עקוב אחר
Nils Krone
כותרת
צוטט על ידי
צוטט על ידי
שנה
Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients
W Arlt, DS Willis, SH Wild, N Krone, EJ Doherty, S Hahner, TS Han, ...
The Journal of Clinical Endocrinology & Metabolism 95 (11), 5110-5121, 2010
4972010
Urine steroid metabolomics as a biomarker tool for detecting malignancy in adrenal tumors
W Arlt, M Biehl, AE Taylor, S Hahner, R Libe, BA Hughes, P Schneider, ...
The Journal of Clinical Endocrinology & Metabolism 96 (12), 3775-3784, 2011
4782011
Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass …
N Krone, BA Hughes, GG Lavery, PM Stewart, W Arlt, CHL Shackleton
The Journal of steroid biochemistry and molecular biology 121 (3-5), 496-504, 2010
4642010
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany
N Krone, A Braun, AA Roscher, D Knorr, HP Schwarz
The Journal of Clinical Endocrinology & Metabolism 85 (3), 1059-1065, 2000
4522000
Genetics of congenital adrenal hyperplasia
N Krone, W Arlt
Best practice & research clinical endocrinology & metabolism 23 (2), 181-192, 2009
3242009
Congenital adrenal hyperplasia—current insights in pathophysiology, diagnostics, and management
HL Claahsen-van der Grinten, PW Speiser, SF Ahmed, W Arlt, RJ Auchus, ...
Endocrine reviews 43 (1), 91-159, 2022
2812022
Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015)
SF Ahmed, JC Achermann, W Arlt, A Balen, G Conway, Z Edwards, ...
Clinical endocrinology 84 (5), 771-788, 2016
2502016
Adrenal insufficiency
ES Husebye, SH Pearce, NP Krone, O Kämpe
The Lancet 397 (10274), 613-629, 2021
2402021
UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development
SF Ahmed, JC Achermann, W Arlt, AH Balen, G Conway, ZL Edwards, ...
Clinical Endocrinology 75 (1), 12-26, 2011
1872011
Inactivating PAPSS2 mutations in a patient with premature pubarche
C Noordam, V Dhir, JC McNelis, F Schlereth, NA Hanley, N Krone, ...
New England Journal of Medicine 360 (22), 2310-2318, 2009
1772009
Premature adrenarche: novel lessons from early onset androgen excess
J Idkowiak, GG Lavery, V Dhir, TG Barrett, PM Stewart, N Krone, W Arlt
European Journal of Endocrinology 165 (2), 189-207, 2011
1672011
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency
N Krone, V Dhir, HE Ivison, W Arlt
Clinical endocrinology 66 (2), 162-172, 2007
1642007
Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency
LA Metherell, D Naville, G Halaby, M Begeot, A Huebner, G Nurnberg, ...
The Journal of Clinical Endocrinology & Metabolism 94 (10), 3865-3871, 2009
1622009
Genetics in endocrinology: approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM …
L Audi, SF Ahmed, N Krone, M Cools, K McElreavey, PM Holterhus, ...
European Journal of Endocrinology 179 (4), R197-R206, 2018
1422018
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency
N Krone, N Reisch, J Idkowiak, V Dhir, HE Ivison, BA Hughes, IT Rose, ...
The Journal of Clinical Endocrinology & Metabolism 97 (2), E257-E267, 2012
1372012
Health problems in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
N Reisch, W Arlt, N Krone
Hormone research in paediatrics 76 (2), 73-85, 2011
1352011
Changes over time in sex assignment for disorders of sex development
Z Kolesinska, SF Ahmed, M Niedziela, J Bryce, M Molinska-Glura, ...
Pediatrics 134 (3), e710-e715, 2014
1342014
Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium‐chain acyl‐CoA dehydrogenase deficiency
EM Maier, B Liebl, W Röschinger, U Nennstiel‐Ratzel, R Fingerhut, ...
Human Mutation 25 (5), 443-452, 2005
1302005
Novel associations in disorders of sex development: findings from the I-DSD Registry
K Cox, J Bryce, J Jiang, M Rodie, R Sinnott, M Alkhawari, W Arlt, L Audi, ...
The Journal of Clinical Endocrinology & Metabolism 99 (2), E348-E355, 2014
1192014
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal …
N Krone, IT Rose, DS Willis, J Hodson, SH Wild, EJ Doherty, S Hahner, ...
The Journal of Clinical Endocrinology & Metabolism 98 (2), E346-E354, 2013
1142013
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מאמרים 1–20