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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 46

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1,302 results

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Page 1
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.
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.
[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 …
Unverricht-Lundborg disease.
Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A. Crespel A, et al. Epileptic Disord. 2016 Sep 1;18(S2):28-37. doi: 10.1684/epd.2016.0841. Epileptic Disord. 2016. PMID: 27582036 Review.
Naegeli-Franceschetti-Jadassohn syndrome: a systematic review of case studies.
Shah HH, Hussain T, Subash A, Qadir RA, Meshram YR, Shahzad M, Sultan W, Hadi Z, Ashfaque F, Anas Z, Rauf SA, Waseem R, Hussain MS, Zuberi MAW. Shah HH, et al. Front Med (Lausanne). 2025 Feb 28;12:1453172. doi: 10.3389/fmed.2025.1453172. eCollection 2025. Front Med (Lausanne). 2025. PMID: 40093016 Free PMC article.
INTRODUCTION: Naegeli-Franceschetti-Jadassohn syndrome (NFJS), also known as Naegeli Syndrome, is a rare autosomal dominant ectodermal dysplasia characterized by mutations in the KRT14 gene. ...
INTRODUCTION: Naegeli-Franceschetti-Jadassohn syndrome (NFJS), also known as Naegeli Syndrome, is a rare autosomal dominant ectoderma …
Franceschetti syndrome.
Kasat V. Kasat V. Contemp Clin Dent. 2011 Jul;2(3):245-8. doi: 10.4103/0976-237X.86480. Contemp Clin Dent. 2011. PMID: 22090774 Free PMC article.
Franceschetti syndrome is an autosomal dominant disorder of craniofacial development with variable expressivity. ...
Franceschetti syndrome is an autosomal dominant disorder of craniofacial development with variable expressivity. ...
[Heterochromia complicata Fuchs].
Hollwich F. Hollwich F. Klin Monbl Augenheilkd. 1988 Feb;192(2):87-96. doi: 10.1055/s-2008-1050081. Klin Monbl Augenheilkd. 1988. PMID: 3283429 Review. German.
In the present author's view, the reason why so many different opinions are held concerning the clinical picture and the etiology is that only a few authors (Franceschetti, Francois, Georgiades, Hollwich, Huber, Kimura, Hogan and Thygeson, Perkins, Sugar and others) have b …
In the present author's view, the reason why so many different opinions are held concerning the clinical picture and the etiology is that on …
1,302 results