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Items: 34

1.

Implantation of the nyxoah bilateral hypoglossal nerve stimulator for obstructive sleep apnea.

Lewis R, Pételle B, Campbell MC, MacKay S, Palme C, Raux G, Sommer JU, Maurer JT.

Laryngoscope Investig Otolaryngol. 2019 Nov 22;4(6):703-707. doi: 10.1002/lio2.312. eCollection 2019 Dec.

2.

Bilateral hypoglossal nerve stimulation for treatment of adult obstructive sleep apnoea.

Eastwood PR, Barnes M, MacKay SG, Wheatley JR, Hillman DR, Nguyên XL, Lewis R, Campbell MC, Pételle B, Walsh JH, Jones AC, Palme CE, Bizon A, Meslier N, Bertolus C, Maddison KJ, Laccourreye L, Raux G, Denoncin K, Attali V, Gagnadoux F, Launois SH.

Eur Respir J. 2020 Jan 9;55(1). pii: 1901320. doi: 10.1183/13993003.01320-2019. Print 2020 Jan.

3.

Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients.

Bastard C, Raux G, Fruchart C, Parmentier F, Vaur D, Penther D, Troussard X, Nagib D, Lepretre S, Tosi M, Frebourg T, Tilly H.

Leukemia. 2007 Jul;21(7):1460-3. Epub 2007 May 10.

PMID:
17495973
4.

Variations in the APP gene promoter region and risk of Alzheimer disease.

Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D.

Neurology. 2007 Feb 27;68(9):684-7.

PMID:
17325276
5.

A simple method for the routine detection of somatic quantitative genetic alterations in colorectal cancer.

Killian A, Di Fiore F, Le Pessot F, Blanchard F, Lamy A, Raux G, Flaman JM, Paillot B, Michel P, Sabourin JC, Tuech JJ, Michot F, Kerckaert JP, Sesboüé R, Frebourg T.

Gastroenterology. 2007 Feb;132(2):645-53. Epub 2006 Dec 3.

PMID:
17258723
6.

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.

Hum Mol Genet. 2007 Jan 1;16(1):83-91. Epub 2006 Nov 29.

PMID:
17135275
7.

Deleterious mutations in exon 1 of MECP2 in Rett syndrome.

Quenard A, Yilmaz S, Fontaine H, Bienvenu T, Moncla A, des Portes V, Rivier F, Mathieu M, Raux G, Jonveaux P, Philippe C.

Eur J Med Genet. 2006 Jul-Aug;49(4):313-22. Epub 2005 Dec 20.

PMID:
16829352
8.

Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.

Lesca G, Burnichon N, Raux G, Tosi M, Pinson S, Marion MJ, Babin E, Gilbert-Dussardier B, Rivière S, Goizet C, Faivre L, Plauchu H, Frébourg T, Calender A, Giraud S; French Rendu-Osler Network.

Hum Mutat. 2006 Jun;27(6):598.

PMID:
16705692
9.

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D.

Nat Genet. 2006 Jan;38(1):24-6. Epub 2005 Dec 20.

PMID:
16369530
10.

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.

Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D.

J Med Genet. 2005 Oct;42(10):793-5. Epub 2005 Jul 20.

11.

Acd, a peptidoglycan hydrolase of Clostridium difficile with N-acetylglucosaminidase activity.

Dhalluin A, Bourgeois I, Pestel-Caron M, Camiade E, Raux G, Courtin P, Chapot-Chartier MP, Pons JL.

Microbiology. 2005 Jul;151(Pt 7):2343-2351. doi: 10.1099/mic.0.27878-0.

PMID:
16000724
12.

Hyperprolinemia is a risk factor for schizoaffective disorder.

Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, D'Amato T, Petit M, Thibaut F, Frébourg T, Campion D.

Mol Psychiatry. 2005 May;10(5):479-85.

PMID:
15494707
13.

A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.

Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D.

Brain. 2004 Sep;127(Pt 9):1979-92. Epub 2004 Jun 23.

PMID:
15215218
14.

Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method.

Tournier I, Raux G, Di Fiore F, Maréchal I, Leclerc C, Martin C, Wang Q, Buisine MP, Stoppa-Lyonnet D, Olschwang S, Frébourg T, Tosi M.

Hum Mutat. 2004 Apr;23(4):379-84.

PMID:
15024732
15.

Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu).

Portet F, Dauvilliers Y, Campion D, Raux G, Hauw JJ, Lyon-Caen O, Camu W, Touchon J.

Neurology. 2003 Oct 28;61(8):1136-7.

PMID:
14581682
16.

The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit.

Houy E, Raux G, Thibaut F, Belmont A, Demily C, Allio G, Haouzir S, Fouldrin G, Petit M, Frebourg T, Campion D.

Mol Psychiatry. 2004 Mar;9(3):320-2.

PMID:
14569275
17.

Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.

Maréchal L, Raux G, Dumanchin C, Lefebvre G, Deslandre E, Girard C, Campion D, Parain D, Frebourg T, Hannequin D.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):114-7.

PMID:
12707948
18.

Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene.

Bougeard G, Brugières L, Chompret A, Gesta P, Charbonnier F, Valent A, Martin C, Raux G, Feunteun J, Bressac-de Paillerets B, Frébourg T.

Oncogene. 2003 Feb 13;22(6):840-6.

PMID:
12584563
19.

The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene.

Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T.

J Med Genet. 2003 Jan;40(1):e7. No abstract available.

20.

The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit.

Raux G, Bonnet-Brilhault F, Louchart S, Houy E, Gantier R, Levillain D, Allio G, Haouzir S, Petit M, Martinez M, Frebourg T, Thibaut F, Campion D.

Mol Psychiatry. 2002;7(9):1006-11.

21.

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.

Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frébourg T.

Hum Mol Genet. 2002 Sep 15;11(19):2243-9.

PMID:
12217952
22.

Pemphigus is not associated with allotypic markers of immunoglobulin kappa.

Zitouni M, Martel P, Ben Ayed M, Raux G, Gilbert D, Joly P, Mokhtar I, Ridha Kamoun M, Turki H, Zahaf A, Mokni M, Ben Osman A, Masmoudi H, Makni S, Tron F.

Genes Immun. 2002 Feb;3(1):50-2.

23.

IGHV3-associated restriction fragment length polymorphisms confer susceptibility to bullous pemphigoid.

Raux G, Gilbert D, Joly P, Martel P, Roujeau JC, Prost C, Lefranc MP, Tron F.

Exp Clin Immunogenet. 2001;18(2):59-66.

PMID:
11340293
24.

A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease.

Martel P, Gilbert D, Drouot L, Prost C, Raux G, Delaporte E, Joly P, Tron F.

Genes Immun. 2001 Feb;2(1):41-3.

25.

Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation.

Raux G, Gantier R, Thomas-Anterion C, Boulliat J, Verpillat P, Hannequin D, Brice A, Frebourg T, Campion D.

Neurology. 2000 Nov 28;55(10):1577-8.

PMID:
11094121
26.

APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.

Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T.

Eur J Hum Genet. 2000 Sep;8(9):713-6.

27.

A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease.

Raux G, Gantier R, Martin C, Pothin Y, Brice A, Frebourg T, Campion D.

Hum Mutat. 2000 Jul;16(1):95. No abstract available.

PMID:
10874324
28.

Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments.

Charbonnier F, Raux G, Wang Q, Drouot N, Cordier F, Limacher JM, Saurin JC, Puisieux A, Olschwang S, Frebourg T.

Cancer Res. 2000 Jun 1;60(11):2760-3.

29.

Association of KM genotype with bullous pemphigoid.

Raux G, Gilbert D, Joly P, Daveau M, Martel P, Christ M, Tron F.

J Autoimmun. 2000 Feb;14(1):79-82.

PMID:
10648118
30.

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T.

Am J Hum Genet. 1999 Sep;65(3):664-70.

31.

Comparison of structural characteristics of antisubnucleosome and anti-DNA monoclonal antibodies derived from lupus mice.

Koutouzov S, Jovelin F, Brard F, Raux G, Tron F, Gilbert D.

Ann N Y Acad Sci. 1997 Apr 5;815:327-30. No abstract available.

PMID:
9186671
32.

Immunoglobin variable-region mRNA direct sequencing: a method to bypass aberrant myeloma light-chain transcripts.

Jovelin F, Brard F, Raux G, Tron F, Gilbert D.

Biotechniques. 1996 Oct;21(4):576, 578, 580. No abstract available.

33.

[Resident medical student 25].

Buisine A, Raux G, Savoie A.

J Sci Med Lille. 1971 Jan;89(1):9-11. French. No abstract available.

PMID:
4928913
34.

[Polyepiphyseal dystrophy with nanism].

BUISINE A, RAUX G.

Arch Fr Pediatr. 1952;9(9):972-4. Undetermined Language. No abstract available.

PMID:
13017679

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