Catala M - Search Results

1

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

2

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.

3

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

4

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.

5

[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.

6

Genetic control of caudal development.

Catala M. Catala M. Clin Genet. 2002 Feb;61(2):89-96. doi: 10.1034/j.1399-0004.2002.610202.x. Clin Genet. 2002. PMID: 11940082 Review.

7

Gross anatomy and development of the peripheral nervous system.

Catala M, Kubis N. Catala M, et al. Handb Clin Neurol. 2013;115:29-41. doi: 10.1016/B978-0-444-52902-2.00003-5. Handb Clin Neurol. 2013. PMID: 23931773 Review.

8

Schnitzler's syndrome associated with sensorimotor neuropathy.

Lebbe C, Rybojad M, Klein F, Oksenhendler E, Catala M, Danon F, Morel P. Lebbe C, et al. Among authors: catala m. J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):316-8. doi: 10.1016/s0190-9622(94)70031-1. J Am Acad Dermatol. 1994. PMID: 7507501

9

[Neurosurgical embryology. Part 5: Temporal landmarks of the development of the central nervous system in humans].

Catala M. Catala M. Neurochirurgie. 2003 Nov;49(5):486-94. Neurochirurgie. 2003. PMID: 14646813 Review. French.

10

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.

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