Παρακολούθηση
Clemens Kamrath
Clemens Kamrath
Justus Liebig Universität Giessen
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα nic-site.de
Τίτλος
Παρατίθεται από
Παρατίθεται από
Έτος
Ketoacidosis in children and adolescents with newly diagnosed type 1 diabetes during the COVID-19 pandemic in Germany
C Kamrath, K Mönkemöller, T Biester, TR Rohrer, K Warncke, ...
Jama 324 (8), 801-804, 2020
3792020
Increased activation of the alternative “backdoor” pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis
C Kamrath, Z Hochberg, MF Hartmann, T Remer, SA Wudy
The Journal of Clinical Endocrinology & Metabolism 97 (3), E367-E375, 2012
2062012
Did the COVID-19 lockdown affect the incidence of pediatric type 1 diabetes in Germany?
SR Tittel, J Rosenbauer, C Kamrath, J Ziegler, F Reschke, J Hammersen, ...
Diabetes care 43 (11), e172, 2020
1932020
Incidence of type 1 diabetes in children and adolescents during the COVID-19 pandemic in Germany: results from the DPV registry
C Kamrath, J Rosenbauer, AJ Eckert, K Siedler, H Bartelt, D Klose, ...
Diabetes Care 45 (8), 1762-1771, 2022
1402022
Impact of the COVID-19 pandemic on long-term trends in the prevalence of diabetic ketoacidosis at diagnosis of paediatric type 1 diabetes: an international multicentre study …
NH Birkebaek, C Kamrath, JM Grimsmann, K Aakesson, V Cherubini, ...
The Lancet Diabetes & Endocrinology 10 (11), 786-794, 2022
692022
Androgen excess is due to elevated 11-oxygenated androgens in treated children with congenital adrenal hyperplasia
C Kamrath, L Wettstaedt, C Boettcher, MF Hartmann, SA Wudy
The Journal of steroid biochemistry and molecular biology 178, 221-228, 2018
692018
A novel entity of clinically isolated adrenal insufficiency caused by a partially inactivating mutation of the gene encoding for P450 side chain cleavage enzyme (CYP11A1)
S Parajes, C Kamrath, IT Rose, AE Taylor, CF Mooij, V Dhir, J Grötzinger, ...
The Journal of Clinical Endocrinology & Metabolism 96 (11), E1798-E1806, 2011
632011
Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing
D Lal, BA Neubauer, MR Toliat, J Altmüller, H Thiele, P Nürnberg, ...
PLoS One 11 (1), e0146040, 2016
472016
Steroid 17α-Hydroxylase Deficiency: Functional Characterization of Four Mutations (A174E, V178D, R440C, L465P) in the CYP17A1 Gene
V Dhir, N Reisch, CM Bleicken, J Lebl, C Kamrath, HP Schwarz, ...
The Journal of Clinical Endocrinology & Metabolism 94 (8), 3058-3064, 2009
452009
Incidence of COVID-19 and risk of diabetic ketoacidosis in new-onset type 1 diabetes
C Kamrath, J Rosenbauer, AJ Eckert, A Pappa, F Reschke, TR Rohrer, ...
Pediatrics 148 (3), 2021
442021
Early versus delayed insulin pump therapy in children with newly diagnosed type 1 diabetes: results from the multicentre, prospective diabetes follow-up DPV registry
C Kamrath, SR Tittel, TM Kapellen, T von Dem Berge, B Heidtmann, ...
The Lancet Child & Adolescent Health 5 (1), 17-25, 2021
412021
Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography–mass spectrometry analysis: reference values for neonates and infants
C Kamrath, MF Hartmann, C Boettcher, KP Zimmer, SA Wudy
The Journal of steroid biochemistry and molecular biology 156, 10-16, 2016
402016
Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy—short version of the updated German best practice guideline (S2e)—AWMF register no. 166-001 …
R Ehren, MR Benz, PT Brinkkötter, J Dötsch, WR Eberl, J Gellermann, ...
Pediatric Nephrology 36 (10), 2971-2985, 2021
382021
The urinary steroidome of treated children with classic 21-hydroxylase deficiency
C Kamrath, L Wettstaedt, C Boettcher, MF Hartmann, SA Wudy
The Journal of Steroid Biochemistry and Molecular Biology 165, 396-406, 2017
372017
Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms
C Kamrath, MF Hartmann, C Boettcher, SA Wudy
The Journal of Pediatrics 165 (2), 280-284, 2014
352014
Frequency of autoantibody-negative type 1 diabetes in children, adolescents, and young adults during the first wave of the COVID-19 pandemic in Germany
C Kamrath, J Rosenbauer, SR Tittel, K Warncke, R Hirtz, C Denzer, ...
Diabetes Care 44 (7), 1540-1546, 2021
342021
The activities of 5α-reductase and 17, 20-lyase determine the direction through androgen synthesis pathways in patients with 21-hydroxylase deficiency
C Kamrath, MF Hartmann, T Remer, SA Wudy
Steroids 77 (13), 1391-1397, 2012
332012
Androgen synthesis in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
C Kamrath, MF Hartmann, SA Wudy
Hormone and Metabolic Research 45 (02), 86-91, 2013
302013
Prevalence of type 1 and type 2 diabetes in children and adolescents in Germany from 2002 to 2020: A study based on electronic health record data from the DPV registry
A Stahl‐Pehe, C Kamrath, N Prinz, T Kapellen, U Menzel, O Kordonouri, ...
Journal of diabetes 14 (12), 840-850, 2022
282022
Incidence and presentation of new-onset type 1 diabetes in children and adolescents from Germany during the COVID-19 pandemic 2020 and 2021: Current data from the DPV Registry
C Baechle, A Eckert, C Kamrath, A Neu, U Manuwald, S Thiele-Schmitz, ...
Diabetes Research and Clinical Practice 197, 110559, 2023
272023
Δεν είναι δυνατή η εκτέλεση της ενέργειας από το σύστημα αυτή τη στιγμή. Προσπαθήστε ξανά αργότερα.
Άρθρα 1–20