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Endocrine, Vol. 40, Iss. 1, 2011-08 ,pp. : 144-145

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Children with Cushing's syndrome: primary pigmented nodular adrenocortical disease should always be suspected

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Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

By Pedroni M.   Gregorio C.   Cortesi L.   Reggiani Bonetti L.   Magnani G.   Simone M.   Medici V.   Priore Oliva C.   Marino M.   Ponz de Leon M.  

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Increased frequency of MEFV gene mutations in patients with primary dysmenorrhea

By Erten Sukran   Altunoglu A.   Keskin H.   Ceylan G.   Yazıcı A.   Dalgaci A.   Uyanık G.   Avsar A.  

Modern Rheumatology, Vol. 23, Iss. 5, 2013-09 ,pp. : 959-962

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Mutations of activin-receptor-like kinase 1 (ALK-1) are not found in patients with pulmonary hypertension and underlying connective tissue disease

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