نتایج جستجو برای: de quervain syndrome

تعداد نتایج: 2118015  

Journal: :International Journal of Research in Medical Sciences 2017

امینی , سیدمحمد, طبیبان , ساسان, عبادی , کاظم, گلشنی , صمد,

Çongenital long-QT syndrome (LQTS) is an inherited disorder that presents with syncope, polymorphic ventricular tachycardia, torsade de pointes and sudden death. The incidence rate of LQTS is 1 to 2 per 100000 and mainly involves children and young individuals. Because of familial and genetic underling and predisposing factors for life threatening arrhythmias in patients, diagnosis and treatm...

Journal: :Postgraduate medical journal 1998
T Bianda C Schmid

We describe a 39-year-old woman presenting with a painless solitary thyroid nodule, initially without signs suggesting thyroiditis. The serum level of thyrotropin was suppressed whereas those of thyroxine and triiodothyronine were normal. Fine needle aspiration cytology showed no signs of inflammation or malignancy. One week later, the patient felt pain and tenderness on her neck, and erythrocy...

2008
T Bianda C Schmid

Accepted 23 April 1998 Summary We describe a 39-year-old woman presenting with a painless solitary thyroid nodule, initially without signs suggesting thyroiditis. The serum level ofthyrotropin was suppressed whereas those of thyroxine and triiodothyronine were normal. Fine needle aspiration cytology showed no signs ofinflammation or malignancy. One week later, the patient felt pain and tenderne...

Farian, Jafarian, Ramin, Mohammad Hossein Marandian, Morteza Lesani, Reza Askari,

Les auteurs prcsentent deux 11ouveaux cas du syndrome associant le diabcte sucre juvenile it !'atro­phic optiquc. Ccs deux malades ages de dix et de quinzc ans avaient un retard statural. La premiere malade hospitalisee pour une mcgavessie est decedce dans le tableau de coma acidocctonique et d'Insuffi­s,rncc rcna!e. Dans la deuxicme observation, outre une sun.lite de perception decouvcrte it r...

Journal: :iranian journal of child neurology 0
z. razavi md,assistant professor, pediatric endocrinologist, hamedan university of medical sciences

objective the diagnosis of de morsier syndrome or septo-optic dysplasia is made on the basis of the diagnosis of optic nerve hypoplasia. septo-optic dysplasia is defined by a variable combination of dysgenesis of midline brain structures including optic nerve hypoplasia and hypothalamic-pituitary dysfunction often associated with a wide variety of brain malformations of cortical development. th...

Journal: :Endocrinología, Diabetes y Nutrición 2020

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