نتایج جستجو برای: endocrinopathy

تعداد نتایج: 599  

Journal: :Indian Journal of Endocrinology and Metabolism 2011

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1994

2010
BARRON BRAINERD

for some real number X, the symbol V denoting the lattice least upper bound. Any ring R is regular [10] if for each xER there is an xaER such that xx°x = x. It is evident that every regular F-ring R contains a maximal bounded sub-F-ring R, the F-ring of all xER satisfying equation (1.1). The relationship between a regular F-ring and its maximal bounded sub-F-ring is analogous to that between th...

Journal: :The Journal of the Association of Physicians of India 2005
K Biswas R Goyal A C Ammini A K Karak C Sarkar N K Mishra V S Mehta

Lymphocytic hypophysitis commonly occurs in females in peripartum period but several unusual presentations have been reported. Here we report a rare case of recurrent lymphocytic hypophysitis in a woman who had subtotal adrenalectomy for hypercortisolism 27 years back. Polyglandular autoimmune endocrinopathy with an uncommon combination of Cushing's syndrome and recurrent hypophysitis is a stro...

Journal: :Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi 2016
Ioana Păvăleanu D Gafiţanu Diana Popovici Letiţia Doina Duceac Maricica Păvăleanu

Polycystic ovary syndrome is a common endocrinopathy characterized by oligo ovulation or anovulation, signs of androgen excess and multiple small ovarian cysts. It includes various metabolic abnormalities: insulin resistance, hyperinsulinemia, impaired glucose tolerance, visceral obesity, inflammation and endothelial dysfunction, hypertension and dyslipidemia. All these metabolic abnormalities ...

2005
Şeref TARGAN Emre ÇEÇEN Füsun ATLIHAN Ceyhun DİZDARER Behçet Uz Ferah GENEL

POEMS syndrome has been defined as an association of plasma celi dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein and skin changes. In this report, we describe a case of POEMS syndrome. A 10-year-old girl presented with polyneoropathy, diabetes mellitus type I, double monoclonal gammopathy (IgA and IgG), hepatomegaly, cardiomegaly, hyperpigmentation, and hypertricosis. To ...

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