Kneppo C - Search Results

Year	Number of Results
2006	3
2010	1
2011	1
2014	3
2015	3
2016	2
2017	1
2018	2
2024	0

1

Multiple prevalent fractures in relation to macroscopic bone architecture in patients with cystic fibrosis.

Stahl M, Holfelder C, Kneppo C, Kieser M, Kasperk C, Schoenau E, Sommerburg O, Tönshoff B. Stahl M, et al. Among authors: kneppo c. J Cyst Fibros. 2018 Jan;17(1):114-120. doi: 10.1016/j.jcf.2016.06.004. Epub 2016 Jun 18. J Cyst Fibros. 2018. PMID: 27324551 Free article.

2

Analysis of the functional muscle-bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomography.

Choukair D, Kneppo C, Feneberg R, Schönau E, Lindner M, Kölker S, Hoffmann GF, Tönshoff B. Choukair D, et al. Among authors: kneppo c. J Inherit Metab Dis. 2017 Mar;40(2):219-226. doi: 10.1007/s10545-016-0002-6. Epub 2016 Nov 22. J Inherit Metab Dis. 2017. PMID: 27878409

3

Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients.

Tefs K, Gueorguieva M, Klammt J, Allen CM, Aktas D, Anlar FY, Aydogdu SD, Brown D, Ciftci E, Contarini P, Dempfle CE, Dostalek M, Eisert S, Gökbuget A, Günhan O, Hidayat AA, Hügle B, Isikoglu M, Irkec M, Joss SK, Klebe S, Kneppo C, Kurtulus I, Mehta RP, Ornek K, Schneppenheim R, Seregard S, Sweeney E, Turtschi S, Veres G, Zeitler P, Ziegler M, Schuster V. Tefs K, et al. Among authors: kneppo c. Blood. 2006 Nov 1;108(9):3021-6. doi: 10.1182/blood-2006-04-017350. Epub 2006 Jul 18. Blood. 2006. PMID: 16849641 Free article.

4

Sequential measurements of IGF-I serum concentrations in adolescents with Laron syndrome treated with recombinant human IGF-I (rhIGF-I).

Breil T, Kneppo C, Bettendorf M; German IGF-I Deficiency Study Group; Müller HL, Kapelari K, Schnabel D, Woelfle J. Breil T, et al. Among authors: kneppo c. J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):895-902. doi: 10.1515/jpem-2018-0139. J Pediatr Endocrinol Metab. 2018. PMID: 29995632

5

Assessment of aortic morphology and compliance in children and adolescents with Ullrich-Turner syndrome (UTS) using magnetic resonance imaging (MRI).

Kneppo C, Eichhorn JG, Ley S, Schenk JP, Gorenflo M, Bettendorf M. Kneppo C, et al. J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):915-22. doi: 10.1515/jpem-2013-0332. J Pediatr Endocrinol Metab. 2014. PMID: 24854524

6

Long-Term Neurodevelopmental Outcome of Children Treated with Tri-Iodothyronine after Cardiac Surgery: Follow-Up of a Double-Blind, Randomized, Placebo-Controlled Study.

Mittnacht J, Choukair D, Kneppo C, Brunner R, Parzer P, Gorenflo M, Bettendorf M. Mittnacht J, et al. Among authors: kneppo c. Horm Res Paediatr. 2015;84(2):130-6. doi: 10.1159/000381711. Epub 2015 May 7. Horm Res Paediatr. 2015. PMID: 25967124 Clinical Trial.

7

Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial.

Dörr HG, Bettendorf M, Binder G, Karges B, Kneppo C, Schmidt H, Voss E, Wabitsch M, Dötsch J. Dörr HG, et al. Among authors: kneppo c. Horm Res Paediatr. 2015;84(4):266-74. doi: 10.1159/000437140. Epub 2015 Aug 7. Horm Res Paediatr. 2015. PMID: 26279111 Free article. Clinical Trial.

8

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy.

Otto EA, Ramaswami G, Janssen S, Chaki M, Allen SJ, Zhou W, Airik R, Hurd TW, Ghosh AK, Wolf MT, Hoppe B, Neuhaus TJ, Bockenhauer D, Milford DV, Soliman NA, Antignac C, Saunier S, Johnson CA, Hildebrandt F; GPN Study Group. Otto EA, et al. J Med Genet. 2011 Feb;48(2):105-16. doi: 10.1136/jmg.2010.082552. Epub 2010 Nov 10. J Med Genet. 2011. PMID: 21068128 Free PMC article.

9

Screening for Pax8 mutations in patients with congenital hypothyroidism in South-West Germany.

Lanzerath K, Bettendorf M, Haag C, Kneppo C, Schulze E, Grulich-Henn J. Lanzerath K, et al. Among authors: kneppo c. Horm Res. 2006;66(2):96-100. doi: 10.1159/000093799. Epub 2006 Jun 7. Horm Res. 2006. PMID: 16763387

10

Analyses of Gonadoblastoma Y (GBY)-locus and of Y centromere in Turner syndrome patients.

Knauer-Fischer S, Besikoglu B, Inta I, Kneppo C, Vogt PH, Bettendorf M. Knauer-Fischer S, et al. Among authors: kneppo c. Exp Clin Endocrinol Diabetes. 2015 Jan;123(1):61-5. doi: 10.1055/s-0034-1387734. Epub 2014 Oct 14. Exp Clin Endocrinol Diabetes. 2015. PMID: 25314650 Clinical Trial.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

12 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

12 results

Results by year