Multiple endocrine dysfunctions in a patient with secondary hemochromatosis
Oueslati, I.; Khiari, K.; Elfaleh, E.; Khessairi, N.; Ben Abdallah, N.éj.
La Tunisie Medicale 97(2): 391-393
2019
ISSN/ISBN: 2724-7031 PMID: 31539101 Document Number: 699713
Document emailed within 1 workday
Related Documents
Hayes, D.; Condon, F.; Henry, M.; Duggan, M.; Mitchell, T. 1993: Sodium clodronate in a patient with the Eisenmenger syndrome, hyperparathyroidism and multiple endocrine adenomatosis Irish Medical Journal 86(4): 133Fassbender, W.J.; Krohn-Grimberghe, B.; Görtz, B.; Litzlbauer, D.; Stracke, H.; Raue, F.; Kaiser, H.E. 2000: Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus Anticancer Research 20(6c): 4877-4887
Vidal Marsal, F.; Sánchez Ripollés, J.M.; Torre Alonso, L.; Beltrán Genescá, A.; Pujol Inglés, F.; Mayayo, E. 1984: Primary hemochromatosis or secondary hemosiderosis? Medicina Clinica 82(13): 601
Hessman, O.; Lindberg, D.; Skogseid, B.; Carling, T.; Hellman, P.; Rastad, J.; Akerström, G.; Westin, G. 1998: Mutation of the multiple endocrine neoplasia type 1 gene in nonfamilial, malignant tumors of the endocrine pancreas Cancer Research 58(3): 377-379
Lehy, T.; Cadiot, G.; Mignon, M.; Ruszniewski, P.; Bonfils, S. 1992: Influence of multiple endocrine neoplasia type 1 on gastric endocrine cells in patients with the Zollinger-Ellison syndrome Gut 33(9): 1275-1279
Peces, R.; Gil, F.; González, F.; Ablanedo, P. 2002: Multiple brown tumors in a female hemodialyzed patient with severe secondary hyperparathyroidism Nefrologia: Publicacion Oficial de la Sociedad Espanola Nefrologia 22(1): 79-82
Naccarato, R.; Rizzo, A.; Sirigu, F.; Polin, R. 1975: Morphological and functional aspects of the liver in idiopathic and secondary hemochromatosis Medecine and Chirurgie Digestives 4(1): 1-8
Rodríguez-Miñón, J.L.; Herrera Pombo, J.L.; Arrieta Alvarez, F. 1979: The forms of so-called secondary diabetes (pancreatitis, cancer, hemochromatosis) Revista Clinica Espanola 153(6): 409-413
Nicolescu, P.; Bălan, A.; Ieremia-Poboran, V.; Petrescu, C.T. 1980: Electron microscope studies of the hepatic lesions of secondary hemochromatosis Morphologie et Embryologie 26(2): 145-148
Miller, M.; Crippin, J.S.; Klintmalm, G. 1996: End stage liver disease in a 13-year old secondary to hepatitis C and hemochromatosis American Journal of Gastroenterology 91(7): 1427-1429
Babović, R.; Milićević, S.ša.; Radovanović, S.ša.; Jančić, J. 2014: Testing of urodynamic dysfunctions in patients with multiple sclerosis Vojnosanitetski Pregled 71(5): 446-450
Blume, K.G.; Beutler, E.; Chillar, R.K.; Fahey, J.L.; Sharkoff, D.; Zia, P.K. 1978: Continuous intravenous deferoxamine infusion. Treatment of secondary hemochromatosis in adults JAMA 239(20): 2149-2151
Goranov, S. 1995: Renal disorders and calcium phosphorus tubular dysfunctions in multiple myeloma Folia Medica 37(4a Suppl): 46
Lutfarakhmanov, I.I.; Mironov, P.I.; Timerbulatov, V.M. 2007: Prognostic value of the pattern of multiple organ dysfunctions in severe acute pancreatitis Anesteziologiia i Reanimatologiia 2007(2): 44-47
Baudouy, P.; Lombrail, P.; Azancot, I.; Piekarski, A.; Martin, E.; Slama, R. 1983: Adiastole caused by a secondary cardiac hemochromatosis. Successful treatment with an iron chelating agent Archives des Maladies du Coeur et des Vaisseaux 76(10): 1240-1246
Chalenko, V.V. 1998: Classification of acute dysfunctions of organs and systems in multiple organ failure syndrome Anesteziologiia i Reanimatologiia 2: 25-30
Farina, G.; Pedrotti, C.; Cerani, P.; Rovati, A.; Strada, E.; Bergamaschi, G.; Montanari, L. 1995: Successful pregnancy following gonadotropin therapy in a young female with juvenile idiopathic hemochromatosis and secondary hypogonadotropic hypogonadism Haematologica 80(4): 335-337
Stierli, J. 1986: A case from practice (65). Patient: C.S., 1932 (hemochromatosis) Schweizerische Rundschau für Medizin Praxis 75(43): 1298-1299
Zdárský, E.; Horák, J.; Stríteský, J.; Heirler, F. 1999: Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards Casopis Lekaru Ceskych 138(16): 497-499
Kubota, K.; Kurabayashi, H.; Tamura, J.; Kawada, E.; Tamura, K.; Nagashima, K.; Shirakura, T. 1992: Change in the thyroid function by use of deferoxamine in a patient with hemochromatosis complicated by hyperthyroidism Journal of Medicine 23(1): 75-77