Livet MO - Search Results

1

Livet MO, Moncla A, Delobel B, Croquette MF, Philip N, Vallée L. Livet MO, et al. Arch Pediatr. 1997 Dec;4(12):1231-7. doi: 10.1016/s0929-693x(97)82615-2. Arch Pediatr. 1997. PMID: 9538429 French.

2

[Neuropsychological phenotypes of genetic diseases].

Livet MO, Cournelle MA, Moncla A, Mancini J. Livet MO, et al. Arch Pediatr. 2000 May;7 Suppl 2:112s-113s. doi: 10.1016/s0929-693x(00)80003-2. Arch Pediatr. 2000. PMID: 10904676 French. No abstract available.

3

[A practical diagnostic approach to mental deficiency in 2002].

des Portes V, Livet MO, Vallée L; Groupe de travail de la Société française de neuropédiatrie (SFNP) sur les retards mantaux. des Portes V, et al. Among authors: livet mo. Arch Pediatr. 2002 Jul;9(7):709-25. doi: 10.1016/s0929-693x(01)00973-3. Arch Pediatr. 2002. PMID: 12162161 Review. French.

4

Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.

Moncla A, Livet MO, Auger M, Mattei JF, Mattei MG, Giraud F. Moncla A, et al. Among authors: livet mo. J Med Genet. 1991 Sep;28(9):627-32. doi: 10.1136/jmg.28.9.627. J Med Genet. 1991. PMID: 1956064 Free PMC article. Review.

5

[Angelman syndrome].

Moncla A, Livet MO, Malzac P, Voelckel MA, Mattei MG, Mattei JF, Giraud F. Moncla A, et al. Among authors: livet mo. Arch Pediatr. 1994 Dec;1(12):1118-26. Arch Pediatr. 1994. PMID: 7849899 Review. French.

6

Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling.

Moncla A, Malzac P, Livet MO, Voelckel MA, Mancini J, Delaroziere JC, Philip N, Mattei JF. Moncla A, et al. Among authors: livet mo. J Med Genet. 1999 Jul;36(7):554-60. J Med Genet. 1999. PMID: 10424818 Free PMC article.

7

[Clinical approach to mental retardation of genetic origin].

Livet MO, Moncla A, Philip N, Chabrol B, Mancini J. Livet MO, et al. Rev Neurol (Paris). 1999 Sep;155(8):593-5. Rev Neurol (Paris). 1999. PMID: 10486850 Review. French.

8

Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients.

Moncla A, Malzac P, Voelckel MA, Auquier P, Girardot L, Mattei MG, Philip N, Mattei JF, Lalande M, Livet MO. Moncla A, et al. Among authors: livet mo. Eur J Hum Genet. 1999 Feb-Mar;7(2):131-9. doi: 10.1038/sj.ejhg.5200258. Eur J Hum Genet. 1999. PMID: 10196695

9

Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approach.

Malzac P, Moncla A, Voelckel MA, Livet MO, Girardot L, Mattei MG, Mattei JF. Malzac P, et al. Among authors: livet mo. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):493-6. doi: 10.1016/0960-8966(93)90103-q. Neuromuscul Disord. 1993. PMID: 7910502

10

[BREV: an assessment battery for cognitive deficits in children 4 to 9 years old. Results of a normative study in 500 children].

Billard C, Gillet P, Galloux A, Piller AG, Livet MO, Motte J, Vallée L, Vol S. Billard C, et al. Among authors: livet mo. Arch Pediatr. 2000 May;7 Suppl 2:128s-130s. doi: 10.1016/s0929-693x(00)80010-x. Arch Pediatr. 2000. PMID: 10904683 French. No abstract available.

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