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Items: 1 to 50 of 225

1.

Merkel cell polyomavirus and Langerhans cell neoplasm.

Murakami I, Wada N, Nakashima J, Iguchi M, Toi M, Hashida Y, Higuchi T, Daibata M, Matsushita M, Iwasaki T, Kuwamoto S, Horie Y, Nagata K, Hayashi K, Oka T, Yoshino T, Imamura T, Morimoto A, Imashuku S, Gogusev J, Jaubert F.

Cell Commun Signal. 2018 Aug 22;16(1):49. doi: 10.1186/s12964-018-0261-y. Review.

2.

Mast cells are associated with exacerbations and eosinophilia in children with severe asthma.

Lezmi G, Galmiche-Rolland L, Rioux S, Jaubert F, Tillie-Leblond I, Scheinmann P, Gosset P, de Blic J.

Eur Respir J. 2016 Nov;48(5):1320-1328. doi: 10.1183/13993003.00947-2016. Epub 2016 Oct 6.

3.

Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics.

Murakami I, Oh Y, Morimoto A, Sano H, Kanzaki S, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Nagata K, Hayashi K, Imashuku S, Gogusev J, Jaubert F, Oka T, Yoshino T.

Clin Proteomics. 2015 Jun 18;12(1):16. doi: 10.1186/s12014-015-9089-2. eCollection 2015.

4.

Interleukin-1 loop model for pathogenesis of Langerhans cell histiocytosis.

Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Nagata K, Horie Y, Hayashi K, Imamura T, Morimoto A, Imashuku S, Gogusev J, Jaubert F, Takata K, Oka T, Yoshino T.

Cell Commun Signal. 2015 Feb 22;13:13. doi: 10.1186/s12964-015-0092-z. Review.

5.

Establishment and characterization of a human parathyroid carcinoma derived cell line.

Gogusev J, Murakami I, Telvi L, Goguin A, Sarfati E, Jaubert F.

Pathol Res Pract. 2015 Apr;211(4):332-40. doi: 10.1016/j.prp.2014.12.008. Epub 2014 Dec 23.

PMID:
25655355
6.

Establishment of a Langerhans cell histiocytosis lesion cell line with dermal dendritic cell characteristics.

Murakami I, Gogusev J, Jaubert F, Matsushita M, Hayashi K, Miura I, Tanaka T, Oka T, Yoshino T.

Oncol Rep. 2015 Jan;33(1):171-8. doi: 10.3892/or.2014.3567. Epub 2014 Oct 24.

PMID:
25351656
7.

High viral load of Merkel cell polyomavirus DNA sequences in Langerhans cell sarcoma tissues.

Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Horie Y, Hayashi K, Gogusev J, Jaubert F, Nakamoto S, Yamakawa M, Nakamine H, Takata K, Oka T, Yoshino T.

Infect Agent Cancer. 2014 May 6;9:15. doi: 10.1186/1750-9378-9-15. eCollection 2014.

8.

Merkel cell polyomavirus DNA sequences in peripheral blood and tissues from patients with Langerhans cell histiocytosis.

Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Horie Y, Hayashi K, Imamura T, Morimoto A, Imashuku S, Gogusev J, Jaubert F, Takata K, Oka T, Yoshino T.

Hum Pathol. 2014 Jan;45(1):119-26. doi: 10.1016/j.humpath.2013.05.028.

PMID:
24321520
9.

IL-17A receptor expression differs between subclasses of Langerhans cell histiocytosis, which might settle the IL-17A controversy.

Murakami I, Morimoto A, Oka T, Kuwamoto S, Kato M, Horie Y, Hayashi K, Gogusev J, Jaubert F, Imashuku S, Al-Kadar LA, Takata K, Yoshino T.

Virchows Arch. 2013 Feb;462(2):219-28. doi: 10.1007/s00428-012-1360-6. Epub 2012 Dec 27.

PMID:
23269323
10.

Results of an international comparison for the activity measurement of 177Lu.

Zimmerman BE, Altzitzoglou T, Antohe A, Arinc A, Bakhshandeiar E, Bergeron DE, Bignell L, Bobin C, Capogni M, Cessna JT, Cozzella ML, da Silva CJ, De Felice P, Dias MS, Dziel T, Fazio A, Fitzgerald R, Iwahara A, Jaubert F, Johansson L, Keightley J, Koskinas MF, Kossert K, Lubbe J, Luca A, Mo L, Nähle O, Ott O, Paepen J, Pommé S, Sahagia M, Simpson BR, Silva FF, van Ammel R, van Staden MJ, van Wyngaardt WM, Yamazaki IM.

Appl Radiat Isot. 2012 Sep;70(9):1825-30. doi: 10.1016/j.apradiso.2012.02.014. Epub 2012 Mar 6.

PMID:
22445396
11.

Foxl-2 in gonad development and pathology.

Jaubert F, Galmiche L, Lortat-Jacob S, Fournet JC, Fellous M.

Arkh Patol. 2011 Jul-Aug;73(4):10-3. Review.

PMID:
22164424
12.

The surgical management of atypical forms of congenital hyperinsulinism.

Capito C, de Lonlay P, Verkarre V, Jaubert F, Rahier J, Nihoul-Fékété C, Aigrain Y.

Semin Pediatr Surg. 2011 Feb;20(1):54-5. doi: 10.1053/j.sempedsurg.2010.10.003.

PMID:
21186006
13.

Laronidase for cardiopulmonary disease in Hurler syndrome 12 years after bone marrow transplantation.

Valayannopoulos V, de Blic J, Mahlaoui N, Stos B, Jaubert F, Bonnet D, Fischer A, de Lonlay P.

Pediatrics. 2010 Nov;126(5):e1242-7. doi: 10.1542/peds.2009-2843. Epub 2010 Oct 25.

PMID:
20974778
14.

Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo-obstruction.

Galmiche L, Jaubert F, Sauvat F, Sarnacki S, Goulet O, Assouline Z, Vedrenne V, Lebre AS, Boddaert N, Brousse N, Chrétien D, Munnich A, Rötig A.

Neurogastroenterol Motil. 2011 Jan;23(1):24-9, e1. doi: 10.1111/j.1365-2982.2010.01595.x. Epub 2010 Sep 14.

PMID:
20879992
15.

Neonatal rhabdomyosarcoma misdiagnosed as a congenital hemangioma.

Megarbane H, Doz F, Manach Y, Fletcher C, Jaubert F, de Prost Y, Hamel-Teillac D.

Pediatr Dermatol. 2011 May-Jun;28(3):299-301. doi: 10.1111/j.1525-1470.2010.01210.x. Epub 2010 Aug 4.

PMID:
20738798
16.

Mediastina Tuberculosis mass in a three-month-old boy.

Boussetta K, Tinsa F, Ghaffari H, Brini I, Aloui N, Jaubert F, Bousnina S.

Tunis Med. 2010 Aug;88(8):602-4.

17.

ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.

Bellanné-Chantelot C, Saint-Martin C, Ribeiro MJ, Vaury C, Verkarre V, Arnoux JB, Valayannopoulos V, Gobrecht S, Sempoux C, Rahier J, Fournet JC, Jaubert F, Aigrain Y, Nihoul-Fékété C, de Lonlay P.

J Med Genet. 2010 Nov;47(11):752-9. doi: 10.1136/jmg.2009.075416. Epub 2010 Aug 3.

PMID:
20685672
18.

Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysis.

Mechri M, Epaud R, Emond S, Coulomb A, Jaubert F, Tarrant A, Feldmann D, Flamein F, Clement A, de Blic J, Taam RA, Brunelle F, le Pointe HD.

Pediatr Pulmonol. 2010 Oct;45(10):1021-9. doi: 10.1002/ppul.21289.

19.

Congenital hyperinsulinism.

Arnoux JB, de Lonlay P, Ribeiro MJ, Hussain K, Blankenstein O, Mohnike K, Valayannopoulos V, Robert JJ, Rahier J, Sempoux C, Bellanné C, Verkarre V, Aigrain Y, Jaubert F, Brunelle F, Nihoul-Fékété C.

Early Hum Dev. 2010 May;86(5):287-94. doi: 10.1016/j.earlhumdev.2010.05.003. Epub 2010 Jun 13. Review.

PMID:
20550977
20.

Application of a stochastic TDCR model based on Geant4 for Cherenkov primary measurements.

Bobin C, Thiam C, Bouchard J, Jaubert F.

Appl Radiat Isot. 2010 Dec;68(12):2366-71. doi: 10.1016/j.apradiso.2010.05.012. Epub 2010 Jun 9.

PMID:
20542706
21.

Unusual virilization in girls with juvenile granulosa cell tumors of the ovary is related to intratumoral aromatase deficiency.

Kalfa N, Méduri G, Philibert P, Patte C, Boizet-Bonhoure B, Thibaut E, Pienkowski C, Jaubert F, Misrahi M, Sultan C.

Horm Res Paediatr. 2010;74(2):83-91. doi: 10.1159/000313396. Epub 2010 Apr 15.

PMID:
20395670
22.

Retrospective French nationwide survey of childhood aggressive vascular anomalies of bone, 1988-2009.

Héritier S, Le Merrer M, Jaubert F, Bigorre M, Gillibert-Yvert M, de Courtivron B, Ziade M, Bertrand Y, Carrie C, Chastagner P, Bost-Bru C, Léonard JC, Ouache M, Boccon-Gibod L, Mary P, de Blic J, Pin I, Wendling D, Revillon Y, Houdoin V, Forin V, Lepointe HD, Languepin J, Wagnon J, Epaud R, Fauroux B, Donadieu J.

Orphanet J Rare Dis. 2010 Feb 3;5:3. doi: 10.1186/1750-1172-5-3.

23.

Study of the influence of the liquid scintillator in the Compton efficiency tracing method.

Cassette P, Jaubert F, Tartes I.

Appl Radiat Isot. 2010 Jul-Aug;68(7-8):1510-4. doi: 10.1016/j.apradiso.2009.11.065. Epub 2009 Dec 2.

PMID:
20045340
24.

NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome".

Guillot L, Carré A, Szinnai G, Castanet M, Tron E, Jaubert F, Broutin I, Counil F, Feldmann D, Clement A, Polak M, Epaud R.

Hum Mutat. 2010 Feb;31(2):E1146-62. doi: 10.1002/humu.21183.

PMID:
20020530
25.

Deletion of Pten in the mouse enteric nervous system induces ganglioneuromatosis and mimics intestinal pseudoobstruction.

Puig I, Champeval D, De Santa Barbara P, Jaubert F, Lyonnet S, Larue L.

J Clin Invest. 2009 Dec;119(12):3586-96. doi: 10.1172/JCI39929. Epub 2009 Nov 2.

26.

Complete androgen insensitivity syndrome: diagnosis and management.

Cheikhelard A, Thibaud E, Morel Y, Jaubert F, Lortat-Jacob S, Polak M, Nihoul-Fekete C.

Expert Rev Endocrinol Metab. 2009 Nov;4(6):565-573. doi: 10.1586/eem.09.31.

PMID:
30780790
27.

Value of 18F-fluoro-L-dopa PET in the preoperative localization of focal lesions in congenital hyperinsulinism.

Capito C, Khen-Dunlop N, Ribeiro MJ, Brunelle F, Aigrain Y, Crétolle C, Jaubert F, De Lonlay P, Nihoul-Fékété C.

Radiology. 2009 Oct;253(1):216-22. doi: 10.1148/radiol.2532081445. Epub 2009 Aug 25.

PMID:
19709999
28.

Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model.

Fourcade L, Mousseau Y, Jaubert F, Sturtz FG.

Neurosci Lett. 2009 Sep 18;461(2):126-30. doi: 10.1016/j.neulet.2009.06.009. Epub 2009 Jun 17.

PMID:
19539706
29.

[Diagnosis and management of 46,XY mixed gonadal dysgenesis and disorder of sexual differentiation].

Verkauskas G, Macianskyte D, Janciauskas D, Preiksa RT, Verkauskiene R, Jaubert F.

Medicina (Kaunas). 2009;45(5):357-64. Lithuanian.

30.

WNT/beta-catenin pathway activation in Wilms tumors: a unifying mechanism with multiple entries?

Corbin M, de Reyniès A, Rickman DS, Berrebi D, Boccon-Gibod L, Cohen-Gogo S, Fabre M, Jaubert F, Faussillon M, Yilmaz F, Sarnacki S, Landman-Parker J, Patte C, Schleiermacher G, Antignac C, Jeanpierre C.

Genes Chromosomes Cancer. 2009 Sep;48(9):816-27. doi: 10.1002/gcc.20686.

PMID:
19530245
31.

Low renal mineralocorticoid receptor expression at birth contributes to partial aldosterone resistance in neonates.

Martinerie L, Viengchareun S, Delezoide AL, Jaubert F, Sinico M, Prevot S, Boileau P, Meduri G, Lombès M.

Endocrinology. 2009 Sep;150(9):4414-24. doi: 10.1210/en.2008-1498. Epub 2009 May 28.

32.

Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome.

de Pontual L, Mathieu Y, Golzio C, Rio M, Malan V, Boddaert N, Soufflet C, Picard C, Durandy A, Dobbie A, Heron D, Isidor B, Motte J, Newburry-Ecob R, Pasquier L, Tardieu M, Viot G, Jaubert F, Munnich A, Colleaux L, Vekemans M, Etchevers H, Lyonnet S, Amiel J.

Hum Mutat. 2009 Apr;30(4):669-76. doi: 10.1002/humu.20935.

PMID:
19235238
33.

Familial interstitial disease with I73T mutation: A mid- and long-term study.

Abou Taam R, Jaubert F, Emond S, Le Bourgeois M, Epaud R, Karila C, Feldmann D, Scheinmann P, de Blic J.

Pediatr Pulmonol. 2009 Feb;44(2):167-75. doi: 10.1002/ppul.20970.

PMID:
19148933
34.

Neonatal bilateral ovarian sex cord stromal tumors.

Capito C, Flechtner I, Thibaud E, Emond S, Kalfa N, Jaubert F, Sarnacki S.

Pediatr Blood Cancer. 2009 Mar;52(3):401-3. doi: 10.1002/pbc.21775.

PMID:
19058207
35.

Serous and seromucinous infantile ovarian cystadenomas--a study of 42 cases.

Massicot R, Rousseau V, Darwish AA, Sauvat F, Jaubert F, Nihoul-Fékété C.

Eur J Obstet Gynecol Reprod Biol. 2009 Jan;142(1):64-7. doi: 10.1016/j.ejogrb.2008.09.007. Epub 2008 Nov 8.

PMID:
18996636
36.

Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutions.

Clément-Ziza M, Munnich A, Lyonnet S, Jaubert F, Besmond C.

RNA. 2008 Dec;14(12):2698-704. doi: 10.1261/rna.1261708. Epub 2008 Oct 22.

37.

Constitutively active Akt1 expression in mouse pancreas requires S6 kinase 1 for insulinoma formation.

Alliouachene S, Tuttle RL, Boumard S, Lapointe T, Berissi S, Germain S, Jaubert F, Tosh D, Birnbaum MJ, Pende M.

J Clin Invest. 2008 Nov;118(11):3629-38. doi: 10.1172/JCI35237. Epub 2008 Oct 9.

38.

Predictive value of postoperative glycosuria after partial elective pancreatectomy in focal congenital hyperinsulinism.

Khen-Dunlop N, Capito C, Valayannopoulos V, Elie C, Ribeiro MJ, Rahier J, Jaubert F, Robert JJ, Aigrain Y, de Lonlay P, Fékété CN.

Diabetes Care. 2008 Oct;31(10):e71. doi: 10.2337/dc08-0596. No abstract available.

PMID:
18820217
39.

Management of Wilms tumors in Drash and Frasier syndromes.

Auber F, Jeanpierre C, Denamur E, Jaubert F, Schleiermacher G, Patte C, Cabrol S, Leverger G, Nihoul-Fékété C, Sarnacki S.

Pediatr Blood Cancer. 2009 Jan;52(1):55-9. doi: 10.1002/pbc.21759.

PMID:
18816692
40.

Herpes-virus infection in patients with Langerhans cell histiocytosis: a case-controlled sero-epidemiological study, and in situ analysis.

Jeziorski E, Senechal B, Molina TJ, Devez F, Leruez-Ville M, Morand P, Glorion C, Mansuy L, Gaudelus J, Debre M, Jaubert F, Seigneurin JM, Thomas C, Joab I, Donadieu J, Geissmann F.

PLoS One. 2008 Sep 23;3(9):e3262. doi: 10.1371/journal.pone.0003262.

41.

Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism.

Damaj L, le Lorch M, Verkarre V, Werl C, Hubert L, Nihoul-Fékété C, Aigrain Y, de Keyzer Y, Romana SP, Bellanne-Chantelot C, de Lonlay P, Jaubert F.

J Clin Endocrinol Metab. 2008 Dec;93(12):4941-7. doi: 10.1210/jc.2008-0673. Epub 2008 Sep 16.

PMID:
18796520
42.

Rhabdomyosarcoma an ubiquitous pediatric tumour.

Verkarre V, Galmiche-Rolland L, Sarnacki S, Jaubert F.

Arkh Patol. 2008 May-Jun;70(3):50-3.

PMID:
18727437
43.

Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in children.

Kalfa N, Fellous M, Boizet-Bonhoure B, Patte C, Duvillard P, Pienkowski C, Jaubert F, Ecochard A, Sultan C.

J Urol. 2008 Oct;180(4 Suppl):1810-3. doi: 10.1016/j.juro.2008.03.097. Epub 2008 Aug 21.

PMID:
18721930
44.

Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.

Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, Jaubert F, Polak M, Nihoul-Fekete C.

J Urol. 2008 Oct;180(4):1496-501. doi: 10.1016/j.juro.2008.06.045. Epub 2008 Aug 16.

PMID:
18710728
45.

Transcription factors involved in pancreas development are expressed in paediatric solid pseudopapillary tumours.

Galmiche L, Sarnacki S, Verkarre V, Boizet B, Duvillie B, Fabre M, Jaubert F.

Histopathology. 2008 Sep;53(3):318-24. doi: 10.1111/j.1365-2559.2008.03108.x. Epub 2008 Jul 29.

PMID:
18671802
46.

[Hyperinsulinism in children: new concepts - the role of imaging].

Brunelle F, Ribeiro M, Boddaert N, Nihoul-Fekete C, Jaubert F, Rahier J, de Lonlay P.

Bull Acad Natl Med. 2008 Jan;192(1):59-70; discussion 71-2. French.

PMID:
18663982
47.

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.

Faussillon M, Murakami I, Bichat M, Telvi L, Jeanpierre C, Nezelof C, Jaubert F, Gogusev J.

Cancer Genet Cytogenet. 2008 Jul;184(1):22-30. doi: 10.1016/j.cancergencyto.2008.02.018.

PMID:
18558285
48.

High cyclin E staining index in blastemal, stromal or epithelial cells is correlated with tumor aggressiveness in patients with nephroblastoma.

Berrebi D, Leclerc J, Schleiermacher G, Zaccaria I, Boccon-Gibod L, Fabre M, Jaubert F, El Ghoneimi A, Jeanpierre C, Peuchmaur M.

PLoS One. 2008 May 21;3(5):e2216. doi: 10.1371/journal.pone.0002216.

49.

Cerebral localization of Rosai-Dorfman disease in a child. Case report.

Di Rocco F, Garnett MR, Puget S, Pueyerredon F, Roujeau T, Jaubert F, Sainte-Rose C.

J Neurosurg. 2007 Aug;107(2 Suppl):147-51. doi: 10.3171/PED-07/08/147.

PMID:
18459887
50.

Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.

Crétolle C, Pelet A, Sanlaville D, Zérah M, Amiel J, Jaubert F, Révillon Y, Baala L, Munnich A, Nihoul-Fékété C, Lyonnet S.

Hum Mutat. 2008 Jul;29(7):903-10. doi: 10.1002/humu.20718.

PMID:
18449898

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