Moutard ML - Search Results

1

Agenesis of corpus callosum: prenatal diagnosis and prognosis.

Moutard ML, Kieffer V, Feingold J, Kieffer F, Lewin F, Adamsbaum C, Gélot A, Campistol I Plana J, van Bogaert P, André M, Ponsot G. Moutard ML, et al. Childs Nerv Syst. 2003 Aug;19(7-8):471-6. doi: 10.1007/s00381-003-0781-6. Epub 2003 Jul 4. Childs Nerv Syst. 2003. PMID: 12845459

2

[Post-transfusion cerebrovascular hemorrhagic complications disclosing homozygote sickle cell anemia].

Buissonniere RF, Moutard ML, Ponsot G. Buissonniere RF, et al. Among authors: moutard ml. Arch Fr Pediatr. 1989 Mar;46(3):195-7. Arch Fr Pediatr. 1989. PMID: 2660767 Review. French.

3

Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardation.

des Portes V, Carrié A, Billuart P, Kieffer V, Bienvenu T, Vinet MC, Beldjord C, Kahn A, Ponsot G, Chelly J, Moutard ML. des Portes V, et al. Among authors: moutard ml. Clin Genet. 1998 Feb;53(2):136-41. doi: 10.1111/j.1399-0004.1998.tb02661.x. Clin Genet. 1998. PMID: 9611075

4

[Obstetrical management of agenesis of the corpus callosum].

Descamps P, Lewin F, Body G, Moutard ML. Descamps P, et al. Among authors: moutard ml. Neurochirurgie. 1998 May;44(1 Suppl):93-5. Neurochirurgie. 1998. PMID: 9757328 Clinical Trial. French.

5

[Prognosis of isolated agenesis of the corpus callosum].

Moutard ML, Lewin F, Baron JM, Kieffer V, Descamps P. Moutard ML, et al. Neurochirurgie. 1998 May;44(1 Suppl):96-8. Neurochirurgie. 1998. PMID: 9757329 Clinical Trial. French.

6

[Role of neuropediatrics in prenatal diagnosis].

Moutard ML, Lewin F, Adamsbaum C, Gélot A, Rodriguez D, Ponsot G. Moutard ML, et al. Arch Pediatr. 2001 May;8 Suppl 2:442s-444s. doi: 10.1016/s0929-693x(01)80103-2. Arch Pediatr. 2001. PMID: 11394145 French. No abstract available.

7

Pontoneocerebellar hypoplasia: definition of MR features.

Goasdoué P, Rodriguez D, Moutard ML, Robain O, Lalande G, Adamsbaum C. Goasdoué P, et al. Among authors: moutard ml. Pediatr Radiol. 2001 Sep;31(9):613-8. doi: 10.1007/s002470100507. Pediatr Radiol. 2001. PMID: 11511999

8

[Prenatal diagnosis of isolated posterior fossa anomalies: attempt at a simplified approach].

Adamsbaum C, Merzoug V, André Ch, Fallet-Bianco C, Lewin F, Kalifa G, Rolland Y, Moutard ML. Adamsbaum C, et al. Among authors: moutard ml. J Radiol. 2002 Mar;83(3):321-8. J Radiol. 2002. PMID: 11979225 Review. French.

9

Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation.

Desguerre I, Pinton F, Nabbout R, Moutard ML, N'Guyen S, Marsac C, Ponsot G, Dulac O. Desguerre I, et al. Among authors: moutard ml. Neuropediatrics. 2003 Jun;34(5):265-9. doi: 10.1055/s-2003-43258. Neuropediatrics. 2003. PMID: 14598233

10

Prenatal diagnosis of cerebral malformation with an uncertain prognosis: a study concerning couple's information and consequences on pregnancy.

Moutard ML, Moutel G, François I, Fauriel I, Feingold J, Ponsot G, Hervé C. Moutard ML, et al. Ann Genet. 2004 Jan-Mar;47(1):41-51. doi: 10.1016/j.anngen.2003.10.004. Ann Genet. 2004. PMID: 15050873

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