Concolino P, Falhammar H
J Endocr Soc. 2025; 9(3):bvaf018.
PMID: 39911519
PMC: 11795198.
DOI: 10.1210/jendso/bvaf018.
Claahsen-van der Grinten H, Adriaansen B, Falhammar H
J Clin Endocrinol Metab. 2025; 110(Supplement_1):S25-S36.
PMID: 39836620
PMC: 11749911.
DOI: 10.1210/clinem/dgae718.
Stanchev P, Dimitrova M, Makakova D, Tilov B
Medicina (Kaunas). 2025; 60(12.
PMID: 39768890
PMC: 11727780.
DOI: 10.3390/medicina60122010.
Krysiak R, Claahsen-van der Grinten H, Reisch N, Touraine P, Falhammar H
Endocr Rev. 2024; 46(1):80-148.
PMID: 39240753
PMC: 11720181.
DOI: 10.1210/endrev/bnae026.
Kulle A, Jurgensen M, Dohnert U, Malich L, Marshall L, Hiort O
Med Genet. 2024; 35(3):181-187.
PMID: 38840817
PMC: 10842577.
DOI: 10.1515/medgen-2023-2037.
Memory in female adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Espinosa Reyes T, Cordero Martin D, Angel Alvarez M, Falhammar H
Endocrine. 2024; 85(3):1379-1386.
PMID: 38727867
DOI: 10.1007/s12020-024-03806-3.
Increased risk of nephrolithiasis: an emerging issue in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Chiarito M, Lattanzio C, DAscanio V, Capalbo D, Cavarzere P, Grandone A
Endocrine. 2024; 84(2):727-734.
PMID: 38536547
PMC: 11076308.
DOI: 10.1007/s12020-024-03792-6.
Editorial: Recent advances in diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Caglar Cetinkaya S
Front Endocrinol (Lausanne). 2023; 14:1332962.
PMID: 38075037
PMC: 10703459.
DOI: 10.3389/fendo.2023.1332962.
Landscape of Adrenal Tumours in Patients with Congenital Adrenal Hyperplasia.
Carsote M, Gheorghe A, Nistor C, Trandafir A, Sima O, Cucu A
Biomedicines. 2023; 11(11).
PMID: 38002081
PMC: 10669095.
DOI: 10.3390/biomedicines11113081.
Cardiovascular risk in Cuban adolescents and young adults with congenital adrenal hyperplasia.
Espinosa Reyes T, Pesantez Velepucha A, Cabrera Rego J, Valdes Gomez W, Dominguez Alonso E, Falhammar H
BMC Endocr Disord. 2023; 23(1):241.
PMID: 37919699
PMC: 10621154.
DOI: 10.1186/s12902-023-01499-9.
Increased Prevalence of Accidents and Injuries in Congenital Adrenal Hyperplasia: A Population-based Cohort Study.
Falhammar H, Linden Hirschberg A, Nordenskjold A, Larsson H, Nordenstrom A
J Clin Endocrinol Metab. 2023; 109(3):e1175-e1184.
PMID: 37862468
PMC: 10876393.
DOI: 10.1210/clinem/dgad624.
Specialty grand challenge in adrenal endocrinology.
Falhammar H
Front Endocrinol (Lausanne). 2023; 14:1237733.
PMID: 37484952
PMC: 10358978.
DOI: 10.3389/fendo.2023.1237733.
Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease Management.
Sarafoglou K, Merke D, Reisch N, Claahsen-van der Grinten H, Falhammar H, Auchus R
J Clin Endocrinol Metab. 2023; 108(9):2154-2175.
PMID: 36950738
PMC: 10438890.
DOI: 10.1210/clinem/dgad134.
Approach of Heterogeneous Spectrum Involving 3beta-Hydroxysteroid Dehydrogenase 2 Deficiency.
Nicola A, Carsote M, Gheorghe A, Petrova E, Popescu A, Staicu A
Diagnostics (Basel). 2022; 12(9).
PMID: 36140569
PMC: 9497988.
DOI: 10.3390/diagnostics12092168.