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Items: 1 to 50 of 460

1.

Genetic counseling for cystic fibrosis: A basic model with new challenges.

Bieth E, Nectoux J, Girardet A, Gruchy N, Mittre H, Laurans M, Guenet D, Brouard J, Gerard M.

Arch Pediatr. 2020 Feb;27 Suppl 1:eS30-eS34. doi: 10.1016/S0929-693X(20)30048-8.

PMID:
32172934
2.

High thromboembolic event rate in patients with locally advanced oesophageal cancer during neoadjuvant therapy. An exploratory analysis of the prospective, randomised intergroup phase III trial SAKK 75/08.

Fehr M, Hawle H, Hayoz S, Thuss-Patience P, Schacher S, Riera Knorrenschild J, Dürr D, Knoefel WT, Rumpold H, Bitzer M, Zweifel M, Samaras P, Mey U, Küng M, Winterhalder R, Eisterer W, Hess V, Gérard MA, Templeton A, Stahl M, Ruhstaller T; Swiss Group for Clinical Cancer Research (SAKK); German Esophageal Cancer Study Group; Austrian Arbeitsgemeinschaft Medikamentöse Tumortherapie (AGMT); Fédération Francophone de Cancérologie Digestive (FFCD) / Fédération de Recherche en Chirurgie (FRENCH).

BMC Cancer. 2020 Feb 28;20(1):166. doi: 10.1186/s12885-020-6623-z.

3.

Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders.

Barbosa S, Greville-Heygate S, Bonnet M, Godwin A, Fagotto-Kaufmann C, Kajava AV, Laouteouet D, Mawby R, Wai HA, Dingemans AJM, Hehir-Kwa J, Willems M, Capri Y, Mehta SG, Cox H, Goudie D, Vansenne F, Turnpenny P, Vincent M, Cogné B, Lesca G, Hertecant J, Rodriguez D, Keren B, Burglen L, Gérard M, Putoux A; C4RCD Research Group, Cantagrel V, Siquier-Pernet K, Rio M, Banka S, Sarkar A, Steeves M, Parker M, Clement E, Moutton S, Tran Mau-Them F, Piton A, de Vries BBA, Guille M, Debant A, Schmidt S, Baralle D.

Am J Hum Genet. 2020 Mar 5;106(3):338-355. doi: 10.1016/j.ajhg.2020.01.018. Epub 2020 Feb 27.

4.

DL4papers: a deep learning approach for the automatic interpretation of scientific articles.

Bugnon L, Yones C, Raad J, Gerard M, Rubiolo M, Merino G, Pividori M, Di Persia L, Milone DH, Stegmayer G.

Bioinformatics. 2020 Feb 24. pii: btaa111. doi: 10.1093/bioinformatics/btaa111. [Epub ahead of print]

PMID:
32091584
5.

Exome sequencing identifies the first genetic determinants of sirenomelia in humans.

Lecoquierre F, Brehin AC, Coutant S, Coursimault J, Bazin A, Finck W, Benoist G, Begorre M, Beneteau C, Cailliez D, Chenal P, De Jong M, Degré S, Devisme L, Francannet C, Gérard B, Jeanne C, Joubert M, Journel H, Laurichesse Delmas H, Layet V, Liquier A, Mangione R, Patrier S, Pelluard F, Petit F, Tillouche N, van Ravenswaaij-Arts C, Frebourg T, Saugier-Veber P, Gruchy N, Nicolas G, Gerard M.

Hum Mutat. 2020 Feb 14. doi: 10.1002/humu.23998. [Epub ahead of print]

PMID:
32058622
6.

Infections due to carbapenemase-producing bacteria, clinical burden, and impact of screening strategies on outcome.

Abramowicz L, Gerard M, Martiny D, Delforge M, De Wit S, Konopnicki D.

Med Mal Infect. 2020 Feb 5. pii: S0399-077X(20)30024-X. doi: 10.1016/j.medmal.2019.12.011. [Epub ahead of print]

PMID:
32035722
7.

[Stereotaxic ablative radiotherapy in stage 1 non-small-cell lung cancer: Results of the phase 3 randomized trial "CHISEL"].

Gerard M, Lerouge D, Le Guevelou J, Thariat J.

Bull Cancer. 2020 Feb;107(2):145-147. doi: 10.1016/j.bulcan.2019.11.001. Epub 2020 Feb 5. French. No abstract available.

PMID:
32035650
8.

Vascularization of tissue-engineered skeletal muscle constructs.

Gholobova D, Terrie L, Gerard M, Declercq H, Thorrez L.

Biomaterials. 2020 Mar;235:119708. doi: 10.1016/j.biomaterials.2019.119708. Epub 2019 Dec 19. Review.

PMID:
31999964
9.

Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.

Marsili L, Overwater E, Hanna N, Baujat G, Baars MJH, Boileau C, Bonneau D, Brehin AC, Capri Y, Cheung HY, Dulfer E, Gerard M, Gouya L, Hilhorst-Hofstee Y, Houweling AC, Isidor B, Le Gloan L, Menke LA, Odent S, Morice-Picard F, Vanlerberghe C, Voorhoeve E, van Tintelen JP, Maugeri A, Arnaud P.

Clin Genet. 2020 Jan 2. doi: 10.1111/cge.13700. [Epub ahead of print]

PMID:
31898322
10.

Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations.

Snanoudj S, Molin A, Colson C, Coudray N, Paulien S, Mittre H, Gérard M, Schaefer E, Goldenberg A, Bacchetta J, Odent S, Naudion S, Demeer B, Faivre L, Gruchy N, Kottler ML, Richard N.

J Bone Miner Res. 2019 Dec 30. doi: 10.1002/jbmr.3948. [Epub ahead of print]

PMID:
31886927
11.

Hadrontherapy Interactions in Molecular and Cellular Biology.

Thariat J, Valable S, Laurent C, Haghdoost S, Pérès EA, Bernaudin M, Sichel F, Lesueur P, Césaire M, Petit E, Ferré AE, Saintigny Y, Skog S, Tudor M, Gérard M, Thureau S, Habrand JL, Balosso J, Chevalier F.

Int J Mol Sci. 2019 Dec 24;21(1). pii: E133. doi: 10.3390/ijms21010133. Review.

12.

Morphometric analysis of fossil bumble bees (Hymenoptera, Apidae, Bombini) reveals their taxonomic affinities.

Dehon M, Engel MS, Gérard M, Aytekin AM, Ghisbain G, Williams PH, Rasmont P, Michez D.

Zookeys. 2019 Nov 21;891:71-118. doi: 10.3897/zookeys.891.36027. eCollection 2019.

13.

Association of In Utero HIV Exposure With Obesity and Reactive Airway Disease in HIV-Negative Adolescents and Young Adults.

Fourman LT, Pan CS, Zheng I, Gerard ME, Sheehab A, Lee H, Stanley TL, Grinspoon SK.

J Acquir Immune Defic Syndr. 2020 Feb 1;83(2):126-134. doi: 10.1097/QAI.0000000000002235.

PMID:
31738195
14.

Shift in size of bumblebee queens over the last century.

Gérard M, Martinet B, Maebe K, Marshall L, Smagghe G, Vereecken NJ, Vray S, Rasmont P, Michez D.

Glob Chang Biol. 2020 Mar;26(3):1185-1195. doi: 10.1111/gcb.14890. Epub 2019 Nov 29.

PMID:
31665557
15.

Decreased number of striatal cholinergic interneurons and motor deficits in dopamine receptor 2-expressing-cell-specific Dyt1 conditional knockout mice.

Yokoi F, Oleas J, Xing H, Liu Y, Dexter KM, Misztal C, Gerard M, Efimenko I, Lynch P, Villanueva M, Alsina R, Krishnaswamy S, Vaillancourt DE, Li Y.

Neurobiol Dis. 2020 Feb;134:104638. doi: 10.1016/j.nbd.2019.104638. Epub 2019 Oct 13.

16.

[How I explore… intrauterine growth restriction].

Paquay P, Gérard M, Pieltain C, Emonts P, Grandfils S.

Rev Med Liege. 2019 Oct;74(10):543-552. French.

PMID:
31609559
17.

Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.

Bar C, Barcia G, Jennesson M, Le Guyader G, Schneider A, Mignot C, Lesca G, Breuillard D, Montomoli M, Keren B, Doummar D, Billette de Villemeur T, Afenjar A, Marey I, Gerard M, Isnard H, Poisson A, Dupont S, Berquin P, Meyer P, Genevieve D, De Saint Martin A, El Chehadeh S, Chelly J, Guët A, Scalais E, Dorison N, Myers CT, Mefford HC, Howell KB, Marini C, Freeman JL, Nica A, Terrone G, Sekhara T, Lebre AS, Odent S, Sadleir LG, Munnich A, Guerrini R, Scheffer IE, Kabashi E, Nabbout R.

Hum Mutat. 2020 Jan;41(1):69-80. doi: 10.1002/humu.23915. Epub 2019 Oct 4.

PMID:
31513310
18.

Skeletal muscle mass correlates with increased toxicity during neoadjuvant radiochemotherapy in locally advanced esophageal cancer: A SAKK 75/08 substudy.

Panje CM, Höng L, Hayoz S, Baracos VE, Herrmann E, Garcia Schüler H, Meier UR, Henke G, Schacher S, Hawle H, Gérard MA, Ruhstaller T, Plasswilm L; Swiss Group for Clinical Cancer Research (SAKK).

Radiat Oncol. 2019 Sep 11;14(1):166. doi: 10.1186/s13014-019-1372-3.

19.

Urinary ketone body loss leads to degeneration of brain white matter in elderly SLC5A8-deficient mice.

Suissa L, Flachon V, Guigonis JM, Olivieri CV, Burel-Vandenbos F, Guglielmi J, Ambrosetti D, Gérard M, Franken P, Darcourt J, Pellerin L, Pourcher T, Lindenthal S.

J Cereb Blood Flow Metab. 2019 Sep 10:271678X19873662. doi: 10.1177/0271678X19873662. [Epub ahead of print]

PMID:
31506013
20.

A patient and family reporting system for perceived ambulatory note mistakes: experience at 3 U.S. healthcare centers.

Bourgeois FC, Fossa A, Gerard M, Davis ME, Taylor YJ, Connor CD, Vaden T, McWilliams A, Spencer MD, Folcarelli P, Bell SK.

J Am Med Inform Assoc. 2019 Dec 1;26(12):1566-1573. doi: 10.1093/jamia/ocz142.

PMID:
31504576
21.

Multiplex targeted high-throughput sequencing in a series of 352 patients with congenital limb malformations.

Jourdain AS, Petit F, Odou MF, Balduyck M, Brunelle P, Dufour W, Boussion S, Brischoux-Boucher E, Colson C, Dieux A, Gérard M, Ghoumid J, Giuliano F, Goldenberg A, Khau Van Kien P, Lehalle D, Morin G, Moutton S, Smol T, Vanlerberghe C, Manouvrier-Hanu S, Escande F.

Hum Mutat. 2020 Jan;41(1):222-239. doi: 10.1002/humu.23912. Epub 2019 Sep 23.

PMID:
31502745
22.

First case of Campylobacter rectus and Solobacterium moorei mixed bacteraemia successfully identified by MALDI TOF-MS.

Genderini FG, Martiny D, Ponthieux F, Argudín MA, Gomez Galdon M, Zaarour A, Garcia C, Libois A, Gérard M, Dauby N.

New Microbes New Infect. 2019 Jul 3;31:100587. doi: 10.1016/j.nmni.2019.100587. eCollection 2019 Sep.

23.

Immunopathological manifestations in Kabuki syndrome: a registry study of 177 individuals.

Margot H, Boursier G, Duflos C, Sanchez E, Amiel J, Andrau JC, Arpin S, Brischoux-Boucher E, Boute O, Burglen L, Caille C, Capri Y, Collignon P, Conrad S, Cormier-Daire V, Delplancq G, Dieterich K, Dollfus H, Fradin M, Faivre L, Fernandes H, Francannet C, Gatinois V, Gerard M, Goldenberg A, Ghoumid J, Grotto S, Guerrot AM, Guichet A, Isidor B, Jacquemont ML, Julia S, Khau Van Kien P, Legendre M, Le Quan Sang KH, Leheup B, Lyonnet S, Magry V, Manouvrier S, Martin D, Morel G, Munnich A, Naudion S, Odent S, Perrin L, Petit F, Philip N, Rio M, Robbe J, Rossi M, Sarrazin E, Toutain A, Van Gils J, Vera G, Verloes A, Weber S, Whalen S, Sanlaville D, Lacombe D, Aladjidi N, Geneviève D.

Genet Med. 2020 Jan;22(1):181-188. doi: 10.1038/s41436-019-0623-x. Epub 2019 Jul 31.

PMID:
31363182
24.

Leaf economics and slow-fast adaptation across the geographic range of Arabidopsis thaliana.

Sartori K, Vasseur F, Violle C, Baron E, Gerard M, Rowe N, Ayala-Garay O, Christophe A, Jalón LG, Masclef D, Harscouet E, Granado MDR, Chassagneux A, Kazakou E, Vile D.

Sci Rep. 2019 Jul 24;9(1):10758. doi: 10.1038/s41598-019-46878-2.

25.

RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation.

Revencu N, Fastre E, Ravoet M, Helaers R, Brouillard P, Bisdorff-Bresson A, Chung CWT, Gerard M, Dvorakova V, Irvine AD, Boon LM, Vikkula M.

J Med Genet. 2020 Jan;57(1):48-52. doi: 10.1136/jmedgenet-2019-106024. Epub 2019 Jul 12.

PMID:
31300548
26.

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.

Nizon M, Laugel V, Flanigan KM, Pastore M, Waldrop MA, Rosenfeld JA, Marom R, Xiao R, Gerard A, Pichon O, Le Caignec C, Gérard M, Dieterich K, Truitt Cho M, McWalter K, Hiatt S, Thompson ML, Bézieau S, Wadley A, Wierenga KJ, Egly JM, Isidor B.

Genet Med. 2019 Nov;21(11):2663. doi: 10.1038/s41436-019-0590-2.

PMID:
31267042
27.

Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome.

Snanoudj S, Mordel P, Dupas Q, Schanen C, Arion A, Gérard M, Read MH, Nait Rabah D, Goux D, Chapon F, Jokic M, Allouche S.

Mol Genet Genomic Med. 2019 Aug;7(8):e815. doi: 10.1002/mgg3.815. Epub 2019 Jun 28.

28.

Hypoxia Imaging and Adaptive Radiotherapy: A State-of-the-Art Approach in the Management of Glioma.

Gérard M, Corroyer-Dulmont A, Lesueur P, Collet S, Chérel M, Bourgeois M, Stefan D, Limkin EJ, Perrio C, Guillamo JS, Dubray B, Bernaudin M, Thariat J, Valable S.

Front Med (Lausanne). 2019 Jun 12;6:117. doi: 10.3389/fmed.2019.00117. eCollection 2019. Review.

29.

FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.

Ader F, De Groote P, Réant P, Rooryck-Thambo C, Dupin-Deguine D, Rambaud C, Khraiche D, Perret C, Pruny JF, Mathieu-Dramard M, Gérard M, Troadec Y, Gouya L, Jeunemaitre X, Van Maldergem L, Hagège A, Villard E, Charron P, Richard P.

Clin Genet. 2019 Oct;96(4):317-329. doi: 10.1111/cge.13594. Epub 2019 Jul 18.

PMID:
31245841
30.

Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.

Nizon M, Laugel V, Flanigan KM, Pastore M, Waldrop MA, Rosenfeld JA, Marom R, Xiao R, Gerard A, Pichon O, Le Caignec C, Gérard M, Dieterich K, Truitt Cho M, McWalter K, Hiatt S, Thompson ML, Bézieau S, Wadley A, Wierenga KJ, Egly JM, Isidor B.

Genet Med. 2019 Dec;21(12):2713-2722. doi: 10.1038/s41436-019-0557-3. Epub 2019 Jun 3. Erratum in: Genet Med. 2019 Jul 3;:.

PMID:
31155615
31.

OpenNotes After 7 Years: Patient Experiences With Ongoing Access to Their Clinicians' Outpatient Visit Notes.

Walker J, Leveille S, Bell S, Chimowitz H, Dong Z, Elmore JG, Fernandez L, Fossa A, Gerard M, Fitzgerald P, Harcourt K, Jackson S, Payne TH, Perez J, Shucard H, Stametz R, DesRoches C, Delbanco T.

J Med Internet Res. 2019 May 6;21(5):e13876. doi: 10.2196/13876.

32.

Kinetic Study on Clogging of a Geothermal Pumping Well Triggered by Mixing-Induced Biogeochemical Reactions.

Burté L, Cravotta CA 3rd, Bethencourt L, Farasin J, Pédrot M, Dufresne A, Gérard MF, Baranger C, Le Borgne T, Aquilina L.

Environ Sci Technol. 2019 May 21;53(10):5848-5857. doi: 10.1021/acs.est.9b00453. Epub 2019 May 10.

PMID:
31038936
33.

Contribution of the FilmArray Respiratory Panel in the management of adult and pediatric patients attending the emergency room during 2015-2016 influenza epidemics: An interventional study.

Busson L, Bartiaux M, Brahim S, Konopnicki D, Dauby N, Gérard M, De Backer P, Van Vaerenbergh K, Mahadeb B, Mekkaoui L, De Foor M, Wautier M, Vandenberg O, Mols P, Levy J, Hallin M.

Int J Infect Dis. 2019 Jun;83:32-39. doi: 10.1016/j.ijid.2019.03.027. Epub 2019 Mar 26.

34.

Prospective evaluation of diagnostic tools for respiratory viruses in children and adults.

Busson L, Bartiaux M, Brahim S, Konopnicki D, Dauby N, Gérard M, De Backer P, Van Vaerenbergh K, Mahadeb B, De Foor M, Wautier M, Vandenberg O, Mols P, Levy J, Hallin M.

J Virol Methods. 2019 Apr;266:1-6. doi: 10.1016/j.jviromet.2019.01.006. Epub 2019 Jan 15.

PMID:
30658123
35.

Duplication of 10q24 locus: broadening the clinical and radiological spectrum.

Holder-Espinasse M, Jamsheer A, Escande F, Andrieux J, Petit F, Sowinska-Seidler A, Socha M, Jakubiuk-Tomaszuk A, Gerard M, Mathieu-Dramard M, Cormier-Daire V, Verloes A, Toutain A, Plessis G, Jonveaux P, Baumann C, David A, Farra C, Colin E, Jacquemont S, Rossi A, Mansour S, Ghali N, Moncla A, Lahiri N, Hurst J, Pollina E, Patch C, Ahn JW, Valat AS, Mezel A, Bourgeot P, Zhang D, Manouvrier-Hanu S.

Eur J Hum Genet. 2019 Apr;27(4):525-534. doi: 10.1038/s41431-018-0326-9. Epub 2019 Jan 8.

36.

Tailored axillary surgery with or without axillary lymph node dissection followed by radiotherapy in patients with clinically node-positive breast cancer (TAXIS): study protocol for a multicenter, randomized phase-III trial.

Henke G, Knauer M, Ribi K, Hayoz S, Gérard MA, Ruhstaller T, Zwahlen DR, Muenst S, Ackerknecht M, Hawle H, Fitzal F, Gnant M, Mátrai Z, Ballardini B, Gyr A, Kurzeder C, Weber WP.

Trials. 2018 Dec 4;19(1):667. doi: 10.1186/s13063-018-3021-9.

37.

Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature.

Vuillaume ML, Moizard MP, Rossignol S, Cottereau E, Vonwill S, Alessandri JL, Busa T, Colin E, Gérard M, Giuliano F, Lambert L, Lefevre M, Kotecha U, Nampoothiri S, Netchine I, Raynaud M, Brioude F, Toutain A.

Hum Mutat. 2018 Dec;39(12):2110-2112. doi: 10.1002/humu.23612. Epub 2018 Sep 17. No abstract available.

PMID:
30447178
38.

Metabolic pathways synthesis based on ant colony optimization.

Gerard MF, Stegmayer G, Milone DH.

Sci Rep. 2018 Nov 6;8(1):16398. doi: 10.1038/s41598-018-34454-z.

39.

NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

Schanze I, Bunt J, Lim JWC, Schanze D, Dean RJ, Alders M, Blanchet P, Attié-Bitach T, Berland S, Boogert S, Boppudi S, Bridges CJ, Cho MT, Dobyns WB, Donnai D, Douglas J, Earl DL, Edwards TJ, Faivre L, Fregeau B, Genevieve D, Gérard M, Gatinois V, Holder-Espinasse M, Huth SF, Izumi K, Kerr B, Lacaze E, Lakeman P, Mahida S, Mirzaa GM, Morgan SM, Nowak C, Peeters H, Petit F, Pilz DT, Puechberty J, Reinstein E, Rivière JB, Santani AB, Schneider A, Sherr EH, Smith-Hicks C, Wieland I, Zackai E, Zhao X, Gronostajski RM, Zenker M, Richards LJ.

Am J Hum Genet. 2018 Nov 1;103(5):752-768. doi: 10.1016/j.ajhg.2018.10.006.

40.

Coculture Method to Obtain Endothelial Networks Within Human Tissue-Engineered Skeletal Muscle.

Gholobova D, Gerard M, Terrie L, Desender L, Shansky J, Vandenburgh H, Thorrez L.

Methods Mol Biol. 2019;1889:169-183. doi: 10.1007/978-1-4939-8897-6_10.

PMID:
30367414
41.

Constitutive androstane receptor 1 is constitutively bound to chromatin and 'primed' for transactivation in hepatocytes.

McMahon M, Ding S, Jimenez LA, Terranova R, Gerard MA, Vitobello A, Moggs J, Henderson CJ, Wolf CR.

Mol Pharmacol. 2019 Jan;95(1):97-105. doi: 10.1124/mol.118.113555. Epub 2018 Oct 25.

42.

Stressful conditions reveal decrease in size, modification of shape but relatively stable asymmetry in bumblebee wings.

Gerard M, Michez D, Debat V, Fullgrabe L, Meeus I, Piot N, Sculfort O, Vastrade M, Smagghe G, Vanderplanck M.

Sci Rep. 2018 Oct 11;8(1):15169. doi: 10.1038/s41598-018-33429-4.

43.

16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.

Allach El Khattabi L, Heide S, Caberg JH, Andrieux J, Doco Fenzy M, Vincent-Delorme C, Callier P, Chantot-Bastaraud S, Afenjar A, Boute-Benejean O, Cordier MP, Faivre L, Francannet C, Gerard M, Goldenberg A, Masurel-Paulet A, Mosca-Boidron AL, Marle N, Moncla A, Le Meur N, Mathieu-Dramard M, Plessis G, Lesca G, Rossi M, Edery P, Delahaye-Duriez A, De Pontual L, Tabet AC, Lebbar A, Suiro L, Ioos C, Natiq A, Chafai Elalaoui S, Missirian C, Receveur A, François-Fiquet C, Garnier P, Yardin C, Laroche C, Vago P, Sanlaville D, Dupont JM, Benzacken B, Pipiras E.

J Med Genet. 2018 Oct 4. pii: jmedgenet-2018-105389. doi: 10.1136/jmedgenet-2018-105389. [Epub ahead of print]

PMID:
30287593
44.

Nut Directs p300-Dependent, Genome-Wide H4 Hyperacetylation in Male Germ Cells.

Shiota H, Barral S, Buchou T, Tan M, Couté Y, Charbonnier G, Reynoird N, Boussouar F, Gérard M, Zhu M, Bargier L, Puthier D, Chuffart F, Bourova-Flin E, Picaud S, Filippakopoulos P, Goudarzi A, Ibrahim Z, Panne D, Rousseaux S, Zhao Y, Khochbin S.

Cell Rep. 2018 Sep 25;24(13):3477-3487.e6. doi: 10.1016/j.celrep.2018.08.069.

45.

Foetal exposure to mitotane/Op'DDD: Post-natal study of four children.

Magkou D, Do Cao C, Bouvattier C, Douillard C, de Marcellus C, Cazabat L, Gérard M, Raffin-Sanson ML, Young J.

Clin Endocrinol (Oxf). 2018 Dec;89(6):805-812. doi: 10.1111/cen.13854. Epub 2018 Oct 16.

PMID:
30222204
46.

Intra-Arterial Image Guidance With Optical Frequency Domain Reflectometry Shape Sensing.

Parent F, Gerard M, Monet F, Loranger S, Soulez G, Kashyap R, Kadoury S.

IEEE Trans Med Imaging. 2019 Feb;38(2):482-492. doi: 10.1109/TMI.2018.2866494. Epub 2018 Aug 22.

PMID:
30136934
47.

Human tissue-engineered skeletal muscle: a novel 3D in vitro model for drug disposition and toxicity after intramuscular injection.

Gholobova D, Gerard M, Decroix L, Desender L, Callewaert N, Annaert P, Thorrez L.

Sci Rep. 2018 Aug 15;8(1):12206. doi: 10.1038/s41598-018-30123-3.

48.

Caudal intercostal block for abdominal surgery in horses.

Gingold BMC, Hassen KM, Milloway MC, Gerard M, Fowler AW.

Vet Rec. 2018 Aug 4;183(5):164-165. doi: 10.1136/vr.k3319. No abstract available.

PMID:
30072466
49.

Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes.

Baert-Desurmont S, Coutant S, Charbonnier F, Macquere P, Lecoquierre F, Schwartz M, Blanluet M, Vezain M, Lanos R, Quenez O, Bou J, Bouvignies E, Fourneaux S, Manase S, Vasseur S, Mauillon J, Gerard M, Marlin R, Bougeard G, Tinat J, Frebourg T, Tournier I.

Eur J Hum Genet. 2018 Nov;26(11):1597-1602. doi: 10.1038/s41431-018-0207-2. Epub 2018 Jul 2.

50.

Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome.

Van Damme T, Pang X, Guillemyn B, Gulberti S, Syx D, De Rycke R, Kaye O, de Die-Smulders CEM, Pfundt R, Kariminejad A, Nampoothiri S, Pierquin G, Bulk S, Larson AA, Chatfield KC, Simon M, Legrand A, Gerard M, Symoens S, Fournel-Gigleux S, Malfait F.

Hum Mol Genet. 2018 Oct 15;27(20):3475-3487. doi: 10.1093/hmg/ddy234.

PMID:
29931299

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