Milh M - Search Results

1

Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.

Busa T, Milh M, Degardin N, Girard N, Sigaudy S, Longy M, Olshchwang S, Sobol H, Chabrol B, Philip N. Busa T, et al. Among authors: milh m. Eur J Paediatr Neurol. 2015 Mar;19(2):188-92. doi: 10.1016/j.ejpn.2014.11.012. Epub 2014 Dec 16. Eur J Paediatr Neurol. 2015. PMID: 25549896

2

Efficacy and tolerance of cannabidiol in the treatment of epilepsy in patients with Rett syndrome.

Desnous B, Beretti T, Muller N, Neveu J, Villeneuve N, Lépine A, Daquin G, Milh M. Desnous B, et al. Among authors: milh m. Epilepsia Open. 2024 Feb;9(1):397-403. doi: 10.1002/epi4.12796. Epub 2023 Nov 15. Epilepsia Open. 2024. PMID: 37485779 Free PMC article.

3

[Epileptic seizures in childhood: from seizure type to diagnosis].

Milh M, Ticus I, Villeneuve N, Hugonencq C, Mancini J, Chabrol B. Milh M, et al. Arch Pediatr. 2008 Feb;15(2):216-22. doi: 10.1016/j.arcped.2007.11.007. Epub 2008 Jan 14. Arch Pediatr. 2008. PMID: 18248967 French.

4

[GLUT-1 deficiency syndrome or De Vivo disease: a case report].

Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B. Ticus I, et al. Among authors: milh m. Arch Pediatr. 2008 Aug;15(8):1296-9. doi: 10.1016/j.arcped.2008.04.024. Epub 2008 Jun 16. Arch Pediatr. 2008. PMID: 18556184 French.

5

Transient brain magnetic resonance imaging hyperintensity in basal ganglia and brain stem of epileptic infants treated with vigabatrin.

Milh M, Villeneuve N, Chapon F, Pineau S, Lamoureux S, Livet MO, Bartoli C, Hugonenq C, Mancini J, Chabrol B, Girard N. Milh M, et al. J Child Neurol. 2009 Mar;24(3):305-15. doi: 10.1177/0883073808324219. J Child Neurol. 2009. PMID: 19258289

6

[Treatment of childhood convulsive status epilepticus: an update].

Milh M, Villeneuve N, Chabrol B. Milh M, et al. Arch Pediatr. 2009 Jun;16(6):790-2. doi: 10.1016/S0929-693X(09)74155-7. Arch Pediatr. 2009. PMID: 19541173 French. No abstract available.

7

[Handicap: definition and classification].

Chabrol B, Halbert C, Milh M, Mancini J. Chabrol B, et al. Among authors: milh m. Arch Pediatr. 2009 Jun;16(6):912-4. doi: 10.1016/S0929-693X(09)74201-0. Arch Pediatr. 2009. PMID: 19541219 French. No abstract available.

8

[Epilepsy in the child].

Milh M, Chabrol B. Milh M, et al. Rev Prat. 2009 May 20;59(5):689-93. Rev Prat. 2009. PMID: 19552211 French. No abstract available.

9

Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia.

Mignon-Ravix C, Cacciagli P, El-Waly B, Moncla A, Milh M, Girard N, Chabrol B, Philip N, Villard L. Mignon-Ravix C, et al. Among authors: milh m. J Med Genet. 2010 Feb;47(2):132-6. doi: 10.1136/jmg.2009.069112. Epub 2009 Jul 26. J Med Genet. 2010. PMID: 19635726

10

[Language disorders in children with morphologic abnormalities of the hippocampus].

Agostini G, Mancini J, Chabrol B, Villeneuve N, Milh M, George F, Maurel B, Girard N. Agostini G, et al. Among authors: milh m. Arch Pediatr. 2010 Jul;17(7):1008-16. doi: 10.1016/j.arcped.2010.03.002. Epub 2010 Apr 20. Arch Pediatr. 2010. PMID: 20409697 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

162 results

Search Page