Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (original) (raw)

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia between 1995. and 2005

Veselin Skrabic

2008

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Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Semra Çetinkaya

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Normal Gestation and Diminished Androgen Responsiveness in an Untreated Patient with 21-Hydroxylase Deficiency

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Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients

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Non-classic congenital adrenal hyperplasia due to 21-hydoxylase deficiency as a cause of infertility and miscarriages

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Testicular Tumors in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Show Functional Features of Adrenocortical Tissue

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Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population

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Adult Patients with Congenital Adrenal Hyperplasia Have Elevated Blood Pressure but Otherwise a Normal Cardiovascular Risk Profile

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Congenital adrenal hyperplasia is a very rare cause of adrenal incidentalomas in Sweden

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Three cases of congenital adrenal hypoplasia: A cause of salt-wasting and mortality in the neonatal period

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Reproductive Outcome of Women With 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia

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Increased Mortality in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

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Successful Pregnancy Following Preimplantation Genetic Diagnosis of Adrenoleukodystrophy by Detection of Mutation on the ABCD1 Gene

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Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry

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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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Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

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A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome

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Malaysian Females With Congenital Adrenal Hyperplasia: Surgical Outcomes and Attitudes

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Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Alma Toromanovic

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A five-year retrospective study in the Children's Hospital of Damascus, Syria

asad alebrahem

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Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report

João Martins

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Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment

Jihad Obeid

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Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in Croatia

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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline

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