Results
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101.
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EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. [electronic resource] by
- Gasser, T
- Finsterer, J
- Baets, J
- Van Broeckhoven, C
- Di Donato, S
- Fontaine, B
- De Jonghe, P
- Lossos, A
- Lynch, T
- Mariotti, C
- Schöls, L
- Spinazzola, A
- Szolnoki, Z
- Tabrizi, S J
- Tallaksen, C M E
- Zeviani, M
- Burgunder, J-M
- Harbo, H F
Producer: 20100817
In:
European journal of neurology vol. 17
Availability: No items available.
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102.
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EFNS guidelines on the molecular diagnosis of mitochondrial disorders. [electronic resource] by
- Finsterer, J
- Harbo, H F
- Baets, J
- Van Broeckhoven, C
- Di Donato, S
- Fontaine, B
- De Jonghe, P
- Lossos, A
- Lynch, T
- Mariotti, C
- Schöls, L
- Spinazzola, A
- Szolnoki, Z
- Tabrizi, S J
- Tallaksen, C M E
- Zeviani, M
- Burgunder, J-M
- Gasser, T
Producer: 20100202
In:
European journal of neurology vol. 16
Availability: No items available.
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103.
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Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. [electronic resource] by
- Richard, I
- Brenguier, L
- Dinçer, P
- Roudaut, C
- Bady, B
- Burgunder, J M
- Chemaly, R
- Garcia, C A
- Halaby, G
- Jackson, C E
- Kurnit, D M
- Lefranc, G
- Legum, C
- Loiselet, J
- Merlini, L
- Nivelon-Chevallier, A
- Ollagnon-Roman, E
- Restagno, G
- Topaloglu, H
- Beckmann, J S
Producer: 19970603
In:
American journal of human genetics vol. 60
Availability: No items available.
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104.
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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. [electronic resource] by
- Fonknechten, N
- Mavel, D
- Byrne, P
- Davoine, C S
- Cruaud, C
- Bönsch, D
- Boentsch, D
- Samson, D
- Coutinho, P
- Hutchinson, M
- McMonagle, P
- Burgunder, J M
- Tartaglione, A
- Heinzlef, O
- Feki, I
- Deufel, T
- Parfrey, N
- Brice, A
- Fontaine, B
- Prud'homme, J F
- Weissenbach, J
- Dürr, A
- Hazan, J
Producer: 20000414
In:
Human molecular genetics vol. 9
Availability: No items available.
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105.
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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. [electronic resource] by
- Brockington, M
- Yuva, Y
- Prandini, P
- Brown, S C
- Torelli, S
- Benson, M A
- Herrmann, R
- Anderson, L V
- Bashir, R
- Burgunder, J M
- Fallet, S
- Romero, N
- Fardeau, M
- Straub, V
- Storey, G
- Pollitt, C
- Richard, I
- Sewry, C A
- Bushby, K
- Voit, T
- Blake, D J
- Muntoni, F
Producer: 20020207
In:
Human molecular genetics vol. 10
Availability: No items available.
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106.
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Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese. [electronic resource] by
- Tan, E K
- Lu, C S
- Peng, R
- Teo, Y Y
- Wu-Chou, Y H
- Chen, R S
- Weng, Y H
- Chen, C M
- Fung, H C
- Tan, L C
- Zhang, Z J
- An, X K
- Lee-Chen, G J
- Lee, M C
- Fook-Chong, S
- Burgunder, J M
- Wu, R M
- Wu, Y R
Producer: 20110829
In:
Neurobiology of aging vol. 31
Availability: No items available.
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107.
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Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls. [electronic resource] by
- Jiang, H
- Sun, Y M
- Hao, Y
- Yan, Y P
- Chen, K
- Xin, S H
- Tang, Y P
- Li, X H
- Jun, T
- Chen, Y Y
- Liu, Z J
- Wang, C R
- Li, H
- Pei, Z
- Shang, H F
- Zhang, B R
- Gu, W H
- Wu, Z Y
- Tang, B S
- Burgunder, J-M
Producer: 20141106
In:
European journal of neurology vol. 21
Availability: No items available.
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