Dergiler / Turkish Journal of Gastroenterology / 2018 / Cilt: 29 - Sayı: 6

Primary intestinal lymphangiectasia and a review of the current literature

Sayfa
714–716
DOI
—
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Bu Makaleye Atıf Yap

ALTIN, Z., ATABAY, Y., ÖZER, S., KARAKOYUN, M., EKMEKÇİ, S., YÜREKLİ, E., AKAR, H. (2018). Primary intestinal lymphangiectasia and a review of the current literature. Turkish Journal of Gastroenterology, Cilt: 29 - Sayı: 6, 714–716. https://ajindex.com/articles/410112

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Kaynakça (4)

  1. Levitt DG, Levitt MD. Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states. Clin Exp Gastroenterol 2017; 10: 147-68.
  2. Vignes S, Bellanger J. Primary intestinal lymphangiectasia (Waldmann’s disease). Orphanet J Rare Dis 2008; 3: 5. Le Bougeant P, Delbrel X, Grenouillet M, Leou S, Djossou F, Beylot J, et al. Familial Waldmann’s disease. Ann Med Interne 2000; 151: 511-2.
  3. Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, et al. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation. Am J Med Genet 1989; 34: 593-600.
  4. Ozeki M, Fukao T, Kondo N. Propranolol for intractable diffuse lymphangiomatosis.