R. Caspari

发表

Comparison of capsule endoscopy and magnetic resonance imaging for the detection of polyps of the small intestine in patients with familial adenomatous polyposis or with Peutz-Jeghers' syndrome.

H. Schild, M. von Falkenhausen, T. Sauerbruch, 2004, Endoscopy.

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

P. Propping, S. Aretz, R. Caspari, 2006, International journal of cancer.

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

P. Propping, A. Hirner, R. Caspari, 2001, Cancer detection and prevention.

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

T. Sauerbruch, P. Propping, M. Knapp, 2002, Pharmacogenetics.

Clinical Protocol 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

P. Albers, T. Sauerbruch, R. Caspari, 2003 .

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

P. Propping, R. Caspari, W. Friedl, 1994, Human molecular genetics.

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

K. Fliessbach, H. Hass, C. Hoppe, 2017, Psycho-oncology.

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

T. Sauerbruch, P. Propping, R. Kruse, 1999, Gut.

Efficacy and Safety of a Personalized Vitamin D3 Loading Dose Followed by Daily 2000 IU in Colorectal Cancer Patients with Vitamin D Insufficiency: Interim Analysis of a Randomized Controlled Trial

B. Schöttker, A. Kopp-Schneider, R. Caspari, 2022, Nutrients.

Patient competencies, coping self‐efficacy, and coping: Do they change during oncological inpatient rehabilitation and beyond?

J. Weis, R. Caspari, H. Bartsch, 2021, Psycho-oncology.

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.

P. Albers, T. Sauerbruch, I. Schmidt-Wolf, 2003, Human gene therapy.

Reliability of presymptomatic test for adenomatous polyposis coli

P. Laurent-Puig, P. Propping, S. Olschwang, 1991, The Lancet.

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

P. Propping, R. Kruse, R. Caspari, 1997 .

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

P. Propping, R. Caspari, E. Mangold, 2005, Journal of Medical Genetics.

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

J. Gebert, P. Propping, G. Möslein, 2001, Gut.

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

U. Spengler, R. Caspari, W. Friedl, 2004, International Journal of Colorectal Disease.

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

P. Propping, S. Aretz, R. Caspari, 2004, European Journal of Human Genetics.

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

K. Schulmann, P. Propping, S. Aretz, 2004, Human mutation.

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

G. Thomas, P. Propping, S. Olschwang, 1995, Human molecular genetics.

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

P. Propping, R. Caspari, E. Mangold, 2001, Gastroenterology.

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

P. Propping, M. Knapp, G. Möslein, 1994, The Lancet.

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

P. Propping, R. Kruse, R. Caspari, 1997, Human mutation.

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

P. Propping, A. Augustin, R. Caspari, 1993, Zeitschrift fur Gastroenterologie.

Protocol of the optimal study: Optimization of polypharmacy in geriatric oncology - A randomized controlled trial

B. Schöttker, R. Caspari, H. Brenner, 2023, BMC Cancer.

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

A. Jauch, P. Propping, R. Caspari, 1996, Human Genetics.

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

P. Propping, S. Krieger, R. Caspari, 1996, Human Genetics.

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

P. Propping, R. Caspari, W. Friedl, 1994, Human molecular genetics.

Protocol of the VICTORIA study: personalized vitamin D supplementation for reducing or preventing fatigue and enhancing quality of life of patients with colorectal tumor - randomized intervention trial

H. Brenner, B. Schöttker, A. Kopp-Schneider, 2020, BMC Cancer.

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

P. Propping, R. Caspari, W. Friedl, 2000, American journal of medical genetics.

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

P. Propping, R. Caspari, W. Friedl, 1996, Human Genetics.

Development Trajectories of Fatigue, Quality of Life, and the Ability to Work among Colorectal Cancer Patients in the First Year after Rehabilitation—First Results of the MIRANDA Study

B. Schöttker, R. Caspari, H. Brenner, 2023, Cancers.

Einfluss klinischer, sozialmedizinischer und psychologischer Faktoren auf die berufliche Reintegration von Patientinnen mit Brustkrebs 6 Monate nach der Rehabilitation

K. Fliessbach, H. Hass, C. Hoppe, 2021, Die Rehabilitation.

Misleading phenotype in kindred with familial adenomatous polyposis

P. Propping, R. Caspari, W. Friedl, 1992, The Lancet.