Results 41 to 50 of about 23,359 (243)
Novas perspectivas no diagnóstico do hipogonadismo pediátrico masculino: a importância do AMH como marcador de células de Sertoli [PDF]
, 2011 Sertoli cells are the most active cell population in the testis during infancy and childhood. In these periods of life, hypogonadism can only be evidenced without stimulation tests, if Sertoli cell function is assessed.
Grinspon, Romina, Rey, Rodolfo Alberto
core +2 more sources
Kallmann syndrome: MRI findings
Indian Journal of Endocrinology and Metabolism, 2013 Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic hypogonadism and anosmia or hyposmia. It is a neuronal migration disorder.
Houneida Zaghouani +5 more
doaj +1 more source
The FIGO ovulatory disorders classification system
International Journal of Gynecology &Obstetrics, Volume 159, Issue 1, Page 1-20, October 2022., 2022 Abstract Ovulatory disorders are common causes of amenorrhea, abnormal uterine bleeding, and infertility, and are frequent manifestations of polycystic ovary syndrome (PCOS). There are many potential causes and contributors to ovulatory dysfunction that challenge clinicians, trainees, educators, and those who perform basic, translational, clinical, and
Malcolm G. Munro +12 more
wiley +1 more source
Medicine Science, 2015 Hypogonadism is a result of testicular/ovarian failure and/or insufficient pituitary stimulation. Various hypothalamo-pituitary abnormalities or lesions can contribute to hypogonadism. Benign or malign tumoural lesions of cellar or paracellar region, may
Dilek Arpaci +6 more
doaj +1 more source
‘It takes a village’ – fertility treatment using donor gametes, embryos and/or surrogacy
The Obstetrician &Gynaecologist, Volume 24, Issue 4, Page 251-259, October 2022., 2022 Key content Fertility treatment using donated gametes and embryos is increasingly common. Indications for the use of donated sperm and oocytes include azoospermia, single women and women in same‐sex relationships, inherited conditions, poor quality embryos or failed fertilisation in previous cycles of assisted reproductive technology, and ovarian ...
Claudia Raperport +6 more
wiley +1 more source
Beyond hormone replacement: quality of life in women with congenital hypogonadotropic hypogonadism. [PDF]
, 2017 Little is known about how women with isolated GnRH deficiency cope with their condition. This study aimed to examine the health and informational needs of women with congenital hypogonadotropic hypogonadism (CHH) and evaluate if their experiences differ ...
Dwyer, A.A. +5 more
core +1 more source
Constitutional delay of growth and puberty in boys: review
Mìžnarodnij Endokrinologìčnij Žurnal, 2019 The review focuses on the diagnosis, clinical and general therapeutic approach to constitutional growth and delayed puberty and hypogonadotrophic hypogonadism in men, which are difficult to distinguish. Clinical history and physical examination should be
A.B. Grossman +4 more
doaj +1 more source
Frontiers in Endocrinology, 2022 BackgroundNR0B1 pathogenic variants can cause congenital adrenal hypoplasia or primary adrenal insufficiency in early childhood usually associated with hypogonadotropic hypogonadism.
Jordan Teoli +28 more
doaj +1 more source
Management of anovulatory infertility [PDF]
, 2012 Anovulatory subfertility is a heterogeneous condition with various underlying causes, which should be identified with appropriate history taking, physical examination and relevant investigations.
Li, RHW, Ng, EHY
core +1 more source
Clinicopathologic assessment of hypogonadism in men with type 2 diabetes mellitus
Indian Journal of Endocrinology and Metabolism, 2016 Objective: To determine the prevalence of hypogonadism in men with type 2 diabetes mellitus and evaluate its clinical and pathologic correlates. Subjects and Methods: In a cross-sectional survey of 200 type 2 diabetic males aged 32-69 years, total ...
Theophilus E Ugwu +3 more
doaj +1 more source