نتایج جستجو برای: acebutolol

تعداد نتایج: 162  

Journal: :Journal of medical genetics 2003
H De Leersnyder J L Bresson M-C de Blois J-C Souberbielle A Mogenet B Delhotal-Landes F Salefranque A Munnich

First described by Smith et al 1 in 1982, Smith-Magenis syndrome (SMS) is a contiguous gene syndrome ascribed to interstitial deletions of chromosome 17p11.2. Clinical features include infantile hypotonia, characteristic craniofacial appearance, brachydactyly, short stature, ocular anomalies, deep, hoarse voice, early speech delay, mental retardation, and behavioural disturbances. 3 Behavioural...

2002
H De Leersnyder J L Bresson M-C de Blois

First described by Smith et al 1 in 1982, Smith-Magenis syndrome (SMS) is a contiguous gene syndrome ascribed to interstitial deletions of chromosome 17p11.2. Clinical features include infantile hypotonia, characteristic craniofacial appearance, brachydactyly, short stature, ocular anomalies, deep, hoarse voice, early speech delay, mental retardation, and behavioural disturbances. 3 Behavioural...

2016
MONA MARIA TALMACIU EDE BODOKI RADU OPREAN

BACKGROUND AND AIM Beta-adrenergic antagonists have been established as first line treatment in the medical management of hypertension, acute coronary syndrome and other cardiovascular diseases, as well as for the prevention of initial episodes of gastrointestinal bleeding in patients with cirrhosis and esophageal varices, glaucoma, and have recently become the main form of treatment of infanti...

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