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Items: 1 to 50 of 61

1.

An unusual altered biodistribution of 18F-FDG on PET/CT: diffuse perimuscular uptake in the setting of acute adrenal crisis.

Özütemiz C, Steinberger D, Froelich JW.

Eur J Nucl Med Mol Imaging. 2019 Apr;46(4):1037-1038. doi: 10.1007/s00259-018-4247-1. Epub 2019 Jan 7. No abstract available.

PMID:
30617962
2.

Postoperative analgesia by adding acupuncture to conventional therapy, a non-randomized controlled trial.

Levy I, Attias S, Cohen L, Stoppelmann N, Steinberger D, Grimberg O, Ben-Arye E, Matter I, Sroka G, Somri M, Schiff E.

J Complement Integr Med. 2018 Oct 12;16(2). pii: /j/jcim.2019.16.issue-2/jcim-2018-0028/jcim-2018-0028.xml. doi: 10.1515/jcim-2018-0028.

PMID:
30312162
3.

Near complete response to Pembrolizumab in microsatellite-stable metastatic sebaceous carcinoma.

Domingo-Musibay E, Murugan P, Giubellino A, Sharma S, Steinberger D, Yuan J, Hunt MA, Lou E, Miller JS.

J Immunother Cancer. 2018 Jun 19;6(1):58. doi: 10.1186/s40425-018-0357-3.

4.

Nurses as boundary actors: Promoting integrative medicine in hospital wards.

Arnon Z, Steinberger D, Attias S, Grimberg O, Peterfreund I, Schiff E, Keshet Y.

Complement Ther Clin Pract. 2018 May;31:96-103. doi: 10.1016/j.ctcp.2018.01.014. Epub 2018 Feb 10.

PMID:
29705488
5.

Implementing pharmacogenomics decision support across seven European countries: The Ubiquitous Pharmacogenomics (U-PGx) project.

Blagec K, Koopmann R, Crommentuijn-van Rhenen M, Holsappel I, van der Wouden CH, Konta L, Xu H, Steinberger D, Just E, Swen JJ, Guchelaar HJ, Samwald M.

J Am Med Inform Assoc. 2018 Jul 1;25(7):893-898. doi: 10.1093/jamia/ocy005.

6.

CORRIGENDUM: Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium.

van der Wouden CH, Cambon-Thomsen A, Cecchin E, Cheung KC, Dávila-Fajardo CL, Deneer VH, Dolžan V, Ingelman-Sundberg M, Jönsson S, Karlsson MO, Kriek M, Mitropoulou C, Patrinos GP, Pirmohamed M, Samwald M, Schaeffeler E, Schwab M, Steinberger D, Stingl J, Sunder-Plassmann G, Toffoli G, Turner RM, van Rhenen MH, Swen JJ, Guchelaar HJ; Ubiquitous Pharmacogenomics Consortium.

Clin Pharmacol Ther. 2017 Jul;102(1):152. doi: 10.1002/cpt.725. No abstract available.

PMID:
30239993
7.

EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO.

Skopkova M, Hennig F, Shin BS, Turner CE, Stanikova D, Brennerova K, Stanik J, Fischer U, Henden L, Müller U, Steinberger D, Leshinsky-Silver E, Bottani A, Kurdiova T, Ukropec J, Nyitrayova O, Kolnikova M, Klimes I, Borck G, Bahlo M, Haas SA, Kim JR, Lotspeich-Cole LE, Gasperikova D, Dever TE, Kalscheuer VM.

Hum Mutat. 2017 Apr;38(4):409-425. doi: 10.1002/humu.23170. Epub 2017 Jan 23.

8.

Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium.

van der Wouden CH, Cambon-Thomsen A, Cecchin E, Cheung KC, Dávila-Fajardo CL, Deneer VH, Dolžan V, Ingelman-Sundberg M, Jönsson S, Karlsson MO, Kriek M, Mitropoulou C, Patrinos GP, Pirmohamed M, Samwald M, Schaeffeler E, Schwab M, Steinberger D, Stingl J, Sunder-Plassmann G, Toffoli G, Turner RM, van Rhenen MH, Swen JJ, Guchelaar HJ; Ubiquitous Pharmacogenomics Consortium.

Clin Pharmacol Ther. 2017 Mar;101(3):341-358. doi: 10.1002/cpt.602. Erratum in: Clin Pharmacol Ther. 2017 Jul;102(1):152.

PMID:
28027596
9.

Evaluation of an investigational wearable injector in healthy human volunteers.

Torjman MC, Machnicki R, Lessin J, Loeum C, Steinberger D, Mycroft S, Joseph JI.

Expert Opin Drug Deliv. 2017 Jan;14(1):7-13. Epub 2016 Nov 4.

PMID:
27809609
10.

Isoniazid-induced polyneuropathy in a tuberculosis patient - implication for individual risk stratification with genotyping?

Stettner M, Steinberger D, Hartmann CJ, Pabst T, Konta L, Hartung HP, Kieseier BC.

Brain Behav. 2015 Aug;5(8):e00326. doi: 10.1002/brb3.326. Epub 2015 May 29.

11.

Repeated mechanical lengthening of intestinal segments in a novel model.

Scott A, Sullins VF, Steinberger D, Rouch JD, Wagner JP, Chiang E, Lee SL, Wu BM, Dunn JC.

J Pediatr Surg. 2015 Jun;50(6):954-7. doi: 10.1016/j.jpedsurg.2015.03.020. Epub 2015 Mar 14.

PMID:
25818320
12.

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, de Brouwer AP, Weinert S, Froyen G, Frints SG, Laumonnier F, Zemojtel T, Love MI, Richard H, Emde AK, Bienek M, Jensen C, Hambrock M, Fischer U, Langnick C, Feldkamp M, Wissink-Lindhout W, Lebrun N, Castelnau L, Rucci J, Montjean R, Dorseuil O, Billuart P, Stuhlmann T, Shaw M, Corbett MA, Gardner A, Willis-Owen S, Tan C, Friend KL, Belet S, van Roozendaal KE, Jimenez-Pocquet M, Moizard MP, Ronce N, Sun R, O'Keeffe S, Chenna R, van Bömmel A, Göke J, Hackett A, Field M, Christie L, Boyle J, Haan E, Nelson J, Turner G, Baynam G, Gillessen-Kaesbach G, Müller U, Steinberger D, Budny B, Badura-Stronka M, Latos-Bieleńska A, Ousager LB, Wieacker P, Rodríguez Criado G, Bondeson ML, Annerén G, Dufke A, Cohen M, Van Maldergem L, Vincent-Delorme C, Echenne B, Simon-Bouy B, Kleefstra T, Willemsen M, Fryns JP, Devriendt K, Ullmann R, Vingron M, Wrogemann K, Wienker TF, Tzschach A, van Bokhoven H, Gecz J, Jentsch TJ, Chen W, Ropers HH, Kalscheuer VM.

Mol Psychiatry. 2016 Jan;21(1):133-48. doi: 10.1038/mp.2014.193. Epub 2015 Feb 3.

13.

Intestinal lengthening in an innovative rodent surgical model.

Sullins VF, Scott A, Wagner JP, Steinberger D, Lee SL, Wu BM, Dunn JC.

J Pediatr Surg. 2014 Dec;49(12):1791-4. doi: 10.1016/j.jpedsurg.2014.09.022. Epub 2014 Oct 1.

PMID:
25487485
14.

Radiology diagnostic exchange agents: clinical term identification and validation.

Shores KB, Konstan JA, Riedl JT, Taylor AJ, Steinberger DJ, Adam TJ.

AMIA Jt Summits Transl Sci Proc. 2013 Mar 18;2013:244-8. eCollection 2013.

15.

Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics.

Wildhardt G, Zirn B, Graul-Neumann LM, Wechtenbruch J, Suckfüll M, Buske A, Bohring A, Kubisch C, Vogt S, Strobl-Wildemann G, Greally M, Bartsch O, Steinberger D.

BMJ Open. 2013 Mar 18;3(3). pii: e001917. doi: 10.1136/bmjopen-2012-001917.

16.

Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection.

Michaelis M, Barth S, Breitling R, Bruch J, Steinberger D, Rothweiler F, Hackmann K, Schröck E, Doerr HW, Griffin DK, Cinatl J, Cinatl J Jr.

Oncogenesis. 2012 Apr 30;1:e10. doi: 10.1038/oncsis.2012.10.

17.

Intracerebral hemorrhage with thrombolytic therapy for acute pulmonary embolism.

Stein PD, Matta F, Steinberger DS, Keyes DC.

Am J Med. 2012 Jan;125(1):50-6. doi: 10.1016/j.amjmed.2011.06.026. Epub 2011 Nov 24.

PMID:
22115025
18.
19.

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain.

Chen J, Wildhardt G, Zhong Z, Röth R, Weiss B, Steinberger D, Decker J, Blum WF, Rappold G.

J Med Genet. 2009 Dec;46(12):834-9. doi: 10.1136/jmg.2009.067785. Epub 2009 Jul 2.

20.

A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome.

Trübenbach J, Wildhardt G, Niebel J, Hawle H, Steinberger D.

Rheumatol Int. 2010 Apr;30(6):805-9. doi: 10.1007/s00296-009-0996-2. Epub 2009 Jun 23.

PMID:
19547977
21.

Gene symbol: LMX1B. Disease: Nail-Patella syndrome.

Al Balwi M, Steinberger D, Al Abdulkareem I, Al Abdi S.

Hum Genet. 2008 Feb;123(1):109-10. No abstract available.

PMID:
18386349
22.

Hypergonadotropic hypogonadism in a patient with inv ins (2;4).

Tzschach A, Ramel C, Kron A, Seipel B, Wüster C, Cordes U, Liehr T, Hoeltzenbein M, Menzel C, Ropers HH, Ullmann R, Kalscheuer V, Decker J, Steinberger D.

Int J Androl. 2009 Jun;32(3):226-30. Epub 2007 Nov 27.

PMID:
18042180
23.

Frequency of GCH1 deletions in Dopa-responsive dystonia.

Zirn B, Steinberger D, Troidl C, Brockmann K, von der Hagen M, Feiner C, Henke L, Müller U.

J Neurol Neurosurg Psychiatry. 2008 Feb;79(2):183-6. Epub 2007 Sep 26.

PMID:
17898029
24.

Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia.

Steinberger D, Trübenbach J, Zirn B, Leube B, Wildhardt G, Müller U.

Neurogenetics. 2007 Jan;8(1):51-5. Epub 2006 Nov 17. Erratum in: Neurogenetics. 2007 Jan;8(1):69.

PMID:
17111153
25.

Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications.

Wylenzek C, Trübenbach J, Gohl P, Wildhardt G, Alkins S, Fausett MB, Decker J, Steinberger D.

Clin Lab Haematol. 2005 Oct;27(5):343-6.

PMID:
16178919
26.

Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis).

Mulliken JB, Gripp KW, Stolle CA, Steinberger D, Müller U.

Plast Reconstr Surg. 2004 Jun;113(7):1899-909.

PMID:
15253176
27.

Heterozygous mutation in 5'-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystonia.

Steinberger D, Blau N, Goriuonov D, Bitsch J, Zuker M, Hummel S, Müller U.

Neurogenetics. 2004 Sep;5(3):187-90. Epub 2004 Jul 6.

PMID:
15241655
28.

Development of the University of Wisconsin donation After Cardiac Death Evaluation Tool.

Lewis J, Peltier J, Nelson H, Snyder W, Schneider K, Steinberger D, Anderson M, Krichevsky A, Anderson J, Ellefson J, D'Alessandro A.

Prog Transplant. 2003 Dec;13(4):265-73.

PMID:
14765718
29.

Genetic mapping of variation in spatial learning in the mouse.

Steinberger D, Reynolds DS, Ferris P, Lincoln R, Datta S, Stanley J, Paterson A, Dawson GR, Flint J.

J Neurosci. 2003 Mar 15;23(6):2426-33.

30.

Mutations of GCH1 in Dopa-responsive dystonia.

Müller U, Steinberger D, Topka H.

J Neural Transm (Vienna). 2002 Mar;109(3):321-8. Review.

PMID:
11956954
31.

Medical billing outsourcing: is it worth the risk?

Steinberger D.

J Ophthalmic Nurs Technol. 2000 Sep-Oct;19(5):218-9. No abstract available.

PMID:
11933317
32.

Standardized evaluation and documentation of findings in patients with craniosynostosis.

Jünger TH, Reicherts M, Steinberger D, Collmann H, Kotrikova B, Zöller J, Howaldt HP.

J Craniomaxillofac Surg. 2001 Feb;29(1):25-32.

PMID:
11467491
33.

Standardized evaluation and documentation of findings in patients with craniosynostosis.

Jünger TH, Reicherts M, Steinberger D, Collmann H, Kotrikova B, Zöller J, Howaldt HP.

J Maxillofac Surg. 2001 Feb;29(1):25-32.

PMID:
11308276
34.

Recordkeeping: helpful ways to reduce practice risk in the event of an audit.

Steinberger D.

J Ophthalmic Nurs Technol. 2000 May-Jun;19(3):112-3. No abstract available.

PMID:
11249239
35.

Dopa-responsive dystonia: mutation analysis of GCH1 and analysis of therapeutic doses of L-dopa. German Dystonia Study Group.

Steinberger D, Korinthenberg R, Topka H, Berghäuser M, Wedde R, Müller U.

Neurology. 2000 Dec 12;55(11):1735-7.

PMID:
11113234
36.

Recommendations lead to effective practice compliance programs.

Steinberger D.

J Ophthalmic Nurs Technol. 2000 Mar-Apr;19(2):60-1. No abstract available.

PMID:
11075073
37.

Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses.

Robson CD, Mulliken JB, Robertson RL, Proctor MR, Steinberger D, Barnes PD, McFarren A, Müller U, Zurakowski D.

AJNR Am J Neuroradiol. 2000 Oct;21(9):1707-17.

38.

Mutation of FGFR2 (cys278phe) in craniolacunia and pansynostosis.

Steinberger D, Müller U, Jünger TH, Howaldt HP, Christophis P.

J Med Genet. 1999 Jun;36(6):499-500. No abstract available.

39.

How to 'surf' for Medicare billing and coding information: use Internet and print sources.

Steinberger D.

J Ophthalmic Nurs Technol. 1999 Sep-Oct;18(5):196-7. No abstract available.

PMID:
10847045
40.

Clinical and molecular genetics of primary dystonias.

Müller U, Steinberger D, Németh AH.

Neurogenetics. 1998 Mar;1(3):165-77. Review.

PMID:
10737119
41.

Two previously unrecognized splicing mutations of GCH1 in Dopa-responsive dystonia: exon skipping and one base insertion.

Weber Y, Steinberger D, Deuschl G, Benecke R, Müller U.

Neurogenetics. 1997 Sep;1(2):125-7.

PMID:
10732814
42.

Features of Antley-Bixler syndrome in an infant born to a mother with pregnancy luteoma.

Roth C, Hinney B, Peter M, Steinberger D, Lakomek M.

Eur J Pediatr. 2000 Mar;159(3):189-92.

PMID:
10664233
43.

PGL3, a third, not maternally imprinted locus in autosomal dominant paraganglioma.

Niemann S, Steinberger D, Müller U.

Neurogenetics. 1999 Sep;2(3):167-70.

PMID:
10541590
44.

Molecular diagnosis of bilateral coronal synostosis.

Mulliken JB, Steinberger D, Kunze S, Müller U.

Plast Reconstr Surg. 1999 Nov;104(6):1603-15. Review.

PMID:
10541159
45.

GCH1 mutation in a patient with adult-onset oromandibular dystonia.

Steinberger D, Topka H, Fischer D, Müller U.

Neurology. 1999 Mar 10;52(4):877-9.

PMID:
10078749
47.

Integrated physical and transcript map of 5q31.3-qter.

Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U.

Eur J Hum Genet. 1998 May-Jun;6(3):266-74.

48.

Dopa responsive dystonia with Turner's syndrome: clinical, genetic, and neuropsychological studies in a family with a new mutation in the GTP-cyclohydrolase I gene.

Nitschke M, Steinberger D, Heberlein I, Otto V, Müller U, Vieregge P.

J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):806-8.

49.

High penetrance and pronounced variation in expressivity of GCH1 mutations in five families with dopa-responsive dystonia.

Steinberger D, Weber Y, Korinthenberg R, Deuschl G, Benecke R, Martinius J, Müller U.

Ann Neurol. 1998 May;43(5):634-9. Erratum in: Ann Neurol 1998 Jul;44(1):147.

PMID:
9585358
50.

The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptor.

Steinberger D, Vriend G, Mulliken JB, Müller U.

Hum Genet. 1998 Feb;102(2):145-50. Erratum in: Hum Genet 1998 Apr;102(4):495.

PMID:
9521581

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