Sort by
Items per page

Send to

Choose Destination

Best matches for Vallée L[au]:

[Iron and Neurodevelopment]. Vallée L et al. Arch Pediatr. (2017)

[Evaluating a child after a febrile seizure: Insights on three important issues]. Auvin S et al. Arch Pediatr. (2017)

Postdrome symptoms in pediatric migraine: A questionnaire retrospective study by phone in 100 patients. Mamouri O et al. Cephalalgia. (2018)

Search results

Items: 1 to 50 of 192


Assessing assistive technology requirements in children with written language disorders. A decision tree to guide counseling.

Cado A, Nicli J, Bourgois B, Vallée L, Lemaitre MP.

Arch Pediatr. 2019 Jan;26(1):48-54. doi: 10.1016/j.arcped.2018.11.007. Epub 2018 Dec 13.


Sensing Coated Iron-Oxide Nanoparticles with Spectral Induced Polarization (SIP): Experiments in Natural Sand Packed Flow-Through Columns.

Mellage A, Holmes AB, Linley S, Vallée L, Rezanezhad F, Thomson N, Gu F, Van Cappellen P.

Environ Sci Technol. 2018 Dec 18;52(24):14256-14265. doi: 10.1021/acs.est.8b03686. Epub 2018 Dec 6.


[Mathematical learning disability: A multiple origin? Examples of Turner and Fragile X syndromes].

Deffrennes C, De Clercq M, Vallée L, Lemaître MP.

Arch Pediatr. 2018 Apr;25(3):223-228. doi: 10.1016/j.arcped.2018.01.001. Epub 2018 Mar 14. Review. French.


Effect of desipramine on patients with breathing disorders in RETT syndrome.

Mancini J, Dubus JC, Jouve E, Roux JC, Franco P, Lagrue E, Castelnau P, Cances C, Chaix Y, Rougeot-Jung C, Cornu C, Desportes V, Vallée L, Bahi-Buisson N, Truillet R, Attolini L, Villard L, Blin O, Micallef J.

Ann Clin Transl Neurol. 2017 Dec 27;5(2):118-127. doi: 10.1002/acn3.468. eCollection 2018 Feb.


[Evaluating a child after a febrile seizure: Insights on three important issues].

Auvin S, Antonios M, Benoist G, Dommergues MA, Corrard F, Gajdos V, Gras Leguen C, Launay E, Salaün A, Titomanlio L, Vallée L, Milh M.

Arch Pediatr. 2017 Nov;24(11):1137-1146. doi: 10.1016/j.arcped.2017.08.018. Epub 2017 Sep 29. French.


Anti-HMGCR Antibody-Related Necrotizing Autoimmune Myopathy Mimicking Muscular Dystrophy.

Tard C, Tiffreau V, Jaillette E, Jouen F, Nelson I, Bonne G, Yaou RB, Romero N, Vallée L, Vermersch P, Nguyen S, Maurage CA, Cuisset JM.

Neuropediatrics. 2017 Dec;48(6):473-476. doi: 10.1055/s-0037-1604402. Epub 2017 Aug 4. No abstract available.


Postdrome symptoms in pediatric migraine: A questionnaire retrospective study by phone in 100 patients.

Mamouri O, Cuvellier JC, Duhamel A, Vallée L, Nguyen The Tich S.

Cephalalgia. 2018 Apr;38(5):943-948. doi: 10.1177/0333102417721132. Epub 2017 Jul 20.


[Iron and Neurodevelopment].

Vallée L.

Arch Pediatr. 2017 May;24(5S):5S18-5S22. doi: 10.1016/S0929-693X(17)24005-6. Review. French.


Trigger Factors in Childhood Migraine: A Prospective Clinic-Based Study From North of France.

Solotareff L, Cuvellier JC, Duhamel A, Vallée L, Tich SNT.

J Child Neurol. 2017 Jul;32(8):754-758. doi: 10.1177/0883073817705251. Epub 2017 Apr 24.


Arithmetic Abilities in Children With Developmental Dyslexia: Performance on French ZAREKI-R Test.

De Clercq-Quaegebeur M, Casalis S, Vilette B, Lemaitre MP, Vallée L.

J Learn Disabil. 2018 May/Jun;51(3):236-249. doi: 10.1177/0022219417690355. Epub 2017 Jan 30.


[Classification of children with specific language impairments: What can we think about them in 2016?]

Avenet S, Lemaître MP, Vallée L.

Arch Pediatr. 2016 Oct;23(10):1085-1093. doi: 10.1016/j.arcped.2016.07.009. Epub 2016 Sep 14. French.


[Multidisciplinary management of children with disabling chronic pain in a French pediatric rehabilitation center: Current management and perspectives].

Roessler N, Allen Debeaurepaire C, Deprez A, Tanche L, Pavageau V, Hamain A, Grave C, Yatzimirsky A, Vallée L, Avez-Couturier J.

Arch Pediatr. 2016 Aug;23(8):806-14. doi: 10.1016/j.arcped.2016.05.016. Epub 2016 Jun 23. French.


Stability of Pediatric Migraine Subtype After a 5-year Follow-Up.

Cuvellier JC, Tourte M, Lucas C, Vallée L.

J Child Neurol. 2016 Aug;31(9):1138-42. doi: 10.1177/0883073816643404. Epub 2016 Apr 12.


Assessment of Procedural Pain in Children Using Analgesia Nociception Index: A Pilot Study.

Avez-Couturier J, De Jonckheere J, Jeanne M, Vallée L, Cuisset JM, Logier R.

Clin J Pain. 2016 Dec;32(12):1100-1104.


Health Care Trajectories for Children With ADHD in France: Results From the QUEST Survey.

Caci H, Cohen D, Bonnot O, Kabuth B, Raynaud JP, Paillé S, Vallée L.

J Atten Disord. 2016 Jan 21. pii: 1087054715618790. [Epub ahead of print]


[Management of fractures in the elderly].

Daire R, Thès A, Vallée L, Fourment M, Potel M, Cudennec T.

Soins Gerontol. 2015 Jul-Aug;(114):13-7. doi: 10.1016/j.sger.2015.05.004. French.


[Lemierre syndrome revealed by torticollis].

Ben Abdallah Chabchoub R, Riquet A, Ramdane A, Vallée L, Raccoussot S.

Arch Pediatr. 2015 May;22(5):540-3. doi: 10.1016/j.arcped.2015.02.019. Epub 2015 Mar 31. French.


New spastic paraplegia phenotype associated to mutation of NFU1.

Tonduti D, Dorboz I, Imbard A, Slama A, Boutron A, Pichard S, Elmaleh M, Vallée L, Benoist JF, Ogier H, Boespflug-Tanguy O.

Orphanet J Rare Dis. 2015 Feb 8;10:13. doi: 10.1186/s13023-015-0237-6.


15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.

Vanlerberghe C, Petit F, Malan V, Vincent-Delorme C, Bouquillon S, Boute O, Holder-Espinasse M, Delobel B, Duban B, Vallee L, Cuisset JM, Lemaitre MP, Vantyghem MC, Pigeyre M, Lanco-Dosen S, Plessis G, Gerard M, Decamp M, Mathieu M, Morin G, Jedraszak G, Bilan F, Gilbert-Dussardier B, Fauvert D, Roume J, Cormier-Daire V, Caumes R, Puechberty J, Genevieve D, Sarda P, Pinson L, Blanchet P, Lemeur N, Sheth F, Manouvrier-Hanu S, Andrieux J.

Eur J Med Genet. 2015 Mar;58(3):140-7. doi: 10.1016/j.ejmg.2015.01.002. Epub 2015 Jan 14.


Vagus nerve stimulation for drug-resistant epilepsy: a European long-term study up to 24 months in 347 children.

Orosz I, McCormick D, Zamponi N, Varadkar S, Feucht M, Parain D, Griens R, Vallée L, Boon P, Rittey C, Jayewardene AK, Bunker M, Arzimanoglou A, Lagae L.

Epilepsia. 2014 Oct;55(10):1576-84. doi: 10.1111/epi.12762. Epub 2014 Sep 17.


Further delineation of eye manifestations in homozygous 15q13.3 microdeletions including TRPM1: a differential diagnosis of ceroid lipofuscinosis.

Masurel-Paulet A, Drumare I, Holder M, Cuisset JM, Vallée L, Defoort S, Bourgois B, Pernes P, Cuvellier JC, Huet F, Chehadeh SE, Thevenon J, Callier P, Thauvin C, Faivre L, Andrieux J.

Am J Med Genet A. 2014 Jun;164A(6):1537-44. doi: 10.1002/ajmg.a.36471. Epub 2014 Mar 25.


[Muscle biopsy in children: Usefulness in 2012].

Cuisset JM, Maurage CA, Carpentier A, Briand G, Thévenon A, Rouaix N, Vallée L.

Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):632-9. doi: 10.1016/j.neurol.2012.11.011. Epub 2013 Aug 28. French.


Clinically severe Epstein-Barr virus encephalitis with mild cerebrospinal fluid abnormalities in an immunocompetent adolescent: a case report.

Engelmann I, Nasser H, Belmiloudi S, Le Guern R, Dewilde A, Vallée L, Hober D.

Diagn Microbiol Infect Dis. 2013 Jun;76(2):232-4. doi: 10.1016/j.diagmicrobio.2013.02.024. Epub 2013 Mar 25.


Medication overuse headache in school-aged children: more common than expected?

Cuvellier JC, Nasser H, Vallée L.

Headache. 2013 Feb;53(2):387-8. doi: 10.1111/j.1526-4610.2012.02291.x. No abstract available.


[Neuropsychological disorders and childhood epilepsies].

Vallée L.

Rev Prat. 2012 Dec;62(10):1406-9. Review. French.


Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1.

Douniol M, Jacquette A, Cohen D, Bodeau N, Rachidi L, Angeard N, Cuisset JM, Vallée L, Eymard B, Plaza M, Héron D, Guilé JM.

Dev Med Child Neurol. 2012 Oct;54(10):905-11. doi: 10.1111/j.1469-8749.2012.04379.x. Epub 2012 Aug 3. Review.


De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature.

Becker K, Di Donato N, Holder-Espinasse M, Andrieux J, Cuisset JM, Vallée L, Plessis G, Jean N, Delobel B, Thuresson AC, Annerén G, Ravn K, Tümer Z, Tinschert S, Schrock E, Jønch AE, Hackmann K.

Eur J Med Genet. 2012 Aug-Sep;55(8-9):490-7. doi: 10.1016/j.ejmg.2012.03.003. Epub 2012 Apr 12. Review.


A patient with myoclonic epilepsy in infancy followed by myoclonic astatic epilepsy.

Auvin S, Lamblin MD, Cuvellier JC, Vallée L.

Seizure. 2012 May;21(4):300-3. doi: 10.1016/j.seizure.2012.01.011. Epub 2012 Feb 17.


A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.

Molin AM, Andrieux J, Koolen DA, Malan V, Carella M, Colleaux L, Cormier-Daire V, David A, de Leeuw N, Delobel B, Duban-Bedu B, Fischetto R, Flinter F, Kjaergaard S, Kok F, Krepischi AC, Le Caignec C, Ogilvie CM, Maia S, Mathieu-Dramard M, Munnich A, Palumbo O, Papadia F, Pfundt R, Reardon W, Receveur A, Rio M, Ronsbro Darling L, Rosenberg C, Sá J, Vallee L, Vincent-Delorme C, Zelante L, Bondeson ML, Annerén G.

J Med Genet. 2012 Feb;49(2):104-9. doi: 10.1136/jmedgenet-2011-100534. Epub 2011 Dec 17.


Neuropsychological evaluation and follow-up of children with cerebellar cortical dysplasia.

Jissendi-Tchofo P, Pandit F, Soto-Ares G, Vallee L.

Dev Med Child Neurol. 2011 Dec;53(12):1119-27. doi: 10.1111/j.1469-8749.2011.04117.x. Epub 2011 Nov 11.


The prevalence of triggers in paediatric migraine: a questionnaire study in 102 children and adolescents.

Neut D, Fily A, Cuvellier JC, Vallée L.

J Headache Pain. 2012 Jan;13(1):61-5. doi: 10.1007/s10194-011-0397-2. Epub 2011 Nov 1.


Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability.

Willemsen MH, Vallès A, Kirkels LA, Mastebroek M, Olde Loohuis N, Kos A, Wissink-Lindhout WM, de Brouwer AP, Nillesen WM, Pfundt R, Holder-Espinasse M, Vallée L, Andrieux J, Coppens-Hofman MC, Rensen H, Hamel BC, van Bokhoven H, Aschrafi A, Kleefstra T.

J Med Genet. 2011 Dec;48(12):810-8. doi: 10.1136/jmedgenet-2011-100294. Epub 2011 Oct 15.


Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, de Leeuw N, de Vries BB, Esko T, Fernandez BA, Fernández-Aranda F, Fernández-Real JM, Gratacòs M, Guilmatre A, Hoyer J, Jarvelin MR, Kooy RF, Kurg A, Le Caignec C, Männik K, Platt OS, Sanlaville D, Van Haelst MM, Villatoro Gomez S, Walha F, Wu BL, Yu Y, Aboura A, Addor MC, Alembik Y, Antonarakis SE, Arveiler B, Barth M, Bednarek N, Béna F, Bergmann S, Beri M, Bernardini L, Blaumeiser B, Bonneau D, Bottani A, Boute O, Brunner HG, Cailley D, Callier P, Chiesa J, Chrast J, Coin L, Coutton C, Cuisset JM, Cuvellier JC, David A, de Freminville B, Delobel B, Delrue MA, Demeer B, Descamps D, Didelot G, Dieterich K, Disciglio V, Doco-Fenzy M, Drunat S, Duban-Bedu B, Dubourg C, El-Sayed Moustafa JS, Elliott P, Faas BH, Faivre L, Faudet A, Fellmann F, Ferrarini A, Fisher R, Flori E, Forer L, Gaillard D, Gerard M, Gieger C, Gimelli S, Gimelli G, Grabe HJ, Guichet A, Guillin O, Hartikainen AL, Heron D, Hippolyte L, Holder M, Homuth G, Isidor B, Jaillard S, Jaros Z, Jiménez-Murcia S, Helas GJ, Jonveaux P, Kaksonen S, Keren B, Kloss-Brandstätter A, Knoers NV, Koolen DA, Kroisel PM, Kronenberg F, Labalme A, Landais E, Lapi E, Layet V, Legallic S, Leheup B, Leube B, Lewis S, Lucas J, MacDermot KD, Magnusson P, Marshall C, Mathieu-Dramard M, McCarthy MI, Meitinger T, Mencarelli MA, Merla G, Moerman A, Mooser V, Morice-Picard F, Mucciolo M, Nauck M, Ndiaye NC, Nordgren A, Pasquier L, Petit F, Pfundt R, Plessis G, Rajcan-Separovic E, Ramelli GP, Rauch A, Ravazzolo R, Reis A, Renieri A, Richart C, Ried JS, Rieubland C, Roberts W, Roetzer KM, Rooryck C, Rossi M, Saemundsen E, Satre V, Schurmann C, Sigurdsson E, Stavropoulos DJ, Stefansson H, Tengström C, Thorsteinsdóttir U, Tinahones FJ, Touraine R, Vallée L, van Binsbergen E, Van der Aa N, Vincent-Delorme C, Visvikis-Siest S, Vollenweider P, Völzke H, Vulto-van Silfhout AT, Waeber G, Wallgren-Pettersson C, Witwicki RM, Zwolinksi S, Andrieux J, Estivill X, Gusella JF, Gustafsson O, Metspalu A, Scherer SW, Stefansson K, Blakemore AI, Beckmann JS, Froguel P.

Nature. 2011 Aug 31;478(7367):97-102. doi: 10.1038/nature10406.


Oral administration of docosahexaenoic acid/eicosapentaeinoic acids is not anticonvulsant in rats: implications for translational research.

Curatolo N, Lecointe C, Bordet R, Vallée L, Galabert C, Gressens P, Auvin S.

Pediatr Res. 2011 Dec;70(6):584-8. doi: 10.1203/PDR.0b013e31823277d9.


Brain regional glucose uptake changes in isolated cerebellar cortical dysplasia: qualitative assessment using coregistrated FDG-PET/MRI.

Jissendi-Tchofo P, Pandit F, Vallée L, Vinchon M, Pruvo JP, Baleriaux D, Soto Ares G.

Cerebellum. 2012 Mar;11(1):280-8. doi: 10.1007/s12311-011-0309-7.


Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.

Micol R, Ben Slama L, Suarez F, Le Mignot L, Beauté J, Mahlaoui N, Dubois d'Enghien C, Laugé A, Hall J, Couturier J, Vallée L, Delobel B, Rivier F, Nguyen K, Billette de Villemeur T, Stephan JL, Bordigoni P, Bertrand Y, Aladjidi N, Pedespan JM, Thomas C, Pellier I, Koenig M, Hermine O, Picard C, Moshous D, Neven B, Lanternier F, Blanche S, Tardieu M, Debré M, Fischer A, Stoppa-Lyonnet D; CEREDIH Network Investigators.

J Allergy Clin Immunol. 2011 Aug;128(2):382-9.e1. doi: 10.1016/j.jaci.2011.03.052. Epub 2011 Jun 12.


Insights into genotype-phenotype correlations in spinal muscular atrophy: a retrospective study of 103 patients.

Petit F, Cuisset JM, Rouaix-Emery N, Cancés C, Sablonnière B, Bieth E, Moerman A, Sukno S, Hardy N, Holder-Espinasse M, Manouvrier-Hanu S, Vallée L.

Muscle Nerve. 2011 Jan;43(1):26-30. doi: 10.1002/mus.21832.


A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay.

Bouquillon S, Andrieux J, Landais E, Duban-Bedu B, Boidein F, Lenne B, Vallée L, Leal T, Doco-Fenzy M, Delobel B.

Eur J Med Genet. 2011 Mar-Apr;54(2):194-7. doi: 10.1016/j.ejmg.2010.11.009. Epub 2010 Dec 9.


Usefulness of video-EEG monitoring in children.

Riquet A, Lamblin MD, Bastos M, Bulteau C, Derambure P, Vallée L, Auvin S.

Seizure. 2011 Jan;20(1):18-22. doi: 10.1016/j.seizure.2010.09.011. Epub 2010 Oct 15.


[Characteristics of tuberous sclerosis in children].

Riquet A, Cuisset JM, Cuvellier JC, Joriot S, Petit F, Vallée L.

Arch Pediatr. 2010 Sep;17(9):1338-45. doi: 10.1016/j.arcped.2010.06.019. Epub 2010 Aug 14. French.


Neuropsychological profile on the WISC-IV of French children with dyslexia.

De Clercq-Quaegebeur M, Casalis S, Lemaitre MP, Bourgois B, Getto M, Vallée L.

J Learn Disabil. 2010 Nov-Dec;43(6):563-74. doi: 10.1177/0022219410375000. Epub 2010 Jul 8.


Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhood.

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.

J Pediatr. 2010 Oct;157(4):623-9, 629.e1. doi: 10.1016/j.jpeds.2010.04.020. Epub 2010 May 31.


Premonitory symptoms in migraine patients.

Pascual J, Quintela E, Cuvellier JC, Mars A, Vallée L.

Cephalalgia. 2010 May;30(5):639; author reply 639-40. doi: 10.1177/0333102409357479. Epub 2010 Mar 17. No abstract available.


Infantile epileptic encephalopathy with late-onset spasms: report of 19 patients.

Auvin S, Lamblin MD, Pandit F, Vallée L, Bouvet-Mourcia A.

Epilepsia. 2010 Jul;51(7):1290-6. doi: 10.1111/j.1528-1167.2010.02534.x. Epub 2010 Mar 18.


Delineation of 15q13.3 microdeletions.

Masurel-Paulet A, Andrieux J, Callier P, Cuisset JM, Le Caignec C, Holder M, Thauvin-Robinet C, Doray B, Flori E, Alex-Cordier MP, Beri M, Boute O, Delobel B, Dieux A, Vallee L, Jaillard S, Odent S, Isidor B, Beneteau C, Vigneron J, Bilan F, Gilbert-Dussardier B, Dubourg C, Labalme A, Bidon C, Gautier A, Pernes P, Pinoit JM, Huet F, Mugneret F, Aral B, Jonveaux P, Sanlaville D, Faivre L.

Clin Genet. 2010 Aug;78(2):149-61. doi: 10.1111/j.1399-0004.2010.01374.x. Epub 2010 Feb 9.


[Liaison pediatric psychiatry: a position in between?].

Medjkane F, Vallée L, Delion P.

Arch Pediatr. 2010 Mar;17(3):209-10. doi: 10.1016/j.arcped.2009.12.006. Epub 2010 Feb 18. French. No abstract available.


The prevalence of premonitory symptoms in paediatric migraine: a questionnaire study in 103 children and adolescents.

Cuvellier JC, Mars A, Vallée L.

Cephalalgia. 2009 Nov;29(11):1197-201. doi: 10.1111/j.1468-2982.2009.01854.x.


Treatment of primary headache in children: a multicenter hospital-based study in France.

Cuvellier JC, Donnet A, Guégan-Massardier E, Nachit-Ouinekh F, Parain D, Vallée L; Céleste Study Group.

J Headache Pain. 2009 Dec;10(6):447-53. doi: 10.1007/s10194-009-0158-7. Epub 2009 Sep 22.


The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers.

Cetin E, Cuisset JM, Tiffreau V, Vallée L, Hurtevent JF, Thevenon A.

Ann Phys Rehabil Med. 2009 Sep-Oct;52(7-8):546-55. doi: 10.1016/ Epub 2009 Aug 18. English, French.

Supplemental Content

Loading ...
Support Center