Results
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42.
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43.
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44.
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Unverricht-Lundborg disease: absence of nonallelic genetic heterogeneity. [electronic resource] by
- Cochius, J I
- Figlewicz, D A
- Kälviäinen, R
- Nousiainen, U
- Farrell, K
- Patry, G
- Söderfeldt, B
- Frydman, M
- Lerman, P
- Andermann, F
Producer: 19931206
In:
Annals of neurology vol. 34
Availability: No items available.
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45.
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Paraoxonase gene polymorphisms and sporadic ALS. [electronic resource] by
- Slowik, A
- Tomik, B
- Wolkow, P P
- Partyka, D
- Turaj, W
- Malecki, M T
- Pera, J
- Dziedzic, T
- Szczudlik, A
- Figlewicz, D A
Producer: 20060926
In:
Neurology vol. 67
Availability: No items available.
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46.
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DD genotype of ACE gene is a risk factor for intracerebral hemorrhage. [electronic resource] by
- Slowik, A
- Turaj, W
- Dziedzic, T
- Haefele, A
- Pera, J
- Malecki, M T
- Glodzik-Sobanska, L
- Szermer, P
- Figlewicz, D A
- Szczudlik, A
Producer: 20050114
In:
Neurology vol. 63
Availability: No items available.
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47.
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48.
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. [electronic resource] by
- Rosen, D R
- Siddique, T
- Patterson, D
- Figlewicz, D A
- Sapp, P
- Hentati, A
- Donaldson, D
- Goto, J
- O'Regan, J P
- Deng, H X
Producer: 19930406
In:
Nature vol. 362
Availability: No items available.
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49.
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Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis. [electronic resource] by
- Pramatarova, A
- Figlewicz, D A
- Krizus, A
- Han, F Y
- Ceballos-Picot, I
- Nicole, A
- Dib, M
- Meininger, V
- Brown, R H
- Rouleau, G A
Producer: 19950413
In:
American journal of human genetics vol. 56
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50.
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51.
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. [electronic resource] by
- Hentati, A
- Bejaoui, K
- Pericak-Vance, M A
- Hentati, F
- Speer, M C
- Hung, W Y
- Figlewicz, D A
- Haines, J
- Rimmler, J
- Ben Hamida, C
Producer: 19941117
In:
Nature genetics vol. 7
Availability: No items available.
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52.
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Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21. [electronic resource] by
- Figlewicz, D A
- McInnis, M G
- Goto, J
- Haines, J L
- Warren, A C
- Krizus, A
- Khodr, N
- Brown, R H
- McKenna-Yasek, D
- Antonarakis, S E
Producer: 19950202
In:
Journal of the neurological sciences vol. 124 Suppl
Availability: No items available.
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53.
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Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. [electronic resource] by
- Siddique, T
- Figlewicz, D A
- Pericak-Vance, M A
- Haines, J L
- Rouleau, G
- Jeffers, A J
- Sapp, P
- Hung, W Y
- Bebout, J
- McKenna-Yasek, D
Producer: 19910530
In:
The New England journal of medicine vol. 324
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54.
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Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group. [electronic resource] by
- Fink, J K
- Heiman-Patterson, T
- Bird, T
- Cambi, F
- Dubé, M P
- Figlewicz, D A
- Fink, J K
- Haines, J L
- Heiman-Patterson, T
- Hentati, A
- Pericak-Vance, M A
- Raskind, W
- Rouleau, G A
- Siddique, T
Producer: 19960725
In:
Neurology vol. 46
Availability: No items available.
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55.
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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. [electronic resource] by
- Hadano, S
- Hand, C K
- Osuga, H
- Yanagisawa, Y
- Otomo, A
- Devon, R S
- Miyamoto, N
- Showguchi-Miyata, J
- Okada, Y
- Singaraja, R
- Figlewicz, D A
- Kwiatkowski, T
- Hosler, B A
- Sagie, T
- Skaug, J
- Nasir, J
- Brown, R H
- Scherer, S W
- Rouleau, G A
- Hayden, M R
- Ikeda, J E
Producer: 20011204
In:
Nature genetics vol. 29
Availability: No items available.
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56.
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A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. [electronic resource] by
- Wills, A-M
- Cronin, S
- Slowik, A
- Kasperaviciute, D
- Van Es, M A
- Morahan, J M
- Valdmanis, P N
- Meininger, V
- Melki, J
- Shaw, C E
- Rouleau, G A
- Fisher, E M C
- Shaw, P J
- Morrison, K E
- Pamphlett, R
- Van den Berg, L H
- Figlewicz, D A
- Andersen, P M
- Al-Chalabi, A
- Hardiman, O
- Purcell, S
- Landers, J E
- Brown, R H
Producer: 20090817
In:
Neurology vol. 73
Availability: No items available.
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