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Showing 1 to 9 of 9 entries
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Laparoscopic lavage for perforated diverticulitis in the LapLav study: population-based registry study.

The British journal of surgery

Samuelsson A, Bock D, Prytz M, Block M, Ehrencrona C, Wedin A, Ahlstedt M, Angenete E, Haglind E.
PMID: 34148084
Br J Surg. 2021 Oct 23;108(10):1236-1242. doi: 10.1093/bjs/znab211.

BACKGROUND: The standard treatment for Hinchey III perforated diverticulitis with peritonitis was resection with or without a stoma, but recent trials have shown that laparoscopic lavage is a reasonable alternative. This registry-based Swedish study investigated results at a national...

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Samuelsson A, Bock D, Prytz M, et al. Laparoscopic lavage for perforated diverticulitis in the LapLav study: population-based registry study. Br J Surg. 2021;108(10):1236-1242doi: 10.1093/bjs/znab211.
Samuelsson, A., Bock, D., Prytz, M., Block, M., Ehrencrona, C., Wedin, A., Ahlstedt, M., Angenete, E., & Haglind, E. (2021). Laparoscopic lavage for perforated diverticulitis in the LapLav study: population-based registry study. The British journal of surgery, 108(10), 1236-1242. https://doi.org/10.1093/bjs/znab211
Samuelsson, A, et al. "Laparoscopic lavage for perforated diverticulitis in the LapLav study: population-based registry study." The British journal of surgery vol. 108,10 (2021): 1236-1242. doi: https://doi.org/10.1093/bjs/znab211
Samuelsson A, Bock D, Prytz M, Block M, Ehrencrona C, Wedin A, Ahlstedt M, Angenete E, Haglind E. Laparoscopic lavage for perforated diverticulitis in the LapLav study: population-based registry study. Br J Surg. 2021 Oct 23;108(10):1236-1242. doi: 10.1093/bjs/znab211. PMID: 34148084.
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Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein.

Molecular genetics & genomic medicine

Dominguez-Valentin M, Drost M, Therkildsen C, Rambech E, Ehrencrona H, Angleys M, Lau Hansen T, de Wind N, Nilbert M, Juel Rasmussen L.
PMID: 25077178
Mol Genet Genomic Med. 2014 Jul;2(4):352-5. doi: 10.1002/mgg3.80. Epub 2014 May 06.

In clinical genetic diagnostics, it is difficult to predict whether genetic mutations that do not greatly alter the primary sequence of the encoded protein causing unknown functional effects on cognate proteins lead to development of disease. Here, we report...

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Dominguez-Valentin M, Drost M, Therkildsen C, et al. Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein. Mol Genet Genomic Med. 2014;2(4):352-5doi: 10.1002/mgg3.80.
Dominguez-Valentin, M., Drost, M., Therkildsen, C., Rambech, E., Ehrencrona, H., Angleys, M., Lau Hansen, T., de Wind, N., Nilbert, M., & Juel Rasmussen, L. (2014). Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein. Molecular genetics & genomic medicine, 2(4), 352-5. https://doi.org/10.1002/mgg3.80
Dominguez-Valentin, Mev, et al. "Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein." Molecular genetics & genomic medicine vol. 2,4 (2014): 352-5. doi: https://doi.org/10.1002/mgg3.80
Dominguez-Valentin M, Drost M, Therkildsen C, Rambech E, Ehrencrona H, Angleys M, Lau Hansen T, de Wind N, Nilbert M, Juel Rasmussen L. Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein. Mol Genet Genomic Med. 2014 Jul;2(4):352-5. doi: 10.1002/mgg3.80. Epub 2014 May 06. PMID: 25077178; PMCID: PMC4113276.
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Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.

Hereditary cancer in clinical practice

Andersson A, Hawranek C, Öfverholm A, Ehrencrona H, Grill K, Hajdarevic S, Melin B, Tham E, Hellquist BN, Rosén A.
PMID: 32944097
Hered Cancer Clin Pract. 2020 Sep 15;18:18. doi: 10.1186/s13053-020-00151-0. eCollection 2020.

BACKGROUND: Targeted surveillance of at-risk individuals in families with increased risk of hereditary cancer is an effective prevention strategy if relatives are identified, informed and enrolled in screening programs. Despite the potential benefits, many eligible at-risk relatives remain uninformed...

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Andersson A, Hawranek C, Öfverholm A, et al. Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden. Hered Cancer Clin Pract. 2020;18:18doi: 10.1186/s13053-020-00151-0.
Andersson, A., Hawranek, C., Öfverholm, A., Ehrencrona, H., Grill, K., Hajdarevic, S., Melin, B., Tham, E., Hellquist, B. N., & Rosén, A. (2020). Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden. Hereditary cancer in clinical practice, 1818. https://doi.org/10.1186/s13053-020-00151-0
Andersson, Andreas, et al. "Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden." Hereditary cancer in clinical practice vol. 18 (2020): 18. doi: https://doi.org/10.1186/s13053-020-00151-0
Andersson A, Hawranek C, Öfverholm A, Ehrencrona H, Grill K, Hajdarevic S, Melin B, Tham E, Hellquist BN, Rosén A. Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden. Hered Cancer Clin Pract. 2020 Sep 15;18:18. doi: 10.1186/s13053-020-00151-0. eCollection 2020. PMID: 32944097; PMCID: PMC7493346.
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The Spectrum of .

Cancers

Figlioli G, Kvist A, Tham E, Soukupova J, Kleiblova P, Muranen TA, Andrieu N, Azzollini J, Balmaña J, Barroso A, Benítez J, Bertelsen B, Blanco A, Bonanni B, Borg Å, Brunet J, Calistri D, Calvello M, Chvojka S, Cortesi L, Darder E, Del Valle J, Diez O, Eon-Marchais S, Fostira F, Gensini F, Houdayer C, Janatova M, Kiiski JI, Konstantopoulou I, Kubelka-Sabit K, Lázaro C, Lesueur F, Manoukian S, Marcinkute R, Mickys U, Moncoutier V, Myszka A, Nguyen-Dumont T, Nielsen FC, Norvilas R, Olah E, Osorio A, Papi L, Peissel B, Peixoto A, Plaseska-Karanfilska D, Pócza T, Rossing M, Rudaitis V, Santamariña M, Santos C, Smichkoska S, Southey MC, Stoppa-Lyonnet D, Teixeira M, Törngren T, Toss A, Urioste M, Vega A, Vlckova Z, Yannoukakos D, Zampiga V, Kleibl Z, Radice P, Nevanlinna H, Ehrencrona H, Janavicius R, Peterlongo P.
PMID: 31991861
Cancers (Basel). 2020 Jan 26;12(2). doi: 10.3390/cancers12020292.

Germline protein truncating variants (PTVs) in the

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Figlioli G, Kvist A, Tham E, et al. The Spectrum of . Cancers (Basel). 2020;12(2)doi: 10.3390/cancers12020292.
Figlioli, G., Kvist, A., Tham, E., Soukupova, J., Kleiblova, P., Muranen, T. A., Andrieu, N., Azzollini, J., Balmaña, J., Barroso, A., Benítez, J., Bertelsen, B., Blanco, A., Bonanni, B., Borg, �. �., Brunet, J., Calistri, D., Calvello, M., Chvojka, S., Cortesi, L., Darder, E., Del Valle, J., Diez, O., Eon-Marchais, S., Fostira, F., Gensini, F., Houdayer, C., Janatova, M., Kiiski, J. I., Konstantopoulou, I., Kubelka-Sabit, K., Lázaro, C., Lesueur, F., Manoukian, S., Marcinkute, R., Mickys, U., Moncoutier, V., Myszka, A., Nguyen-Dumont, T., Nielsen, F. C., Norvilas, R., Olah, E., Osorio, A., Papi, L., Peissel, B., Peixoto, A., Plaseska-Karanfilska, D., Pócza, T., Rossing, M., Rudaitis, V., Santamariña, M., Santos, C., Smichkoska, S., Southey, M. C., Stoppa-Lyonnet, D., Teixeira, M., Törngren, T., Toss, A., Urioste, M., Vega, A., Vlckova, Z., Yannoukakos, D., Zampiga, V., Kleibl, Z., Radice, P., Nevanlinna, H., Ehrencrona, H., Janavicius, R., & Peterlongo, P. (2020). The Spectrum of . Cancers, 12(2), . https://doi.org/10.3390/cancers12020292
Figlioli, Gisella, et al. "The Spectrum of ." Cancers vol. 12,2 (2020). doi: https://doi.org/10.3390/cancers12020292
Figlioli G, Kvist A, Tham E, Soukupova J, Kleiblova P, Muranen TA, Andrieu N, Azzollini J, Balmaña J, Barroso A, Benítez J, Bertelsen B, Blanco A, Bonanni B, Borg Å, Brunet J, Calistri D, Calvello M, Chvojka S, Cortesi L, Darder E, Del Valle J, Diez O, Eon-Marchais S, Fostira F, Gensini F, Houdayer C, Janatova M, Kiiski JI, Konstantopoulou I, Kubelka-Sabit K, Lázaro C, Lesueur F, Manoukian S, Marcinkute R, Mickys U, Moncoutier V, Myszka A, Nguyen-Dumont T, Nielsen FC, Norvilas R, Olah E, Osorio A, Papi L, Peissel B, Peixoto A, Plaseska-Karanfilska D, Pócza T, Rossing M, Rudaitis V, Santamariña M, Santos C, Smichkoska S, Southey MC, Stoppa-Lyonnet D, Teixeira M, Törngren T, Toss A, Urioste M, Vega A, Vlckova Z, Yannoukakos D, Zampiga V, Kleibl Z, Radice P, Nevanlinna H, Ehrencrona H, Janavicius R, Peterlongo P. The Spectrum of . Cancers (Basel). 2020 Jan 26;12(2). doi: 10.3390/cancers12020292. PMID: 31991861; PMCID: PMC7073216.
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Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey.

Journal of community genetics

Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Schmidt MK, Dolbeault S, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutlzer R.
PMID: 29508368
J Community Genet. 2019 Jan;10(1):61-71. doi: 10.1007/s12687-018-0362-8. Epub 2018 Mar 05.

The BOADICEA breast cancer (BC) risk assessment model and its associated Web Application v3 (BWA) tool are being extended to incorporate additional genetic and non-genetic BC risk factors. From an online survey through the BOADICEA website and UK, Dutch,...

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Brédart A, Kop JL, Antoniou AC, et al. Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. J Community Genet. 2018;10(1):61-71doi: 10.1007/s12687-018-0362-8.
Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., De Pauw, A., Tischkowitz, M., Ehrencrona, H., Schmidt, M. K., Dolbeault, S., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D., & Schmutlzer, R. (2019). Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. Journal of community genetics, 10(1), 61-71. https://doi.org/10.1007/s12687-018-0362-8
Brédart, Anne, et al. "Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey." Journal of community genetics vol. 10,1 (2019): 61-71. doi: https://doi.org/10.1007/s12687-018-0362-8
Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Schmidt MK, Dolbeault S, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutlzer R. Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. J Community Genet. 2019 Jan;10(1):61-71. doi: 10.1007/s12687-018-0362-8. Epub 2018 Mar 05. PMID: 29508368; PMCID: PMC6325038.
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Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.

Familial cancer

Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Dolbeault S, Robieux L, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutlzer R.
PMID: 29071503
Fam Cancer. 2018 Jul;17(3):469. doi: 10.1007/s10689-017-0051-5.

The article "Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries" written by Anne Brédart · Jean‑Luc Kop · Antonis C. Antoniou · Alex P. Cunningham · Antoine De Pauw ·Marc Tischkowitz ·...

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Brédart A, Kop JL, Antoniou AC, et al. Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries. Fam Cancer. 2018;17(3):469doi: 10.1007/s10689-017-0051-5.
Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., De Pauw, A., Tischkowitz, M., Ehrencrona, H., Dolbeault, S., Robieux, L., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D., & Schmutlzer, R. (2018). Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries. Familial cancer, 17(3), 469. https://doi.org/10.1007/s10689-017-0051-5
Brédart, Anne, et al. "Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries." Familial cancer vol. 17,3 (2018): 469. doi: https://doi.org/10.1007/s10689-017-0051-5
Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Dolbeault S, Robieux L, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutlzer R. Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries. Fam Cancer. 2018 Jul;17(3):469. doi: 10.1007/s10689-017-0051-5. PMID: 29071503; PMCID: PMC6828123.
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Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome.

Journal of community genetics

Henriksson I, Henriksson K, Ehrencrona H, Gebre-Medhin S.
PMID: 30251116
J Community Genet. 2019 Apr;10(2):259-266. doi: 10.1007/s12687-018-0385-1. Epub 2018 Sep 24.

Overlapping phenotypes between different hereditary colorectal cancer (CRC) syndromes together with a growing demand for cancer genetic testing and improved sequencing technology call for adjusted patient selection and adapted diagnostic routines. Here we present a retrospective evaluation of family...

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Henriksson I, Henriksson K, Ehrencrona H, et al. Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome. J Community Genet. 2018;10(2):259-266doi: 10.1007/s12687-018-0385-1.
Henriksson, I., Henriksson, K., Ehrencrona, H., & Gebre-Medhin, S. (2019). Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome. Journal of community genetics, 10(2), 259-266. https://doi.org/10.1007/s12687-018-0385-1
Henriksson, Isabelle, et al. "Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome." Journal of community genetics vol. 10,2 (2019): 259-266. doi: https://doi.org/10.1007/s12687-018-0385-1
Henriksson I, Henriksson K, Ehrencrona H, Gebre-Medhin S. Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome. J Community Genet. 2019 Apr;10(2):259-266. doi: 10.1007/s12687-018-0385-1. Epub 2018 Sep 24. PMID: 30251116; PMCID: PMC6435770.
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Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey.

Journal of community genetics

Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Schmidt MK, Dolbeault S, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutzler R.
PMID: 31332717
J Community Genet. 2019 Oct;10(4):531. doi: 10.1007/s12687-019-00431-w.

The published online version contains mistake in author list. The correct presentation of the name Rita Schmutlzer is Rita Schmutzler.

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Brédart A, Kop JL, Antoniou AC, et al. Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. J Community Genet. 2019;10(4):531doi: 10.1007/s12687-019-00431-w.
Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., De Pauw, A., Tischkowitz, M., Ehrencrona, H., Schmidt, M. K., Dolbeault, S., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D., & Schmutzler, R. (2019). Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. Journal of community genetics, 10(4), 531. https://doi.org/10.1007/s12687-019-00431-w
Brédart, Anne, et al. "Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey." Journal of community genetics vol. 10,4 (2019): 531. doi: https://doi.org/10.1007/s12687-019-00431-w
Brédart A, Kop JL, Antoniou AC, Cunningham AP, De Pauw A, Tischkowitz M, Ehrencrona H, Schmidt MK, Dolbeault S, Rhiem K, Easton DF, Devilee P, Stoppa-Lyonnet D, Schmutzler R. Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey. J Community Genet. 2019 Oct;10(4):531. doi: 10.1007/s12687-019-00431-w. PMID: 31332717; PMCID: PMC6754473.
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Effect of Short-Term Homebased Pre- and Postoperative Exercise on Recovery after Colorectal Cancer Surgery (PHYSSURG-C): A Randomized Clinical Trial.

Annals of surgery

Onerup A, Andersson J, Angenete E, Bock D, Börjesson M, Ehrencrona C, Olsén MF, Larsson PA, de la Croix H, Wedin A, Haglind E.
PMID: 33843798
Ann Surg. 2021 Apr 09; doi: 10.1097/SLA.0000000000004901. Epub 2021 Apr 09.

OBJECTIVE: To determine the effect of a short-term, unsupervised exercise intervention before and after colorectal cancer surgery on self-assessed physical recovery.SUMMARY BACKGROUND DATA: Preoperative exercise interventions could help improve recovery after colorectal cancer surgery and is currently recommended.METHODS: A...

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Onerup A, Andersson J, Angenete E, et al. Effect of Short-Term Homebased Pre- and Postoperative Exercise on Recovery after Colorectal Cancer Surgery (PHYSSURG-C): A Randomized Clinical Trial. Ann Surg. 2021;doi: 10.1097/SLA.0000000000004901.
Onerup, A., Andersson, J., Angenete, E., Bock, D., Börjesson, M., Ehrencrona, C., Olsén, M. F., Larsson, P. A., de la Croix, H., Wedin, A., & Haglind, E. (2021). Effect of Short-Term Homebased Pre- and Postoperative Exercise on Recovery after Colorectal Cancer Surgery (PHYSSURG-C): A Randomized Clinical Trial. Annals of surgery, . https://doi.org/10.1097/SLA.0000000000004901
Onerup, Aron, et al. "Effect of Short-Term Homebased Pre- and Postoperative Exercise on Recovery after Colorectal Cancer Surgery (PHYSSURG-C): A Randomized Clinical Trial." Annals of surgery vol. (2021). doi: https://doi.org/10.1097/SLA.0000000000004901
Onerup A, Andersson J, Angenete E, Bock D, Börjesson M, Ehrencrona C, Olsén MF, Larsson PA, de la Croix H, Wedin A, Haglind E. Effect of Short-Term Homebased Pre- and Postoperative Exercise on Recovery after Colorectal Cancer Surgery (PHYSSURG-C): A Randomized Clinical Trial. Ann Surg. 2021 Apr 09; doi: 10.1097/SLA.0000000000004901. Epub 2021 Apr 09. PMID: 33843798.
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