Nils Krone
Titolo
Citata da
Citata da
Anno
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
3782000
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
3352010
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
3252011
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 massá…
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
3152010
Genetics of congenital adrenal hyperplasia
N Krone, W Arlt
Best practice & research clinical endocrinology & metabolism 23 (2), 181-192, 2009
2252009
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
1512011
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
1362009
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
1342016
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, 2011
1262011
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
1172009
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
1132011
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency
N Krone, V Dhir, HE Ivison, W Arlt
Clinical endocrinology 66 (2), 162-172, 2007
1132007
Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium‐chain acyl‐CoA dehydrogenase deficiency
EM Maier, B Liebl, W R÷schinger, U Nennstiel‐Ratzel, R Fingerhut, ...
Human mutation 25 (5), 443-452, 2005
1072005
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
882014
Management of congenital adrenal hyperplasia: results of the ESPE questionnaire
FG Riepe, N Krone, M Viemann, CJ Partsch, WG Sippell
Hormone Research in Paediatrics 58 (4), 196-205, 2002
842002
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenalá…
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
832013
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
822012
Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia
N Krone, A Braun, S Weinert, M Peter, AA Roscher, CJ Partsch, ...
Clinical Chemistry 48 (6), 818-825, 2002
792002
Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11βá…
S Parajes, L Loidi, N Reisch, V Dhir, IT Rose, R Hampel, M Quinkler, ...
The Journal of Clinical Endocrinology & Metabolism 95 (2), 779-788, 2010
752010
Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287P
V Dhir, HE Ivison, N Krone, CHL Shackleton, AJ Doherty, PM Stewart, ...
Molecular Endocrinology 21 (8), 1958-1968, 2007
742007
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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