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Results: 1 to 20 of 25

1.

Neurostructural correlates of two subtypes of specific phobia: a voxel-based morphometry study.

Hilbert K, Evens R, Maslowski NI, Wittchen HU, Lueken U.

Psychiatry Res. 2015 Feb 28;231(2):168-75. doi: 10.1016/j.pscychresns.2014.12.003. Epub 2014 Dec 12.

PMID:
25561374
2.

Diagnostic classification of specific phobia subtypes using structural MRI data: a machine-learning approach.

Lueken U, Hilbert K, Wittchen HU, Reif A, Hahn T.

J Neural Transm. 2015 Jan;122(1):123-34. doi: 10.1007/s00702-014-1272-5. Epub 2014 Jul 19.

PMID:
25037587
3.

Fear processing in dental phobia during crossmodal symptom provocation: an fMRI study.

Hilbert K, Evens R, Maslowski NI, Wittchen HU, Lueken U.

Biomed Res Int. 2014;2014:196353. doi: 10.1155/2014/196353. Epub 2014 Mar 11.

4.

Neural structures, functioning and connectivity in Generalized Anxiety Disorder and interaction with neuroendocrine systems: a systematic review.

Hilbert K, Lueken U, Beesdo-Baum K.

J Affect Disord. 2014 Apr;158:114-26. doi: 10.1016/j.jad.2014.01.022. Epub 2014 Feb 12. Review.

PMID:
24655775
5.

Neural substrates of defensive reactivity in two subtypes of specific phobia.

Lueken U, Hilbert K, Stolyar V, Maslowski NI, Beesdo-Baum K, Wittchen HU.

Soc Cogn Affect Neurosci. 2014 Nov;9(11):1668-75. doi: 10.1093/scan/nst159. Epub 2013 Oct 29.

PMID:
24174207
6.

Investigating the genetic and environmental bases of biases in threat recognition and avoidance in children with anxiety problems.

Lau JY, Hilbert K, Goodman R, Gregory AM, Pine DS, Viding EM, Eley TC.

Biol Mood Anxiety Disord. 2012 Jul 12;2(1):12. doi: 10.1186/2045-5380-2-12.

7.

Separation of water-soluble polymers using capillary-channeled polymer fiber stationary phases.

Hilbert KJ, Marcus RK.

J Sep Sci. 2010 Nov;33(22):3571-7. doi: 10.1002/jssc.201000519.

PMID:
20972973
8.

Mutations in MMP9 and MMP13 determine the mode of inheritance and the clinical spectrum of metaphyseal anadysplasia.

Lausch E, Keppler R, Hilbert K, Cormier-Daire V, Nikkel S, Nishimura G, Unger S, Spranger J, Superti-Furga A, Zabel B.

Am J Hum Genet. 2009 Aug;85(2):168-78. doi: 10.1016/j.ajhg.2009.06.014. Epub 2009 Jul 16. Erratum in: Am J Hum Genet. 2009 Sep;85(3):420.

9.

The Faces Symbol Test, a newly developed screening instrument to assess cognitive decline related to multiple sclerosis: first results of the Berlin Multi-Centre FST Validation Study.

Scherer P, Penner IK, Rohr A, Boldt H, Ringel I, Wilke-Burger H, Burger-Deinerth E, Isakowitsch K, Zimmermann M, Zahrnt S, Hauser R, Hilbert K, Tiel-Wilck K, Anvari K, Behringer A, Peglau I, Friedrich H, Plenio A, Benesch G, Ehret R, Nippert I, Finke G, Schulz I, Bergtholdt B, Breitkopf S, Kaskel P, Reischies F, Kugler J.

Mult Scler. 2007 Apr;13(3):402-11. Epub 2007 Jan 29.

PMID:
17439910
10.

Du Pan syndrome phenotype caused by heterozygous pathogenic mutations in CDMP1 gene.

Szczaluba K, Hilbert K, Obersztyn E, Zabel B, Mazurczak T, Kozlowski K.

Am J Med Genet A. 2005 Nov 1;138(4):379-83.

PMID:
16222676
11.

Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies.

Zankl A, Neumann L, Ignatius J, Nikkels P, Schrander-Stumpel C, Mortier G, Omran H, Wright M, Hilbert K, Bonafé L, Spranger J, Zabel B, Superti-Furga A.

Am J Med Genet A. 2005 Feb 15;133A(1):61-7.

PMID:
15643621
12.

Spondyloperipheral dysplasia is caused by truncating mutations in the C-propeptide of COL2A1.

Zankl A, Zabel B, Hilbert K, Wildhardt G, Cuenot S, Xavier B, Ha-Vinh R, Bonafé L, Spranger J, Superti-Furga A.

Am J Med Genet A. 2004 Aug 30;129A(2):144-8.

PMID:
15316962
13.

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.

Physiol Genomics. 2000 Jan 24;2(1):9-12.

PMID:
11015576
14.

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.

Genomics. 2000 Jul 15;67(2):179-87.

PMID:
10903843
15.

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.

Hum Genet. 1997 Aug;100(2):215-9.

PMID:
9254852
16.

Mouse CD24 as a signaling molecule for integrin-mediated cell binding: functional and physical association with src-kinases.

Sammar M, Gulbins E, Hilbert K, Lang F, Altevogt P.

Biochem Biophys Res Commun. 1997 May 19;234(2):330-4.

PMID:
9177270
17.

Two different PAX3 gene mutations causing Waardenburg syndrome type I.

Wildhardt G, Winterpacht A, Hilbert K, Menger H, Zabel B.

Mol Cell Probes. 1996 Jun;10(3):229-31.

PMID:
8799378
18.

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.

Am J Med Genet. 1996 May 3;63(1):123-8.

PMID:
8723097
19.

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.

J Med Virol. 1995 Dec;47(4):336-41.

PMID:
8636700
20.

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

Winterpacht A, Hilbert K, Schwarze U, Zabel B.

Hum Genet. 1995 Apr;95(4):437-9.

PMID:
7705841
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