Catala M - Search Results

1

PINK1 and FLNA mutations association: A role for atypical parkinsonism?

Degos B, Toussaint A, Lesage S, Brice A, Vidailhet M, Beldjord C, Catala M. Degos B, et al. Among authors: catala m. Parkinsonism Relat Disord. 2016 May;26:78-80. doi: 10.1016/j.parkreldis.2016.02.023. Epub 2016 Mar 2. Parkinsonism Relat Disord. 2016. PMID: 26969111 No abstract available.

2

Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): a prospective study of 130 patients with inherited peripheral neuropathies.

Ravisé N, Dubourg O, Tardieu S, Aurias F, Mercadiel M, Coullin P, Ruberg M, Catala M, Lesourd S, Brice A, LeGuern E. Ravisé N, et al. Among authors: catala m. Am J Med Genet A. 2003 Apr 1;118A(1):43-8. doi: 10.1002/ajmg.a.10190. Am J Med Genet A. 2003. PMID: 12605439

3

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.

des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrié A, Gelot A, Dupuis E, Motte J, Berwald-Netter Y, Catala M, Kahn A, Beldjord C, Chelly J. des Portes V, et al. Among authors: catala m. Cell. 1998 Jan 9;92(1):51-61. doi: 10.1016/s0092-8674(00)80898-3. Cell. 1998. PMID: 9489699 Free article.

4

Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.

Brioude F, Netchine I, Praz F, Le Jule M, Calmel C, Lacombe D, Edery P, Catala M, Odent S, Isidor B, Lyonnet S, Sigaudy S, Leheup B, Audebert-Bellanger S, Burglen L, Giuliano F, Alessandri JL, Cormier-Daire V, Laffargue F, Blesson S, Coupier I, Lespinasse J, Blanchet P, Boute O, Baumann C, Polak M, Doray B, Verloes A, Viot G, Le Bouc Y, Rossignol S. Brioude F, et al. Among authors: catala m. Hum Mutat. 2015 Sep;36(9):894-902. doi: 10.1002/humu.22824. Epub 2015 Aug 6. Hum Mutat. 2015. PMID: 26077438

5

A male fetus with aqueductal stenosis and four accessory spleens. A case report with a tentative genetic explanation.

Catala M, Aubert V, Lesourd S, Héron D, Vauthier-Brouzes D, Harpey JP. Catala M, et al. Pediatr Neurosurg. 1996 Jul;25(1):36-40. doi: 10.1159/000121094. Pediatr Neurosurg. 1996. PMID: 9055333

6

Agenesis of the corpus callosum.

Catala M, Lesourd S. Catala M, et al. J Neurosurg. 1997 May;86(5):914. doi: 10.3171/jns.1997.86.5.0914. J Neurosurg. 1997. PMID: 9126915 No abstract available.

7

The role of primary cilia in corpus callosum formation is mediated by production of the Gli3 repressor.

Laclef C, Anselme I, Besse L, Catala M, Palmyre A, Baas D, Paschaki M, Pedraza M, Métin C, Durand B, Schneider-Maunoury S. Laclef C, et al. Among authors: catala m. Hum Mol Genet. 2015 Sep 1;24(17):4997-5014. doi: 10.1093/hmg/ddv221. Epub 2015 Jun 12. Hum Mol Genet. 2015. PMID: 26071364

8

[Neurosurgical Embryology. Part 2: Recent data on normal and pathological development of the cortex].

Catala M. Catala M. Neurochirurgie. 2003 Sep;49(4):431-40. Neurochirurgie. 2003. PMID: 14526254 French.

9

From conception to the child.

Catala M. Catala M. Childs Nerv Syst. 1999 Nov;15(11-12):613-9. doi: 10.1007/s003810050449. Childs Nerv Syst. 1999. PMID: 10603001 Review.

10

[Neurotrophins and the development of the peripheral nervous system].

Catala M. Catala M. Rev Neurol (Paris). 1997 Feb;153(1):73-5. Rev Neurol (Paris). 1997. PMID: 9296163 Review. French. No abstract available.

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