Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation

By Nascif Sergio   Vieira Teresa   Ramos-Dias João   Lengyel Ana-Maria   Abucham Julio  

Pituitary, Vol. 9, Iss. 1, 2006-03 ,pp. : 47-52

Springer Publishing Company

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The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

By Vieira Teresa   Silva Magnus   Abucham Julio  

Endocrine Journal, Vol. 30, Iss. 3, 2006-12 ,pp. : 365-369

Humana Press, Inc

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Long-term follow-up of combined pituitary hormone deficiency in two siblings with a Prophet of Pit-1 gene mutation

By Georgopoulos Neoklis A.   Katsikis Ilias   Giamalis Petros   Koika Vasiliki   Adonakis George   Kourtis Anargyros   Kourounis George   Panidis Dimitrios  

Gynecological Endocrinology, Vol. 22, Iss. 12, 2006-12 ,pp. : 704-709

Informa Healthcare

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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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Polymorphism in the HMOX1 Gene is Associated with High Levels of Fetal Hemoglobin in Brazilian Patients with Sickle Cell Anemia

By Gil Gislene P.   Ananina Galina   Oliveira Mariana B.   Costa Fernando F.   Silva Márcio J.   Santos Magnun N. N.   Bezerra Marcos A. C.   Hatzlhofer Betânia L. D.   Araujo Aderson S.   Melo Mônica B.  

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 315-324

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