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Vitamin D Modulates the Response of Bronchial Epithelial Cells Exposed to Cigarette Smoke Extract.

Mathyssen C, Serré J, Sacreas A, Everaerts S, Maes K, Verleden S, Verlinden L, Verstuyf A, Pilette C, Gayan-Ramirez G, Vanaudenaerde B, Janssens W.

Nutrients. 2019 Sep 6;11(9). pii: E2138. doi: 10.3390/nu11092138.


Airway morphometry in COPD with bronchiectasis: a view on all airway generations.

Everaerts S, McDonough JE, Verleden SE, Josipovic I, Boone M, Dubbeldam A, Mathyssen C, Serré J, Dupont LJ, Gayan-Ramirez G, Verschakelen J, Hogg JC, Verleden GM, Vanaudenaerde BM, Janssens W.

Eur Respir J. 2019 Nov 7;54(5). pii: 1802166. doi: 10.1183/13993003.02166-2018. Print 2019 Nov.


Targeting Vitamin D Deficiency to Limit Exacerbations in Respiratory Diseases: Utopia or Strategy With Potential?

Maes K, Serré J, Mathyssen C, Janssens W, Gayan-Ramirez G.

Calcif Tissue Int. 2019 Jul 26. doi: 10.1007/s00223-019-00591-4. [Epub ahead of print] Review.


Hydroxychloroquine-induced podocytopathy mimicking Fabry disease.

Serre J, Buob D, Boffa JJ.

BMJ Case Rep. 2019 May 13;12(5). pii: e228876. doi: 10.1136/bcr-2018-228876.


C5b9 Deposition in Glomerular Capillaries Is Associated With Poor Kidney Allograft Survival in Antibody-Mediated Rejection.

Goutaudier V, Perrochia H, Mucha S, Bonnet M, Delmas S, Garo F, Garrigue V, Lepreux S, Pernin V, Serre JE, Szwarc I, Merville P, Ramounau-Pigot A, René C, Visentin J, Morgan BP, Frémeaux-Bacchi V, Mourad G, Couzi L, Le Quintrec M.

Front Immunol. 2019 Mar 8;10:235. doi: 10.3389/fimmu.2019.00235. eCollection 2019.


Data on inflammatory cytokines and pathways involved in clearance of Nontypeable Haemophilus influenzae from the lungs during cigarette smoking and vitamin D deficiency.

Serré J, Mathyssen C, Ajime TT, Korf H, Maes K, Heulens N, Gysemans C, Mathieu C, Vanaudenaerde B, Janssens W, Gayan-Ramirez G.

Data Brief. 2018 Dec 18;22:703-708. doi: 10.1016/j.dib.2018.12.048. eCollection 2019 Feb.


Airway infection with Nontypeable Haemophilus influenzae is more rapidly eradicated in vitamin D deficient mice.

Serré J, Mathyssen C, Ajime TT, Korf H, Maes K, Heulens N, Gysemans C, Mathieu C, Vanaudenaerde B, Janssens W, Gayan-Ramirez G.

J Steroid Biochem Mol Biol. 2019 Mar;187:42-51. doi: 10.1016/j.jsbmb.2018.10.021. Epub 2018 Nov 3.


Increased IgA Expression in Lung Lymphoid Follicles in Severe Chronic Obstructive Pulmonary Disease.

Ladjemi MZ, Martin C, Lecocq M, Detry B, Nana FA, Moulin C, Weynand B, Fregimilicka C, Bouzin C, Thurion P, Carlier F, Serré J, Gayan-Ramirez G, Delos M, Ocak S, Burgel PR, Pilette C.

Am J Respir Crit Care Med. 2019 Mar 1;199(5):592-602. doi: 10.1164/rccm.201802-0352OC.


Heparin-free renal replacement therapy for chronic hemodialyzed patients at high risk for bleeding: a comparison of on-line predilution hemodiafiltration with conventional hemodialysis.

Brunot V, Serre JE, Mourad G, Klouche K, Pernin V.

Hemodial Int. 2018 Oct;22(4):463-473. doi: 10.1111/hdi.12668. Epub 2018 May 10.


Stricturing Crohn's disease-like colitis in a patient treated with belatacept.

Bozon A, Jeantet G, Rivière B, Funakoshi N, Dufour G, Combes R, Valats JC, Delmas S, Serre JE, Bismuth M, Ramos J, Le Quintrec M, Blanc P, Pineton de Chambrun G.

World J Gastroenterol. 2017 Dec 28;23(48):8660-8665. doi: 10.3748/wjg.v23.i48.8660.


Nurse-led vaccination program dramatically improves pneumococcal vaccination coverage among patients with autoimmune inflammatory disorders.

Serre J, François C, der Haegen MCV, Papo T, Goulenok T, Sacre K.

Eur J Intern Med. 2017 Sep;43:e43-e45. doi: 10.1016/j.ejim.2017.05.023. Epub 2017 May 26. No abstract available.


Pregnancy outcomes in simultaneous pancreas and kidney transplant recipients: a national French survey study.

Normand G, Brunner F, Badet L, Buron F, Catton M, Massardier J, Esposito L, Grimbert P, Mourad G, Serre JE, Caillard S, Karam G, Cantarovich D, Morelon E, Thaunat O.

Transpl Int. 2017 Sep;30(9):893-902. doi: 10.1111/tri.12983. Epub 2017 Jun 15.


Mortality Associated with Night and Weekend Admissions to ICU with On-Site Intensivist Coverage: Results of a Nine-Year Cohort Study (2006-2014).

Brunot V, Landreau L, Corne P, Platon L, Besnard N, Buzançais A, Daubin D, Serre JE, Molinari N, Klouche K.

PLoS One. 2016 Dec 29;11(12):e0168548. doi: 10.1371/journal.pone.0168548. eCollection 2016.


Primary sclerosing cholangitis: a new cause of distal renal tubular acidosis.

Goutaudier V, Szwarc I, Serre JE, Pageaux GP, Argilés À, Ribstein J.

Clin Kidney J. 2016 Dec;9(6):811-813. Epub 2016 Aug 31.


[Infectious and neoplasic complications after kidney transplantation].

Mourad G, Serre JE, Alméras C, Basel O, Garrigue V, Pernin V, Le Quintrec M.

Nephrol Ther. 2016 Nov;12(6):468-487. doi: 10.1016/j.nephro.2016.06.003. Epub 2016 Sep 24. French.


Treatment Response and Outcomes in Post-transplantation Lymphoproliferative Disease vs Lymphoma in Immunocompetent Patients.

Trusson R, Serre JE, Szwarc I, Brunot V, Garrigue V, Delmas S, Kanouni T, Cartron G, Mourad G.

Transplant Proc. 2016 Jul-Aug;48(6):1927-33. doi: 10.1016/j.transproceed.2016.03.045.


Genome Editing and Dialogic Responsibility: "What's in a Name?".

Blasimme A, Anegon I, Concordet JP, De Vos J, Dubart-Kupperschmitt A, Fellous M, Fouchet P, Frydman N, Giovannangeli C, Jouannet P, Serre JL, Steffann J, Rial-Sebbag E, Thomsen M, Cambon-Thomsen A.

Am J Bioeth. 2015;15(12):54-7. doi: 10.1080/15265161.2015.1103811. No abstract available.


Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.

Jalkh N, Sahbatou M, Chouery E, Megarbane A, Leutenegger AL, Serre JL.

Eur J Hum Genet. 2015 Oct;23(10):1434. doi: 10.1038/ejhg.2015.17. No abstract available.


[The prenatal diagnosis is not the eugenics].

Simon-Bouy B, Serre JL.

Gynecol Obstet Fertil. 2015 Apr;43(4):263-5. doi: 10.1016/j.gyobfe.2015.02.013. Epub 2015 Mar 26. French. No abstract available.


Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.

Jalkh N, Sahbatou M, Chouery E, Megarbane A, Leutenegger AL, Serre JL.

Eur J Hum Genet. 2015 Oct;23(10):1364-9. doi: 10.1038/ejhg.2014.246. Epub 2014 Nov 26. Erratum in: Eur J Hum Genet. 2015 Oct;23(10):1434.


Guide to good practices to ensure privacy protection in secondary use of medical records.

Riou C, Fresson J, Serre JL, Avillach P, Leneveut L, Quantin C; groupe de travail CIMES, CUESP, CNIM, CCTIRS, CNIL.

Rev Epidemiol Sante Publique. 2014 Jun;62(3):207-14. doi: 10.1016/j.respe.2014.03.005. Epub 2014 Jun 2. No abstract available.


[Anonymous sperm donation does not increase the risk for unions between relatives nor the incidence of autosomal recessive diseases due to consanguinity].

Serre JL, Leutenegger AL, Bernheim A, Fellous M, Rouen A, Kunstmann JM, Hyon C, Siffroi JP.

Gynecol Obstet Fertil. 2014 Apr;42(4):200-4. doi: 10.1016/j.gyobfe.2014.02.005. Epub 2014 Mar 26. French. No abstract available.


Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity?

Serre JL, Leutenegger AL, Bernheim A, Fellous M, Rouen A, Siffroi JP.

Hum Reprod. 2014 Mar;29(3):394-9. doi: 10.1093/humrep/det452. Epub 2013 Dec 16.


Maintaining calcineurin inhibition after the diagnosis of post-transplant lymphoproliferative disorder improves renal graft survival.

Serre JE, Michonneau D, Bachy E, Noël LH, Dubois V, Suberbielle C, Kreis H, Legendre C, Mamzer-Bruneel MF, Morelon E, Thaunat O.

Kidney Int. 2014 Jan;85(1):182-90. doi: 10.1038/ki.2013.253. Epub 2013 Jun 26.


[A mini-invasive approach to renal autotransplantation in the management of loin pain hematuria syndrome].

Almaiman H, Serre JE, Abid N, Fouque D, Martin X.

Prog Urol. 2013 May;23(6):389-93. doi: 10.1016/j.purol.2012.11.010. Epub 2013 Jan 3. French.


Simultaneous simulations of uptake in plants and leaching to groundwater of cadmium and lead for arable land amended with compost or farmyard manure.

Legind CN, Rein A, Serre J, Brochier V, Haudin CS, Cambier P, Houot S, Trapp S.

PLoS One. 2012;7(10):e47002. doi: 10.1371/journal.pone.0047002. Epub 2012 Oct 4.


[Rapidly progressive ANCA positive glomerulonephritis as the presenting feature of infectious endocarditis].

Hanf W, Serre JE, Salmon JH, Fabien N, Ginon I, Dijoud F, Trolliet P.

Rev Med Interne. 2011 Dec;32(12):e116-8. doi: 10.1016/j.revmed.2010.12.017. Epub 2011 Jan 31. French.


A whole-genome scan in a large family with leukodystrophy and oligodontia reveals linkage to 10q22.

Chouery E, Delague V, Jalkh N, Salem N, Kfoury J, Rodriguez D, Chabrol B, Boespflug-Tanguy O, Lévy N, Serre JL, Mégarbané A.

Neurogenetics. 2011 Feb;12(1):73-8. doi: 10.1007/s10048-010-0256-3. Epub 2010 Aug 19.


Involvement of the modifier gene of a human Mendelian disorder in a negative selection process.

Jéru I, Hayrapetyan H, Duquesnoy P, Cochet E, Serre JL, Feingold J, Grateau G, Sarkisian T, Jeanpierre M, Amselem S.

PLoS One. 2009 Oct 30;4(10):e7676. doi: 10.1371/journal.pone.0007676.


Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles.

Fauvert D, Brun-Heath I, Lia-Baldini AS, Bellazi L, Taillandier A, Serre JL, de Mazancourt P, Mornet E.

BMC Med Genet. 2009 Jun 6;10:51. doi: 10.1186/1471-2350-10-51.


[Treatment of information on personal health data for research purposes: nobody should ignore the law].

Bonaïti-Pellié C, Arveux P, Billette de Villemeur A, Dantchev N, Elbaz A, Fabre-Guillevin E, Fresson J, Saura C, Saurel-Cubizolles MJ, Serre JL, Simon D, Stucker I, Thélot B, Tubert-Bitter P, Zureik M.

Med Sci (Paris). 2009 Jan;25(1):93-7. doi: 10.1051/medsci/200925193. French. No abstract available.


Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling.

Simon-Bouy B, Taillandier A, Fauvert D, Brun-Heath I, Serre JL, Armengod CG, Bialer MG, Mathieu M, Cousin J, Chitayat D, Liebelt J, Feldman B, Gérard-Blanluet M, Körtge-Jung S, King C, Laivuori H, Le Merrer M, Mehta S, Jern C, Sharif S, Prieur F, Gillessen-Kaesbach G, Zankl A, Mornet E.

Prenat Diagn. 2008 Nov;28(11):993-8. doi: 10.1002/pd.2088.


A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12.

Chouery E, Kfoury J, Delague V, Jalkh N, Bejjani P, Serre JL, Mégarbané A.

Neurogenetics. 2008 Oct;9(4):287-93. doi: 10.1007/s10048-008-0142-4. Epub 2008 Aug 8.


Mutations in TREM2 lead to pure early-onset dementia without bone cysts.

Chouery E, Delague V, Bergougnoux A, Koussa S, Serre JL, Mégarbané A.

Hum Mutat. 2008 Sep;29(9):E194-204. doi: 10.1002/humu.20836.


A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein.

Lia-Baldini AS, Brun-Heath I, Carrion C, Simon-Bouy B, Serre JL, Nunes ME, Mornet E.

Hum Genet. 2008 May;123(4):429-32. doi: 10.1007/s00439-008-0480-1. Epub 2008 Mar 14.


A case of lethal hypophosphatasia providing new insights into the perinatal benign form of hypophosphatasia and expression of the ALPL gene.

Brun-Heath I, Chabrol E, Fox M, Drexler K, Petit C, Taillandier A, De Mazancourt P, Serre JL, Mornet E.

Clin Genet. 2008 Mar;73(3):245-50. Epub 2007 Oct 7.


Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasia.

Brun-Heath I, Lia-Baldini AS, Maillard S, Taillandier A, Utsch B, Nunes ME, Serre JL, Mornet E.

Eur J Med Genet. 2007 Sep-Oct;50(5):367-78. Epub 2007 Jul 21.


Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutations.

Jalkh N, Génin E, Chouery E, Delague V, Medlej-Hashim M, Idrac CA, Mégarbané A, Serre JL.

Ann Hum Genet. 2008 Jan;72(Pt 1):41-7. Epub 2007 Aug 16.


[Various topics in population genetics].

Serre JL.

Presse Med. 2007 Mar;36 Spec No 1:1S26-31. Review. French.


Characterization of missense mutations and large deletions in the ALPL gene by sequencing and quantitative multiplex PCR of short fragments.

Spentchian M, Brun-Heath I, Taillandier A, Fauvert D, Serre JL, Simon-Bouy B, Carvalho F, Grochova I, Mehta SG, Müller G, Oberstein SL, Ogur G, Sharif S, Mornet E.

Genet Test. 2006 Winter;10(4):252-7.


Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations.

Medlej-Hashim M, Serre JL, Corbani S, Saab O, Jalkh N, Delague V, Chouery E, Salem N, Loiselet J, Lefranc G, Mégarbané A.

Eur J Med Genet. 2005 Oct-Dec;48(4):412-20. Epub 2005 Jun 20.


Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype-phenotype correlations.

Brun-Heath I, Taillandier A, Serre JL, Mornet E.

Mol Genet Metab. 2005 Mar;84(3):273-7. Epub 2004 Dec 19.


Childhood hypophosphatasia due to a de novo missense mutation in the tissue-nonspecific alkaline phosphatase gene.

Taillandier A, Sallinen SL, Brun-Heath I, De Mazancourt P, Serre JL, Mornet E.

J Clin Endocrinol Metab. 2005 Apr;90(4):2436-9. Epub 2005 Jan 25.


[Towards an improved antenatal screening for cystic fibrosis].

Serre JL, Feingold J, Simon-Bouy B, Muller F.

Rev Epidemiol Sante Publique. 2003 Apr;51(2):245-53. French.


Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL gene.

Spentchian M, Merrien Y, Herasse M, Dobbie Z, Gläser D, Holder SE, Ivarsson SA, Kostiner D, Mansour S, Norman A, Roth J, Stipoljev F, Taillemite JL, van der Smagt JJ, Serre JL, Simon-Bouy B, Taillandier A, Mornet E.

Hum Mutat. 2003 Jul;22(1):105-6.


Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: results of a French molecular collaborative study based on 641 prospective cases.

Muller F, Simon-Bouy B, Girodon E, Monnier N, Malinge MC, Serre JL; French Collaborative Group.

Am J Med Genet. 2002 Jun 15;110(2):109-15.


Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations.

Medlej-Hashim M, Petit I, Adib S, Chouery E, Salem N, Delague V, Rawashdeh M, Mansour I, Lefranc G, Naman R, Loiselet J, Lecron JC, Serre JL, Mégarbané A.

Eur J Hum Genet. 2001 Nov;9(11):849-54.


A molecular approach to dominance in hypophosphatasia.

Lia-Baldini AS, Muller F, Taillandier A, Gibrat JF, Mouchard M, Robin B, Simon-Bouy B, Serre JL, Aylsworth AS, Bieth E, Delanote S, Freisinger P, Hu JC, Krohn HP, Nunes ME, Mornet E.

Hum Genet. 2001 Jul;109(1):99-108.


Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia.

Taillandier A, Lia-Baldini AS, Mouchard M, Robin B, Muller F, Simon-Bouy B, Serre JL, Bera-Louville A, Bonduelle M, Eckhardt J, Gaillard D, Myhre AG, Körtge-Jung S, Larget-Piet L, Malou E, Sillence D, Temple IK, Viot G, Mornet E.

Hum Mutat. 2001;18(1):83-4.


Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.

Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F.

Ann Hum Genet. 2001 Jan;65(Pt 1):35-41.

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