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Did you mean: (Menetriers disease)?
(Ménétrier disease)
828 results
  • Ménétrier's disease : a case of successful treatment using long-acting octreotide. [Case Reports]
    Acta Gastroenterol Belg 2019 Jul-Sep; 82(3):429-432Nunes G, Barosa R, … Fonseca J
  • The authors describe a 31 years old male, admitted for hematemesis, epigastric pain and lower limb edema. Laboratorial data showed haemoglobin 18.4g/dl, total proteins 2.8g/dl, albumin 1.6g/dl and hipogammaglobulinaemia. 24h urinary proteins were normal. HIV and CMV serology were negative. Upper GI endoscopy revealed markedly enlarged gastric folds covered by abundant exudative fluid. Endoscopic …
  • Hyperplastic and fibrosing gastropathy resembling Ménétrier disease in a cat. [Case Reports]
    JFMS Open Rep 2019 Jul-Dec; 5(2):2055116919861248Barker EN, Holdsworth AS, … Hayward NJ
  • A 3.5-year-old domestic shorthair cat presented with a 6 month history of weight loss and polyphagia. Clinical examination revealed a markedly reduced body condition score (2/9) and a quiet demeanour. Laboratory abnormalities comprised a mild non-regenerative anaemia, stress leukogram, hypoproteinaemia due to hypoalbuminaemia, azotaemia, hypokalaemia, total hypocalcaemia and sub-maximally concent…
  • Menetrier's disease (protein-losing gastropathy) in a child with acute lymphoblastic leukemia. [Case Reports]
    Int J Pediatr Adolesc Med 2019; 6(1):38-40Fouda A, Kamath B, … Punnett A
  • A 3-year-old boy with high-risk precursor-B ALL presented with abdominal pain, vomiting, and hypoalbuminemia just before his second scheduled course of high-dose methotrexate in interim maintenance. Examination was significant for epigastric tenderness and periorbital edema. Abdominal imaging revealed a circumferential thickening of the stomach with an increased mucosal enhancement and a mild cir…
  • Ménétrier's disease presenting as recurrent unprovoked venous thrombosis: a case report. [Case Reports]
    J Med Case Rep 2019; 13(1):14Greenblatt HK, Nguyen BK
  • CONCLUSIONS: This case describes an acquired thrombophilic state in a patient with Ménétrier's disease and profound hypoalbuminemia. Although this association is rarely described, we discuss the probable mechanisms leading to our patient's thrombosis. Specifically, we posit that his gastrointestinal protein loss led to a deficiency of several anticoagulant proteins and a compensatory elevation in factor VIII, as occurs in nephrotic syndrome and inflammatory bowel disease. Of note, this patient's recurrent venous thrombosis was the initial clinical sign of his gastrointestinal pathology.
  • A microglial cell model for acyl-CoA oxidase 1 deficiency. [Journal Article]
    Biochim Biophys Acta Mol Cell Biol Lipids 2019; 1864(4):567-576Raas Q, Saih FE, … Savary S
  • Acyl-CoA oxidase 1 (ACOX1) deficiency is a rare and severe peroxisomal leukodystrophy associated with a very long-chain fatty acid (VLCFA) β-oxidation defect. This neurodegenerative disease lacks relevant cell models to further decipher the pathomechanisms in order to identify novel therapeutic targets. Since peroxisomal defects in microglia appear to be a key component of peroxisomal leukodystro…
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