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Results by year

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

Year Number of Results
1965 2
1966 1
1967 1
1969 1
1970 1
1971 3
1972 1
1974 1
1975 5
1976 7
1977 9
1978 7
1979 18
1980 15
1981 11
1982 19
1983 29
1984 49
1985 33
1986 38
1987 36
1988 39
1989 50
1990 51
1991 50
1992 36
1993 51
1994 56
1995 65
1996 61
1997 59
1998 63
1999 67
2000 78
2001 64
2002 69
2003 77
2004 53
2005 69
2006 87
2007 61
2008 69
2009 60
2010 85
2011 67
2012 77
2013 102
2014 101
2015 108
2016 107
2017 105
2018 109
2019 99
2020 118
2021 121
2022 115
2023 99
2024 96

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2,918 results

Results by year

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Page 1
CREST syndrome.
Kumar A, Sharma A, Agarwal A. Kumar A, et al. Postgrad Med J. 2021 Nov;97(1153):746. doi: 10.1136/postgradmedj-2020-138817. Epub 2020 Sep 3. Postgrad Med J. 2021. PMID: 32883767 No abstract available.
Crest Syndrome.
Kumar P, Das A. Kumar P, et al. Skinmed. 2016 Feb 1;14(1):43. eCollection 2016. Skinmed. 2016. PMID: 27072730 No abstract available.
Biventricular affection in CREST syndrome.
Brugger M, Steger A, Okrojek R, Gaa J, Ibrahim T. Brugger M, et al. Eur Heart J Cardiovasc Imaging. 2021 Aug 14;22(9):e146. doi: 10.1093/ehjci/jeab068. Eur Heart J Cardiovasc Imaging. 2021. PMID: 33963836 No abstract available.
[CREST syndrome].
Meyer O. Meyer O. Ann Med Interne (Paris). 2002 May;153(3):183-8. Ann Med Interne (Paris). 2002. PMID: 12218901 French.
Antinuclear antibodies recognizing chromosomal centromere proteins are characteristic of CREST syndrome and are present in more than 50% of the cases. The prognosis of CREST syndrome is relatively good with a long lasting disease duration (>10 years …
Antinuclear antibodies recognizing chromosomal centromere proteins are characteristic of CREST syndrome and are present in mor …
[CREST syndrome].
Ohtani H, Imai H. Ohtani H, et al. Ryoikibetsu Shokogun Shirizu. 1997;(17 Pt 2):377-9. Ryoikibetsu Shokogun Shirizu. 1997. PMID: 9277943 Review. Japanese. No abstract available.
CREST Syndrome in Systemic Sclerosis Patients - Is Dystrophic Calcinosis a Key Element to a Positive Diagnosis?
Bobeica C, Niculet E, Craescu M, Parapiru EL, Musat CL, Dinu C, Chiscop I, Nechita L, Debita M, Stefanescu V, Stefanopol IA, Nechifor A, Pelin AM, Balan G, Chirobocea S, Vasile CI, Tatu AL. Bobeica C, et al. J Inflamm Res. 2022 Jun 9;15:3387-3394. doi: 10.2147/JIR.S361667. eCollection 2022. J Inflamm Res. 2022. PMID: 35706527 Free PMC article.
INTRODUCTION: CREST syndrome is a clinical entity associated with systemic sclerosis, which meets at least three of the five clinical features: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia. Three of these clinical featu …
INTRODUCTION: CREST syndrome is a clinical entity associated with systemic sclerosis, which meets at least three of the five c …
Pseudo-ainhum in a patient with CREST syndrome.
Darlenski R, Popov Y, Dourmishev L, Balabanova M, Vassileva S. Darlenski R, et al. Int J Dermatol. 2020 Sep;59(9):1163-1164. doi: 10.1111/ijd.15014. Epub 2020 Jun 18. Int J Dermatol. 2020. PMID: 32557599 No abstract available.
[CREST or CREIST syndrome?].
Lévesque H, Marie I. Lévesque H, et al. J Mal Vasc. 1999 Feb;24(1):7-9. J Mal Vasc. 1999. PMID: 10192029 Review. French. No abstract available.
Familial CREST syndrome.
McColl GJ, Buchanan RR. McColl GJ, et al. J Rheumatol. 1994 Apr;21(4):754-6. J Rheumatol. 1994. PMID: 8035406 Review.
The familial occurrence of scleroderma is uncommon particularly the limited (CREST) form. We describe 2 families in which such an association occurred. Family pedigree 1 consists of 2 of 3 sisters with CREST scleroderma. ...Family pedigree 2 includes a grandmother a …
The familial occurrence of scleroderma is uncommon particularly the limited (CREST) form. We describe 2 families in which such an ass …
PACK syndrome: A case series and review.
Collins B, Dillon D, Silver RM. Collins B, et al. Am J Med Sci. 2023 Apr;365(4):321-328. doi: 10.1016/j.amjms.2022.12.005. Epub 2022 Dec 16. Am J Med Sci. 2023. PMID: 36535538 Review.
A rare overlap syndrome between CREST (calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome and primary biliary cholangitis (PBC) is described as PACK syndrome, an acronym for primary biliary cholangitis, …
A rare overlap syndrome between CREST (calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectas …
2,918 results