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Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

author

Henrik Falhammar

1970 -

published in: Endocrine

date of publication: 2016-12-07

main subject: congenital disorder, congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Cites articles 200

Too many entities requested (205). Only 200 are displayed.

Date

Title

Authors

2016-03-05

Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiency.

Riza Koksal Ozgul
2016-01-06

Hospital Admission Patterns in Children with CAH: Admission Rates and Adrenal Crises Decline with Age

Henrik Falhammar, Craig F Munns
2016-02-26

CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY PRESENTING AS ADRENAL INCIDENTALOMA: A SYSTEMATIC REVIEW AND META-ANALYSIS.

Henrik Falhammar
2016-09-01

A 42-year-old man presented with adrenal incidentaloma due to non-classic congenital adrenal hyperplasia with a novel CYP21A2 mutation.

Henrik Falhammar
2016-01-01

Congenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child
2015-06-17

Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome

Henrik Falhammar, Anna Nordenström
2015-09-04

Biochemical and genetic diagnosis of 21-hydroxylase deficiency

Henrik Falhammar, Anna Nordenström
2015-06-26

Congenital adrenal hyperplasia and risk for psychiatric disorders in girls and women born between 1915 and 2010: A total population study

Mikael Landén, Angelica Lindén Hirschberg, Agneta Nordenskjöld, Hedvig Engberg, Agnieszka Butwicka, Henrik Falhammar, Paul Lichtenstein, Anna Nordenström
2015-06-30

Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study

Agneta Nordenskjöld, Angelica Lindén Hirschberg, Henrik Falhammar, Catarina Almqvist, Anna Nordenström
2015-03-30

Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey

Thierry Brue, Jérome Bertherat, Olivier Chabre, Didier Dewailly, Delphine Drui, Sophie Christin-Maitre, Jacques Young, Yves Reznik, Claire Bouvattier, Véronique Kerlan, Philippe Emy, Igor Tauveron, Jean-Marc Kuhn, Frank Schillo
2015-06-29

CLINICAL OUTCOMES IN ADRENAL INCIDENTALOMA: EXPERIENCE FROM ONE CENTER.

Henrik Falhammar
2015-02-05

Modified-release hydrocortisone decreases BMI and HbA1c in patients with primary and secondary adrenal insufficiency

Marcus Quinkler
2015-05-15

Height augmentation in 11β-hydroxylase deficiency congenital adrenal hyperplasia
2014-10-18

The CYP11B subfamily

Lina Schiffer, Frank Hannemann, Rita Bernhardt, Simone Brixius-Anderko, Antje Eiden-Plach
2014-01-23

Non-functioning adrenal incidentalomas caused by 21-hydroxylase deficiency or carrier status?

Henrik Falhammar
2014-01-29

Suboptimal psychosocial outcomes in patients with congenital adrenal hyperplasia: epidemiological studies in a nonbiased national cohort in Sweden.

Henrik Falhammar, Agneta Nordenskjöld, Anna Nordenström, Angelica Lindén Hirschberg, Paul Lichtenstein
2014-01-10

Quality of life, social situation, and sexual satisfaction, in adult males with congenital adrenal hyperplasia

Henrik Falhammar
2014-03-13

Uniparental disomy of chromosome 8 leading to homozygosity of a CYP11B1 mutation in a patient with congenital adrenal hyperplasia: implication for a rare etiology of an autosomal recessive disorder

Tsutomu Ogata
2014-04-10

Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency.
2014-12-01

Increased mortality in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Henrik Falhammar, Agneta Nordenskjöld, Anna Nordenström, Catarina Almqvist, Angelica Lindén Hirschberg
2014-06-28

Cortical bone mineral density in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Diala El-Maouche
2014-04-10

Testicular adrenal rest tumor in 11-Beta-hydroxylase deficiency driven congenital adrenal hyperplasia
2013-02-26

One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study

Henrik Falhammar, Sebastian Gidlöf, Anna Nordenström
2013-08-12

A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism

Wiebke Arlt, Wolfgang Högler, Nils Krone
2013-02-12

Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
2013-02-15

Bone mineral density, bone markers, and fractures in adult males with congenital adrenal hyperplasia

Kerstin Brismar, Helena Filipsson Nyström, Henrik Falhammar
2013-05-21

Voice problems due to virilization in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Henrik Falhammar, Agneta Nordenskjöld, Ulrika Nygren
2013-12-03

Increased psychiatric morbidity in men with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Henrik Falhammar, Mikael Landén, Agneta Nordenskjöld, Anna Nordenström, Paul Lichtenstein, Agnieszka Butwicka
2013-09-11

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

Paul-Martin Holterhus, Joachim Grötzinger, Antonio Balsamo
2013-05-01

Prevalence and long-term follow-up outcomes of testicular adrenal rest tumours in children and adolescent males with congenital adrenal hyperplasia
2012-01-07

Clinical outcomes in the management of congenital adrenal hyperplasia

Henrik Falhammar
2012-09-18

Clinical characteristics of a cohort of 244 patients with congenital adrenal hyperplasia

Article - wd:Q39032544

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