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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1977 1
1979 1
1980 1
1981 1
1984 2
1985 1
1987 1
1988 1
1990 1
1991 1
1992 1
1993 1
1994 1
1997 3
1998 1
1999 2
2000 2
2001 2
2002 2
2003 2
2004 2
2005 4
2007 1
2008 8
2009 3
2010 7
2011 4
2012 3
2013 5
2014 5
2015 7
2016 8
2017 6
2018 3
2019 3
2020 9
2021 11
2022 11
2023 6
2024 1

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124 results

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Page 1
Cronkhite-Canada Syndrome.
Kwon J, Fluxá-Cardenas D, Francis D. Kwon J, et al. Clin Gastroenterol Hepatol. 2022 Jun;20(6):e1224-e1225. doi: 10.1016/j.cgh.2021.08.054. Epub 2021 Sep 4. Clin Gastroenterol Hepatol. 2022. PMID: 34492384 No abstract available.
Cronkhite-Canada syndrome.
Vashistha N, Chakravarty S, Singhal D. Vashistha N, et al. Gastrointest Endosc. 2017 Nov;86(5):922-923. doi: 10.1016/j.gie.2017.05.028. Epub 2017 May 30. Gastrointest Endosc. 2017. PMID: 28576394 No abstract available.
Cronkhite-Canada syndrome: treatment responses and improved overall survival.
Pham JT, Kisiel JB, Sweetser S. Pham JT, et al. Int J Colorectal Dis. 2023 Feb 13;38(1):39. doi: 10.1007/s00384-023-04332-w. Int J Colorectal Dis. 2023. PMID: 36781513
BACKGROUND: Cronkhite-Canada syndrome (CCS) is considered a relentlessly progressive disease with high mortality rates. ...
BACKGROUND: Cronkhite-Canada syndrome (CCS) is considered a relentlessly progressive disease with high mortality rates. …
Hamartomatous polyposis syndromes.
Calva D, Howe JR. Calva D, et al. Surg Clin North Am. 2008 Aug;88(4):779-817, vii. doi: 10.1016/j.suc.2008.05.002. Surg Clin North Am. 2008. PMID: 18672141 Free PMC article. Review.
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homolog gene (PTEN) hamartoma tumor syndromes (Cowden and Bannayan-Riley-Ruvalcaba syndromes), which are autosomal-dominantly inherited, and …
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homo …
Gastrointestinal polyposis with associated cutaneous manifestations.
Duarte M, Milikowski C. Duarte M, et al. Pathology. 2022 Mar;54(2):157-166. doi: 10.1016/j.pathol.2021.08.009. Epub 2021 Nov 9. Pathology. 2022. PMID: 34763900 Review.
In this review, we have focused on Lynch syndrome (hereditary nonpolyposis colon cancer and Muir-Torre syndrome), familial adenomatous polyposis, the hamartomatous polyposis syndromes that include Peutz-Jeghers syndrome and the PTEN hamartoma syndromes, which include Cowden syndr …
In this review, we have focused on Lynch syndrome (hereditary nonpolyposis colon cancer and Muir-Torre syndrome), familial adenomatous polyp …
Cronkhite-Canada syndrome: An investigation in clinical features and pathogenesis.
Zhu LP, Zhong WL, Wang ZG, Sun KD, Liu QLF, Zhao J, Zhao JW, Chen X, Wang BM. Zhu LP, et al. J Dig Dis. 2021 Nov;22(11):663-671. doi: 10.1111/1751-2980.13062. J Dig Dis. 2021. PMID: 34697888
OBJECTIVE: This study aimed to investigate the clinical features and potential pathogenesis of a rare nonhereditary polyposis syndrome, Cronkhite-Canada syndrome (CCS). METHODS: Medical records of eight patients with CCS who were admitted to our hospital from …
OBJECTIVE: This study aimed to investigate the clinical features and potential pathogenesis of a rare nonhereditary polyposis syndrome, C …
Cronkhite-Canada Syndrome Mimicking COVID-19-related Symptoms.
Miyawaki K, Komori T, Ishida Y, Sakaguchi Y, Honjo H, Kudo M, Otsuka A. Miyawaki K, et al. Acta Derm Venereol. 2022 Nov 7;102:adv00812. doi: 10.2340/actadv.v102.3402. Acta Derm Venereol. 2022. PMID: 36250761 Free PMC article. No abstract available.
Cronkhite-Canada Syndrome: A Case Report.
Sapkota P, Gurung RB, Shrestha A, Paudel I, Shrestha P. Sapkota P, et al. JNMA J Nepal Med Assoc. 2022 May 5;60(249):473-477. doi: 10.31729/jnma.7407. JNMA J Nepal Med Assoc. 2022. PMID: 35633239 Free PMC article.
Cronkhite-Canada Syndrome is a rare disease characterised by diffuse gastrointestinal polyposis, abdominal pain, diarrhoea, cutaneous and mucosal hyperpigmentation, alopecia, and onychodystrophy. Here we report a case of a 40-year-old female with Cronkhite …
Cronkhite-Canada Syndrome is a rare disease characterised by diffuse gastrointestinal polyposis, abdominal pain, diarrh …
Cronkhite-Canada syndrome.
Kim YS, Chun HJ, Jeen YT, Um SH, Kim CD, Hyun JH. Kim YS, et al. Gastrointest Endosc. 2004 Sep;60(3):432-3. doi: 10.1016/s0016-5107(04)01703-1. Gastrointest Endosc. 2004. PMID: 15332040 No abstract available.
Endoscopic and Pathological Characteristics of Cronkhite- Canada Syndrome: A Retrospective Analysis of 76 Cases.
Wang W, Shao Y, Zhao DH, Xue F, Ma XB, Li Q, Liu CX. Wang W, et al. Turk J Gastroenterol. 2022 Jan;33(1):19-29. doi: 10.5152/tjg.2021.20667. Turk J Gastroenterol. 2022. PMID: 35040784 Free PMC article.
BACKGROUND: Cronkhite-Canada syndrome (CCS) is a disease of unknown etiology characterized by the presence of multiple gastrointestinal polyps, chronic diarrhea, loss of appetite, alopecia, onychodystrophy, and cutaneous hyperpigmentation. ...
BACKGROUND: Cronkhite-Canada syndrome (CCS) is a disease of unknown etiology characterized by the presence of multiple …
124 results