Associated Papers
Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes.
Gach A et al.
Reproductive Biology and Endocrinology : Rb&e, 2020
Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons.
Balasubramanian R et al.
Neuroendocrinology, 2010
Diversity in fibroblast growth factor receptor 1 regulation: learning from the investigation of Kallmann syndrome.
Kim SH et al.
Journal of Neuroendocrinology, 2008
Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome.
Tsai PS et al.
Nature Clinical Practice. Endocrinology & Metabolism, 2006
Isolated gonadotropic deficiency with and without anosmia: a developmental defect or a neuroendocrine regulation abnormality of the gonadotropic axis.
de Roux N
Hormone Research, 2005
Kallmann syndrome: fibroblast growth factor signaling insufficiency?
Dodé C et al.
Journal of Molecular Medicine (berlin, Germany), 2004
Analysis of the KAL1 gene in 19 Japanese patients with Kallmann syndrome.
Izumi Y et al.
Endocrine Journal, 2001
A novel nonsense mutation of the KAL gene in two brothers with Kallmann syndrome.
Jansen C et al.
Hormone Research, 2000
A novel mutation of the KAL1 gene in Kallmann syndrome.
Izumi Y et al.
Endocrine Journal, 1999
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