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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 79
2001 64
2002 69
2003 77
2004 52
2005 69
2006 87
2007 61
2008 69
2009 60
2010 85
2011 67
2012 77
2013 101
2014 101
2015 108
2016 107
2017 105
2018 108
2019 98
2020 84
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2,501 results
Results by year
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Page 1
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.
CREST Syndrome: Clinical Expression of the Disease.
Arana-Guajardo A, Villarreal-Alarcón M. Arana-Guajardo A, et al. J Clin Rheumatol. 2017 Aug;23(5):285. doi: 10.1097/RHU.0000000000000491. J Clin Rheumatol. 2017. PMID: 28742726 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 …
PBC and related extrahepatic diseases.
Floreani A, Cazzagon N. Floreani A, et al. Best Pract Res Clin Gastroenterol. 2018 Jun-Aug;34-35:49-54. doi: 10.1016/j.bpg.2018.05.013. Epub 2018 May 23. Best Pract Res Clin Gastroenterol. 2018. PMID: 30343710 Review.
Botulinum toxin for treatment of Raynaud phenomenon in CREST syndrome.
Berk-Krauss J, Christman MP, Franks A, Sicco KL, Liebman TN. Berk-Krauss J, et al. Dermatol Online J. 2018 Dec 15;24(12):13030/qt9zr1318w. Dermatol Online J. 2018. PMID: 30677800 Free article.
Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome is a form of a rare, clinical subtype of systemic sclerosis, known as limited systemic sclerosis. Limited systemic sclerosis, including CREST syndrom
Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome is a form of a rare …
[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.
[Systemic sclerosis].
Schinke S, Riemekasten G. Schinke S, et al. Internist (Berl). 2019 Dec;60(12):1251-1269. doi: 10.1007/s00108-019-00699-7. Internist (Berl). 2019. PMID: 31754753 Review. German.
Systemic Sclerosis (CREST syndrome).
Adigun R, Goyal A, Bansal P, Hariz A. Adigun R, et al. 2020 Aug 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. StatPearls. 2020 Jan–. PMID: 28613625 Free Books & Documents. Review.
Scleroderma can be divided into two forms, Localized Scleroderma (Morphea, Linear Scleroderma and Scleroderma en coup de sabre), or Systemic sclerosis, which can further be classified as either Limited cutaneous Systemic Sclerosis (formerly known as the CREST syndrome
Scleroderma can be divided into two forms, Localized Scleroderma (Morphea, Linear Scleroderma and Scleroderma en coup de sabre), or Systemic …
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 2 includes a grandmother and grandson with CREST scleroderma as well as a family member with Ra …
The familial occurrence of scleroderma is uncommon particularly the limited (CREST) form. We describe 2 families in which such an ass …
[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.
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