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Journal of Pediatric Gastroenterology and Nutrition
Volumn 28, Issue 2, 1999, Pages 203-205
Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia
Author keywords

[No Author keywords available]
Indexed keywords

ANTHROPOMETRY; ARTICLE; CASE REPORT; CESAREAN SECTION; CLINICAL FEATURE; DIAGNOSTIC APPROACH ROUTE; DIARRHEA; DISEASE ASSOCIATION; ELECTRON MICROSCOPY; FEMALE; HUMAN; HYPOCHONDROPLASIA; INFANT; INTESTINE VILLUS ATROPHY; JEJUNUM BIOPSY; PRIORITY JOURNAL; RADIODIAGNOSIS;
EID: 0032976239     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-199902000-00022     Document Type: Article
Times cited : (10)
References (12)
  • 1
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    • Davidson GP, Cutz E, Hamilton JR, Gall DG. Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villous atrophy. Gastroenterology 1978;5:783-90.
    • (1978) Gastroenterology , vol.5 , pp. 783-790
    • Davidson, G.P.1    Cutz, E.2    Hamilton, J.R.3    Gall, D.G.4
  • 2
    • 0026695199 scopus 로고
    • Familial microvillus atrophy: A clinicopathological survey of 23 cases
    • Phillips AD, Schmitz J. Familial microvillus atrophy: A clinicopathological survey of 23 cases. J Pediatr Gastroenterol Nutr 1992;14:380-96.
    • (1992) J Pediatr Gastroenterol Nutr , vol.14 , pp. 380-396
    • Phillips, A.D.1    Schmitz, J.2
  • 4
    • 0024509966 scopus 로고
    • Microvillus inclusion disease: An inherited defect of brush-border assembly and differentiation
    • Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG. Microvillus inclusion disease: An inherited defect of brush-border assembly and differentiation. N Engl J Med 1989;320:646-51.
    • (1989) N Engl J Med , vol.320 , pp. 646-651
    • Cutz, E.1    Rhoads, J.M.2    Drumm, B.3    Sherman, P.M.4    Durie, P.R.5    Forstner, G.G.6
  • 5
    • 0028298272 scopus 로고
    • Alterations in epithelial polarity and the pathogenesis of disease states
    • Fish EM, Molitoris BA. Alterations in epithelial polarity and the pathogenesis of disease states. N Engl J Med 1994;330:1580-8.
    • (1994) N Engl J Med , vol.330 , pp. 1580-1588
    • Fish, E.M.1    Molitoris, B.A.2
  • 7
    • 0018707359 scopus 로고
    • Hypochondroplasia: Clinical and radiological aspects in 39 cases
    • Hall BD, Spranger J. Hypochondroplasia: Clinical and radiological aspects in 39 cases. Radiology 1979;133:95-100.
    • (1979) Radiology , vol.133 , pp. 95-100
    • Hall, B.D.1    Spranger, J.2
  • 8
    • 0023892634 scopus 로고
    • Hypochondroplasie: Revue de 80 cas
    • Maroteaux JP, Falzon P. Hypochondroplasie: Revue de 80 cas. Arch Fr Pediatr 1988;45:105-9.
    • (1988) Arch Fr Pediatr , vol.45 , pp. 105-109
    • Maroteaux, J.P.1    Falzon, P.2
  • 9
    • 0029032394 scopus 로고
    • A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
    • Bellus GA, McIntosh I, Smith EA, et al. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nat Genet 1995;785:357-9.
    • (1995) Nat Genet , vol.785 , pp. 357-359
    • Bellus, G.A.1    McIntosh, I.2    Smith, E.A.3
  • 10
    • 0029785459 scopus 로고    scopus 로고
    • Clinical and genetic heterogeneity of hypochondroplasia
    • Rousseau F, Bonaventure J, Legai-Mallet L, et al. Clinical and genetic heterogeneity of hypochondroplasia. J Med Genet 1996; 33:749-52.
    • (1996) J Med Genet , vol.33 , pp. 749-752
    • Rousseau, F.1    Bonaventure, J.2    Legai-Mallet, L.3
  • 11
    • 0344254137 scopus 로고
    • Forfar JO, Arneil JC. London: Churchill Livingstone
    • Tanner JM. In: Forfar JO, Arneil JC. Textbook of pediatrics. London: Churchill Livingstone, 1973.
    • (1973) Textbook of Pediatrics
    • Tanner, J.M.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.