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

Year Number of Results
1991 1
1992 1
1996 1
1997 3
1998 1
1999 1
2000 4
2001 2
2002 7
2003 3
2004 8
2005 5
2006 5
2007 16
2008 3
2009 2
2010 6
2011 5
2012 8
2013 3
2014 3
2015 3
2016 2
2017 2
2018 6
2019 2
2020 3
2021 1
2022 3
2023 1
2024 0

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98 results

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Page 1
Delineating septo-optic dysplasia.
Lubinsky M, Encha-Razavi F. Lubinsky M, et al. Among authors: encha razavi f. Birth Defects Res. 2022 Dec 1;114(20):1343-1353. doi: 10.1002/bdr2.2095. Epub 2022 Oct 6. Birth Defects Res. 2022. PMID: 36200678 Review.
Features of the developing brain.
Encha-Razavi F, Sonigo P. Encha-Razavi F, et al. Childs Nerv Syst. 2003 Aug;19(7-8):426-8. doi: 10.1007/s00381-003-0765-6. Epub 2003 Jun 19. Childs Nerv Syst. 2003. PMID: 12827416 Review.
TCTN3 mutations cause Mohr-Majewski syndrome.
Thomas S, Legendre M, Saunier S, Bessières B, Alby C, Bonnière M, Toutain A, Loeuillet L, Szymanska K, Jossic F, Gaillard D, Yacoubi MT, Mougou-Zerelli S, David A, Barthez MA, Ville Y, Bole-Feysot C, Nitschke P, Lyonnet S, Munnich A, Johnson CA, Encha-Razavi F, Cormier-Daire V, Thauvin-Robinet C, Vekemans M, Attié-Bitach T. Thomas S, et al. Among authors: encha razavi f. Am J Hum Genet. 2012 Aug 10;91(2):372-8. doi: 10.1016/j.ajhg.2012.06.017. Am J Hum Genet. 2012. PMID: 22883145 Free PMC article.
Pitfalls of the morphologic approach.
Encha-Razavi F, Chelly J. Encha-Razavi F, et al. J Neuropathol Exp Neurol. 2006 Mar;65(3):302; author reply 302-3. doi: 10.1097/01.jnen.0000223199.72823.27. J Neuropathol Exp Neurol. 2006. PMID: 16651892 No abstract available.
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome.
Quélin C, Loget P, Verloes A, Bazin A, Bessières B, Laquerrière A, Patrier S, Grigorescu R, Encha-Razavi F, Delahaye S, Jouannic JM, Carbonne B, D'Hervé D, Aubry MC, Macé G, Harvey T, Ville Y, Viot G, Joyé N, Odent S, Attié-Bitach T, Wolf C, Chevy F, Benlian P, Gonzales M. Quélin C, et al. Among authors: encha razavi f. Eur J Med Genet. 2012 Feb;55(2):81-90. doi: 10.1016/j.ejmg.2011.12.002. Epub 2011 Dec 22. Eur J Med Genet. 2012. PMID: 22226660 Free article.
Stress-induced unfolded protein response contributes to Zika virus-associated microcephaly.
Gladwyn-Ng I, Cordón-Barris L, Alfano C, Creppe C, Couderc T, Morelli G, Thelen N, America M, Bessières B, Encha-Razavi F, Bonnière M, Suzuki IK, Flamand M, Vanderhaeghen P, Thiry M, Lecuit M, Nguyen L. Gladwyn-Ng I, et al. Among authors: encha razavi f. Nat Neurosci. 2018 Jan;21(1):63-71. doi: 10.1038/s41593-017-0038-4. Epub 2017 Dec 11. Nat Neurosci. 2018. PMID: 29230053
PAX2 mutations in fetal renal hypodysplasia.
Martinovic-Bouriel J, Benachi A, Bonnière M, Brahimi N, Esculpavit C, Morichon N, Vekemans M, Antignac C, Salomon R, Encha-Razavi F, Attié-Bitach T, Gubler MC. Martinovic-Bouriel J, et al. Among authors: encha razavi f. Am J Med Genet A. 2010 Apr;152A(4):830-5. doi: 10.1002/ajmg.a.33133. Am J Med Genet A. 2010. PMID: 20358591
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Gardner JF, Cushion TD, Niotakis G, Olson HE, Grant PE, Scott RH, Stoodley N, Cohen JS, Naidu S, Attie-Bitach T, Bonnières M, Boutaud L, Encha-Razavi F, Palmer-Smith SM, Mugalaasi H, Mullins JGL, Pilz DT, Fry AE. Gardner JF, et al. Among authors: encha razavi f. Brain Sci. 2018 Aug 7;8(8):145. doi: 10.3390/brainsci8080145. Brain Sci. 2018. PMID: 30087272 Free PMC article.
98 results