Congenital Adrenal Hyperplasia (original) (raw)
Congenital Adrenal Hyperplasia Due to 21 Hydroxy Deficiency in a Female Newborn With Ambiguous Genitalia Who Had a False-Negative Newborn Screening and Delayed Salt Wasting
Sunil Nayak
2010
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Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
L. Ghizzoni, Phyllis Speiser
Clinical Endocrinology, 1998
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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
Phyllis W Speiser
The Journal of Clinical Endocrinology Metabolism, 2013
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Disorders of Sex Development of Adrenal Origin
Gabriela Finkielstain
Frontiers in Endocrinology, 2021
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Congenital Adrenal Hyperplasia in Patients with Disorders of Sexual Differentiation
Warda Fatima
THE JOURNAL OF MICROBIOLOGY AND MOLECULAR GENETICS
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Congenital Adrenal Hyperplasia due to 21Hydroxylase Deficiency
Phyllis Speiser
2010
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Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Alessandra Vottero
Journal of Clinical …, 1996
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Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Henrik Falhammar
Endocrine, 2016
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Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report
João Martins
Journal of Medical Case Reports, 2013
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Congenital Adrenal Hyperplasia - The Main Effect of 21-Hydroxylase Deficiency
Davide Carvalho
IntechOpen eBooks, 2022
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Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency
A. al-Ashwal
Annals of Saudi medicine
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Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Helmuth Dörr
Hormone Research in Paediatrics, 2011
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CONGENITAL ADRENAL HYPERPLASIA OWING TO 21-HYDROXYLASE DEFICIENCY
Phyllis Speiser
Endocrinology and Metabolism Clinics of North America, 2001
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An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity
Sten Ivarsson
The Journal of Clinical Endocrinology & Metabolism, 2002
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A child with hypertension and ambiguous genitalia - an uncommon variant of congenital adrenal hyperplasia: a case report
vivek pant
Journal of medical case reports, 2017
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Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Gu-Hwan Kim
Annals of pediatric endocrinology & metabolism, 2016
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Congenital Adrenal Hyperplasia due to 21--Hydroxylase Deficiency in Saudi Arabia
amer alali
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CONGENITAL ADRENAL HYPERPLASIA DUE TO 21HYDROXYLASE (21-OHase) DEFICIENCY: PHENOTYPE/GENOTYPE CORRELATIONS IN NEWBORN SCREENING.??? 553
Sunil Nayak
Pediatric Research, 1996
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Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Alma Toromanovic
European Journal of Pediatrics, 2009
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Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment
Jihad Obeid
Journal of Steroid Biochemistry and Molecular Biology, 1999
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Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-Deoxycortisol in Classic Congenital Adrenal Hyperplasia: Clinical and Hormonal Correlations and Identification of Patients with 11β-Hydroxylase Deficiency among a Large Group with Alleged 21-Hydroxylase Deficiency
Claudio Kater
The Journal of Clinical Endocrinology & Metabolism, 2006
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CLINICAL PROFILE OF PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 21 HYDROXYLASE DEFIICIENCY
National Journal of Medical Research, Dr. Asif Ahmed
National Journal of Medical Research, 2016
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Association between genotype, clinical presentation, and severity of congenital adrenal hyperplasia: a review
Professor Abdulmoein E Al Agha
The Turkish journal of pediatrics, 2012
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Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
Fred C. G. J. Sweep
Frontiers in Endocrinology, 2022
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Newly Proposed Hormonal Criteria via Genotypic Proof for Type II 3β-Hydroxysteroid Dehydrogenase Deficiency
Raphael David
The Journal of Clinical Endocrinology & Metabolism, 2002
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Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Case Report
Yunis Mohamed
Scholars Journal of Medical Case Reports
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Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology
Philip Ransley
The Journal of Clinical Endocrinology & Metabolism, 2003
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