Related references
Note: Only part of the references are listed.Normal and Premature Adrenarche
Robert L. Rosenfield
ENDOCRINE REVIEWS (2021)
Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia
Malgorzata Gabriela Wasniewska et al.
HORMONE RESEARCH IN PAEDIATRICS (2020)
Central Precocious Puberty as a Presenting Sign of Nonclassical Congenital Adrenal Hyperplasia: Clinical Characteristics
Bar Neeman et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2019)
Diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency
Anna Nordenstrom et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2019)
Basal levels of 17-hydroxyprogesterone can distinguish children with isolated precocious pubarche
Anna Grandone et al.
PEDIATRIC RESEARCH (2018)
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline
Phyllis W. Speiser et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2018)
Girls with a History of Premature Adrenarche Have Advanced Growth and Pubertal Development at the Age of 12 Years
Jani Liimatta et al.
FRONTIERS IN ENDOCRINOLOGY (2017)
Premature adrenarche: Etiology, clinical findings, and consequences
Raimo Voutilainen et al.
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY (2015)
In children with premature adrenarche, bone age advancement by 2 or more years is common and generally benign
Daniel J. DeSalvo et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2013)
Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche
Carla Bizzarri et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2012)
Bone Age Advancement in Prepubertal Children With Obesity and Premature Adrenarche: Possible Potentiating Factors
Aviva B. Sopher et al.
OBESITY (2011)
Precocious Pubarche: Distinguishing Late-Onset Congenital Adrenal Hyperplasia from Premature Adrenarche
Jean-Baptiste Armengaud et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
Extensive clinical experience - Nonclassical 21-hydroxylase deficiency
Maria I. New
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Decreased androgen receptor gene methylation in premature pubarche: A novel pathogenetic mechanism?
A Vottero et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency
D Török et al.
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES (2003)
Italian cross-sectional growth charts for height, weight and BMI (6-20y)
E Cacciari et al.
EUROPEAN JOURNAL OF CLINICAL NUTRITION (2002)
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TASS Bachega et al.
CLINICAL ENDOCRINOLOGY (2000)