The relationship between olfactory function, rhinencephalon and forebrain changes in Kallmann syndrome (KS) have not been adequately investigated. We evaluated a large cohort of male KS patients using Sniffin' Sticks and MRI in order to study olfactory bulb (OB) volume, olfactory sulcus (OS) depth, cortical thickness close to the OS, and olfactory phenotype
Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotrophic hypogonad...
The present study refers to the magnetic resonance characteristics observed in a group of three pati...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
The relationship between olfactory function, rhinencephalon and forebrain changes in Kallmann syndro...
BACKGROUND: The relationship between olfactory function, rhinencephalon and forebrain changes in Kal...
Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic...
This large MR imaging study on male patients with Kallmann syndrome featured significant morphologic...
© 2015, Hellenic Endocrine Society. All rights reserved.OBJECTIVE: Kallmann syndrome (KS) is a genet...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotrophic hypogonad...
The present study refers to the magnetic resonance characteristics observed in a group of three pati...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
The relationship between olfactory function, rhinencephalon and forebrain changes in Kallmann syndro...
BACKGROUND: The relationship between olfactory function, rhinencephalon and forebrain changes in Kal...
Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic...
This large MR imaging study on male patients with Kallmann syndrome featured significant morphologic...
© 2015, Hellenic Endocrine Society. All rights reserved.OBJECTIVE: Kallmann syndrome (KS) is a genet...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotrophic hypogonad...
The present study refers to the magnetic resonance characteristics observed in a group of three pati...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...