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Items: 1 to 50 of 293

1.

Three Consecutive Pregnancies in a Patient with Chronic Autoimmune Thyroid Disease Associated with Hypothyroidism and Extremely High Levels of Anti-Thyrotropin Receptor Antibodies.

Grulet H, Barraud S, Chikh K, Souchon PF, Claris O, Bouvier R, Trouillas J, Gabriel R, Bory JP, Schvartz C, Orgiazzi J, Delemer B.

Thyroid. 2019 May;29(5):743-747. doi: 10.1089/thy.2018.0098.

PMID:
30973063
2.

Exercise Frequency Determines Heart Rate Variability Gains in Older People: A Meta-Analysis and Meta-Regression.

Raffin J, Barthélémy JC, Dupré C, Pichot V, Berger M, Féasson L, Busso T, Da Costa A, Colvez A, Montuy-Coquard C, Bouvier R, Bongue B, Roche F, Hupin D.

Sports Med. 2019 May;49(5):719-729. doi: 10.1007/s40279-019-01097-7. Review.

PMID:
30945205
3.

Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.

Mary L, Chennen K, Stoetzel C, Antin M, Leuvrey A, Nourisson E, Alanio-Detton E, Antal MC, Attié-Bitach T, Bouvagnet P, Bouvier R, Buenerd A, Clémenson A, Devisme L, Gasser B, Gilbert-Dussardier B, Guimiot F, Khau Van Kien P, Leroy B, Loget P, Martinovic J, Pelluard F, Perez MJ, Petit F, Pinson L, Rooryck-Thambo C, Poch O, Dollfus H, Schaefer E, Muller J.

Clin Genet. 2019 Mar;95(3):384-397. doi: 10.1111/cge.13500.

PMID:
30614526
4.

Helicenes Grafted with 1,1,4,4-Tetracyanobutadiene Moieties: π-Helical Push-Pull Systems with Strong Electronic Circular Dichroism and Two-Photon Absorption.

Bouvier R, Durand R, Favereau L, Srebro-Hooper M, Dorcet V, Roisnel T, Vanthuyne N, Vesga Y, Donnelly J, Hernandez F, Autschbach J, Trolez Y, Crassous J.

Chemistry. 2018 Sep 25;24(54):14484-14494. doi: 10.1002/chem.201802763. Epub 2018 Sep 3.

5.

Fifteen Minutes Daily Brisk Walk May Be a New Best Target in Very Old Adults: Age Is Not an Excuse to Not Exercise.

Raffin J, Barthelemy JC, Barth N, Garet M, Busso T, Feasson L, Devun A, Montuy-Coquard C, Thillays M, Poillerat R, Bouvier R, Bongue B, Roche F, Hupin D.

J Am Med Dir Assoc. 2018 Mar;19(3):273-275. doi: 10.1016/j.jamda.2017.12.097. No abstract available.

PMID:
29402653
6.

[Iris metastasis of prostatic adenocarcinoma: A case report].

Bouvier R, Jany B, Gozlan S, Promelle V, Sevestre H, Milazzo S.

J Fr Ophtalmol. 2018 Feb;41(2):e63-e65. doi: 10.1016/j.jfo.2017.05.020. French. No abstract available.

PMID:
29398144
7.

DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma.

Sheffield NC, Pierron G, Klughammer J, Datlinger P, Schönegger A, Schuster M, Hadler J, Surdez D, Guillemot D, Lapouble E, Freneaux P, Champigneulle J, Bouvier R, Walder D, Ambros IM, Hutter C, Sorz E, Amaral AT, de Álava E, Schallmoser K, Strunk D, Rinner B, Liegl-Atzwanger B, Huppertz B, Leithner A, de Pinieux G, Terrier P, Laurence V, Michon J, Ladenstein R, Holter W, Windhager R, Dirksen U, Ambros PF, Delattre O, Kovar H, Bock C, Tomazou EM.

Nat Med. 2017 Mar;23(3):386-395. doi: 10.1038/nm.4273. Epub 2017 Jan 30.

8.

[Atypical vernal shield ulcer in a 3-year-old child].

Benarous A, Iscar C, Roussel C, Bouvier R, Sevestre H, Bremond-Gignac D.

J Fr Ophtalmol. 2016 May;39(5):e133-6. doi: 10.1016/j.jfo.2015.04.026. Epub 2016 May 5. French. No abstract available.

PMID:
27155912
9.

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome and recurrent intrauterine fetal death.

Vasiljevic A, Poreau B, Bouvier R, Lachaux A, Arnoult C, Fauré J, Cordier MP, Ray PF.

Lancet. 2015 May 23;385(9982):2120. doi: 10.1016/S0140-6736(15)60773-5. No abstract available.

PMID:
26009232
10.

Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis.

Rossi M, Hall CM, Bouvier R, Collardeau-Frachon S, Le Breton F, Bucourt M, Cordier MP, Vianey-Saban C, Parenti G, Andria G, Le Merrer M, Edery P, Offiah AC.

Pediatr Radiol. 2015 Jul;45(7):965-76. doi: 10.1007/s00247-014-3257-9. Epub 2015 Feb 3. Review.

PMID:
25646736
11.

Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failure.

Heissat S, Collardeau-Frachon S, Baruteau J, Dubruc E, Bouvier R, Fabre M, Cordier MP, Broué P, Guigonis V, Debray D.

J Pediatr. 2015 Jan;166(1):66-73. doi: 10.1016/j.jpeds.2014.09.030. Epub 2014 Oct 23.

PMID:
25444000
12.

Microscopic and ultrastructural features in Wolcott-Rallison syndrome, a permanent neonatal diabetes mellitus: about two autopsy cases.

Collardeau-Frachon S, Vasiljevic A, Jouvet A, Bouvier R, Senée V, Nicolino M.

Pediatr Diabetes. 2015 Nov;16(7):510-20. doi: 10.1111/pedi.12201. Epub 2014 Aug 18.

PMID:
25131821
13.

Fetal phenotype associated with the 22q11 deletion.

Noël AC, Pelluard F, Delezoide AL, Devisme L, Loeuillet L, Leroy B, Martin A, Bouvier R, Laquerriere A, Jeanne-Pasquier C, Bessieres-Grattagliano B, Mechler C, Alanio E, Leroy C, Gaillard D.

Am J Med Genet A. 2014 Nov;164A(11):2724-31. doi: 10.1002/ajmg.a.36720. Epub 2014 Aug 8.

PMID:
25111715
14.

Transient neonatal liver disease after maternal antenatal intravenous Ig infusions in gestational alloimmune liver disease associated with neonatal haemochromatosis.

Baruteau J, Heissat S, Broué P, Collardeau-Frachon S, Bouvier R, Fabre M, Debiec H, Ronco P, Uzan M, Narcy P, Cordier MP, Lachaux A, Lamireau T, Elleau C, Filet JP, Mitanchez D, Dupuy MP, Salaün JF, Odent S, Davison J, Debray D, Guigonis V.

J Pediatr Gastroenterol Nutr. 2014 Nov;59(5):629-35. doi: 10.1097/MPG.0000000000000514.

PMID:
25079484
15.

First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond–Blackfan anemia.

Da Costa L, Chanoz-Poulard G, Simansour M, French M, Bouvier R, Prieur F, Couque N, Delezoide AL, Leblanc T, Mohandas N, Touraine R.

Am J Hematol. 2013 Apr;88(4):340-1. No abstract available.

16.

Increasing diversion of household hazardous wastes and materials through mandatory retail take-back.

Wagner TP, Toews P, Bouvier R.

J Environ Manage. 2013 Jul 15;123:88-97. doi: 10.1016/j.jenvman.2013.03.020. Epub 2013 Apr 12.

PMID:
23583869
17.

Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.

Madariaga L, Morinière V, Jeanpierre C, Bouvier R, Loget P, Martinovic J, Dechelotte P, Leporrier N, Thauvin-Robinet C, Jensen UB, Gaillard D, Mathieu M, Turlin B, Attie-Bitach T, Salomon R, Gübler MC, Antignac C, Heidet L.

Clin J Am Soc Nephrol. 2013 Jul;8(7):1179-87. doi: 10.2215/CJN.10221012. Epub 2013 Mar 28.

18.

Hepatocyte nuclear factor 1β controls nephron tubular development.

Massa F, Garbay S, Bouvier R, Sugitani Y, Noda T, Gubler MC, Heidet L, Pontoglio M, Fischer E.

Development. 2013 Feb;140(4):886-96. doi: 10.1242/dev.086546.

19.

First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond-Blackfan anemia.

Da Costa L, Chanoz-Poulard G, Simansour M, French M, Bouvier R, Prieur F, Couque N, Delezoide AL, Leblanc T, Mohandas N, Touraine R.

Am J Hematol. 2013 Feb;88(2):160. doi: 10.1002/ajh.23366. No abstract available. Erratum in: Am J Hematol. 2013 Apr;88(4):340-1.

20.

Long-term critical issues in pediatric renal transplant recipients: a single-center experience.

Harambat J, Ranchin B, Bertholet-Thomas A, Mestrallet G, Bacchetta J, Badet L, Basmaison O, Bouvier R, Demède D, Dubourg L, Floret D, Martin X, Cochat P.

Transpl Int. 2013 Feb;26(2):154-61. doi: 10.1111/tri.12014. Epub 2012 Dec 10.

21.

French retrospective multicentric study of neonatal hemochromatosis: importance of autopsy and autoimmune maternal manifestations.

Collardeau-Frachon S, Heissat S, Bouvier R, Fabre M, Baruteau J, Broue P, Cordier MP, Debray D, Debiec H, Ronco P, Guigonis V.

Pediatr Dev Pathol. 2012 Nov-Dec;15(6):450-70. doi: 10.2350/12-02-1155-OA.1. Epub 2012 Aug 17.

PMID:
22901025
22.

NEK1 and DYNC2H1 are both involved in short rib polydactyly Majewski type but not in Beemer Langer cases.

El Hokayem J, Huber C, Couvé A, Aziza J, Baujat G, Bouvier R, Cavalcanti DP, Collins FA, Cordier MP, Delezoide AL, Gonzales M, Johnson D, Le Merrer M, Levy-Mozziconacci A, Loget P, Martin-Coignard D, Martinovic J, Mortier GR, Perez MJ, Roume J, Scarano G, Munnich A, Cormier-Daire V.

J Med Genet. 2012 Apr;49(4):227-33. doi: 10.1136/jmedgenet-2011-100717.

PMID:
22499340
23.

Clear cell ependymoma with trisomy 19 developing bone metastases.

Payet M, Conter C, Labrousse F, De Paula AM, Marabelle A, Branger DF, Bouvier R, Frappaz D.

Childs Nerv Syst. 2012 May;28(5):739-42. doi: 10.1007/s00381-011-1656-x. Epub 2011 Dec 30. No abstract available.

PMID:
22207400
24.

Prevalence of liver complications in children receiving long-term parenteral nutrition.

Peyret B, Collardeau S, Touzet S, Loras-Duclaux I, Yantren H, Michalski MC, Chaix J, Restier-Miron L, Bouvier R, Lachaux A, Peretti N.

Eur J Clin Nutr. 2011 Jun;65(6):743-9. doi: 10.1038/ejcn.2011.26. Epub 2011 Mar 23.

PMID:
21427734
25.

[Aetiology and prognosis of prenatally diagnosed megacystis regarding gestational age at discovery. A six-year retrospective study].

Peyrière MP, Roth P, Combourieu D, Vavasseur C, Bouvier R, Guibaud L, Gaucherand P.

Gynecol Obstet Fertil. 2010 Nov;38(11):663-7. doi: 10.1016/j.gyobfe.2010.09.008. Epub 2010 Oct 28. French.

PMID:
21035372
26.

BBS10 mutations are common in 'Meckel'-type cystic kidneys.

Putoux A, Mougou-Zerelli S, Thomas S, Elkhartoufi N, Audollent S, Le Merrer M, Lachmeijer A, Sigaudy S, Buenerd A, Fernandez C, Delezoide AL, Gubler MC, Salomon R, Saad A, Cordier MP, Vekemans M, Bouvier R, Attie-Bitach T.

J Med Genet. 2010 Dec;47(12):848-52. doi: 10.1136/jmg.2010.079392. Epub 2010 Aug 30.

PMID:
20805367
27.

[Hypoplasia adrenal congenita of anencephalic type: two cases with pituitary abnormalities and review of literature].

Folligan K, Roume J, Razavi F, Sepaniak S, Bouvier R, Morel Y, Trouillas J.

Morphologie. 2011 Mar;95(308):26-33. doi: 10.1016/j.morpho.2010.07.003. Review. French.

PMID:
20801702
28.

[Granulomatous pulmonary involvement preceding diagnosis of Crohn disease: a pediatric case report].

Roblin E, Pecciarini N, Yantren H, Dubois R, Hameury F, Bellon G, Bouvier R, Lachaux A.

Arch Pediatr. 2010 Sep;17(9):1308-12. doi: 10.1016/j.arcped.2010.06.006. Epub 2010 Aug 14. French.

PMID:
20709507
29.

Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?

Léticée N, Bessières-Grattagliano B, Dupré T, Vuillaumier-Barrot S, de Lonlay P, Razavi F, El Khartoufi N, Ville Y, Vekemans M, Bouvier R, Seta N, Attié-Bitach T.

Mol Genet Metab. 2010 Oct-Nov;101(2-3):253-7. doi: 10.1016/j.ymgme.2010.06.009. Epub 2010 Jun 22. Review.

PMID:
20638314
30.

Occurrence of inflammatory bowel disease during treatment of juvenile idiopathic arthritis with etanercept: a French retrospective study.

Dallocchio A, Canioni D, Ruemmele F, Duquesne A, Scoazec JY, Bouvier R, Paraf F, Languepin J, Wouters CH, Guillot M, Quartier P, Bader-Meunier B; SOFREMIP.

Rheumatology (Oxford). 2010 Sep;49(9):1694-8. doi: 10.1093/rheumatology/keq136. Epub 2010 May 14.

PMID:
20472717
31.

Recurrence of a dysgerminoma in Frasier syndrome.

Mestrallet G, Bertholet-Thomas A, Ranchin B, Bouvier R, Frappaz D, Cochat P.

Pediatr Transplant. 2011 May;15(3):e53-5. doi: 10.1111/j.1399-3046.2010.01273.x.

PMID:
20408995
32.

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.

Denamur E, Delezoide AL, Alberti C, Bourillon A, Gubler MC, Bouvier R, Pascaud O, Elion J, Grandchamp B, Michel-Calemard L, Missy P, Zaccaria I, Le Nagard H, Gerard B, Loirat C; Société Française de Foetopathologie, Barbet J, Beaufrère AM, Berchel C, Bessières B, Boudjemaa S, Buenerd A, Carles D, Clemenson A, Dechelotte P, Devisme L, Dijoud F, Espérandieu O, Fallet C, Gonzalès M, Hillion Y, Jacob B, Joubert M, Kermanach P, Lallemand A, Laquerrière A, Laurent N, Liprandi A, Loeuillet L, Loget P, Martinovic J, Ménez F, Narcy F, Roux JJ, Rouleau-Dubois C, Sinico M, Tantau J, Wann AR.

Kidney Int. 2010 Feb;77(4):350-8. doi: 10.1038/ki.2009.440. Epub 2009 Nov 25.

33.

Severe dysphagia in children with eosinophilic esophagitis and esophageal stricture: an indication for balloon dilation?

Robles-Medranda C, Villard F, le Gall C, Lukashok H, Rivet C, Bouvier R, Dumortier J, Lachaux A.

J Pediatr Gastroenterol Nutr. 2010 May;50(5):516-20. doi: 10.1097/MPG.0b013e3181b66dbd.

PMID:
19934772
34.

Long-term treatment reduction and steroids withdrawal in children with autoimmune hepatitis: a single centre experience on 55 children.

Dumortier J, Arita CT, Rivet C, LeGall C, Bouvier R, Fabien N, Guillaud O, Collardeau-Frachon S, Scoazec JY, Lachaux A.

Eur J Gastroenterol Hepatol. 2009 Dec;21(12):1413-8. doi: 10.1097/MEG.0b013e32832ad5f7.

PMID:
19907227
35.

Malignancy incidence after renal transplantation in children: a 20-year single-centre experience.

Koukourgianni F, Harambat J, Ranchin B, Euvrard S, Bouvier R, Liutkus A, Cochat P.

Nephrol Dial Transplant. 2010 Feb;25(2):611-6. doi: 10.1093/ndt/gfp497. Epub 2009 Oct 10.

PMID:
19820249
36.

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation.

Mougou-Zerelli S, Thomas S, Szenker E, Audollent S, Elkhartoufi N, Babarit C, Romano S, Salomon R, Amiel J, Esculpavit C, Gonzales M, Escudier E, Leheup B, Loget P, Odent S, Roume J, Gérard M, Delezoide AL, Khung S, Patrier S, Cordier MP, Bouvier R, Martinovic J, Gubler MC, Boddaert N, Munnich A, Encha-Razavi F, Valente EM, Saad A, Saunier S, Vekemans M, Attié-Bitach T.

Hum Mutat. 2009 Nov;30(11):1574-82. doi: 10.1002/humu.21116.

37.

A first report of collagenous gastritis, sprue, and colitis in a 9-month-old infant: 14 years of clinical, endoscopic, and histologic follow-up.

Billiémaz K, Robles-Medranda C, Le Gall C, Gay C, Mory O, Clémenson A, Bouvier R, Teyssier G, Lachaux A.

Endoscopy. 2009;41 Suppl 2:E233-4. doi: 10.1055/s-2008-1077440. Epub 2009 Sep 15. No abstract available.

PMID:
19757370
38.

Elevated aminotransaminases as the first manifestation of sarcoidosis.

Nawfal G, Budin C, Bouvier R, Lachaux A.

Case Rep Med. 2009;2009:193785. doi: 10.1155/2009/193785. Epub 2009 May 26.

39.

Autoimmune hypoparathyroidism in a 12-year-old girl with McKusick cartilage hair hypoplasia.

Bacchetta J, Ranchin B, Brunet AS, Bouvier R, Duquesne A, Edery P, Fabien N, Peretti N.

Pediatr Nephrol. 2009 Dec;24(12):2449-53. doi: 10.1007/s00467-009-1256-0. Epub 2009 Jul 22.

PMID:
19626344
40.

Chylomicron retention disease: a long term study of two cohorts.

Peretti N, Roy CC, Sassolas A, Deslandres C, Drouin E, Rasquin A, Seidman E, Brochu P, Vohl MC, Labarge S, Bouvier R, Samson-Bouma ME, Charcosset M, Lachaux A, Levy E.

Mol Genet Metab. 2009 Jun;97(2):136-42. doi: 10.1016/j.ymgme.2009.02.003. Epub 2009 Feb 20.

PMID:
19285442
41.

Hepatic stem-like phenotype and interplay of Wnt/beta-catenin and Myc signaling in aggressive childhood liver cancer.

Cairo S, Armengol C, De Reyniès A, Wei Y, Thomas E, Renard CA, Goga A, Balakrishnan A, Semeraro M, Gresh L, Pontoglio M, Strick-Marchand H, Levillayer F, Nouet Y, Rickman D, Gauthier F, Branchereau S, Brugières L, Laithier V, Bouvier R, Boman F, Basso G, Michiels JF, Hofman P, Arbez-Gindre F, Jouan H, Rousselet-Chapeau MC, Berrebi D, Marcellin L, Plenat F, Zachar D, Joubert M, Selves J, Pasquier D, Bioulac-Sage P, Grotzer M, Childs M, Fabre M, Buendia MA.

Cancer Cell. 2008 Dec 9;14(6):471-84. doi: 10.1016/j.ccr.2008.11.002.

42.

Campomelic dysplasia: echographic suspicion in the first trimester of pregnancy and final diagnosis of two cases.

Massardier J, Roth P, Michel-Calemard L, Rudigoz RC, Bouvier R, Dijoud F, Arnould P, Combourieu D, Gaucherand P.

Fetal Diagn Ther. 2008;24(4):452-7. doi: 10.1159/000176299. Epub 2008 Nov 26.

PMID:
19033726
43.

First report of rapidly progressive glomerulonephritis in tumor necrosis factor receptor-associated periodic syndrome.

Harambat J, Desjonqueres M, Garaix F, Cochat P, Ranchin B, Cimaz R, Dodé C, Bouvier R.

Arthritis Rheum. 2008 Oct;58(10):3275-6. doi: 10.1002/art.23887. No abstract available.

44.

[Malignancy risk and Wiedemann-Beckwith syndrome: what follow-up to provide?].

Santiago J, Muszlak M, Samson C, Goulois E, Glorion A, Atale A, Ranaivoarivony V, Hebert JC, Bouvier R, Cordier MP.

Arch Pediatr. 2008 Sep;15(9):1498-502. doi: 10.1016/j.arcped.2008.06.009. Epub 2008 Jul 31. French.

PMID:
18674889
45.

Spontaneous esophageal perforation in eosinophilic esophagitis in children.

Robles-Medranda C, Villard F, Bouvier R, Dumortier J, Lachaux A.

Endoscopy. 2008 Sep;40 Suppl 2:E171. doi: 10.1055/s-2007-995801. No abstract available.

PMID:
18668459
46.

'Renal hypersensitivity' to inulin and IgA nephropathy.

Bacchetta J, Villard F, Vial T, Dubourg L, Bouvier R, Kassaï B, Cochat P.

Pediatr Nephrol. 2008 Oct;23(10):1883-5. doi: 10.1007/s00467-008-0819-9. Epub 2008 Jun 6.

PMID:
18535847
47.

Nephronophthisis-like nephritis associated with fibrous dysplasia of bone.

Bacchetta J, Chapurlat R, Bouvier R, Antignac C, Dubourg L, Kohler R, Delmas PD, Cochat P.

Pediatr Nephrol. 2008 Sep;23(9):1559-63. doi: 10.1007/s00467-008-0850-x. Epub 2008 May 30.

PMID:
18512082
48.

Mid-term results demonstrate salvage high-intensity focused ultrasound (HIFU) as an effective and acceptably morbid salvage treatment option for locally radiorecurrent prostate cancer.

Murat FJ, Poissonnier L, Rabilloud M, Belot A, Bouvier R, Rouviere O, Chapelon JY, Gelet A.

Eur Urol. 2009 Mar;55(3):640-7. doi: 10.1016/j.eururo.2008.04.091. Epub 2008 May 9.

PMID:
18508188
49.

[Locally recurrent prostatic adenocarcinoma after exclusive radiotherapy: results of high intensity focused ultrasound].

Poissonnier L, Murat FJ, Belot A, Bouvier R, Rabilloud M, Rouviere O, Chapelon JY, Gelet A.

Prog Urol. 2008 Apr;18(4):223-9. doi: 10.1016/j.purol.2008.02.006. Epub 2008 May 2. French.

PMID:
18501302
50.

Renal translocation carcinomas: clinicopathologic, immunohistochemical, and gene expression profiling analysis of 31 cases with a review of the literature.

Camparo P, Vasiliu V, Molinie V, Couturier J, Dykema KJ, Petillo D, Furge KA, Comperat EM, Lae M, Bouvier R, Boccon-Gibod L, Denoux Y, Ferlicot S, Forest E, Fromont G, Hintzy MC, Laghouati M, Sibony M, Tucker ML, Weber N, Teh BT, Vieillefond A.

Am J Surg Pathol. 2008 May;32(5):656-70. doi: 10.1097/PAS.0b013e3181609914.

PMID:
18344867

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