Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1935 1
1944 1
1945 4
1946 13
1947 20
1948 12
1949 23
1950 14
1951 11
1952 15
1953 13
1954 14
1955 16
1956 12
1957 22
1958 11
1959 13
1960 11
1961 10
1962 9
1963 8
1964 11
1965 15
1966 14
1967 11
1968 24
1969 11
1970 12
1971 5
1972 9
1973 1
1974 4
1975 4
1976 7
1977 4
1978 3
1979 4
1980 9
1981 7
1982 6
1983 12
1984 4
1985 7
1986 5
1987 2
1988 4
1989 10
1990 4
1991 7
1992 4
1993 14
1994 12
1995 13
1996 15
1997 13
1998 11
1999 11
2000 6
2001 12
2002 18
2003 15
2004 13
2005 16
2006 31
2007 36
2008 23
2009 34
2010 34
2011 30
2012 39
2013 28
2014 48
2015 40
2016 35
2017 30
2018 25
2019 41
2020 42
2021 61
2022 35
2023 56
2024 50
2025 36

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,292 results

Results by year

Filters applied: . Clear all
Page 1
[Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics].
Bondarenko MT, Zhorzholadze NV, Sheremet NL, Ronzina IA, Galoian NS, Loginova AN, Chukhrova AL, Poliakov AV. Bondarenko MT, et al. Vestn Oftalmol. 2014 Mar-Apr;130(2):72-6. Vestn Oftalmol. 2014. PMID: 24864504 Review. Russian.
The article presents a review of literature on Stargardt's disease and abiotrophy of Franceschetti. Etiopathogenetic, clinical and molecular genetic characteristics are covered. ...
The article presents a review of literature on Stargardt's disease and abiotrophy of Franceschetti. Etiopathogenetic, clinical and mo …
Mandibulofacial Dysostosis.
McElrath AD, Winters R. McElrath AD, et al. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 32965901 Free Books & Documents.
The syndrome was described by Berry (1889), Treacher Collins (1900), and Franceschetti and Klein (1949) ergo the names Berry's syndrome and Franceschetti-Zwahlen-Klein syndrome are also used in older literature. Treacher Collins syndrome (TCS) is the more preferred …
The syndrome was described by Berry (1889), Treacher Collins (1900), and Franceschetti and Klein (1949) ergo the names Berry's syndro …
[Franceschetti's syndrome].
Berardi G, Fornaci M, Rossi R. Berardi G, et al. Minerva Pediatr. 1970 Mar 24;22(12):553-5. Minerva Pediatr. 1970. PMID: 5422059 Italian. No abstract available.
[Franceschetti's syndrome].
[No authors listed] [No authors listed] Jibiinkoka. 1967 Dec;39(12):1289-91. Jibiinkoka. 1967. PMID: 5628541 Japanese. No abstract available.
Sialidoses.
Franceschetti S, Canafoglia L. Franceschetti S, et al. Epileptic Disord. 2016 Sep 1;18(S2):89-93. doi: 10.1684/epd.2016.0845. Epileptic Disord. 2016. PMID: 27621198 Review.
Inherited Reticulate Pigmentary Disorders.
Lin MH, Chou PC, Lee IC, Yang SF, Yu HS, Yu S. Lin MH, et al. Genes (Basel). 2023 Jun 20;14(6):1300. doi: 10.3390/genes14061300. Genes (Basel). 2023. PMID: 37372478 Free PMC article. Review.
Inherited RPDs include dyschromatosis symmetrica hereditaria (DSH), dyschromatosis universalis hereditaria (DUH), reticulate acropigmentation of Kitamura (RAK), Dowling-Degos disease (DDD), dyskeratosis congenita (DKC), Naegeli-Franceschetti-Jadassohn syndrome (NFJS), derm …
Inherited RPDs include dyschromatosis symmetrica hereditaria (DSH), dyschromatosis universalis hereditaria (DUH), reticulate acropigmentatio …
Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family.
Tubaigy SM, Hassan HM. Tubaigy SM, et al. J Forensic Sci. 2014 Mar;59(2):555-8. doi: 10.1111/1556-4029.12316. Epub 2013 Nov 21. J Forensic Sci. 2014. PMID: 24261749 Review.
Subsequent medical investigations suggested that he and his two brothers displayed most of the features of the Naegeli-Franceschetti-Jadassohn (NFJ) syndrome. These features included skin changes with hypo- and hyperpigmentation, hypohidrosis, dystrophy of the nails, diffu …
Subsequent medical investigations suggested that he and his two brothers displayed most of the features of the Naegeli-Franceschetti- …
Franceschetti hereditary recurrent corneal erosion.
Lisch W, Bron AJ, Munier FL, Schorderet DF, Tiab L, Lange C, Saikia P, Reinhard T, Weiss JS, Gundlach E, Pleyer U, Lisch C, Auw-Haedrich C. Lisch W, et al. Am J Ophthalmol. 2012 Jun;153(6):1073-81.e4. doi: 10.1016/j.ajo.2011.12.011. Epub 2012 Mar 7. Am J Ophthalmol. 2012. PMID: 22402249
PURPOSE: To describe new affected individuals of Franceschetti's original pedigree of hereditary recurrent erosion and to classify a unique entity called Franceschetti corneal dystrophy. ...CONCLUSION: We have extended the pedigree of Franceschetti cor …
PURPOSE: To describe new affected individuals of Franceschetti's original pedigree of hereditary recurrent erosion and to clas …
A. Franceschetti.
François J. François J. Am J Ophthalmol. 1968 Jul;66(1):134-5. doi: 10.1016/0002-9394(68)91813-8. Am J Ophthalmol. 1968. PMID: 4872988 No abstract available.
1,292 results