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Items: 1 to 50 of 78

1.

NeuroCog FX study: A multicenter cohort study on cognitive dysfunction in patients with early breast cancer.

Rick O, Reuß-Borst M, Dauelsberg T, Hass HG, König V, Caspari R, Götz-Keil G, Pfitzner J, Kerschgens C, Fliessbach K, Hoppe C.

Psychooncology. 2018 Aug;27(8):2016-2022. doi: 10.1002/pon.4763. Epub 2018 Jun 1.

PMID:
29771474
2.

Race, then and now: 1918 revisited.

Caspari R.

Am J Phys Anthropol. 2018 Apr;165(4):924-938. doi: 10.1002/ajpa.23417. No abstract available.

PMID:
29574831
3.

The Dubois syndrome.

Caspari R, Wolpoff MH.

Hist Philos Life Sci. 2012;34(1-2):33-42.

PMID:
23272593
4.

Diagnostic characteristics of S100A8/A9 in a multicenter study of patients with acute right lower quadrant abdominal pain.

Mills AM, Huckins DS, Kwok H, Baumann BM, Ruddy RM, Rothman RE, Schrock JW, Lovecchio F, Krief WI, Hexdall A, Caspari R, Cohen B, Lewis RJ.

Acad Emerg Med. 2012 Jan;19(1):48-55. doi: 10.1111/j.1553-2712.2011.01259.x. Epub 2012 Jan 5.

5.

The evolution of grandparents.

Caspari R.

Sci Am. 2011 Aug;305(2):44-9. No abstract available.

PMID:
21827124
6.

Arthroscopic laser meniscectomy in a gas medium. 1985.

Whipple TL, Caspari RB, Meyers JE.

Arthroscopy. 2010 Dec;26(12):1571-6. doi: 10.1016/j.arthro.2010.08.021. No abstract available.

PMID:
21112477
7.

1918: Three perspectives on race and human variation.

Caspari R.

Am J Phys Anthropol. 2009 May;139(1):5-15. doi: 10.1002/ajpa.20975.

PMID:
19226644
8.

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.

9.

New reconstruction of Krapina 5, a male Neandertal cranial vault from Krapina, Croatia.

Caspari R, Radovcić J.

Am J Phys Anthropol. 2006 Jul;130(3):294-307.

PMID:
16395724
10.

Is human longevity a consequence of cultural change or modern biology?

Caspari R, Lee SH.

Am J Phys Anthropol. 2006 Apr;129(4):512-7.

PMID:
16342259
11.

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.

12.
13.

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
14.

Older age becomes common late in human evolution.

Caspari R, Lee SH.

Proc Natl Acad Sci U S A. 2004 Jul 27;101(30):10895-900. Epub 2004 Jul 13.

15.

E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, beta-catenin and cyclooxygenase-2 expression.

Jungck M, Grünhage F, Spengler U, Dernac A, Mathiak M, Caspari R, Friedl W, Sauerbruch T.

Int J Colorectal Dis. 2004 Sep;19(5):438-45. Epub 2004 Feb 21.

PMID:
14986031
16.

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

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

Eur J Hum Genet. 2004 Jan;12(1):52-8.

17.

Allogeneic dendritic cells fused with tumor cells: preclinical results and outcome of a clinical phase I/II trial in patients with metastatic renal cell carcinoma.

Märten A, Renoth S, Heinicke T, Albers P, Pauli A, Mey U, Caspari R, Flieger D, Hanfland P, Von Ruecker A, Eis-Hübinger AM, Müller S, Schwaner I, Lohmann U, Heylmann G, Sauerbruch T, Schmidt-Wolf IG.

Hum Gene Ther. 2003 Mar 20;14(5):483-94.

PMID:
12691613
18.

Differences in pelvic floor area between African American and European American women.

Baragi RV, Delancey JO, Caspari R, Howard DH, Ashton-Miller JA.

Am J Obstet Gynecol. 2002 Jul;187(1):111-5.

PMID:
12114898
19.

Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis.

Lamberti C, Jungck M, Laarmann M, Knapp M, Caspari R, Friedl W, Sauerbruch T, Propping P, Kruse R.

Pharmacogenetics. 2002 Jan;12(1):49-54.

PMID:
11773864
20.

Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis.

Friedl W, Mangold E, Caspari R, Lamberti C, Propping P.

Gastroenterology. 2001 Aug;121(2):503-4. No abstract available.

PMID:
11494977
21.

Detection of APC and k-ras mutations in the serum of patients with colorectal cancer.

Lauschke H, Caspari R, Friedl W, Schwarz B, Mathiak M, Propping P, Hirner A.

Cancer Detect Prev. 2001;25(1):55-61.

PMID:
11270422
22.

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P.

Gut. 2001 Apr;48(4):515-21.

23.

Palmitate oxidation rate and action on glycogen synthase in myoblasts from insulin-resistant subjects.

Mott DM, Hoyt C, Caspari R, Stone K, Pratley R, Bogardus C.

Am J Physiol Endocrinol Metab. 2000 Sep;279(3):E561-9.

24.

Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26.

Caspari R, Uhlhaas S, Friedl W, Knapp M, Propping P.

Am J Med Genet. 2000 Aug 14;93(4):290-3.

PMID:
10946355
25.

Multiregional, not multiple origins.

Wolpoff MH, Hawks J, Caspari R.

Am J Phys Anthropol. 2000 May;112(1):129-36.

26.

[Therapy and after-care of familial adenomatous polyposis and hereditary colorectal carcinoma without polyposis].

Lamberti C, Jungck M, Caspari R, Schmidt-Wolf I, Sauerbruch T.

Dtsch Med Wochenschr. 2000 Feb 18;125(7):189-91. German. No abstract available.

PMID:
10719394
27.

[The diagnosis of hereditary colorectal carcinomas].

Caspari R, Jungck M, Lamberti C, Schmidt-Wolf IG, Friedl W, Propping P.

Dtsch Med Wochenschr. 2000 Feb 11;125(6):153-8. Review. German. No abstract available.

PMID:
10700879
28.

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.

Lamberti C, Kruse R, Ruelfs C, Caspari R, Wang Y, Jungck M, Mathiak M, Malayeri HR, Friedl W, Sauerbruch T, Propping P.

Gut. 1999 Jun;44(6):839-43.

29.

Arthroscopic transglenoid multiple suture repair: 2 to 8 year results in 150 shoulders.

Torchia ME, Caspari RB, Asselmeier MA, Beach WR, Gayari M.

Arthroscopy. 1997 Oct;13(5):609-19.

PMID:
9343651
30.

The arthroscopic treatment of posterior shoulder instability: two-year results of a multiple suture technique.

McIntyre LF, Caspari RB, Savoie FH 3rd.

Arthroscopy. 1997 Aug;13(4):426-32.

PMID:
9276047
31.

The arthroscopic treatment of multidirectional shoulder instability: two-year results of a multiple suture technique.

McIntyre LF, Caspari RB, Savoie FH 3rd.

Arthroscopy. 1997 Aug;13(4):418-25.

PMID:
9276046
32.

The role of phenylalanine at position 6 in glucagon's mechanism of biological action: multiple replacement analogues of glucagon.

Azizeh BY, Ahn JM, Caspari R, Shenderovich MD, Trivedi D, Hruby VJ.

J Med Chem. 1997 Aug 1;40(16):2555-62.

PMID:
9258362
33.
34.

Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.

Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W.

Hum Mutat. 1997;10(3):241-4. No abstract available.

PMID:
9298827
35.

[Early detection of colorectal carcinoma].

Caspari R, Mezger J, Sauerbruch T.

Med Klin (Munich). 1996 May 15;91(5):321; author reply 321-2. German. No abstract available.

PMID:
8709913
36.

Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein.

Friedl W, Meuschel S, Caspari R, Lamberti C, Krieger S, Sengteller M, Propping P.

Hum Genet. 1996 May;97(5):579-84.

PMID:
8655134
37.

Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patients.

Mandl M, Caspari R, Jauch A, Böker T, Raschke H, Sengteller M, Propping P, Friedl W.

Hum Genet. 1996 Feb;97(2):204-8.

PMID:
8566954
38.

The arthroscopic treatment of anterior and multidirectional shoulder instability.

McIntyre LF, Caspari RB, Savoie FH.

Instr Course Lect. 1996;45:47-56. Review. No abstract available.

PMID:
8727721
39.

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.

Caspari R, Olschwang S, Friedl W, Mandl M, Boisson C, Böker T, Augustin A, Kadmon M, Möslein G, Thomas G, et al.

Hum Mol Genet. 1995 Mar;4(3):337-40.

PMID:
7795585
40.

Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene.

Paffenholz R, Mandl M, Caspari R, Sengteller M, Propping P, Friedl W.

Hum Mol Genet. 1994 Sep;3(9):1703-4. No abstract available.

PMID:
7833936
41.

A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis.

Mandl M, Kadmon M, Sengteller M, Caspari R, Propping P, Friedl W.

Hum Mol Genet. 1994 Jun;3(6):1009-11. No abstract available.

PMID:
7951213
42.

Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer.

Caspari R, Friedl W, Mandl M, Möslein G, Kadmon M, Knapp M, Jacobasch KH, Ecker KW, Kreissler-Haag D, Timmermanns G, et al.

Lancet. 1994 Mar 12;343(8898):629-32. Erratum in: Lancet 1994 Apr 2;343(8901):863.

PMID:
7906810
43.

[Diagnosis of familial adenomatosis polyposis].

Friedl W, Caspari R, Propping P.

Dtsch Med Wochenschr. 1994 Jan 7;119(1-2):27-30. Review. German. No abstract available.

PMID:
8281879
44.

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P.

Hum Mol Genet. 1994 Jan;3(1):181-4.

PMID:
8162022
45.

Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.

Caspari R, Friedl W, Böker T, Augustin A, Mandl M, Jaeger K, Gallkowski K, Propping P.

Z Gastroenterol. 1993 Nov;31(11):646-52.

PMID:
8291275
46.

Arthroscopic management of rotator cuff disease.

Beach WR, Caspari RB.

Orthopedics. 1993 Sep;16(9):1007-15. Review.

PMID:
8234069
47.

Arthroscopic manifestations of shoulder subluxation and dislocation.

Caspari RB, Geissler WB.

Clin Orthop Relat Res. 1993 Jun;(291):54-66. Review.

PMID:
8504614
48.

A review of allograft processing and sterilization techniques and their role in transmission of the human immunodeficiency virus.

Asselmeier MA, Caspari RB, Bottenfield S.

Am J Sports Med. 1993 Mar-Apr;21(2):170-5. Review.

PMID:
8465908
49.

Arthroscopic anterior shoulder capsulorrhaphy.

Caspari RB, Beach WR.

Sports Med Arthrosc Rev. 1993 Winter;1(4):237-41.

PMID:
17630536
50.

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