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

Year Number of Results
1950 2
1952 1
1953 1
1954 1
1955 4
1956 3
1957 6
1958 1
1959 1
1960 3
1961 6
1962 6
1963 10
1964 7
1965 8
1966 3
1967 5
1968 4
1969 4
1970 3
1971 11
1972 9
1973 2
1974 6
1975 5
1976 6
1977 4
1978 4
1979 10
1980 9
1981 12
1982 10
1983 12
1984 8
1985 16
1986 17
1987 15
1988 16
1989 24
1990 13
1991 11
1992 10
1993 18
1994 11
1995 7
1996 16
1997 9
1998 7
1999 10
2000 10
2001 7
2002 14
2003 6
2004 3
2005 6
2006 3
2007 3
2008 5
2009 8
2010 5
2011 14
2012 24
2013 48
2014 44
2015 46
2016 36
2017 42
2018 61
2019 49
2020 61
2021 65
2022 57
2023 77
2024 87
2025 80

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1,107 results

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Page 1
Progression of skin lesions in Warburg-Cinotti syndrome.
Ours CA, Biesecker LG, Darling TN. Ours CA, et al. JAAD Case Rep. 2021 Dec 15;20:47-49. doi: 10.1016/j.jdcr.2021.12.006. eCollection 2022 Feb. JAAD Case Rep. 2021. PMID: 35036505 Free PMC article. No abstract available.
Warburg-Cinotti disease variant p.Tyr740Cys enhances catalytic activity of DDR2 kinase.
Hao Z, Leitinger B. Hao Z, et al. PLoS One. 2025 Nov 19;20(11):e0336895. doi: 10.1371/journal.pone.0336895. eCollection 2025. PLoS One. 2025. PMID: 41259339 Free PMC article.
Missense mutations in the DDR2 kinase domain cause Warburg-Cinotti syndrome in an autosomal dominant manner. Warburg-Cinotti syndrome is a severe connective tissue disorder, characterised by a range of manifestations including joint contractures of the hand, corneal …
Missense mutations in the DDR2 kinase domain cause Warburg-Cinotti syndrome in an autosomal dominant manner. Warburg-Cinotti s …
In Reply.
Cinotti R, Roquilly A, Asehnoune K. Cinotti R, et al. Anesthesiology. 2018 Mar;128(3):687. doi: 10.1097/ALN.0000000000002072. Anesthesiology. 2018. PMID: 29438256 No abstract available.
An update on remimazolam and anaphylaxis.
Cinotti R. Cinotti R. Eur J Anaesthesiol. 2023 Mar 1;40(3):153-154. doi: 10.1097/EJA.0000000000001794. Eur J Anaesthesiol. 2023. PMID: 36722186 No abstract available.
Fulguration-induced tattoo.
Cinotti E, Bruzziches F, Habougit C, Berot V, Tognetti L, Rubegni P, Perrot JL. Cinotti E, et al. Clin Exp Dermatol. 2020 Oct;45(7):911-912. doi: 10.1111/ced.14288. Epub 2020 Jun 23. Clin Exp Dermatol. 2020. PMID: 32415991 No abstract available.
Progressive conjunctival invasion of cornea in a child with Warburg-Cinotti Syndrome: a case report.
Ben H, Liu X, Zhang P, Hong J. Ben H, et al. BMC Ophthalmol. 2024 Aug 2;24(1):322. doi: 10.1186/s12886-024-03596-2. BMC Ophthalmol. 2024. PMID: 39095787 Free PMC article.
BACKGROUND: Warburg-Cinotti syndrome is a rare syndrome caused by de novo or inherited variants in discoding domain receptor tyrosine kinase 2 (DDR2). ...Whole exome sequencing revealed a hemizygous variant in the DDR2 gene, which is consistent with Warburg-Cinotti …
BACKGROUND: Warburg-Cinotti syndrome is a rare syndrome caused by de novo or inherited variants in discoding domain receptor tyrosine …
Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome.
Xu L, Jensen H, Johnston JJ, Di Maria E, Kloth K, Cristea I, Sapp JC, Darling TN, Huryn LA, Tranebjærg L, Cinotti E, Kubisch C, Rødahl E, Bruland O, Biesecker LG, Houge G, Bredrup C. Xu L, et al. Am J Hum Genet. 2018 Dec 6;103(6):976-983. doi: 10.1016/j.ajhg.2018.10.013. Epub 2018 Nov 15. Am J Hum Genet. 2018. PMID: 30449416 Free PMC article.
We propose this progressive, fibrotic condition should be designated as Warburg-Cinotti syndrome....
We propose this progressive, fibrotic condition should be designated as Warburg-Cinotti syndrome....
The Immunogenetics of Psoriasis.
Trovato E, Rubegni P, Cinotti E. Trovato E, et al. Adv Exp Med Biol. 2022;1367:105-117. doi: 10.1007/978-3-030-92616-8_4. Adv Exp Med Biol. 2022. PMID: 35286693
1,107 results