Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families:Case report

By Sato Naoko  

Human Reproduction, Vol. 20, Iss. 8, 2005-08 ,pp. : 2173-2178

Oxford University Press

Access to resources Recommend Favorite

A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1

By Miura Kiyonori   Miura Shoko   Yoshiura Koh-ichiro   Seminara Stephanie   Hamaguchi Daisuke   Niikawa Norio   Masuzaki Hideaki  

Human Reproduction, Vol. 25, Iss. 4, 2010-04 ,pp. : 1076-1080

Oxford University Press

Access to resources Recommend Favorite

Homozygous 20210G/A Prothrombin Gene Mutation Associated with Bilateral Iliac Vein Thrombosis: A Case Report

By Vaya A.   Garca M.   Mira Y.   Ferrando F.   Villa P.   Estelles A.   Aznar J.  

Thrombosis Research, Vol. 104, Iss. 4, 2001-11 ,pp. : 293-296

Elsevier

Access to resources Recommend Favorite

Testosterone patch improves ovarian follicular response to gonadotrophins in a patient with Kallmann's syndrome: A Case Report

By Sipe Christopher S.   Van Voorhis Bradley J.  

Human Reproduction, Vol. 22, Iss. 5, 2007-05 ,pp. : 1380-1383

Oxford University Press

Access to resources Recommend Favorite

Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: Case Report

By Juul A.   Aksglaede L.   Lund A.M.   Duno M.   Skakkebk N.E.   Rajpert-De Meyts E.  

Human Reproduction, Vol. 22, Iss. 7, 2007-07 ,pp. : 1907-1911

Oxford University Press

Access to resources Recommend Favorite