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

Year Number of Results
1977 1
1982 1
1983 2
1984 1
1985 4
1987 2
1988 5
1989 3
1990 1
1991 3
1992 1
1993 5
1994 6
1995 3
1996 4
1997 4
1998 6
1999 4
2000 2
2001 2
2002 2
2003 2
2004 2
2005 1
2006 5
2007 6
2008 4
2009 2
2010 4
2011 4
2012 7
2013 11
2014 8
2015 11
2016 7
2017 5
2018 5
2019 5
2020 2
2021 3
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Search Results

139 results
Results by year
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Page 1
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Among authors: tadini g. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome.
Wang H, Humbatova A, Liu Y, Qin W, Lee M, Cesarato N, Kortüm F, Kumar S, Romano MT, Dai S, Mo R, Sivalingam S, Motameny S, Wu Y, Wang X, Niu X, Geng S, Bornholdt D, Kroisel PM, Tadini G, Walter SD, Hauck F, Girisha KM, Calza AM, Bottani A, Altmüller J, Buness A, Yang S, Sun X, Ma L, Kutsche K, Grzeschik KH, Betz RC, Lin Z. Wang H, et al. Among authors: tadini g. Am J Hum Genet. 2020 Jul 2;107(1):34-45. doi: 10.1016/j.ajhg.2020.05.006. Epub 2020 Jun 3. Am J Hum Genet. 2020. PMID: 32497488 Free PMC article.
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.
Oji V, Tadini G, Akiyama M, Blanchet Bardon C, Bodemer C, Bourrat E, Coudiere P, DiGiovanna JJ, Elias P, Fischer J, Fleckman P, Gina M, Harper J, Hashimoto T, Hausser I, Hennies HC, Hohl D, Hovnanian A, Ishida-Yamamoto A, Jacyk WK, Leachman S, Leigh I, Mazereeuw-Hautier J, Milstone L, Morice-Picard F, Paller AS, Richard G, Schmuth M, Shimizu H, Sprecher E, Van Steensel M, Taïeb A, Toro JR, Vabres P, Vahlquist A, Williams M, Traupe H. Oji V, et al. Among authors: tadini g. J Am Acad Dermatol. 2010 Oct;63(4):607-41. doi: 10.1016/j.jaad.2009.11.020. J Am Acad Dermatol. 2010. PMID: 20643494 Review.
Hutchinson-Gilford progeria.
Brena M, Besagni F, Gelmetti C, Tadini G. Brena M, et al. Among authors: tadini g. G Ital Dermatol Venereol. 2015 Jun;150(3):339-41. G Ital Dermatol Venereol. 2015. PMID: 25946677 No abstract available.
Discoveries and controversies in cutaneous mosaicism.
Castori M, Tadini G. Castori M, et al. Among authors: tadini g. G Ital Dermatol Venereol. 2016 Jun;151(3):251-65. Epub 2016 Apr 12. G Ital Dermatol Venereol. 2016. PMID: 27070303 Review.
Intellectual Disability: When the Hypertrichosis Is a Clue.
Pezzani L, Milani D, Tadini G. Pezzani L, et al. Among authors: tadini g. J Pediatr Genet. 2015 Sep;4(3):154-8. doi: 10.1055/s-0035-1564442. Epub 2015 Sep 28. J Pediatr Genet. 2015. PMID: 27617126 Free PMC article. Review.
PENS syndrome: a new neurocutaneous phenotype.
Tadini G, Restano L, Happle R, Itin P. Tadini G, et al. Dermatology. 2012;224(1):24-30. doi: 10.1159/000336794. Epub 2012 Mar 9. Dermatology. 2012. PMID: 22414678
139 results