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Items: 33

1.

Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study.

Frémeaux-Bacchi V, Sellier-Leclerc AL, Vieira-Martins P, Limou S, Kwon T, Lahoche A, Novo R, Llanas B, Nobili F, Roussey G, Cailliez M, Ulinski T, Deschênes G, Alberti C, Weill FX, Mariani P, Loirat C.

Clin J Am Soc Nephrol. 2019 Mar 7;14(3):364-377. doi: 10.2215/CJN.05830518. Epub 2019 Jan 23.

PMID:
30674459
2.

Hepatocarcinoma and Cholestasis Associated to Germline Hemizygous Deletion of Gene HNF1B.

de Leusse C, Maues De Paula A, Aschero A, Parache C, Hery G, Cailliez M, Missirian C, Fabre A.

J Pediatr Gastroenterol Nutr. 2019 May;68(5):e85. doi: 10.1097/MPG.0000000000002015. No abstract available.

PMID:
29727438
3.

Patterns of Clinical Response to Eculizumab in Patients With C3 Glomerulopathy.

Le Quintrec M, Lapeyraque AL, Lionet A, Sellier-Leclerc AL, Delmas Y, Baudouin V, Daugas E, Decramer S, Tricot L, Cailliez M, Dubot P, Servais A, Mourey-Epron C, Pourcine F, Loirat C, Frémeaux-Bacchi V, Fakhouri F.

Am J Kidney Dis. 2018 Jul;72(1):84-92. doi: 10.1053/j.ajkd.2017.11.019. Epub 2018 Feb 9.

PMID:
29429752
4.

C5 nephritic factors drive the biological phenotype of C3 glomerulopathies.

Marinozzi MC, Chauvet S, Le Quintrec M, Mignotet M, Petitprez F, Legendre C, Cailliez M, Deschenes G, Fischbach M, Karras A, Nobili F, Pietrement C, Dragon-Durey MA, Fakhouri F, Roumenina LT, Fremeaux-Bacchi V.

Kidney Int. 2017 Nov;92(5):1232-1241. doi: 10.1016/j.kint.2017.04.017. Epub 2017 Jul 14.

PMID:
28712854
5.

Clinical and Genetic Spectrum of Bartter Syndrome Type 3.

Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, Simian C, Deschenes G, Kwon T, Bertholet-Thomas A, Bobrie G, Borde JS, Bourdat-Michel G, Decramer S, Cailliez M, Krug P, Cozette P, Delbet JD, Dubourg L, Chaveau D, Fila M, Jourde-Chiche N, Knebelmann B, Lavocat MP, Lemoine S, Djeddi D, Llanas B, Louillet F, Merieau E, Mileva M, Mota-Vieira L, Mousson C, Nobili F, Novo R, Roussey-Kesler G, Vrillon I, Walsh SB, Teulon J, Blanchard A, Vargas-Poussou R.

J Am Soc Nephrol. 2017 Aug;28(8):2540-2552. doi: 10.1681/ASN.2016101057. Epub 2017 Apr 5.

6.

Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation.

Fakhouri F, Fila M, Provôt F, Delmas Y, Barbet C, Châtelet V, Rafat C, Cailliez M, Hogan J, Servais A, Karras A, Makdassi R, Louillet F, Coindre JP, Rondeau E, Loirat C, Frémeaux-Bacchi V.

Clin J Am Soc Nephrol. 2017 Jan 6;12(1):50-59. doi: 10.2215/CJN.06440616. Epub 2016 Oct 31.

7.

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.

Mansour-Hendili L, Blanchard A, Le Pottier N, Roncelin I, Lourdel S, Treard C, González W, Vergara-Jaque A, Morin G, Colin E, Holder-Espinasse M, Bacchetta J, Baudouin V, Benoit S, Bérard E, Bourdat-Michel G, Bouchireb K, Burtey S, Cailliez M, Cardon G, Cartery C, Champion G, Chauveau D, Cochat P, Dahan K, De la Faille R, Debray FG, Dehoux L, Deschenes G, Desport E, Devuyst O, Dieguez S, Emma F, Fischbach M, Fouque D, Fourcade J, François H, Gilbert-Dussardier B, Hannedouche T, Houillier P, Izzedine H, Janner M, Karras A, Knebelmann B, Lavocat MP, Lemoine S, Leroy V, Loirat C, Macher MA, Martin-Coignard D, Morin D, Niaudet P, Nivet H, Nobili F, Novo R, Faivre L, Rigothier C, Roussey-Kesler G, Salomon R, Schleich A, Sellier-Leclerc AL, Soulami K, Tiple A, Ulinski T, Vanhille P, Van Regemorter N, Jeunemaître X, Vargas-Poussou R.

Hum Mutat. 2015 Aug;36(8):743-52. doi: 10.1002/humu.22804. Epub 2015 Jun 11. Review.

PMID:
25907713
8.

Rituximab fails where eculizumab restores renal function in C3nef-related DDD.

Rousset-Rouvière C, Cailliez M, Garaix F, Bruno D, Laurent D, Tsimaratos M.

Pediatr Nephrol. 2014 Jun;29(6):1107-11. doi: 10.1007/s00467-013-2711-5. Epub 2014 Jan 10.

PMID:
24408225
9.

Diagnosis of Streptococcus pneumoniae-associated hemolytic uremic syndrome.

Loupiac A, Elayan A, Cailliez M, Adra AL, Decramer S, Thouret MC, Harambat J, Guigonis V.

Pediatr Infect Dis J. 2013 Oct;32(10):1045-9. doi: 10.1097/INF.0b013e31829ee872.

PMID:
24067551
10.

Long-term outcome of children treated with rituximab for idiopathic nephrotic syndrome.

Tellier S, Brochard K, Garnier A, Bandin F, Llanas B, Guigonis V, Cailliez M, Pietrement C, Dunand O, Nathanson S, Bertholet-Thomas A, Ichay L, Decramer S.

Pediatr Nephrol. 2013 Jun;28(6):911-8. doi: 10.1007/s00467-012-2406-3. Epub 2013 Jan 23.

PMID:
23340857
11.

Cystinosin is a melanosomal protein that regulates melanin synthesis.

Chiaverini C, Sillard L, Flori E, Ito S, Briganti S, Wakamatsu K, Fontas E, Berard E, Cailliez M, Cochat P, Foulard M, Guest G, Niaudet P, Picardo M, Bernard FX, Antignac C, Ortonne JP, Ballotti R.

FASEB J. 2012 Sep;26(9):3779-89. doi: 10.1096/fj.11-201376. Epub 2012 May 30.

PMID:
22649030
12.

In vivo reflectance confocal microscopy of the skin: a noninvasive means of assessing body cystine accumulation in infantile cystinosis.

Chiavérini C, Kang HY, Sillard L, Berard E, Niaudet P, Guest G, Cailliez M, Bahadoran P, Lacour JP, Ballotti R, Ortonne JP.

J Am Acad Dermatol. 2013 Apr;68(4):e111-e116. doi: 10.1016/j.jaad.2011.08.010. Epub 2011 Oct 2.

PMID:
21963264
13.

Mycophenolate mofetil for steroid-dependent nephrotic syndrome: a phase II Bayesian trial.

Baudouin V, Alberti C, Lapeyraque AL, Bensman A, André JL, Broux F, Cailliez M, Decramer S, Niaudet P, Deschênes G, Jacqz-Aigrain E, Loirat C.

Pediatr Nephrol. 2012 Mar;27(3):389-96. doi: 10.1007/s00467-011-2006-7. Epub 2011 Sep 28.

PMID:
21947272
14.

Population pharmacokinetics and Bayesian estimator of mycophenolic acid in children with idiopathic nephrotic syndrome.

Zhao W, Elie V, Baudouin V, Bensman A, André JL, Brochard K, Broux F, Cailliez M, Loirat C, Jacqz-Aigrain E.

Br J Clin Pharmacol. 2010 Apr;69(4):358-66. doi: 10.1111/j.1365-2125.2010.03615.x.

15.

[How to delay progression of chronic renal failure?].

Garaix F, Rousset Rouvière C, Cailliez M, Bruno D, Tsimaratos M.

Arch Pediatr. 2009 Jun;16(6):703-5. doi: 10.1016/S0929-693X(09)74119-3. French. No abstract available.

PMID:
19541137
16.

[Kidney and vaculitis in children].

Rousset-Rouvière C, Garaix F, Cailliez M, Bruno D, Coulibaly B, Daniel L, Tsimaratos M.

Arch Pediatr. 2009 Jun;16(6):529-31. doi: 10.1016/S0929-693X(09)74055-2. French. No abstract available.

PMID:
19541073
17.

Enteric-coated mycophenolate sodium in de novo pediatric renal transplant patients.

Niaudet P, Charbit M, Loirat C, Lapeyraque AL, Tsimaratos M, Cailliez M, Foulard M, Dehennault M, Marquet P, Chaouche-Teyara K, Lemay D.

Pediatr Nephrol. 2009 Feb;24(2):395-402. doi: 10.1007/s00467-008-1031-7. Epub 2008 Nov 5.

PMID:
18985393
18.

[Mycophenolate mofetil restores renal function and spares steroids during idiopathic nephrotic syndrome in children. A cohort study].

Cailliez M, Bruno D, Daniel L, Afaneti M, Bérard E, Sarles J, Tsimaratos M.

Nephrol Ther. 2008 Feb;4(1):15-20. Epub 2007 Dec 21. French.

PMID:
18096455
19.

Anakinra is safe and effective in controlling hyperimmunoglobulinaemia D syndrome-associated febrile crisis.

Cailliez M, Garaix F, Rousset-Rouvière C, Bruno D, Kone-Paut I, Sarles J, Chabrol B, Tsimaratos M.

J Inherit Metab Dis. 2006 Dec;29(6):763. Epub 2006 Nov 10.

PMID:
17103011
20.

Crescentic glomerulonephritis is part of hyperimmunoglobulinemia D syndrome.

Cailliez M, Garaix F, Rousset-Rouvière C, Bruno D, Daniel L, Chabrol B, Sarles J, Tsimaratos M.

Pediatr Nephrol. 2006 Dec;21(12):1917-8. Epub 2006 Sep 1. No abstract available.

PMID:
16947033
21.

Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

Vargas-Poussou R, Houillier P, Le Pottier N, Strompf L, Loirat C, Baudouin V, Macher MA, Déchaux M, Ulinski T, Nobili F, Eckart P, Novo R, Cailliez M, Salomon R, Nivet H, Cochat P, Tack I, Fargeot A, Bouissou F, Kesler GR, Lorotte S, Godefroid N, Layet V, Morin G, Jeunemaître X, Blanchard A.

J Am Soc Nephrol. 2006 May;17(5):1437-43. Epub 2006 Apr 12.

22.

[Neonatal screening of glucose-6-phosphate dehydrogenase deficiency in umbilical cord blood].

Kaddari F, Sawadogo M, Sancho J, Lelong M, Jaby D, Paulin C, Nkana K, Cailliez M.

Ann Biol Clin (Paris). 2004 Jul-Aug;62(4):446-50. French.

23.

[Multicenter study of commercial kits for the determination of human IgG subclasses, using the ELISA technique].

Pontet F, Pressac M, Musset L, Tapon-Bretaudière J, Jehl C, Cailliez M, Bienvenu F.

Ann Biol Clin (Paris). 1994;52(7-8):555-60. French.

PMID:
7840432
24.

[Sero-immunologic diagnosis of human African trypanosomiasis: cross reactions of various parasitoses and hyperglobulinemias].

Poupin F, Cailliez M, Petithory JC, Savel J.

Bull Soc Pathol Exot Filiales. 1983 Aug-Oct;76(4):393-405. French.

PMID:
6627552
25.

[Use of multidimensional technics of analysis in the study of specific immunoglobulins in human African trypanosomiasis].

Cailliez M, Poupin F, Pages JP, Savel J.

C R Seances Soc Biol Fil. 1982;176(5):643-9. French.

PMID:
6220766
26.

[Blood proteins in African trypanosomiasis: variations and statistical interpretations].

Cailliez M, Poupin F, Pages JP, Savel J.

C R Seances Soc Biol Fil. 1982;176(5):633-42. French.

PMID:
6220765
27.

[A comparative study of the morphology of the Trypanosoma brucei brucei trypomastigote using photonic microscopy and scanning electron microscopy (author's transl)].

Gorenflot A, Poupin F, Cailliez M, Piette C, Savel J, Piette M.

Ann Pharm Fr. 1980;38(2):105-18. French. No abstract available.

PMID:
7416690
28.

[Human african trypanosomiasis. Immunoenzymological diagnosis].

Cailliez M, Poupin F, Savel J, Carrie C, Petithory JC.

Nouv Presse Med. 1979 Feb 10;8(7):522-3. French. No abstract available.

PMID:
379814
29.

[Comparative study of immunoenzyme technics, ELISA and on formed antigens, in the immunologic diagnosis of African trypanosomiasis].

Poupin F, Cailliez M, Carrie C, Petithory JC, Savel J.

Bull Soc Pathol Exot Filiales. 1978 Nov-Dec;71(6):430-40. French.

PMID:
385160
30.

[Hyaline membrane disease: early diagnosis by determination of lecithin/sphingomyelin ratio in the gastric fluid of the newborn].

Retbi JM, Allemon MC, Pilliot M, Dayras JC, Cailliez M, Genest AF.

Nouv Presse Med. 1978 Jun 24;7(25):2263. French. No abstract available.

PMID:
673800
31.

[Comparative value of immunofluorescence and immunoenzymology on figured antigen in the immunological diagnosis of African trypanosomiasis].

Cailliez M, Poupin F, Carrié C, Petithory JC, Savel J.

Bull Soc Pathol Exot Filiales. 1977 Jul-Aug;70(4):391-8. French.

PMID:
352560
32.

[Electrosyneresis in the diagnosis of African trypanosomiasis].

Poupin F, Cailliez M, Petithory JC, Savel J.

Bull Soc Pathol Exot Filiales. 1976 Jan-Feb;69(1):76-83. French.

PMID:
825237
33.

[Preparation of a standardized antigenic extract from several strains of African trypansomes].

Cailliez M, Poupin F, Petithory JC, Savel J.

Bull Soc Pathol Exot Filiales. 1975 Jan-Feb;68(1):67-73. French.

PMID:
1242121

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