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Results: 15

1.

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.

PMID:
25596525
2.

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.

Maillard AM, Ruef A, Pizzagalli F, Migliavacca E, Hippolyte L, Adaszewski S, Dukart J, Ferrari C, Conus P, Männik K, Zazhytska M, Siffredi V, Maeder P, Kutalik Z, Kherif F, Hadjikhani N, Beckmann JS, Reymond A, Draganski B, Jacquemont S; 16p11.2 European Consortium.

Mol Psychiatry. 2015 Feb;20(1):140-7. doi: 10.1038/mp.2014.145. Epub 2014 Nov 25.

3.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

Zufferey F, Sherr EH, Beckmann ND, Hanson E, Maillard AM, Hippolyte L, Macé A, Ferrari C, Kutalik Z, Andrieux J, Aylward E, Barker M, Bernier R, Bouquillon S, Conus P, Delobel B, Faucett WA, Goin-Kochel RP, Grant E, Harewood L, Hunter JV, Lebon S, Ledbetter DH, Martin CL, Männik K, Martinet D, Mukherjee P, Ramocki MB, Spence SJ, Steinman KJ, Tjernagel J, Spiro JE, Reymond A, Beckmann JS, Chung WK, Jacquemont S; Simons VIP Consortium; 16p11.2 European Consortium.

J Med Genet. 2012 Oct;49(10):660-8. doi: 10.1136/jmedgenet-2012-101203. Erratum in: J Med Genet. 2014 Jul;51(7):478.

4.

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.

PMID:
20616371
5.

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

Walters RG, Jacquemont S, Valsesia A, de Smith AJ, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa JS, Chèvre JC, Lecoeur C, Vatin V, Bouquillon S, Buxton JL, Boute O, Holder-Espinasse M, Cuisset JM, Lemaitre MP, Ambresin AE, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel JL, Le Caignec C, David A, Isidor B, Cordier MP, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova EG, Henning E, Keogh J, Ellis RJ, Macdermot KD, van Haelst MM, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy RF, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen AL, McCarthy MI, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles ME, O'Rahilly S, Farooqi IS, Männik K, Jarvelin MR, Pattou F, Meyre D, Walley AJ, Coin LJ, Blakemore AI, Froguel P, Beckmann JS.

Nature. 2010 Feb 4;463(7281):671-5. doi: 10.1038/nature08727.

6.

New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.

Devos D, Vuillaume I, de Becdelievre A, de Martinville B, Dhaenens CM, Cuvellier JC, Cuisset JM, Vallée L, Lemaitre MP, Bourteel H, Hachulla E, Wallaert B, Destée A, Defebvre L, Sablonnière B.

Mov Disord. 2006 Dec;21(12):2237-40.

PMID:
17044090
7.

[A study of 100 consecutive children presenting with learning disabilities].

Cuvellier JC, Pandit F, Casalis S, Lemaître MP, Cuisset JM, Platof A, Vallée L.

Arch Pediatr. 2004 Mar;11(3):201-6. French.

PMID:
14992765
8.

MRI in children with mental retardation.

Soto-Ares G, Joyes B, Lemaître MP, Vallée L, Pruvo JP.

Pediatr Radiol. 2003 May;33(5):334-45. Epub 2003 Mar 11.

PMID:
12695867
9.

Late shunt infection: incidence, pathogenesis, and therapeutic implications.

Vinchon M, Lemaitre MP, Vallée L, Dhellemmes P.

Neuropediatrics. 2002 Aug;33(4):169-73.

PMID:
12368984
10.

["Conservative" treatment in the multiply handicapped child].

Vallée L, Lemaitre MP, Pernes P.

Arch Pediatr. 2002 Apr;9 Suppl 1:60s-65s. French.

PMID:
11998415
11.

[Childhood epilepsy syndromes and diseases].

Vallée L, Lemaître MP, Bastos M, Lamblin MD.

Rev Neurol (Paris). 2002 May;158(5 Pt 2):4S9-14. French.

PMID:
11997745
12.

[Epilepsy in the child. Etiology, diagnosis, prognosis, treatment].

Vallée L, Lemaître MP.

Rev Prat. 2001 May 31;51(10):1145-50. French. No abstract available.

PMID:
11468916
13.

[Dysphonia disclosing laryngeal tuberculosis associated with latent pulmonary tuberculosis].

Lemaître MP, Portet L, Londéro A, Lettré MJ, Vincent D, Pradalier A.

Rev Med Interne. 1995;16(5):371-2. French. No abstract available.

PMID:
7597326
14.

Atmospheric physics and Earth observations: sample performance of the grille spectrometer.

Lemaitre MP, Laurent J, Besson J, Girard A, Lippens C, Muller C, Vercheval J, Ackerman M.

Science. 1984 Jul 13;225(4658):171-2.

PMID:
17837928
15.

Profils experimentaux de I'horizon infrarouge de la terre.

Girard A, Lemaitre MP.

Appl Opt. 1970 Apr 1;9(4):903-12. doi: 10.1364/AO.9.000903.

PMID:
20076301
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