Hilbert K - Search Results

1

Containment of a Large SARS-CoV-2 Outbreak Among Healthcare Workers in a Pediatric Intensive Care Unit.

Knoll RL, Klopp J, Bonewitz G, Gröndahl B, Hilbert K, Kohnen W, Weise K, Plachter B, Hitzler W, Kowalzik F, Runkel S, Zepp F, Winter J, Cacicedo ML, Gehring S. Knoll RL, et al. Among authors: hilbert k. Pediatr Infect Dis J. 2020 Nov;39(11):e336-e339. doi: 10.1097/INF.0000000000002866. Pediatr Infect Dis J. 2020. PMID: 32826719

2

Long-Term, CD4⁺ Memory T Cell Response to SARS-CoV-2.

Wirsching S, Harder L, Heymanns M, Gröndahl B, Hilbert K, Kowalzik F, Meyer C, Gehring S. Wirsching S, et al. Among authors: hilbert k. Front Immunol. 2022 Apr 20;13:800070. doi: 10.3389/fimmu.2022.800070. eCollection 2022. Front Immunol. 2022. PMID: 35514974 Free PMC article.

3

Meconium Microbiome of Very Preterm Infants across Germany.

Klopp J, Ferretti P, Meyer CU, Hilbert K, Haiß A, Marißen J, Henneke P, Hudalla H, Pirr S, Viemann D, Zemlin M, Forslund SK, Härtel C, Bork P, Gehring S, Van Rossum T; the PRIMAL Consortium. Klopp J, et al. Among authors: hilbert k. mSphere. 2022 Feb 23;7(1):e0080821. doi: 10.1128/msphere.00808-21. Epub 2022 Jan 12. mSphere. 2022. PMID: 35019670 Free PMC article.

4

Selection of a precore mutant after vertical transmission of different hepatitis B virus variants is correlated with fulminant hepatitis in infants.

Bahn A, Hilbert K, Martiné U, Westedt J, von Weizsäcker F, Wirth S. Bahn A, et al. Among authors: hilbert k. J Med Virol. 1995 Dec;47(4):336-41. doi: 10.1002/jmv.1890470408. J Med Virol. 1995. PMID: 8636700

5

A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia.

Zabel B, Hilbert K, Stöss H, Superti-Furga A, Spranger J, Winterpacht A. Zabel B, et al. Among authors: hilbert k. Am J Med Genet. 1996 May 3;63(1):123-8. doi: 10.1002/(SICI)1096-8628(19960503)63:1<123::AID-AJMG22>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8723097

6

Two different PAX3 gene mutations causing Waardenburg syndrome type I.

Wildhardt G, Winterpacht A, Hilbert K, Menger H, Zabel B. Wildhardt G, et al. Among authors: hilbert k. Mol Cell Probes. 1996 Jun;10(3):229-31. doi: 10.1006/mcpr.1996.0032. Mol Cell Probes. 1996. PMID: 8799378

7

Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation.

Winterpacht A, Hilbert K, Schwarze U, Zabel B. Winterpacht A, et al. Among authors: hilbert k. Hum Genet. 1995 Apr;95(4):437-9. doi: 10.1007/BF00208971. Hum Genet. 1995. PMID: 7705841

8

Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysis.

Wüchner C, Hilbert K, Zabel B, Winterpacht A. Wüchner C, et al. Among authors: hilbert k. Hum Genet. 1997 Aug;100(2):215-9. doi: 10.1007/s004390050493. Hum Genet. 1997. PMID: 9254852

9

A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia.

Winterpacht A, Hilbert K, Stelzer C, Schweikardt T, Decker H, Segerer H, Spranger J, Zabel B. Winterpacht A, et al. Among authors: hilbert k. Physiol Genomics. 2000 Jan 24;2(1):9-12. doi: 10.1152/physiolgenomics.2000.2.1.9. Physiol Genomics. 2000. PMID: 11015576

10

Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family.

Enklaar T, Esswein M, Oswald M, Hilbert K, Winterpacht A, Higgins M, Zabel B, Prawitt D. Enklaar T, et al. Among authors: hilbert k. Genomics. 2000 Jul 15;67(2):179-87. doi: 10.1006/geno.2000.6234. Genomics. 2000. PMID: 10903843

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