Figlewicz DA - Search Results

1

Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.

Parboosingh JS, Rouleau GA, Meninger V, McKenna-Yasek D, Brown RH Jr, Figlewicz DA. Parboosingh JS, et al. Among authors: figlewicz da. Neuromuscul Disord. 1995 Jan;5(1):7-10. doi: 10.1016/0960-8966(94)e0022-z. Neuromuscul Disord. 1995. PMID: 7719145 Free article.

2

SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.

Rouleau GA, Clark AW, Rooke K, Pramatarova A, Krizus A, Suchowersky O, Julien JP, Figlewicz D. Rouleau GA, et al. Ann Neurol. 1996 Jan;39(1):128-31. doi: 10.1002/ana.410390119. Ann Neurol. 1996. PMID: 8572658

3

Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21.

Figlewicz DA, McInnis MG, Goto J, Haines JL, Warren AC, Krizus A, Khodr N, Brown RH Jr, McKenna-Yasek D, Antonarakis SE, et al. Figlewicz DA, et al. J Neurol Sci. 1994 Jul;124 Suppl:90-5. doi: 10.1016/0022-510x(94)90190-2. J Neurol Sci. 1994. PMID: 7807155

4

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis.

Figlewicz DA, Krizus A, Martinoli MG, Meininger V, Dib M, Rouleau GA, Julien JP. Figlewicz DA, et al. Hum Mol Genet. 1994 Oct;3(10):1757-61. doi: 10.1093/hmg/3.10.1757. Hum Mol Genet. 1994. PMID: 7849698

5

A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis.

Pramatarova A, Goto J, Nanba E, Nakashima K, Takahashi K, Takagi A, Kanazawa I, Figlewicz DA, Rouleau GA. Pramatarova A, et al. Among authors: figlewicz da. Hum Mol Genet. 1994 Nov;3(11):2061-2. Hum Mol Genet. 1994. PMID: 7874127 No abstract available.

6

Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

Pramatarova A, Figlewicz DA, Krizus A, Han FY, Ceballos-Picot I, Nicole A, Dib M, Meininger V, Brown RH, Rouleau GA. Pramatarova A, et al. Among authors: figlewicz da. Am J Hum Genet. 1995 Mar;56(3):592-6. Am J Hum Genet. 1995. PMID: 7887412 Free PMC article.

7

The Cu/Zn superoxide dismutase gene in ALS and parkinsonism-dementia of Guam.

Figlewicz DA, Garruto RM, Krizus A, Yanagihara R, Rouleau GA. Figlewicz DA, et al. Neuroreport. 1994 Jan 31;5(5):557-60. doi: 10.1097/00001756-199401000-00006. Neuroreport. 1994. PMID: 8025243

8

The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis.

Goto J, Figlewicz DA, Haines JL, Brown RH Jr, Khodr N, Rouleau GA. Goto J, et al. Among authors: figlewicz da. Neuromuscul Disord. 1993 Mar;3(2):157-60. doi: 10.1016/0960-8966(93)90008-8. Neuromuscul Disord. 1993. PMID: 8358240

9

Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis.

Garofalo O, Figlewicz DA, Leigh PN, Powell JF, Meininger V, Dib M, Rouleau GA. Garofalo O, et al. Among authors: figlewicz da. Neuromuscul Disord. 1993 May;3(3):195-9. doi: 10.1016/0960-8966(93)90059-s. Neuromuscul Disord. 1993. PMID: 8400860

10

Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis.

Rooke K, Figlewicz DA, Han FY, Rouleau GA. Rooke K, et al. Among authors: figlewicz da. Neurology. 1996 Mar;46(3):789-90. doi: 10.1212/wnl.46.3.789. Neurology. 1996. PMID: 8618684

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