Laplanche JL - Search Results

1

[Biochemical mechanisms in the physiopathology of migraine].

Manivet P, Soliman HR, Callebert J, Laplanche JL, Launay JM. Manivet P, et al. Among authors: laplanche jl. Pathol Biol (Paris). 2000 Sep;48(7):630-41. Pathol Biol (Paris). 2000. PMID: 11072641 Review. French.

2

[Proteins, genes and early diagnosis of Alzheimer's disease].

Laplanche JL, Chatelain J, Launay JM, Dreux C. Laplanche JL, et al. Ann Biol Clin (Paris). 1990;48(5):281-5. Ann Biol Clin (Paris). 1990. PMID: 2195924 Review. French.

3

Serotonin and human immunodeficiency viruses.

Launay JM, Copel L, Callebert J, Corvaïa N, Bricaire F, Laplanche JL, Saal F, Peries J. Launay JM, et al. Among authors: laplanche jl. Nouv Rev Fr Hematol (1978). 1989;31(2):159-61. Nouv Rev Fr Hematol (1978). 1989. PMID: 2771632

4

[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies].

Laplanche JL, Beaudry P, Ripoll L, Launay JM. Laplanche JL, et al. Pathol Biol (Paris). 1995 Feb;43(2):104-13. Pathol Biol (Paris). 1995. PMID: 7777379 Review. French.

5

[Molecular genetics of familial and sporadic forms of human prion diseases].

Laplanche JL, Launay JM, Dreux C. Laplanche JL, et al. Ann Pharm Fr. 1995;53(5):193-200. Ann Pharm Fr. 1995. PMID: 7503507 Review. French.

6

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases.

Peoc'h K, Guérin C, Brandel JP, Launay JM, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Neurosci Lett. 2000 Jun 2;286(2):144-8. doi: 10.1016/s0304-3940(00)01100-9. Neurosci Lett. 2000. PMID: 10825657

7

Deletion in prion protein gene in a Moroccan family.

Laplanche JL, Chatelain J, Launay JM, Gazengel C, Vidaud M. Laplanche JL, et al. Nucleic Acids Res. 1990 Nov 25;18(22):6745. doi: 10.1093/nar/18.22.6745. Nucleic Acids Res. 1990. PMID: 1979164 Free PMC article.

8

Two novel insertions in the prion protein gene in patients with late-onset dementia.

Laplanche JL, Delasnerie-Lauprêtre N, Brandel JP, Dussaucy M, Chatelain J, Launay JM. Laplanche JL, et al. Hum Mol Genet. 1995 Jun;4(6):1109-11. doi: 10.1093/hmg/4.6.1109. Hum Mol Genet. 1995. PMID: 7655470 No abstract available.

9

14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

Beaudry P, Cohen P, Brandel JP, Delasnerie-Lauprêtre N, Richard S, Launay JM, Laplanche JL. Beaudry P, et al. Among authors: laplanche jl. Dement Geriatr Cogn Disord. 1999 Jan-Feb;10(1):40-6. doi: 10.1159/000017095. Dement Geriatr Cogn Disord. 1999. PMID: 10068257 Clinical Trial.

10

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.

Peoc'h K, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-Lauprêtre N, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Hum Mutat. 2000 May;15(5):482. doi: 10.1002/(SICI)1098-1004(200005)15:5<482::AID-HUMU16>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10790216

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