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SERVICE DE PEDIATRIE DE SPECIALITES ET DE MEDECINE INFANTILEC.H.U. Timone - Enfants / Rue Sain-Pierre / 13385 Marseille 05
Téléphone : 04-91-38-68-07 / 0491386806
Fax : 04-91-38-68-09
Courriel : bchabrol@ap-hm.fr
Equipes Acueil des Masters Contrats Liste des Personnels Publications des 2 dernières années Thèses
| Effectifs |
Enseignants - Chercheurs et Ingénieurs Universitaires : 5
Médecins hospitaliers : 7
Chercheurs et Ingénieurs (INSERM, CNRS, autres) :
Personnel Administratif et Technique Universitaire :
Personnel Administratif et Technique (INSERM, CNRS, autres) :
Internes : 6
Etudiants (3ème cycle,Post-Doc, Boursiers...) :
| Equipes de recherche |
- MALADIES METABOLIQUES DE L'ENFANT - (Responsable : Brigitte CHABROL-GIRAUD)
- TROUBLE D'APPRENTISSAGE DU LANGAGE - (Responsable : Julien MANCINI)
- CENTRE DE REFERENCE DES MALADIES HEREDITAIRES DU METABOLISME - (Responsable : Aline CANO)
- TROUBLES D'APPRENTISSAGE DU LANGAGE : TRAITEMENT TEMPOREL, INVESTIGATIONS CLINIQUES ET
- APPLICATIONS THERAPEUTIQUES - (Responsable : Michel HABIB )
- PRISE EN CHARGE DES TROUBLES DES APPRENTISSAGES DE L'ENFANT - (Responsable : Catherine HUGONENQ)
- GERMES EMERGENTS ET LEURS TRAITEMENTS DANS LA MUCOVISCIDOSE - (Responsable : Jean-Christophe DUBUS )
| BOSDURE Emmanuelle - PH | 04-91-38-68-07 |
| BRUN-HENIN Florence - PH (temps partiel) | 04-91-38-68-08 |
| CANO Aline - PH | 04-91-38-48-00 |
| CHABROL-GIRAUD Brigitte - PU-PH | 04-91-38-68-06 |
| DAVID Marion - CCA | 04-91-38-68-07 |
| DUBUS Jean-Christophe - PU-PH | 04-91-38-68-07 |
| HABIB Michel - PH | 04-91-38-68-08 |
| HALBERT Cécile - CCA | 04-91-38-68-07 |
| HUGONENQ Catherine - PH | 04-91-38-45-27 |
| MANCINI/MALLAN Josette - PU-PH | 04-91-38-68-07 |
| MILH Mathieu - PH | 04-91-38-68-13 |
| PECH Catherine - PH (temps partiel) | 04-91-38-68-08 |
| Publications des 2 dernières années |
| - | Anheim M, Monga B, Fleury M, Charles P, Barbot C, Salih M, Delaunoy JP, Fritsch M, Arning L, Synofzik M, Schöls L, Sequeiros J, Goizet C, Marelli C, Le Ber I, Koht J, Gazulla J, De Bleecker J, Mukhtar M, Drouot N, Ali-Pacha L, Benhassine T, Chbicheb M, M'Zahem A, Hamri A, Chabrol B, Pouget J, Murphy R,Watanabe M, Coutinho P, Tazir M, Durr A, Brice A, Tranchant C, Koenig M. Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain. 2009;132(Pt 10):2688-98. |
| - | Armougom F, Bittar F, Stremler N, Rolain JM, Robert C, Dubus JC, Sarles J, Raoult D, La Scola B. Microbial diversity in the sputum of a cystic fibrosis patient studied with 16S rDNA pyrosequencing. Eur J Clin Microbiol Infect Dis. 2009 Sep;28(9):1151-4. |
| - | Broeders ME, Sanchis J, Levy ML, Crompton GK, Dekhuijzen PN; ADMIT Working Group. The ADMIT series--issues in inhalation therapy. 2. Improving technique and clinical effectiveness. Prim Care Respir J. 2009 Jun;18(2):76-82. |
| - | Burgel PR, de Blic J, Chanez P, Delacourt C, Devillier P, Didier A, Dubus JC, Frachon I, Garcia G, Humbert M, Laurent F, Louis R, Magnan A, Mahut B, Perez T, Roche N, Tillie-Leblond I, Tunon de Lara M, Dusser D. Update on the roles of distal airways in asthma. Eur Respir Rev. 2009 Jun 1;18(112):80-95. |
| - | Cardoso C, Boys A, Parrini E, Mignon-Ravix C, McMahon JM, Khantane S, Bertini E, Pallesi E, Missirian C, Zuffardi O, Novara F, Villard L, Giglio S, Chabrol B, Slater HR, Moncla A, Scheffer IE, Guerrini R. Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion. Neurology. 2009;72:784-92. |
| - | Chabrol B, Halbert C, Milh M, Mancini J. Handicap: définition et classification. Arch Pediatr. 2009 ;16:912-4. |
| - | Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A; French Dystonia Network. Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia. Brain. 2009;132(Pt 7):1753-63. |
| - | de Blic J, Deschildre A, Pin I, Dubus JC; GRAPP. [When and how to modify the management of asthma in children over the age of 4]. Rev Mal Respir. 2009 Oct;26(8):827-35. |
| - | Delacourt C, Dubus JC, de Blic J. [Involvement of distal airways in asthma: lessons from pediatric cohorts]. Rev Mal Respir. 2009 Feb;26(2):147-52. |
| - | Devillier P, Naline E, Dubus JC. [Why and how to measure and optimize lung deposition of inhaled drugs]. Rev Mal Respir. 2009 Dec;26(10):1127-37. |
| - | Halbert C, Chabrol B. Essais cliniques dans les maladies neuromusculaires de l'enfant. Arch Pediatr. 2009;16:684-6. |
| - | Heijerman H, Westerman E, Conway S, Touw D, Döring G; consensus working group. Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus. J Cyst Fibros. 2009 Sep;8(5):295-315. |
| - | Khammar A, Stremler N, Dubus JC, Gross G, Sarles J, Reynaud R. [Value of continuous glucose monitoring in screening for diabetes in cystic fibrosis]. Arch Pediatr. 2009 Dec;16(12):1540-6. |
| - | Laforêt P, Acquaviva-Bourdain C, Rigal O, Brivet M, Penisson-Besnier I, Chabrol B, Chaigne D, Boespflug-Tanguy O, Laroche C, Bedat-Millet AL, Behin A, Delevaux I, Lombès A, Andresen BS, Eymard B, Vianey-Saban C. Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency. Neuromuscul Disord. 2009;19:324-9. |
| - | Lavorini F, Levy ML, Dekhuijzen PN, Crompton GK; ADMIT Working Group. Inhaler choice and inhalation technique: key factors for asthma control. Prim Care Respir J. 2009 Dec;18(4):241-2. |
| - | Mikaeloff Y, Caridade G, Suissa S, Tardieu M; KIDSEP Study Group. Clinically observed chickenpox and the risk of childhood-onset multiple sclerosis. Am J Epidemiol. 2009;169:1260-6. |
| - | Milh M, Chabrol B. Epilepsie chez l'enfant. Rev Prat. 2009; 59:689-93. |
| - | Milh M, Chabrol B. Epilepsie de l'enfant. Rev Prat. 2009;59:689-93 |
| - | Milh M, Villeneuve N, Chabrol B. Mise au point : traitement de l'état de mal épileptique de l'enfant. Arch Pediatr. 2009;16:790-2. |
| - | Milh M, Villeneuve N, Chapon F, Pineau S, Lamoureux S, Livet MO, Bartoli C, Hugonenq C, Mancini J, Chabrol B, Girard N. Transient brain magnetic resonance imaging hyperintensity in basal ganglia and brain stem of epileptic infants treated with vigabatrin. J Child Neurol. 2009;24:305-15. |
| - | Milh M, Villeneuve N, Chabrol B. Traitement de l'état de mal convuslif aspects actuelss. Arch Pediatr. 2009;16:790-2. |
| - | Nicolino M, Byrne B, Wraith JE, Leslie N, Mandel H, Freyer DR, Arnold GL, Pivnick EK, Ottinger CJ, Robinson PH, Loo JC, Smitka M, Jardine P, Tatò L, Chabrol B, McCandless S, Kimura S, Mehta L, Bali D, Skrinar A, Morgan C, Rangachari L, Corzo D, Kishnani PS. Clinical outcomes after long-term treatmentwith alglucosidase alfa in infants and children with advanced Pompe disease.Genet Med. 2009;11:210-9 |
| - | Ramachandran N, Munteanu I, Wang P, Aubourg P, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B, Pellissier JF, Minetti C, Udd B, Fardeau M, Tailor CS, Mahuran DJ, Kissel JT, Kalimo H, Levy N, Manolson MF, Ackerley CA, Minassian BA. VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification. Cell. 2009;137:235-46. |
| - | Rolain JM, François P, Hernandez D, Bittar F, Richet H, Fournous G, Mattenberger Y, Bosdure E, Stremler N, Dubus JC, Sarles J, Reynaud-Gaubert M, Boniface S, Schrenzel J, Raoult D. Genomic analysis of an emerging multiresistant Staphylococcus aureus strain rapidly spreading in cystic fibrosis patients revealed the presence of an antibiotic inducible bacteriophage. Biol Direct. 2009Jan 13;4:1. |
| - | Sabouraud P, Cuisset JM, Cances C, Chabrier S, Antoine JC, Richelme C, Chabrol B, Desguerre I, Rivier F; Commission Maladies Neuromusculaires de la Société Française de Neurologie Pédiatrique. Approche diagnostique d'une élévation des créatine-kinase chez l'enfant. Arch Pediatr. 2009;16:678-80. |
| - | Saillour Y, Carion N, Quelin C, Leger PL, Boddaert N, Elie C, Toutain A, Mercier S, Barthez MA, Milh M, Joriot S, des Portes V, Philip N, Broglin D, Roubertie A, Pitelet G, Moutard ML, Pinard JM, Cances C, Kaminska A, Chelly J, Beldjord C, Bahi-Buisson N. LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity. Arch Neurol. 2009;66:1007-15. |
| - | Tessonnier L, Guedj E, Cano A, Cammilleri S, Dragulescu A, Chabrol B, Mundler O. Multiple distal pulmonary arterial thromboses revealed by lung scintigraphy in a patient with homocystinuria and normal multidetector CT pulmonary angiography. Clin Nucl Med. 2009 ;34:42-3. |
| - | Tyzio R, Khalilov I, Represa A, Crepel V, Zilberter Y, Rheims S, Aniksztejn L, Cossart R, Nardou R, Mukhtarov M, Minlebaev M, Epsztein J, Milh M, Becq H, Jorquera I, Bulteau C, Fohlen M, Oliver V, Dulac O, Dorfmüller G, Delalande O, Ben-Ari Y, Khazipov R. Inhibitory actions of the gamma-aminobutyric acid in pediatric Sturge-Weber syndrome. Ann Neurol. 2009;66:209-18. |
| - | Zeidan S, Gorincour G, Potier A, Ughetto F, Dubus JC, Chrestian MA, Grosse C, Gamerre M, Guys JM, de Lagausie P. Congenital lung malformation: evaluation of prenatal and postnatal radiological findings. Respirology. 2009 Sep;14(7):1005-11. |
| - | Zeidan S, Hery G, Lacroix F, Gorincour G, Potier A, Dubus JC, Guys JM, de Lagausie P. Intraloba sequestration associated with cystic adenomatoid malformation: diagnostic and thoracoscopic pitfalls. Surg Endosc. 2009 Aug;23(8):1750-3. |
| - | David M, Luc-Vanuxem C, Loundou A, Bosdure E, Auquier P, Dubus JC. [Assessment of the French Consensus Conference for Acute Viral Bronchiolitis on outpatient management: progress between 2003 and 2008]. Arch Pediatr. 2010 Feb;17(2):125-31. |
| - | Forler J, Carsin A, Arlaud K, Bosdure E, Viard L, Paut O, Camboulives J, Dubus JC. [Respiratory complications of accidental drownings in children]. Arch Pediatr. 2010 Jan;17(1):14-8. |
| - | Abel L, Plancoulaine S, Jouanguy E, Zhang SY, Mahfoufi N, Nicolas N, Sancho-Shimizu V, Alcaïs A, Guo Y, Cardon A, Boucherit S, Obach D, Clozel T, Lorenzo L, Amsallem D, Berquin P, Blanc T, Bost-Bru C, Chabrier S, Chabrol B, Cheuret E, Dulac O, Evrard P, Héron B, Lazaro L, Mancini J, Pedespan JM, Rivier F, Vallée L, Lebon P, Rozenberg F, Casanova JL, Tardieu M.Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhood.J Pediatr. 2010 Oct;157(4):623-9, 629.e1 |
| - | Agostini G, Mancini J, Chabrol B, Villeneuve N, Milh M, George F, Maurel B B, Girard N. Troubles du langage chez les enfants porteurs d'anomalies morphologiques de l'hippocampe. Arch Pediatr. 2010;17:1008-16 |
| - | Bittar F, Stremler N, Audié JP, Dubus JC, Sarles J, Raoult D, Rolain JM. Nocardia farcinica lung infection in a patient with cystic fibrosis: a case report. J Med Case Reports. 2010 Mar 8;4:84. |
| - | Bittar F, Cassagne C, Bosdure E, Stremler N, Dubus JC, Sarles J, Reynaud-Gaubert M, Raoult D, Rolain JM. Outbreak of Corynebacterium pseudodiphtheriticum infection in cystic fibrosis patients, France. Emerg Infect Dis. 2010 Aug;16(8):1231-6. |
| - | Blau N, Bélanger-Quintana A, Demirkol M, Feillet F, Giovannini M, MacDonald A, Trefz FK, van Spronsen F; European PKU centers. Management of phenylketonuria in Europe: survey results from 19 countries. Mol Genet Metab. 2010;99:109-15. |
| - | Busa T, Stremler-Le Bel N, Bosdure E, Bittar F, Rolain JM, Dubus JC. Hygiene of nasal masks used at home for non-invasive ventilation in children. J Hosp Infect. 2010 Oct;76(2):187-8. |
| - | Cacciagli P, Haddad MR, Mignon-Ravix C, El-Waly B, Moncla A, Missirian C, Chabrol B, Villard L.Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype. Eur J Hum Genet. 2010 Dec; 18(12) :1360-3 |
| - | Carsin A, Mely L, Chrestian MA, Devred P, de Lagausie P, Guys JM, Dubus JC. Association of three different congenital malformations in a same pulmonary lobe in a 5-year-old girl. Pediatr Pulmonol. 2010 Aug;45(8):832-5. |
| - | Chabrol B.[Therapies in the Niemann-Pick type C disease].Arch Pediatr. 2010 Jun;17 Suppl 2:S54-7 |
| - | Collongues N, Marignier R, Zéphir H, Papeix C, Blanc F, Ritleng C, Tchikviladzé M, Outteryck O, Vukusic S, Fleury M, Fontaine B, Brassat D, Clanet M, Milh M, Pelletier J, Audoin B, Ruet A, Lebrun-Frenay C, Thouvenot E, Camu W, Debouverie M, Créange A, Moreau T, Labauge P, Castelnovo G, Edan G, Le Page E, Defer G, Barroso B, Heinzlef O, Gout O, Rodriguez D, Wiertlewski S, Laplaud D, Borgel F, Tourniaire P, Grimaud J, Brochet B, Vermersch P, Confavreux C, de Seze J. Neuromyelitis optica in France: a multicenter study of 125 patients. Neurology. 2010;74:736-42. |
| - | Colonnese MT, Kaminska A, Minlebaev M, Milh M, Bloem B, Lescure S, Moriette G, Chiron C, Ben-Ari Y, Khazipov R. A conserved switch in sensory processing prepares developing neocortex for vision. Neuron. 2010;67:480-98 |
| - | Danvin C, Bosdure E, Brémond V, Rousset-Rouvière C, Loundou DA, Barreau-Baumstark K, Dubus JC. [BCG and infants with a high risk of tuberculosis: a study of the vaccination rate in Marseille after suspension of the BCG requirement]. Arch Pediatr. 2010 Nov;17(11):1510-5. |
| - | David M, Luc-Vanuxem C, Loundou A, Bosdure E, Auquier P, Dubus JC. [Assessment of the French Consensus Conference for Acute Viral Bronchiolitis on outpatient management: progress between 2003 and 2008]. Arch Pediatr. 2010 Feb;17(2):125-31. |
| - | Denis D, Girard N, Toesca E, Zanin E, Gambarelli N, Lebranchu P, Mancini J [MRI in congenital nystagmus]. J Fr Ophtalmol. 2010 Mar;33(3):189-205. |
| - | Dubus JC, Bosdure E, David M, Stremler-Lebel N. [Nanoparticles and health]. Arch Pediatr. 2010 Jun;17(6):600-1. |
| - | Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A, Pientka FK, Hellenbroich Y, Kalscheuer VM, Kohlhase J, Moog U, Rappold G, Rauch A, Ropers HH, von Spiczak S, Tönnies H, Villeneuve N, Villard L, Zabel B, Zenker M, Laube B, Reis A, Wieczorek D, Van Maldergem L, Kutsche K. Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet. 2010;42:1021-6 |
| - | Fernandez C, Halbert C, De Paula AM, Lacroze V, Froissart R, Figarella-Branger D, Chabrol B, Pellissier JF. Non-lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations. Muscle Nerve. 2010;41:269-71. |
| - | Forler J, Carsin A, Arlaud K, Bosdure E, Viard L, Paut O, Camboulives J, Dubus JC. [Respiratory complications of accidental drownings in children]. Arch Pediatr. 2010 Jan;17(1):14-8. |
| - | Fuhrman C, Delacourt C, De Blic J, Dubus JC, Thumerelle C, Marguet C, Delmas MC. [Hospital admissions for asthma exacerbation in children]. Arch Pediatr. 2010 Apr;17(4):366-72. |
| - | Jennesson M, Milh M, Villeneuve N, Guedj E, Marie PY, Vignal JP, Raffo E, Vespignani H, Mancini J, Maillard L. Posterior glucose hypometabolism in Lafora disease: early and late FDG-PET assessment. Epilepsia. 2010 Apr;51(4):708-11. |
| - | Jover M, Schmitz C, Centelles L, Chabrol B, Assaiante C.Anticipatory postural adjustments in a bimanual load-lifting task in children with developmental coordination disorder.Dev Med Child Neurol. 2010 Sep;52(9):850-5. |
| - | Jubin V, Ranque S, Stremler Le Bel N, Sarles J, Dubus JC. Risk factors for Aspergillus colonization and allergic bronchopulmonary aspergillosis in children with cystic fibrosis. Pediatr Pulmonol. 2010 Aug;45(8):764-71. |
| - | Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V, Gubser-Mercati D, Funalot B, Brueton L, Sanchez Del Pozo J, Muñoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, Sarda P, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A, Dollfus H. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. Hum Mutat. 2010 ;31:113-26. |
| - | Le Guillou S, Casalta JP, Fraisse A, Kreitmann B, Chabrol B, Dubus JC, Bosdure E. [Infective endocarditis in children without underlying heart disease: a retrospective study analyzing 11 cases]. Arch Pediatr. 2010 Jul;17(7):1047-55. |
| - | Leen WG, Klepper J, Verbeek MM, Leferink M, Hofste T, van Engelen BG, Wevers RA, Arthur T, Bahi-Buisson N, Ballhausen D, Bekhof J, van Bogaert P, Carrilho I, Chabrol B, Champion MP, Coldwell J, Clayton P, Donner E, Evangeliou A, Ebinger F, Farrell K, Forsyth RJ, de Goede CG, Gross S, Grunewald S, Holthausen H, Jayawant S, Lachlan K, Laugel V, Leppig K, Lim MJ, Mancini G, Marina AD, Martorell L, McMenamin J, Meuwissen ME, Mundy H, Nilsson NO, Panzer A, Poll-The BT, Rauscher C, Rouselle CM, Sandvig I, Scheffner T, Sheridan E, Simpson N, Sykora P, Tomlinson R, Trounce J, Webb D, Weschke B, Scheffer H, Willemsen MA Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder..Brain. 2010 Mar;133(Pt 3):655-70. |
| - | Lesca G, Boutry-Kryza N, de Toffol B, Milh M, Steschenko D, Lemesle-Martin M, Maillard L, Foletti G, Rudolf G, Nielsen JE, á Rogvi-Hansen B, Erdal J, Mancini J, Thauvin-Robinet C, M'Rrabet A, Ville D, Szepetowski P, Raffo E, Hirsch E, Ryvlin P, Calender A, Genton P. Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease. Epilepsia. 2010;51:1691-8 |
| - | Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A. Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. J Med Genet. 2010;47:49-53. |
| - | Mignon-Ravix C, Cacciagli P, El-Waly B, Moncla A, Milh M, Girard N, Chabrol B, Philip N, Villard L. Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia. J Med Genet. 2010; 47:132-6. |
| - | Mourdi N, Dubus JC, Bavoux F, Boyer-Gervoise M, Jean-Pastor MJ, Chalumeau M. [Mucolytic drugs: towards a contraindication in infants]. Arch Pediatr. 2010 Jun;17(6):735-6. |
| - | Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK; RettSearch Consortium. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. 2010 Dec;68(6):944-50 |
| - | Pedersen S, Dubus JC, Crompton GK; ADMIT Working Group. The ADMIT series--issues in inhalation therapy. 5) Inhaler selection in children with asthma. Prim Care Respir J. 2010 Sep;19(3):209-16. |
| - | Raoult D, Fenollar F, Rolain JM, Minodier P, Bosdure E, Li W, Garnier JM, Richet H. Tropheryma whipplei in children with gastroenteritis. Emerg Infect Dis. 2010 May;16(5):776-82. |
| - | Rouzier C, Le Guédard-Méreuze S, Fragaki K, Serre V, Miro J, Tuffery-Giraud S, Chaussenot A, Bannwarth S, Caruba C, Ostergaard E, Pellissier JF, Richelme C, Espil C, Chabrol B, Paquis-Flucklinger V The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein.J Med Genet. 2010 Oct;47(10):670-6. |
| - | Santos A, Duret M, Mancini J, Busuttil M, Deruelle C. Does preterm birth affect global and configural processing differently? Dev Med Child Neurol. 2010 Mar;52(3):293-8. |
| - | Sauvaget E, Dellamonica J, Arlaud K, Sanfiorenzo C, Bernardin G, Padovani B, Viard L, Dubus JC. Idiopathic acute eosinophilic pneumonia requiring ECMO in a teenager smoking tobacco and cannabis. Pediatr Pulmonol. 2010 Dec;45(12):1246-9. |
| - | Steenweg ME, Jakobs C, Errami A, van Dooren SJ, Adeva Bartolomé MT, Aerssens P, Augoustides-Savvapoulou P, Baric I, Baumann M, Bonafé L, Chabrol B, Clarke JT, Clayton P, Coker M, Cooper S, Falik-Zaccai T, Gorman M, Hahn A, Hasanoglu A, King MD, de Klerk HB, Korman SH, Lee C, Meldgaard Lund A, Mejaski-Bosnjak V, Pascual-Castroviejo I, Raadhyaksha A, Rootwelt T, Roubertie A, Ruiz-Falco ML, Scalais E, Schimmel U, Seijo-Martinez M, Suri M, Sykut-Cegielska J, Trefz FK, Uziel G, Valayannopoulos V, Vianey-Saban C, Vlaho S, Vodopiutz J, Wajner M, Walter J, Walter-Derbort C, Yapici Z, Zafeiriou DI, Spreeuwenberg MD, Celli J, den Dunnen JT, van der Knaap MS, Salomons GS. An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study. Hum Mutat. 2010;31(4):380-390. |
| - | Viehweger E, Boulay C, Halbert C, Zürcher L, Bollini G, Chabrol B, Jouve JL.[Preoperative workup in severely handicapped children: evaluation and therapeutic approaches].Arch Pediatr. 2010 Jun;17(6):638-9. |
| - | Vincken W, Dekhuijzen PR, Barnes P; ADMIT Group. The ADMIT series - Issues in inhalation therapy. 4) How to choose inhaler devices for the treatment of COPD. Prim Care Respir J. 2010 Mar;19(1):10-20. |
| - | Ziegler JC, Pech-Georgel C, Dufau S, Grainger J. Rapid processing of letters, digits and symbols: what purely visual-attentional deficit in developmental dyslexia? Dev Sci. 2010 Jul;13(4):F8-F14. |
© Faculté de Médecine de Marseill l Mentions légales l Mise à jour du 23 février 2012