo, G.5    Rigon, F.6    Cacciari, E.7
  • 25
    • 33746417581 scopus 로고    scopus 로고
    • Type I diabetes mellitus, Hashimoto's thyroiditis and celiac disease in an adolescent with Down syndrome
    • 10.1111/j.1442-200X.2006.02238.x, 16911096
    • Kinik ST, Ozçay F, Varan B. Type I diabetes mellitus, Hashimoto's thyroiditis and celiac disease in an adolescent with Down syndrome. Pediatr Int 2006, 48:433-435. 10.1111/j.1442-200X.2006.02238.x, 16911096.
    • (2006) Pediatr Int , vol.48 , pp. 433-435
    • Kinik, S.T.1    Ozçay, F.2    Varan, B.3
  • 26
    • 38949155319 scopus 로고    scopus 로고
    • Celiac disease and autoimmune thyroid disease
    • 10.3121/cmr.2007.738, 2111403, 18056028
    • Ch'ng CL, Jones MK, Kingham JG. Celiac disease and autoimmune thyroid disease. Clin Med Res 2007, 5:184-192. 10.3121/cmr.2007.738, 2111403, 18056028.
    • (2007) Clin Med Res , vol.5 , pp. 184-192
    • Ch'ng, C.L.1    Jones, M.K.2    Kingham, J.G.3
  • 27
    • 20544460101 scopus 로고    scopus 로고
    • HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms
    • 10.1016/j.trim.2005.03.021, 15982560
    • Thorsby E, Lie BA. HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms. Transpl Immunol 2005, 14:175-182. 10.1016/j.trim.2005.03.021, 15982560.
    • (2005) Transpl Immunol , vol.14 , pp. 175-182
    • Thorsby, E.1    Lie, B.A.2
  • 28
    • 0036131163 scopus 로고    scopus 로고
    • HLA-DQ typing in the diagnosis of celiac disease
    • 10.1111/j.1572-0241.2002.05471.x, 11922565
    • Kaukinen K, Partanen J, Mäki M, Collin P. HLA-DQ typing in the diagnosis of celiac disease. Am J Gastroenterol 2002, 97:695-699. 10.1111/j.1572-0241.2002.05471.x, 11922565.
    • (2002) Am J Gastroenterol , vol.97 , pp. 695-699
    • Kaukinen, K.1    Partanen, J.2    Mäki, M.3    Collin, P.4
  • 29
    • 15944398017 scopus 로고    scopus 로고
    • Use of HLA typing in diagnosing celiac disease in patients with type 1 diabetes
    • 10.2337/diacare.28.4.806, 15793177
    • Doolan A, Donaghue K, Fairchild J, Wong M, Williams AJ. Use of HLA typing in diagnosing celiac disease in patients with type 1 diabetes. Diabetes Care 2005, 28:806-809. 10.2337/diacare.28.4.806, 15793177.
    • (2005) Diabetes Care , vol.28 , pp. 806-809
    • Doolan, A.1    Donaghue, K.2    Fairchild, J.3    Wong, M.4    Williams, A.J.5
  • 30
    • 0033970092 scopus 로고    scopus 로고
    • Search for coeliac disease susceptibility loci on 7q11.23 candidate region: absence of association with the ELN17 microsatellite marker
    • 10.1159/000022911, 10686497
    • Grillo R, Petronzelli F, Mora B, Bonamico M, Mazzilli MC. Search for coeliac disease susceptibility loci on 7q11.23 candidate region: absence of association with the ELN17 microsatellite marker. Hum Hered 2000, 50:180-183. 10.1159/000022911, 10686497.
    • (2000) Hum Hered , vol.50 , pp. 180-183
    • Grillo, R.1    Petronzelli, F.2    Mora, B.3    Bonamico, M.4    Mazzilli, M.C.5
  • 32
    • 0037381091 scopus 로고    scopus 로고
    • HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease
    • 10.1016/S0198-8859(03)00027-2, 12651074, European Genetics Cluster on Celiac Disease
    • Karell K, Louka AS, Moodie SJ, Ascher H, Clot F, Greco L, Ciclitira PJ, Sollid LM, Partanen J, . European Genetics Cluster on Celiac Disease HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease. Hum Immunol 2003, 64:469-477. 10.1016/S0198-8859(03)00027-2, 12651074, European Genetics Cluster on Celiac Disease.
    • (2003) Hum Immunol , vol.64 , pp. 469-477
    • Karell, K.1    Louka, A.S.2    Moodie, S.J.3    Ascher, H.4    Clot, F.5    Greco, L.6    Ciclitira, P.J.7    Sollid, L.M.8    Partanen, J.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.