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

Year Number of Results
2005 1
2008 1
2009 3
2010 2
2011 1
2012 2
2013 2
2014 3
2015 4
2016 2
2017 2
2018 1
2019 2
2020 6
2021 3
2022 4
2023 2
2024 0

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37 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: pelluard f. 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.
Morphological and genetic causes of fetal cardiomyopathies.
Kohaut E, Ader F, Rooryck C, Pelluard F, Bonnière M, André G, Sauvestre F, Roth P, Khraiche D, Bessières B, Attié-Bitach T, Richard P. Kohaut E, et al. Among authors: pelluard f. Clin Genet. 2023 Jul;104(1):63-72. doi: 10.1111/cge.14333. Epub 2023 May 20. Clin Genet. 2023. PMID: 37209000
Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals.
Aubert-Mucca M, Huber C, Baujat G, Michot C, Zarhrate M, Bras M, Boutaud L, Malan V, Attie-Bitach T; Clinical Contributors; Cormier-Daire V. Aubert-Mucca M, et al. J Med Genet. 2023 Apr;60(4):337-345. doi: 10.1136/jmg-2022-108435. Epub 2022 Aug 4. J Med Genet. 2023. PMID: 35927022
An Atypical Case of Congenital Erythropoietic Porphyria.
Sudrié-Arnaud B, Legendre M, Snanoudj S, Pelluard F, Bekri S, Tebani A. Sudrié-Arnaud B, et al. Among authors: pelluard f. Genes (Basel). 2021 Nov 19;12(11):1828. doi: 10.3390/genes12111828. Genes (Basel). 2021. PMID: 34828434 Free PMC article.
[Placental pathology of uteroplacental vascular deficiency].
Carles D, Pelluard F, André G, Naudion S, Poingt M, Castain C, Sauvestre F. Carles D, et al. Among authors: pelluard f. Ann Pathol. 2013 Aug;33(4):230-6. doi: 10.1016/j.annpat.2013.04.018. Epub 2013 Jul 31. Ann Pathol. 2013. PMID: 23954115 Review. French.
Early fetal presentation of Koolen-de Vries: Case report with literature review.
Sauvestre F, Marguet F, Rooryck C, Vuillaume ML, Cardinaud F, Laquerrière A, André G, Pelluard F. Sauvestre F, et al. Among authors: pelluard f. Eur J Med Genet. 2017 Nov;60(11):605-609. doi: 10.1016/j.ejmg.2017.08.012. Epub 2017 Aug 12. Eur J Med Genet. 2017. PMID: 28811189 Review.
Pathological Findings in Feto-maternal Hemorrhage.
Carles D, André G, Pelluard F, Martin O, Sauvestre F. Carles D, et al. Among authors: pelluard f. Pediatr Dev Pathol. 2014 Mar-Apr;17(2):102-6. doi: 10.2350/13-12-1419-OA.1. Epub 2014 Feb 27. Pediatr Dev Pathol. 2014. PMID: 24575782
Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data.
Lamouroux A, Dauge C, Wells C, Mousty E, Pinson L, Cavé H, Capri Y, Faure JM, Grosjean F, Sauvestre F, Attié-Bitach T, Pelluard F, Geneviève D. Lamouroux A, et al. Among authors: pelluard f. Prenat Diagn. 2022 May;42(5):574-582. doi: 10.1002/pd.6133. Epub 2022 Mar 22. Prenat Diagn. 2022. PMID: 35278234
37 results