Concepedia

Astrid Thilén

AT

13

Publications

1.3K

Citations

13

H-Index

1957

Active since

Affiliations

Karolinska Institutet(Current)

Ryhov Hospital Jönköping

Karolinska University Hospital

Astrid Thilén is an author at Karolinska Institutet specializing in medicine, pediatrics, and adrenal disease.

Top concepts

Publications per year

1957–2013

13

Publications

13

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.

Anna Wedell, Astrid Thilén, E. Martin Ritzén et al. · The Journal of Clinical Endocrinology & Metabolism · 1994 · 355 citations

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

Sebastian Gidlöf, Henrik Falhammar, Astrid Thilén et al. · The Lancet Diabetes & Endocrinology · 2013 · 177 citations

, , +5

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder

Songya Pang, A. Campbell Clark, Eurico Camargo Neto et al. · Screening · 1993 · 161 citations

, , +9

Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in Sweden

Astrid Thilén, Anna Nordenström, Lars Hagenfeldt et al. · PEDIATRICS · 1998 · 145 citations

Genotyping Is a Valuable Diagnostic Complement to Neonatal Screening for Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency<sup>1</sup>

Anna Nordenström, Astrid Thilén, Lars Hagenfeldt et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 99 citations · Full text

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