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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
2022 0
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Search Results

139 results
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Page 1
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation.
Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, Blakeley J, Babovic-Vuksanovic D, Cunha KS, Ferner R, Fisher MJ, Friedman JM, Gutmann DH, Kehrer-Sawatzki H, Korf BR, Mautner VF, Peltonen S, Rauen KA, Riccardi V, Schorry E, Stemmer-Rachamimov A, Stevenson DA, Tadini G, Ullrich NJ, Viskochil D, Wimmer K, Yohay K; International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC), Huson SM, Evans DG, Plotkin SR. Legius E, et al. Among authors: tadini g. Genet Med. 2021 Aug;23(8):1506-1513. doi: 10.1038/s41436-021-01170-5. Epub 2021 May 19. Genet Med. 2021. PMID: 34012067 Free PMC article.
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.
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.
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.
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.
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
Ear nose throat manifestations in hypoidrotic ectodermal dysplasia.
Callea M, Teggi R, Yavuz I, Tadini G, Priolo M, Crovella S, Clarich G, Grasso DL. Callea M, et al. Among authors: tadini g. Int J Pediatr Otorhinolaryngol. 2013 Nov;77(11):1801-4. doi: 10.1016/j.ijporl.2013.09.004. Epub 2013 Sep 13. Int J Pediatr Otorhinolaryngol. 2013. PMID: 24080322 Review.
139 results