[HTML][HTML] Luteinizing hormone beta mutation and hypogonadism in men and women

A Lofrano-Porto, GB Barra, LA Giacomini… - … England Journal of …, 2007 - Mass Medical Soc
Selective luteinizing hormone deficiency due to mutations in the luteinizing hormone beta-
subunit gene (LHB) is a rare cause of hypogonadism. We describe the clinical features of a …

The effect of bisphenol A on puberty: a critical review of the medical literature

A Leonardi, M Cofini, D Rigante, L Lucchetti… - International Journal of …, 2017 - mdpi.com
Many scientific studies have revealed a trend towards an earlier onset of puberty and have
disclosed an increasing number of children that display precocious puberty. As an …

CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development

G Pinto, V Abadie, R Mesnage, J Blustajn… - The Journal of …, 2005 - academic.oup.com
Context: CHARGE (coloboma, heart defect, choanal atresia, retarded growth and
development, g enital hypoplasia, ear abnormalities, and/or hearing loss defect) syndrome …

A marker of growth differs between adolescents with high vs. low sugar preference

SE Coldwell, TK Oswald, DR Reed - Physiology & behavior, 2009 - Elsevier
Sweet preference is higher in childhood than adulthood but the mechanism for this
developmental shift is not known. The objective of this study was to assess perceptual …

[HTML][HTML] Development of precocious puberty in children: Surmised medicinal plant treatment

XX Han, FY Zhao, KR Gu, GP Wang, J Zhang… - Biomedicine & …, 2022 - Elsevier
Precocious puberty in children is one of the common endocrine diseases in paediatrics.
Epidemiological surveys have shown that the number of children with precocious puberty …

Puberty: gonadarche and adrenarche

SF Witchel, AK Topaloglu - Yen and Jaffe's reproductive endocrinology, 2019 - Elsevier
Puberty in humans is defined as the period of becoming capable of reproducing. It is marked
by maturation of the genital organs, development of secondary sex characteristics …

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

AP Abreu, EB Trarbach, M de Castro… - The Journal of …, 2008 - academic.oup.com
Context: Physiological activation of the prokineticin pathway has a critical role in olfactory
bulb morphogenesis and GnRH secretion in mice. Objective: To investigate PROK2 and …

Puberty and its disorders

PA Lee, CP Houk - Pediatric endocrinology, 2007 - taylorfrancis.com
Puberty is the stage of growth leading to sexual maturity and reproductive capacity. In girls,
the initial physical changes are breast development; in boys, testicular growth—both …

Central precocious puberty: current treatment options

F Antoniazzi, G Zamboni - Pediatric Drugs, 2004 - Springer
Central precocious puberty (CPP) is characterized by early pubertal changes, acceleration
of growth velocity, and rapid bone maturation that often result in reduced adult height. An …

A single luteinizing hormone determination 2 hours after depot leuprolide is useful for therapy monitoring of gonadotropin-dependent precocious puberty in girls

VN Brito, AC Latronico, IJP Arnhold… - The Journal of …, 2004 - academic.oup.com
Long-acting GnRH analogs represent the standard treatment for gonadotropin-dependent
precocious puberty. The aim of this study was to determine the hormonal parameters for …