Baron H - Search Results

1

Transgenic mice expressing polyoma virus large T antigen in astrocytes develop severe dysmyelination of the central nervous system.

Baron-Van Evercooren A, Jensen NA, Wyss MT, Cuzin F, Rassoulzadegan M, Brucher JM, Baron H. Baron-Van Evercooren A, et al. Among authors: baron h. Lab Invest. 1992 Jan;66(1):39-53. Lab Invest. 1992. PMID: 1309929

2

Neurological disorder in transgenic mice that express the large T antigen of polyoma virus in the nervous system.

Jensen NA, Baron-Van Evercooren A, Mattei MG, Galiana E, Guron C, Pinçon-Raymond M, Baron H, Rouget P, Cuzin F, Rassoulzadegan M. Jensen NA, et al. Among authors: baron van evercooren a, baron h. Mol Biol Med. 1989 Dec;6(6):493-500. Mol Biol Med. 1989. PMID: 2561375

3

Antiserum to scrapie-associated fibril protein reacts with amyloid plaques in familial transmissible dementia.

Baron H, Baron-Van Evercooren A, Brucher JM. Baron H, et al. Among authors: baron van evercooren a. J Neuropathol Exp Neurol. 1988 Mar;47(2):158-65. doi: 10.1097/00005072-198803000-00008. J Neuropathol Exp Neurol. 1988. PMID: 2892894

4

[Gerstmann-Sträussler-Scheinker disease. Pathologal and genetic study].

Genthon R, Gray F, Salama J, Duyckaerts C, Belin C, Brucher JM, Baron H, Delaporte P. Genthon R, et al. Among authors: baron h. Rev Neurol (Paris). 1992;148(5):335-42. Rev Neurol (Paris). 1992. PMID: 1448647 Review. French.

5

[Cerebellar amyloid plaques in Alzheimer's disease].

Brucher JM, Gillain C, Baron H. Brucher JM, et al. Among authors: baron h. Acta Neurol Belg. 1989 May-Oct;89(3-4):286-93. Acta Neurol Belg. 1989. PMID: 2516979 French.

6

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family.

Goldfarb LG, Brown P, Vrbovská A, Baron H, McCombie WR, Cathala F, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: baron h. J Neurol Sci. 1992 Sep;111(2):189-94. doi: 10.1016/0022-510x(92)90067-u. J Neurol Sci. 1992. PMID: 1431985

7

Coexistence of Creutzfeldt-Jakob disease and Alzheimer's disease in the same patient.

Brown P, Jannotta F, Gibbs CJ Jr, Baron H, Guiroy DC, Gajdusek DC. Brown P, et al. Among authors: baron h. Neurology. 1990 Feb;40(2):226-8. doi: 10.1212/wnl.40.2.226. Neurology. 1990. PMID: 2405293

8

Creutzfeldt-Jakob disease: a case of 16 years' duration.

Cutler NR, Brown PW, Narayan T, Parisi JE, Janotta F, Baron H. Cutler NR, et al. Among authors: baron h. Ann Neurol. 1984 Jan;15(1):107-10. doi: 10.1002/ana.410150121. Ann Neurol. 1984. PMID: 6370097

9

Improved conformation-dependent immunoassay: suitability for human prion detection with enhanced sensitivity.

Bellon A, Seyfert-Brandt W, Lang W, Baron H, Gröner A, Vey M. Bellon A, et al. Among authors: baron h. J Gen Virol. 2003 Jul;84(Pt 7):1921-1925. doi: 10.1099/vir.0.18996-0. J Gen Virol. 2003. PMID: 12810888

10

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, Cervenakova L, Baron H, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: baron h. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10926-30. doi: 10.1073/pnas.88.23.10926. Proc Natl Acad Sci U S A. 1991. PMID: 1683708 Free PMC article.

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