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Year Number of Results
1918 1
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1951 7
1952 9
1953 17
1954 12
1955 20
1956 10
1957 14
1958 6
1959 13
1960 5
1961 5
1962 3
1963 3
1964 11
1965 5
1966 9
1967 9
1968 11
1969 8
1970 7
1971 7
1972 2
1973 4
1974 5
1975 8
1976 9
1977 15
1978 11
1979 21
1980 10
1981 13
1982 15
1983 12
1984 18
1985 13
1986 20
1987 19
1988 9
1989 11
1990 22
1991 22
1992 23
1993 34
1994 29
1995 40
1996 43
1997 39
1998 64
1999 74
2000 83
2001 90
2002 85
2003 85
2004 81
2005 134
2006 114
2007 121
2008 138
2009 163
2010 168
2011 146
2012 210
2013 228
2014 219
2015 231
2016 239
2017 220
2018 241
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2020 383
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5,449 results

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Page 1
Filippi syndrome: further clinical characterization.
Battaglia A, Filippi T, Pusceddu S, Williams CA. Battaglia A, et al. Am J Med Genet A. 2008 Jul 15;146A(14):1848-52. doi: 10.1002/ajmg.a.32400. Am J Med Genet A. 2008. PMID: 18553552 Review.
We report on a child with Filippi syndrome who shows syndactyly of fingers and toes, severe pre- and post-natal growth retardation, postnatal microcephaly, epilepsy, and severe mental retardation with speech impairment. ...
We report on a child with Filippi syndrome who shows syndactyly of fingers and toes, severe pre- and post-natal growth retardation, p …
The Filippi's Glands of Giant Silk Moths: To Be or Not to Be?
Sehadova H, Zavodska R, Zurovec M, Sauman I. Sehadova H, et al. Insects. 2021 Nov 19;12(11):1040. doi: 10.3390/insects12111040. Insects. 2021. PMID: 34821840 Free PMC article.
The Filippi's glands (FGs), formerly "Lyonet's glands", are paired accessory organs associated with the silk glands. ...
The Filippi's glands (FGs), formerly "Lyonet's glands", are paired accessory organs associated with the silk glands. ...
Filippi syndrome: a new case with skeletal abnormalities.
Héron D, Billette de Villemeur T, Munnich A, Lyonnet S. Héron D, et al. J Med Genet. 1995 Aug;32(8):659-61. doi: 10.1136/jmg.32.8.659. J Med Genet. 1995. PMID: 7473664 Free PMC article. Review.
This multiple congenital anomalies/mental retardation pattern very much resembles that described by Filippi. This observation confirms that this syndrome is a distinct, probably autosomal recessive entity....
This multiple congenital anomalies/mental retardation pattern very much resembles that described by Filippi. This observation confirm …
Filippi Syndrome: Report of a Rare Case.
Goyal L, Goyal JP, Bhakhri BK, Chug A. Goyal L, et al. J Clin Diagn Res. 2015 Dec;9(12):SD01-3. doi: 10.7860/JCDR/2015/14550.6945. Epub 2015 Dec 1. J Clin Diagn Res. 2015. PMID: 26813917 Free PMC article.
Filippi syndrome is an autosomal recessive condition characterized by syndactyly of fingers and toes, microcephaly, growth retardation and abnormal facies. ...In addition he had some dental abnormalities like missing bilateral lateral incisors and delayed eruption of teeth …
Filippi syndrome is an autosomal recessive condition characterized by syndactyly of fingers and toes, microcephaly, growth retardatio …
Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease.
Bas H, Durmaz CD, Tombak MC, Cetin GO, Karaer K. Bas H, et al. Am J Med Genet A. 2024 Sep;194(9):e63654. doi: 10.1002/ajmg.a.63654. Epub 2024 May 13. Am J Med Genet A. 2024. PMID: 38738944
Filippi syndrome is a rare genetic disorder characterized by growth and neurodevelopmental delays, dysmorphism, and selective limb abnormalities. ...In this article, we present three new patients of Filippi syndrome with unusual clinical and genetic aspects. These p …
Filippi syndrome is a rare genetic disorder characterized by growth and neurodevelopmental delays, dysmorphism, and selective limb ab …
Filippi syndrome: report of three additional cases.
Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA. Williams MS, et al. Am J Med Genet. 1999 Nov 19;87(2):128-33. Am J Med Genet. 1999. PMID: 10533026 Review.
We report on three unrelated individuals with Filippi syndrome. All have microcephaly, minor facial anomalies, variable syndactyly of digits, growth impairment, and developmental delay. One patient also has polydactyly, which has not been reported previously in the Fili …
We report on three unrelated individuals with Filippi syndrome. All have microcephaly, minor facial anomalies, variable syndactyly of …
Leptin and aging.
Filippi BM, Lam TK. Filippi BM, et al. Aging (Albany NY). 2014 Feb;6(2):82-3. doi: 10.18632/aging.100637. Aging (Albany NY). 2014. PMID: 24561396 Free PMC article. No abstract available.
Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literature.
Franceschini P, Licata D, Guala A, Di Cara G, Franceschini D. Franceschini P, et al. Genet Couns. 2002;13(3):343-52. Genet Couns. 2002. PMID: 12416644 Review.
Filippi syndrome is a specific Multiple Congenital Abnormalities/Mental Retardation (MCA/MR) complex which must not be confused with other so called "craniodigital syndromes", a heterogeneous group of pathological conditions simply lumped for the combination of different c …
Filippi syndrome is a specific Multiple Congenital Abnormalities/Mental Retardation (MCA/MR) complex which must not be confused with …
5,449 results