نتایج جستجو برای: addison disease

تعداد نتایج: 1490684  

Journal: :Brain & development 2010
Laura Bannach Jardim Andrew Chaves Feitosa da Silva Deborah Blank Maria Mercedes Villanueva Luisa Renck Mariana La Bella Costa Carmen Regla Vargas Marion Deon Daniel la M Coelho Leonardo Vedolin Cláudio Galvão de Castro Lauro Gregianin Carmem Bonfim Roberto Giugliani

UNLABELLED X-linked adenoleukodystrophy is a genetic disease that affects the degradation of very long-chain fatty acids. In male patients, common pictures are the cerebral form (CALD), myeloneuropathy (AMN), and Addison-only. OBJECTIVE To describe the clinical course of affected male patients from South Brazil between 1993 and 2007. METHODS Affected male patients and their maternal lineage...

Journal: :Communications of the Association for Information Systems 2007

Journal: :Proceedings of the Royal Society of Medicine 1955

Journal: :Swiss Medical Forum ‒ Schweizerisches Medizin-Forum 2009

Journal: :Blood 1948
R L HADEN

‘947. HEINLE, R. W., AND WELCH, A. D. : J. A. M. A. 133. 739, 1947. 6. HEINLE, R. W., AND \VELCH, A. D.:J. A. M. A. 133. 739, 1947. VILTER, C. F., VITLER, R. \V., AND Spias, T. D. :J. Lab. & Clin. Med. 32 162., 1947. MEYER, L. M.: BLOOD 2. 50, 1947. . A warning regarding the use of folic acid. Editorial, N. E.J. Med. .13: 713, 1947. 8. SUAREZ, R.: Editorial correspondence, N. E. J. Med. 238.34,...

Journal: :Yearbook of pediatric endocrinology 2021

CONTEXT: Oral once-daily dual-release hydrocortisone (DR-HC) replacement therapy has demonstrated an improved metabolic profile compared to conventional 3-times-daily (TID-HC) among patients with primary adrenal insufficiency. This effect might be related a more physiological cortisol profile, but also modified pattern of metabolism. OBJECTIVE: work aimed study metabolism during DR-HC and TID-H...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1999
B M van Geel J Assies E B Haverkort J H Koelman B Verbeeten R J Wanders P G Barth

OBJECTIVES X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder of peroxisomal fatty acid oxidation, biochemically characterised by the accumulation of saturated very long chain fatty acids (VLCFAs), particularly hexacosanoic acid (C26:0). Dietary treatment with a 4:1 mixture of glyceroltrioleate and glyceroltrierucate ("Lorenzo's oil") normalises plasma VLCFA concentrations, but neit...

Journal: :Postgraduate medical journal 1989
P G Hardo

Hiccups has not been previously reported as a manifestation of Addison's disease. We report two cases where persistent hiccups was an early feature of Addison's disease. Steroid replacement cured the symptoms in both patients with no recurrence.

Journal: :Yearbook of pediatric endocrinology 2021

In this narrative review, the authors discuss potential role of novel regenerative therapies for treatment adrenal insufficiency, including gene therapy and cell replacement strategies. More specifically, heterogeneity in function patients with Addison disease, numerous case reports spontaneous remission. The cite recent studies showing that, shortly after onset residual might be restored using...

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