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PubPharm (100)
1
Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency
enthalten in:
Journal of clinical research in pediatric endocrinology
| 2024
von
Garrelfs, M.
|
Rinne, T.
|
Hillebrand, J.
| +10
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2
Reference intervals for serum 11-oxygenated androgens in children
enthalten in:
European journal of endocrinology
| 2024
von
Adriaansen, B.
|
Oude Alink, S.
|
Swinkels, D.
| +5
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3
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development
enthalten in:
EBioMedicine
| 2024
von
Kouri, C.
|
Sommer, G.
|
Martinez de Lapiscina, I.
| +73
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4
Evaluation of Ex Vivo Adrenocorticotropic Hormone Responsiveness of Human Fetal Testis
enthalten in:
Endocrinology
| 2023
von
Schröder, M.
|
Greenald, D.
|
Lodewijk, R.
| +5
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5
Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia : a retrospective multicenter cohort study
enthalten in:
European journal of endocrinology
| 2023
von
Schröder, M.
|
Neacşu, M.
|
Adriaansen, B.
| +29
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6
Quality of life in men with Klinefelter syndrome : a multicentre study
enthalten in:
Endocrine connections
| 2023
von
Franik, S.
|
Fleischer, K.
|
Kortmann, B.
| +12
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7
Children and adolescents with gender questions : dilemmas in the hormonal treatment by multidisciplinary teams
enthalten in:
Nederlands tijdschrift voor geneeskunde
| 2023
von
Claahsen-van der Grinten, H.
|
Hannema, S.
|
Klink, D.
| +4
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8
Novel likely pathogenic variant in NR5A1 gene in a Tanzanian child with 46,XY differences of sex development, inherited from the mosaic father
enthalten in:
Endocrinology, diabetes & metabolism case reports
| 2023
von
Damji, R.
|
Alimohamed, M.
|
Claahsen-van der Grinten, H.
| +2
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9
Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
enthalten in:
Clinical endocrinology
| 2023
von
Waaijers, S.
|
Utari, A.
|
van der Doelen, R.
| +7
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10
Corrigendum : Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country
enthalten in:
Frontiers in endocrinology
| 2023
von
Utari, A.
|
Faradz, S.
|
Ediati, A.
| +6
ErratumFor: Front Endocrinol (Lausanne). 2022 Dec 15;13:1015973. - PMID 36589846
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The Journal of clinical endocrinology and metab...
10
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7
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Hormone research in paediatrics
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Annales d'endocrinologie
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Thema
72
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congenital adrenal hyperplasia
13
Research Support, Non-U.S. Gov't
11
Hydrocortisone
11
WI4X0X7BPJ
10
Glucocorticoids
10
Review
9
17-alpha-Hydroxyprogesterone
9
409J2J96VR
9
68-96-2
9
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9
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8
21-hydroxylase deficiency
8
Case Reports
7
Steroids
6
EC 1.14.14.16
6
Steroid 21-Hydroxylase
5
CAH
4
3XMK78S47O
4
9002-60-2
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2020-
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