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Items: 1 to 50 of 73

1.

Contribution of three-dimensional ultrasound and three-dimensional helical computer tomography in the prenatal diagnosis of Stickler Syndrome.

Gueneuc A, Spaggiari E, Millischer AE, Michot C, O'Gorman N, Ville Y.

Ultrasound Obstet Gynecol. 2018 Sep 25. doi: 10.1002/uog.20127. [Epub ahead of print]

PMID:
30251283
2.

Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasia.

Michot C, Le Goff C, Blair E, Blanchet P, Capri Y, Gilbert-Dussardier B, Goldenberg A, Henderson A, Isidor B, Kayserili H, Kinning E, Le Merrer M, Lyonnet S, Odent S, Simsek-Kiper PO, Quelin C, Savarirayan R, Simon M, Splitt M, Verhagen JMA, Verloes A, Munnich A, Baujat G, Cormier-Daire V.

Eur J Hum Genet. 2018 Nov;26(11):1611-1622. doi: 10.1038/s41431-018-0135-1. Epub 2018 Jul 13.

PMID:
30006632
3.

Targeted therapy in patients with PIK3CA-related overgrowth syndrome.

Venot Q, Blanc T, Rabia SH, Berteloot L, Ladraa S, Duong JP, Blanc E, Johnson SC, Hoguin C, Boccara O, Sarnacki S, Boddaert N, Pannier S, Martinez F, Magassa S, Yamaguchi J, Knebelmann B, Merville P, Grenier N, Joly D, Cormier-Daire V, Michot C, Bole-Feysot C, Picard A, Soupre V, Lyonnet S, Sadoine J, Slimani L, Chaussain C, Laroche-Raynaud C, Guibaud L, Broissand C, Amiel J, Legendre C, Terzi F, Canaud G.

Nature. 2018 Jun;558(7711):540-546. doi: 10.1038/s41586-018-0217-9. Epub 2018 Jun 13.

PMID:
29899452
4.

Perinatal and infantile hypophosphatasia: clinical features and treatment.

Baujat G, Michot C, Le Quan Sang KH, Cormier-Daire V.

Arch Pediatr. 2017 May;24(5S2):5S61-5S65. doi: 10.1016/S0929-693X(18)30016-2.

PMID:
29405934
5.

Identification of PITX3 mutations in individuals with various ocular developmental defects.

Zazo Seco C, Plaisancié J, Lupasco T, Michot C, Pechmeja J, Delanne J, Cottereau E, Ayuso C, Corton M, Calvas P, Ragge N, Chassaing N.

Ophthalmic Genet. 2018 Jun;39(3):314-320. doi: 10.1080/13816810.2018.1430243. Epub 2018 Feb 6.

PMID:
29405783
6.

FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta.

Doyard M, Bacrot S, Huber C, Di Rocco M, Goldenberg A, Aglan MS, Brunelle P, Temtamy S, Michot C, Otaify GA, Haudry C, Castanet M, Leroux J, Bonnefont JP, Munnich A, Baujat G, Lapunzina P, Monnot S, Ruiz-Perez VL, Cormier-Daire V.

J Med Genet. 2018 Apr;55(4):278-284. doi: 10.1136/jmedgenet-2017-104999. Epub 2018 Jan 22.

PMID:
29358272
7.

Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1.

Bacrot S, Mechler C, Talhi N, Martin-Coignard D, Roth P, Michot C, Ichkou A, Alibeu O, Nitschke P, Thomas S, Vekemans M, Razavi F, Boutaud L, Attie-Bitach T.

Birth Defects Res. 2018 Apr 3;110(6):538-542. doi: 10.1002/bdr2.1191. Epub 2018 Jan 8.

PMID:
29316359
8.

Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.

Heide S, Chantot-Bastaraud S, Keren B, Harbison MD, Azzi S, Rossignol S, Michot C, Lackmy-Port Lys M, Demeer B, Heinrichs C, Newfield RS, Sarda P, Van Maldergem L, Trifard V, Giabicani E, Siffroi JP, Le Bouc Y, Netchine I, Brioude F.

J Med Genet. 2018 Mar;55(3):205-213. doi: 10.1136/jmedgenet-2017-104919. Epub 2017 Dec 9.

PMID:
29223973
9.

[About twins: Epidemiological, genetic, and obstetrical aspects, specific risks, and outcome].

Tauzin M, Felix A, Michot C, Dedieu C, Aoust L, Fortas F, Guillier C, Ngo J, Wachter PY, Petermann L, Kermorvant-Duchemin E.

Arch Pediatr. 2017 Dec;24(12):1299-1311. doi: 10.1016/j.arcped.2017.09.023. Epub 2017 Nov 21. Review. French.

PMID:
29169712
10.

Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databases.

Baujat G, Choquet R, Bouée S, Jeanbat V, Courouve L, Ruel A, Michot C, Le Quan Sang KH, Lapidus D, Messiaen C, Landais P, Cormier-Daire V.

Orphanet J Rare Dis. 2017 Jun 30;12(1):123. doi: 10.1186/s13023-017-0674-5.

11.

Phenotypes and genotypes in individuals with SMC1A variants.

Huisman S, Mulder PA, Redeker E, Bader I, Bisgaard AM, Brooks A, Cereda A, Cinca C, Clark D, Cormier-Daire V, Deardorff MA, Diderich K, Elting M, van Essen A, FitzPatrick D, Gervasini C, Gillessen-Kaesbach G, Girisha KM, Hilhorst-Hofstee Y, Hopman S, Horn D, Isrie M, Jansen S, Jespersgaard C, Kaiser FJ, Kaur M, Kleefstra T, Krantz ID, Lakeman P, Landlust A, Lessel D, Michot C, Moss J, Noon SE, Oliver C, Parenti I, Pie J, Ramos FJ, Rieubland C, Russo S, Selicorni A, Tümer Z, Vorstenbosch R, Wenger TL, van Balkom I, Piening S, Wierzba J, Hennekam RC.

Am J Med Genet A. 2017 Aug;173(8):2108-2125. doi: 10.1002/ajmg.a.38279. Epub 2017 May 26.

PMID:
28548707
12.

Sleep-disordered breathing and its management in children with achondroplasia.

Tenconi R, Khirani S, Amaddeo A, Michot C, Baujat G, Couloigner V, De Sanctis L, James S, Zerah M, Cormier-Daire V, Fauroux B.

Am J Med Genet A. 2017 Apr;173(4):868-878. doi: 10.1002/ajmg.a.38130. Epub 2017 Feb 27.

PMID:
28239978
13.

Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing.

Kuentz P, St-Onge J, Duffourd Y, Courcet JB, Carmignac V, Jouan T, Sorlin A, Abasq-Thomas C, Albuisson J, Amiel J, Amram D, Arpin S, Attie-Bitach T, Bahi-Buisson N, Barbarot S, Baujat G, Bessis D, Boccara O, Bonnière M, Boute O, Bursztejn AC, Chiaverini C, Cormier-Daire V, Coubes C, Delobel B, Edery P, Chehadeh SE, Francannet C, Geneviève D, Goldenberg A, Haye D, Isidor B, Jacquemont ML, Khau Van Kien P, Lacombe D, Martin L, Martinovic J, Maruani A, Mathieu-Dramard M, Mazereeuw-Hautier J, Michot C, Mignot C, Miquel J, Morice-Picard F, Petit F, Phan A, Rossi M, Touraine R, Verloes A, Vincent M, Vincent-Delorme C, Whalen S, Willems M, Marle N, Lehalle D, Thevenon J, Thauvin-Robinet C, Hadj-Rabia S, Faivre L, Vabres P, Rivière JB.

Genet Med. 2017 Sep;19(9):989-997. doi: 10.1038/gim.2016.220. Epub 2017 Feb 2.

PMID:
28151489
14.

Gain-of-function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome.

Lin AE, Michot C, Cormier-Daire V, L'Ecuyer TJ, Matherne GP, Barnes BH, Humberson JB, Edmondson AC, Zackai E, O'Connor MJ, Kaplan JD, Ebeid MR, Krier J, Krieg E, Ghoshhajra B, Lindsay ME.

Am J Med Genet A. 2016 Oct;170(10):2617-31. doi: 10.1002/ajmg.a.37739. Epub 2016 Jun 14. Review.

PMID:
27302097
15.

Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.

Calmels N, Greff G, Obringer C, Kempf N, Gasnier C, Tarabeux J, Miguet M, Baujat G, Bessis D, Bretones P, Cavau A, Digeon B, Doco-Fenzy M, Doray B, Feillet F, Gardeazabal J, Gener B, Julia S, Llano-Rivas I, Mazur A, Michot C, Renaldo-Robin F, Rossi M, Sabouraud P, Keren B, Depienne C, Muller J, Mandel JL, Laugel V.

Orphanet J Rare Dis. 2016 Mar 22;11:26. doi: 10.1186/s13023-016-0408-0.

16.

A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome.

Nizon M, Henry M, Michot C, Baumann C, Bazin A, Bessières B, Blesson S, Cordier-Alex MP, David A, Delahaye-Duriez A, Delezoïde AL, Dieux-Coeslier A, Doco-Fenzy M, Faivre L, Goldenberg A, Layet V, Loget P, Marlin S, Martinovic J, Odent S, Pasquier L, Plessis G, Prieur F, Putoux A, Rio M, Testard H, Bonnefont JP, Cormier-Daire V.

Clin Genet. 2016 May;89(5):584-9. doi: 10.1111/cge.12720. Epub 2016 Feb 3.

17.

Comments about the paper entitled "Lessons to be learned from an analysis of ammonium nitrate disasters in the last 100 years" by Pittman et al. (J. Hazard. Mater. 280 (2014) 472-477).

Marlair G, Michot C, Turcotte R, Singh S.

J Hazard Mater. 2016 Feb 13;303:177-80. doi: 10.1016/j.jhazmat.2015.05.040. Epub 2015 Jul 10. No abstract available.

PMID:
26293422
18.

RPL10 mutation segregating in a family with X-linked syndromic Intellectual Disability.

Thevenon J, Michot C, Bole C, Nitschke P, Nizon M, Faivre L, Munnich A, Lyonnet S, Bonnefont JP, Portes VD, Amiel J.

Am J Med Genet A. 2015 Aug;167A(8):1908-12. doi: 10.1002/ajmg.a.37094. Epub 2015 Apr 6.

PMID:
25846674
19.

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.

Abi Habib W, Azzi S, Brioude F, Steunou V, Thibaud N, Das Neves C, Le Jule M, Chantot-Bastaraud S, Keren B, Lyonnet S, Michot C, Rossi M, Pasquier L, Gicquel C, Rossignol S, Le Bouc Y, Netchine I.

Hum Mol Genet. 2014 Nov 1;23(21):5763-73. doi: 10.1093/hmg/ddu290. Epub 2014 Jun 10.

PMID:
24916376
20.

Bilateral amastia in a female with X-linked hypohidrotic ectodermal dysplasia.

Al Marzouqi F, Michot C, Dos Santos S, Bonnefont JP, Bodemer C, Hadj-Rabia S.

Br J Dermatol. 2014 Sep;171(3):671-3. doi: 10.1111/bjd.13023. Epub 2014 Aug 11. No abstract available.

PMID:
24689965
21.

Myhre syndrome.

Le Goff C, Michot C, Cormier-Daire V.

Clin Genet. 2014 Jun;85(6):503-13. doi: 10.1111/cge.12365. Epub 2014 Apr 2. Review.

PMID:
24580733
22.

Myhre and LAPS syndromes: clinical and molecular review of 32 patients.

Michot C, Le Goff C, Mahaut C, Afenjar A, Brooks AS, Campeau PM, Destree A, Di Rocco M, Donnai D, Hennekam R, Heron D, Jacquemont S, Kannu P, Lin AE, Manouvrier-Hanu S, Mansour S, Marlin S, McGowan R, Murphy H, Raas-Rothschild A, Rio M, Simon M, Stolte-Dijkstra I, Stone JR, Sznajer Y, Tolmie J, Touraine R, van den Ende J, Van der Aa N, van Essen T, Verloes A, Munnich A, Cormier-Daire V.

Eur J Hum Genet. 2014 Nov;22(11):1272-7. doi: 10.1038/ejhg.2013.288. Epub 2014 Jan 15. Erratum in: Eur J Hum Genet. 2014 Nov;22(11):1340.

23.

Infant deaths in slings.

Madre C, Rambaud C, Avran D, Michot C, Sachs P, Dauger S.

Eur J Pediatr. 2014 Dec;173(12):1659-61. doi: 10.1007/s00431-013-2238-6. Epub 2013 Dec 18.

PMID:
24343674
24.

Parental mosaicism is a pitfall in preimplantation genetic diagnosis of dominant disorders.

Steffann J, Michot C, Borghese R, Baptista-Fernandes M, Monnot S, Bonnefont JP, Munnich A.

Eur J Hum Genet. 2014 May;22(5):711-2. doi: 10.1038/ejhg.2013.164. Epub 2013 Sep 11.

25.

Finger creases lend a hand in Kabuki syndrome.

Michot C, Corsini C, Sanlaville D, Baumann C, Toutain A, Philip N, Busa T, Holder M, Faivre L, Odent S, Delrue MA, Till M, Jacquemont ML, Cordier MP, Goldenberg A, Sanchez E, Alix E, Poisson S, Kayirangwa H, Lacombe D, Gilbert-Dussardier B, Pelet A, Roume J, Jacquette A, Isidor B, Giuliano F, Burglen L, Fradin M, Schaefer E, Alembick Y, Doray B, Moncla A, Héron D, Willems M, Pinson L, Le Quan Sang KH, Le Merrer M, Cormier-Daire V, Sarda P, Amiel J, Lyonnet S, Geneviève D.

Eur J Med Genet. 2013 Oct;56(10):556-60. doi: 10.1016/j.ejmg.2013.07.005. Epub 2013 Aug 7.

26.

Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts.

Michot C, Mamoune A, Vamecq J, Viou MT, Hsieh LS, Testet E, Lainé J, Hubert L, Dessein AF, Fontaine M, Ottolenghi C, Fouillen L, Nadra K, Blanc E, Bastin J, Candon S, Pende M, Munnich A, Smahi A, Djouadi F, Carman GM, Romero N, de Keyzer Y, de Lonlay P.

Biochim Biophys Acta. 2013 Dec;1832(12):2103-14. doi: 10.1016/j.bbadis.2013.07.021. Epub 2013 Aug 6.

27.

Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid.

Essaoui M, Nizon M, Beaujard MP, Carrier A, Tantau J, de Blois MC, Fontaine S, Michot C, Amiel J, Bernard JP, Attié-Bitach T, Vekemans M, Turleau C, Ville Y, Malan V.

Eur J Med Genet. 2013 Sep;56(9):502-5. doi: 10.1016/j.ejmg.2013.06.007. Epub 2013 Jul 4.

PMID:
23832107
28.

Clinical and molecular spectrum of renal malformations in Kabuki syndrome.

Courcet JB, Faivre L, Michot C, Burguet A, Perez-Martin S, Alix E, Amiel J, Baumann C, Cordier MP, Cormier-Daire V, Delrue MA, Gilbert-Dussardier B, Goldenberg A, Jacquemont ML, Jaquette A, Kayirangwa H, Lacombe D, Le Merrer M, Toutain A, Odent S, Moncla A, Pelet A, Philip N, Pinson L, Poisson S, Kim-Han le QS, Roume J, Sanchez E, Willems M, Till M, Vincent-Delorme C, Mousson C, Vinault S, Binquet C, Huet F, Sarda P, Salomon R, Lyonnet S, Sanlaville D, Geneviève D.

J Pediatr. 2013 Sep;163(3):742-6. doi: 10.1016/j.jpeds.2013.02.032. Epub 2013 Mar 25.

PMID:
23535010
29.

Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia.

Michot C, Hubert L, Romero NB, Gouda A, Mamoune A, Mathew S, Kirk E, Viollet L, Rahman S, Bekri S, Peters H, McGill J, Glamuzina E, Farrar M, von der Hagen M, Alexander IE, Kirmse B, Barth M, Laforet P, Benlian P, Munnich A, JeanPierre M, Elpeleg O, Pines O, Delahodde A, de Keyzer Y, de Lonlay P.

J Inherit Metab Dis. 2012 Nov;35(6):1119-28. doi: 10.1007/s10545-012-9461-6. Epub 2012 Apr 6.

PMID:
22481384
30.

Fatal rhabdomyolysis in 2 children with LPIN1 mutations.

Bergounioux J, Brassier A, Rambaud C, Bustarret O, Michot C, Hubert L, Arnoux JB, Laquerriere A, Bekri S, Galene-Gromez S, Bonnet D, Hubert P, de Lonlay P.

J Pediatr. 2012 Jun;160(6):1052-4. doi: 10.1016/j.jpeds.2012.02.033. Epub 2012 Apr 4.

PMID:
22480698
31.

Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis.

Michot C, Le Goff C, Goldenberg A, Abhyankar A, Klein C, Kinning E, Guerrot AM, Flahaut P, Duncombe A, Baujat G, Lyonnet S, Thalassinos C, Nitschke P, Casanova JL, Le Merrer M, Munnich A, Cormier-Daire V.

Am J Hum Genet. 2012 Apr 6;90(4):740-5. doi: 10.1016/j.ajhg.2012.03.003. Epub 2012 Mar 29.

32.

Synovium CD20 expression is a potential new predictor of bone erosion progression in very-early arthritis treated by sequential DMARDs monotherapy -- a pilot study from the VErA cohort.

Lanfant-Weybel K, Michot C, Daveau R, Milliez PY, Auquit-Auckbur I, Fardellone P, Brazier M, Mejjad O, Daragon A, Krzanowska K, Jouen F, Tron F, Le Loarer F, Le Loët X, Vittecoq O.

Joint Bone Spine. 2012 Dec;79(6):574-80. doi: 10.1016/j.jbspin.2011.11.006. Epub 2012 Mar 27.

PMID:
22459417
33.

Aggressive cutaneous infection with Mycobacterium marinum in two patients receiving anti-tumor necrosis factor-alfa agents.

Caron J, Michot C, Fabre S, Godreuil S, Guillot B, Dereure O.

J Am Acad Dermatol. 2011 Nov;65(5):1060-2. doi: 10.1016/j.jaad.2008.12.041. No abstract available.

PMID:
22000874
34.

[Neonatal renal venous thrombosis: the recent experience of Robert-Debré hospital].

Michot C, Garnier A, Neve M, Naudin J, Tsapis M, Dauger S.

Arch Pediatr. 2011 Oct;18(10):1055-61. doi: 10.1016/j.arcped.2011.07.011. Epub 2011 Sep 1. French.

PMID:
21889320
35.

Acute bullous irritant contact dermatitis caused by EMLA® cream.

Kluger N, Raison-Peyron N, Michot C, Guillot B, Bessis D.

Contact Dermatitis. 2011 Sep;65(3):181-3. doi: 10.1111/j.1600-0536.2011.01944.x. No abstract available.

PMID:
21827512
36.

A soft chemistry approach to coating of LiFePO4 with a conducting polymer.

Lepage D, Michot C, Liang G, Gauthier M, Schougaard SB.

Angew Chem Int Ed Engl. 2011 Jul 18;50(30):6884-7. doi: 10.1002/anie.201101661. Epub 2011 Jun 10. No abstract available.

PMID:
21671323
37.

Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4.

Valayannopoulos V, Michot C, Rodriguez D, Hubert L, Saillour Y, Labrune P, de Laveaucoupet J, Brunelle F, Amiel J, Lyonnet S, Enza-Razavi F, Attié-Bitach T, Lacombe D, Bahi-Buisson N, Desguerre I, Chelly J, Burglen L, Boddaert N, de Lonlay P.

Brain. 2012 Jan;135(Pt 1):e199; author reply e200. doi: 10.1093/brain/awr108. Epub 2011 May 23. No abstract available.

PMID:
21609947
38.

Chronic renal graft rejection-associated bullous pemphigoid: A cross-reactive immune response?

Devaux S, Michot C, Mourad G, Guillot B, Dereure O.

Acta Derm Venereol. 2011 Jan;91(1):82-3. doi: 10.2340/00015555-0954. No abstract available.

39.

[PEComas: report of five abdominopelvic cases].

Houlle S, Lemoine F, Francois A, Michot C, Sabourin JC.

Ann Pathol. 2010 Oct;30(5):350-6. doi: 10.1016/j.annpat.2010.06.004. Epub 2010 Oct 8. French.

PMID:
21055522
40.

LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood.

Michot C, Hubert L, Brivet M, De Meirleir L, Valayannopoulos V, Müller-Felber W, Venkateswaran R, Ogier H, Desguerre I, Altuzarra C, Thompson E, Smitka M, Huebner A, Husson M, Horvath R, Chinnery P, Vaz FM, Munnich A, Elpeleg O, Delahodde A, de Keyzer Y, de Lonlay P.

Hum Mutat. 2010 Jul;31(7):E1564-73. doi: 10.1002/humu.21282.

PMID:
20583302
41.

High prevalence of hypophosphataemia at PICU admission in non-malnourished children.

Loudenot A, Michot C, Alberti C, Armoogum P, Tsapis M, Dauger S.

Intensive Care Med. 2010 Aug;36(8):1443-4. doi: 10.1007/s00134-010-1898-1. Epub 2010 May 12. No abstract available.

PMID:
20461502
42.

Anatomical basis of the suprascapular nerve entrapment, and clinical relevance of the supraspinatus fascia.

Duparc F, Coquerel D, Ozeel J, Noyon M, Gerometta A, Michot C.

Surg Radiol Anat. 2010 Mar;32(3):277-84. doi: 10.1007/s00276-010-0631-7. Epub 2010 Feb 21.

PMID:
20309668
43.

Lenalidomide-induced acute acneiform folliculitis of the head and neck: not only the anti-EGF receptor agents.

Michot C, Guillot B, Dereure O.

Dermatology. 2010;220(1):49-50. doi: 10.1159/000258050. Epub 2009 Nov 11. No abstract available.

44.

[Multiple Bowen disease of the lower limbs in elderly women: a rare clinical subset involving therapeutic difficulties].

Maury G, Girard C, Michot C, Guillot B, Dereure O.

Ann Dermatol Venereol. 2009 Jun-Jul;136(6-7):508-12. doi: 10.1016/j.annder.2009.04.011. Epub 2009 May 27. French.

PMID:
19560611
45.

Migraine with aura induced by efalizumab.

Kluger N, Heroum C, Michot C, Guillot B, Bessis D.

Clin Exp Dermatol. 2009 Oct;34(7):e401-2. doi: 10.1111/j.1365-2230.2009.03378.x. Epub 2009 Jun 22. No abstract available.

PMID:
19549238
46.

Subcutaneous panniculitis-like T-cell lymphoma in a patient receiving etanercept for rheumatoid arthritis.

Michot C, Costes V, Gerard-Dran D, Guillot B, Combes B, Dereure O.

Br J Dermatol. 2009 Apr;160(4):889-90. doi: 10.1111/j.1365-2133.2009.09044.x. Epub 2009 Feb 16. No abstract available.

PMID:
19222452
47.

[Neonatal renal venous thrombosis in 2008].

Dauger S, Michot C, Garnier A, Hurtaud-Roux MF.

Arch Pediatr. 2009 Feb;16(2):132-41. doi: 10.1016/j.arcped.2008.11.014. Epub 2009 Jan 15. Review. French.

PMID:
19150233
48.

A teaching programme to improve compliance with guidelines about management of hypovolaemia in the emergency department.

Dauger S, Holvoet L, Pinto-Da-Costa N, Michot C, Aizenfisz S, Angoulvant F.

Acta Paediatr. 2008 Dec;97(12):1746-8. doi: 10.1111/j.1651-2227.2008.01068.x. Epub 2008 Oct 6. No abstract available.

PMID:
18945277
49.

Do routine catheter-tip cultures in the paediatric intensive care unit impact management?

Dauger S, Mariani-Kurkdjian P, Michot C, Neve M, Aizenfisz S.

Intensive Care Med. 2009 Apr;35(4):758-9. doi: 10.1007/s00134-008-1340-0. Epub 2008 Oct 22. No abstract available.

PMID:
18941735
50.

[Continuous monitoring unit in a university hospital: an operating survey].

Dauger S, Michot C, Pinto Da Costa N.

Arch Pediatr. 2008 Jun;15(5):683-5. doi: 10.1016/S0929-693X(08)71875-X. French. No abstract available.

PMID:
18582714

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