George Kanakis

Dr. George Kanakis


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 May 2019 in Andrology
Verified
Journal Article
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GKGeorge Kanakis
George Kanakis
LNL. Nordkap
L. Nordkap
ABA. K. Bang
A. K. Bang
Aldo E. CalogeroAldo E. Calogero
Aldo E. Calogero
GBG. Bártfai
G. Bártfai
NJNiels Jørgensen
Niels Jørgensen

1 September 2018 in Metabolism
Verified
Journal Article
Closed access
GKGeorge Kanakis
George Kanakis
ENEberhard Nieschlag
Eberhard Nieschlag

1 December 2012 in Best Practice & Research Clinical Gastroenterology
Verified
Journal Article
Closed access
GKGeorge Kanakis
George Kanakis
Gregory KaltsasGregory Kaltsas
Gregory Kaltsas

1 July 2019 in Maturitas
Verified
Journal Article
Closed access
GKGeorge Kanakis
George Kanakis
CTChristos P. Tsametis
Christos P. Tsametis
DGDimitrios G. Goulis
Dimitrios G. Goulis

5 October 2020 in Andrology
Verified
Journal Article
Open access
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MTMarta Tenuta
Marta Tenuta
FCFrancesco Carlomagno
Francesco Carlomagno
BCBiagio Cangiano
Biagio Cangiano
GKGeorge Kanakis
George Kanakis
CPCarlotta Pozza
Carlotta Pozza
DGDaniele Gianfrilli
Daniele Gianfrilli
Background: The hypothalamic‐pituitary‐gonadal (HPG) and hypothalamic‐pituitary‐somatotropic (HPS) axes are strongly interconnected. Interactions between these axes are complex and poorly understood. These interactions are characterized by redundancies in reciprocal influences at each level of regulation and the combination of endocrine and paracrine effects that change during development.Objectives: To comprehensively review the crosstalk between the HPG and HPS axes and related pathological and clinical aspects during various life stages of male subjects.Materials and methods: A thorough search of publications available in PubMed was performed using proper keywords.Results: Molecular studies confirmed the expressions of growth hormone (GH) and insulin‐like growth factor‐I (IGF‐I) receptors on the HPG axis and reproductive organs, indicating a possible interaction between HPS and HPG axes at various levels. Insulin growth factors participate in sexual differentiation during fetal development, indicating that normal HPS axis activity is required for proper testicular development. IGF‐I contributes to correct testicular position during minipuberty, determines linear growth during childhood, and promotes puberty onset and pace through gonadotropin‐releasing hormone activation. IGF‐I levels are high during transition age, even when linear growth is almost complete, suggesting its role in reproductive tract maturation. Patients with GH deficiency (GHD) and insensitivity (GHI) exhibit delayed puberty and impaired genital development; replacement therapy in such patients induces proper pubertal development. In adults, few studies have suggested that lower IGF‐I levels are associated with impaired sperm parameters.Discussion and conclusion: The role of GH‐IGF‐I in testicular development remains largely unexplored. However, it is important to evaluate gonadic development in children with GHD. Additionally, HPS axis function should be evaluated in children with urogenital malformation or gonadal development alterations. Correct diagnosis and prompt therapeutic intervention are needed for healthy puberty, attainment of complete gonadal development during transition age, and fertility potential in adulthood.

1 February 2012 in Endocrine-Related Cancer
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Journal Article
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AKAnna Koumarianou
Anna Koumarianou
SAStavroula Antoniou
Stavroula Antoniou
GKGeorge Kanakis
George Kanakis
NENikolaos Economopoulos
Nikolaos Economopoulos
DRDimitra Rontogianni
Dimitra Rontogianni
Gregory KaltsasGregory Kaltsas
Gregory Kaltsas
Combination treatment with metronomic temozolomide