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

Year Number of Results
1988 1
1989 2
1990 2
1991 4
1992 4
1993 1
1994 4
1995 4
1996 2
1997 3
1998 1
1999 1
2000 3
2001 2
2002 3
2003 3
2004 3
2005 5
2006 4
2007 8
2008 4
2009 3
2010 8
2011 3
2012 6
2013 2
2014 5
2015 4
2016 2
2017 2
2018 4
2019 2
2020 4
2021 3
2022 2
2023 1
2024 1

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106 results

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Page 1
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: fallet bianco c. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
Neuropathology of holoprosencephaly.
Fallet-Bianco C. Fallet-Bianco C. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):214-228. doi: 10.1002/ajmg.c.31623. Am J Med Genet C Semin Med Genet. 2018. PMID: 30182440 Review.
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.
Krochmalnek E, Accogli A, St-Onge J, Addour-Boudrahem N, Prakash G, Kim SH, Brunette-Clement T, Alhajaj G, Mougharbel L, Bruneau E, Myers KA, Dubeau F, Karamchandani J, Farmer JP, Atkinson J, Hall J, Chantal Poulin C, Rosenblatt B, Lafond-Lapalme J, Weil A, Fallet-Bianco C, Albrecht S, Sonenberg N, Riviere JB, Dudley RW, Srour M. Krochmalnek E, et al. Among authors: fallet bianco c. Neurol Genet. 2023 Oct 26;9(6):e200103. doi: 10.1212/NXG.0000000000200103. eCollection 2023 Dec. Neurol Genet. 2023. PMID: 37900581 Free PMC article.
The fetal cerebellum: development and common malformations.
Garel C, Fallet-Bianco C, Guibaud L. Garel C, et al. Among authors: fallet bianco c. J Child Neurol. 2011 Dec;26(12):1483-92. doi: 10.1177/0883073811420148. Epub 2011 Sep 27. J Child Neurol. 2011. PMID: 21954430 Review.
MRI of the fetal posterior fossa.
Adamsbaum C, Moutard ML, André C, Merzoug V, Ferey S, Quéré MP, Lewin F, Fallet-Bianco C. Adamsbaum C, et al. Among authors: fallet bianco c. Pediatr Radiol. 2005 Feb;35(2):124-40. doi: 10.1007/s00247-004-1316-3. Epub 2004 Nov 23. Pediatr Radiol. 2005. PMID: 15565345 Review.
Perinatal-lethal Gaucher disease.
Mignot C, Gelot A, Bessières B, Daffos F, Voyer M, Menez F, Fallet Bianco C, Odent S, Le Duff D, Loget P, Fargier P, Costil J, Josset P, Roume J, Vanier MT, Maire I, Billette de Villemeur T. Mignot C, et al. Among authors: fallet bianco c. Am J Med Genet A. 2003 Jul 30;120A(3):338-44. doi: 10.1002/ajmg.a.20117. Am J Med Genet A. 2003. PMID: 12838552
Human disorders of cortical development: from past to present.
Francis F, Meyer G, Fallet-Bianco C, Moreno S, Kappeler C, Socorro AC, Tuy FP, Beldjord C, Chelly J. Francis F, et al. Among authors: fallet bianco c. Eur J Neurosci. 2006 Feb;23(4):877-93. doi: 10.1111/j.1460-9568.2006.04649.x. Eur J Neurosci. 2006. PMID: 16519653 Review.
Cytomegalovirus-induced brain malformations in fetuses.
Teissier N, Fallet-Bianco C, Delezoide AL, Laquerrière A, Marcorelles P, Khung-Savatovsky S, Nardelli J, Cipriani S, Csaba Z, Picone O, Golden JA, Van Den Abbeele T, Gressens P, Adle-Biassette H. Teissier N, et al. Among authors: fallet bianco c. J Neuropathol Exp Neurol. 2014 Feb;73(2):143-58. doi: 10.1097/NEN.0000000000000038. J Neuropathol Exp Neurol. 2014. PMID: 24423639
Rare ACTG1 variants in fetal microlissencephaly.
Poirier K, Martinovic J, Laquerrière A, Cavallin M, Fallet-Bianco C, Desguerre I, Valence S, Grande-Goburghun J, Francannet C, Deleuze JF, Boland A, Chelly J, Bahi-Buisson N. Poirier K, et al. Among authors: fallet bianco c. Eur J Med Genet. 2015 Aug;58(8):416-8. doi: 10.1016/j.ejmg.2015.06.006. Epub 2015 Jul 16. Eur J Med Genet. 2015. PMID: 26188271
106 results