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Items: 1 to 50 of 240

1.

Effects of Experience on Spatial Frequency Tuning in the Visual System: Behavioral, Visuocortical, and Alpha-band Responses.

Friedl WM, Keil A.

J Cogn Neurosci. 2020 Jan 14:1-17. doi: 10.1162/jocn_a_01524. [Epub ahead of print]

PMID:
31933434
2.

Complications and imaging artifacts related to MRI in patients with intramedullary osteosynthesis after proximal femur fracture.

Raven TF, Boxriker S, Mammadov J, Petrov K, Moghaddam A, Friedl W.

J Orthop Surg (Hong Kong). 2019 Sep-Dec;27(3):2309499019879055. doi: 10.1177/2309499019879055.

PMID:
31615327
3.

Nailing of lower extremity fractures.

Friedl W, Gradl G.

Injury. 2019 Aug;50 Suppl 3:1-3. doi: 10.1016/j.injury.2019.07.007. Epub 2019 Aug 1. No abstract available.

PMID:
31378547
4.

Human-Robotic Variable-Stiffness Grasps of Small-Fruit Containers Are Successful Even Under Severely Impaired Sensory Feedback.

Haas M, Friedl W, Stillfried G, Höppner H.

Front Neurorobot. 2018 Oct 31;12:70. doi: 10.3389/fnbot.2018.00070. eCollection 2018.

5.

[Fracture or avulsion of the extensor tendon: Anatomy of the extensor apparatus of the hand].

Friedl W.

Unfallchirurg. 2016 Jan;119(1):78. doi: 10.1007/s00113-015-0123-7. German. No abstract available.

PMID:
26732260
6.

Real-Time Volumetric Phase Monitoring: Advancing Chemical Analysis by Countercurrent Separation.

Pauli GF, Pro SM, Chadwick LR, Burdick T, Pro L, Friedl W, Novak N, Maltby J, Qiu F, Friesen JB.

Anal Chem. 2015 Jul 21;87(14):7418-25. doi: 10.1021/acs.analchem.5b01613. Epub 2015 Jul 8.

7.

MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.

Aretz S, Tricarico R, Papi L, Spier I, Pin E, Horpaopan S, Cordisco EL, Pedroni M, Stienen D, Gentile A, Panza A, Piepoli A, de Leon MP, Friedl W, Viel A, Genuardi M.

Eur J Hum Genet. 2014 Jul;22(7):923-9. doi: 10.1038/ejhg.2012.309. Epub 2013 Jan 30.

8.

Experimental and computational insights into the stabilization of low-valent main group elements using crown ethers and related ligands.

Macdonald CL, Bandyopadhyay R, Cooper BF, Friedl WW, Rossini AJ, Schurko RW, Eichhorn SH, Herber RH.

J Am Chem Soc. 2012 Mar 7;134(9):4332-45. doi: 10.1021/ja211135s. Epub 2012 Feb 22.

PMID:
22296458
9.

"Crowned" univalent indium complexes as donors? Experimental and computational insights on the valence isomers of EE'X4 species.

Cooper BF, Hamaed H, Friedl WW, Stinchcombe MR, Schurko RW, Macdonald CL.

Chemistry. 2011 May 23;17(22):6148-61. doi: 10.1002/chem.201002946. Epub 2011 Apr 15.

PMID:
21500291
10.

Peutz-Jeghers syndrome: a systematic review and recommendations for management.

Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV.

Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499.

PMID:
20581245
11.

Radial Palsy Caused by Ganglion of the Elbow.

Vasak N, Dorr J, Freund M, Friedl W.

Eur J Trauma Emerg Surg. 2010 Jun;36(3):254-6. doi: 10.1007/s00068-009-9023-2. Epub 2009 Sep 10.

PMID:
26815870
12.

Treatment of fractures of the fifth metatarsal with the XS-nail retrospective study and comparison with tension-band wiring.

Renner C, Whyte J, Singh S, Friedl W.

Arch Orthop Trauma Surg. 2010 Sep;130(9):1149-56. doi: 10.1007/s00402-009-1025-3. Epub 2010 Jan 5.

PMID:
20049608
13.

CLCN2 variants in idiopathic generalized epilepsy.

Kleefuss-Lie A, Friedl W, Cichon S, Haug K, Warnstedt M, Alekov A, Sander T, Ramirez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H.

Nat Genet. 2009 Sep;41(9):954-5. doi: 10.1038/ng0909-954. No abstract available.

PMID:
19710712
14.

Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review.

Kaufmann A, Vogt S, Uhlhaas S, Stienen D, Kurth I, Hameister H, Mangold E, Kötting J, Kaminsky E, Propping P, Friedl W, Aretz S.

J Mol Diagn. 2009 Mar;11(2):131-9. doi: 10.2353/jmoldx.2009.080129. Epub 2009 Feb 5. Review.

15.

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families.

Frank B, Burwinkel B, Bermejo JL, Försti A, Hemminki K, Houlston R, Mangold E, Rahner N, Friedl W, Friedrichs N, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Morak M, Keller G, Schackert HK, Krüger S, Goecke T, Moeslein G, Kloor M, Gebert J, Kunstmann E, Schulmann K, Rüschoff J, Propping P; German HNPCC Consortium.

Cancer Lett. 2008 Nov 18;271(1):153-7. doi: 10.1016/j.canlet.2008.05.043. Epub 2008 Jul 10.

PMID:
18619730
16.

Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus.

Rahner N, Höefler G, Högenauer C, Lackner C, Steinke V, Sengteller M, Friedl W, Aretz S, Propping P, Mangold E, Walldorf C.

Am J Med Genet A. 2008 May 15;146A(10):1314-9. doi: 10.1002/ajmg.a.32210. Review.

PMID:
18409202
17.

Guidelines for the clinical management of familial adenomatous polyposis (FAP).

Vasen HF, Möslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Järvinen H, Mecklin JP, Møller P, Myrhøi T, Nagengast FM, Parc Y, Phillips R, Clark SK, de Leon MP, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen J.

Gut. 2008 May;57(5):704-13. doi: 10.1136/gut.2007.136127. Epub 2008 Jan 14.

PMID:
18194984
18.

Opinion on moderate/low cancer genetic risk markers in medical practice.

Aretz S, Friedl W.

Hered Cancer Clin Pract. 2008 Jun 15;6(2):61-3. doi: 10.1186/1897-4287-6-2-61. No abstract available.

19.

Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.

Rahner N, Friedrichs N, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C.

J Pathol. 2008 Jan;214(1):10-6.

PMID:
17973250
20.

High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.

Aretz S, Stienen D, Uhlhaas S, Stolte M, Entius MM, Loff S, Back W, Kaufmann A, Keller KM, Blaas SH, Siebert R, Vogt S, Spranger S, Holinski-Feder E, Sunde L, Propping P, Friedl W.

J Med Genet. 2007 Nov;44(11):702-9. Epub 2007 Sep 14.

21.

Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.

Rahner N, Friedrichs N, Wehner M, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C.

Acta Oncol. 2007;46(6):763-9.

PMID:
17653898
22.

May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?

Liu X, Shan X, Friedl W, Uhlhaas S, Propping P, Li J, Wang Y.

Acta Oncol. 2007;46(6):757-62.

PMID:
17653897
23.

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).

Aretz S, Stienen D, Friedrichs N, Stemmler S, Uhlhaas S, Rahner N, Propping P, Friedl W.

Hum Mutat. 2007 Oct;28(10):985-92.

PMID:
17486639
24.

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

Vasen HF, Möslein G, Alonso A, Bernstein I, Bertario L, Blanco I, Burn J, Capella G, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Mecklin JP, Møller P, Nagengast F, Parc Y, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Wijnen J.

J Med Genet. 2007 Jun;44(6):353-62. Epub 2007 Feb 27. Review.

25.

A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification.

Pagenstecher C, Gadzicki D, Stienen D, Uhlhaas S, Mangold E, Rahner N, Arslan-Kirchner M, Propping P, Friedl W, Aretz S.

J Mol Diagn. 2007 Feb;9(1):122-6.

26.

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

Mangold E, Rahner N, Friedrichs N, Buettner R, Pagenstecher C, Aretz S, Friedl W, Ruzicka T, Propping P, Rütten A, Kruse R.

Br J Dermatol. 2007 Jan;156(1):158-62. No abstract available.

PMID:
17199584
27.

Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany.

Lamberti C, Mangold E, Pagenstecher C, Jungck M, Schwering D, Bollmann M, Vogel J, Kindermann D, Nikorowitsch R, Friedrichs N, Schneider B, Houshdaran F, Schmidt-Wolf IG, Friedl W, Propping P, Sauerbruch T, Büttner R, Mathiak M.

Digestion. 2006;74(1):58-67. Epub 2006 Mar 3.

PMID:
17095871
28.

Intramedullary locking compression nail for the treatment of an olecranon fracture.

Gehr J, Friedl W.

Oper Orthop Traumatol. 2006 Sep;18(3):199-213. English, German.

PMID:
16953346
29.

[Fracture of the neck of the talus in a child].

Gehr J, Friedl W.

Unfallchirurg. 2006 Oct;109(10):910-3. German.

PMID:
16944078
30.

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.

Krüger S, Engel C, Bier A, Mangold E, Pagenstecher C, Doeberitz Mv, Holinski-Feder E, Moeslein G, Keller G, Kunstmann E, Friedl W, Plaschke J, Rüschoff J, Schackert HK; German HNPCC-Consortium.

Cancer Lett. 2006 May 18;236(2):191-7.

PMID:
16832876
31.

[Intramedullary locked fixation and compression nail (IP-XS-Nail): treatment of ankle joint fractures].

Gehr J, Friedl W.

Oper Orthop Traumatol. 2006 Jun;18(2):155-70. English, German.

PMID:
16820987
32.

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.

Aretz S, Uhlhaas S, Goergens H, Siberg K, Vogel M, Pagenstecher C, Mangold E, Caspari R, Propping P, Friedl W.

Int J Cancer. 2006 Aug 15;119(4):807-14.

33.

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

Pagenstecher C, Wehner M, Friedl W, Rahner N, Aretz S, Friedrichs N, Sengteller M, Henn W, Buettner R, Propping P, Mangold E.

Hum Genet. 2006 Mar;119(1-2):9-22. Epub 2005 Dec 8.

PMID:
16341550
34.

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T.

Pediatr Blood Cancer. 2006 Nov;47(6):811-8.

PMID:
16317745
35.

An unexpected Cowden syndrome case found among members of a large familial adenomatous polyposis kindred.

Mehenni H, Friedl W, Nelen MR, Hutter P, Brundler MA.

Eur J Gastroenterol Hepatol. 2005 Dec;17(12):1407-12.

PMID:
16292097
36.

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.

Aretz S, Stienen D, Uhlhaas S, Loff S, Back W, Pagenstecher C, McLeod DR, Graham GE, Mangold E, Santer R, Propping P, Friedl W.

Hum Mutat. 2005 Dec;26(6):513-9.

PMID:
16287113
37.

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining.

Mangold E, Pagenstecher C, Friedl W, Fischer HP, Merkelbach-Bruse S, Ohlendorf M, Friedrichs N, Aretz S, Buettner R, Propping P, Mathiak M.

J Pathol. 2005 Dec;207(4):385-95.

PMID:
16216036
38.

[Detection of germline mutations in the APC gene with the protein truncation test].

Liu XR, Shan XN, Friedl W, Uhlhaas S, Li JT, Propping P, Wang YP.

Yi Chuan Xue Bao. 2005 Sep;32(9):903-8. Chinese.

PMID:
16201232
39.

[Soft tissue protective, stable osteosynthesis of fractures after elbow ankylosis. Two case reports].

Gehr J, Friedl W.

Unfallchirurg. 2005 Nov;108(11):998-1000. German.

PMID:
16133290
40.

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.

Krüger S, Silber AS, Engel C, Görgens H, Mangold E, Pagenstecher C, Holinski-Feder E, von Knebel Doeberitz M, Moeslein G, Dietmaier W, Stemmler S, Friedl W, Rüschoff J, Schackert HK; German Hereditary Non-Polyposis Colorectal Cancer Consortium.

Lancet Oncol. 2005 Aug;6(8):566-72.

PMID:
16054567
41.

Analysis of germline mutations in the APC gene in familial adenomatous polyposis patients.

Liu XR, Shan XN, Friedl W, Uhlhaas S, Propping P, Wang YP.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):261-4.

PMID:
15952110
42.

Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer.

Zhu M, Li J, Zhang X, Liu X, Friedl W, Zhang Y, Wu X, Propping P, Wang Y.

Cancer Genet Cytogenet. 2005 Jul 1;160(1):61-7.

PMID:
15949572
43.

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.

Wehner M, Mangold E, Sengteller M, Friedrichs N, Aretz S, Friedl W, Propping P, Pagenstecher C.

Eur J Hum Genet. 2005 Aug;13(8):983-6.

44.

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.

Mangold E, Pagenstecher C, Friedl W, Mathiak M, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Müller-Koch Y, Keller G, Schackert HK, Krüger S, Goecke T, Moeslein G, Kloor M, Gebert J, Kunstmann E, Schulmann K, Rüschoff J, Propping P.

Int J Cancer. 2005 Sep 20;116(5):692-702.

45.

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis.

Aretz S, Stienen D, Uhlhaas S, Pagenstecher C, Mangold E, Caspari R, Propping P, Friedl W.

J Med Genet. 2005 Feb;42(2):185-92. No abstract available.

46.

Bronchioloalveolar carcinoma: a new cancer in Peutz-Jeghers syndrome.

von Herbay A, Arens N, Friedl W, Vogt-Moykopf I, Kayser K, Müller KM, Back W.

Lung Cancer. 2005 Feb;47(2):283-8.

PMID:
15639728
47.

Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.

Friedl W, Aretz S.

Hered Cancer Clin Pract. 2005 Sep 15;3(3):95-114. doi: 10.1186/1897-4287-3-3-95.

48.

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W.

Hum Mutat. 2004 Nov;24(5):370-80.

PMID:
15459959
49.

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.

Mangold E, Pagenstecher C, Leister M, Mathiak M, Rütten A, Friedl W, Propping P, Ruzicka T, Kruse R.

J Med Genet. 2004 Jul;41(7):567-72. No abstract available.

50.

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