Chapman J - Search Results

1

Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease.

Blumen SC, Brais B, Korczyn AD, Medinsky S, Chapman J, Asherov A, Nisipeanu P, Codère F, Bouchard JP, Fardeau M, Tomé FM, Rouleau GA. Blumen SC, et al. Among authors: chapman j. Ann Neurol. 1999 Jul;46(1):115-8. Ann Neurol. 1999. PMID: 10401788

2

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Blumen SC, Korczyn AD, Lavoie H, Medynski S, Chapman J, Asherov A, Nisipeanu P, Inzelberg R, Carasso RL, Bouchard JP, Tomé FM, Rouleau GA, Brais B. Blumen SC, et al. Among authors: chapman j. Neurology. 2000 Nov 14;55(9):1267-70. doi: 10.1212/wnl.55.9.1267. Neurology. 2000. PMID: 11087766

3

Routine and quantitative EEG analysis in Gilles de la Tourette's syndrome.

Neufeld MY, Berger Y, Chapman J, Korczyn AD. Neufeld MY, et al. Among authors: chapman j. Neurology. 1990 Dec;40(12):1837-9. doi: 10.1212/wnl.40.12.1837. Neurology. 1990. PMID: 2247231

4

The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation.

Chapman J, Ben-Israel J, Goldhammer Y, Korczyn AD. Chapman J, et al. Neurology. 1994 Sep;44(9):1683-6. doi: 10.1212/wnl.44.9.1683. Neurology. 1994. PMID: 7936296

5

A simple and efficient method for apolipoprotein E genotype determination.

Chapman J, Estupiñan J, Asherov A, Goldfarb LG. Chapman J, et al. Neurology. 1996 May;46(5):1484-5. doi: 10.1212/wnl.46.5.1484-a. Neurology. 1996. PMID: 8628509 No abstract available.

6

Pruritus in Creutzfeldt-Jakob disease.

Shabtai H, Nisipeanu P, Chapman J, Korczyn AD. Shabtai H, et al. Among authors: chapman j. Neurology. 1996 Apr;46(4):940-1. doi: 10.1212/wnl.46.4.940. Neurology. 1996. PMID: 8780068

7

Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease.

Rosenmann H, Kahana E, Korczyn AD, Kahana I, Chapman J, Gabizon R. Rosenmann H, et al. Among authors: chapman j. Neurology. 1999 Oct 12;53(6):1328-9. doi: 10.1212/wnl.53.6.1328. Neurology. 1999. PMID: 10522892

8

Preliminary observations on APOE epsilon4 allele and progression of disability in multiple sclerosis.

Chapman J, Sylantiev C, Nisipeanu P, Korczyn AD. Chapman J, et al. Arch Neurol. 1999 Dec;56(12):1484-7. doi: 10.1001/archneur.56.12.1484. Arch Neurol. 1999. PMID: 10593303

9

Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutation.

Simon ES, Kahana E, Chapman J, Treves TA, Gabizon R, Rosenmann H, Zilber N, Korczyn AD. Simon ES, et al. Among authors: chapman j. Ann Neurol. 2000 Feb;47(2):257-60. Ann Neurol. 2000. PMID: 10665501

10

The very high prevalence of AD in an Arab population is not explained by APOE epsilon4 allele frequency.

Bowirrat A, Friedland RP, Chapman J, Korczyn AD. Bowirrat A, et al. Among authors: chapman j. Neurology. 2000 Sep 12;55(5):731. doi: 10.1212/wnl.55.5.731. Neurology. 2000. PMID: 10980749 No abstract available.

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