共 9 条
[1]
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2
[J].
Durr, A
;
Davoine, CS
;
Paternotte, C
;
vonFellenberg, J
;
Cogilnicean, S
;
Coutinho, P
;
Lamy, C
;
Bourgeois, S
;
Prudhomme, JF
;
Penet, C
;
Mas, JL
;
Burgunder, JM
;
Hazan, J
;
Weissenbach, J
;
Brice, A
;
Fontaine, B
.
BRAIN,
1996, 119
:1487-1496

Durr, A
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Davoine, CS
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Paternotte, C
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

vonFellenberg, J
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Cogilnicean, S
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Coutinho, P
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Lamy, C
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Bourgeois, S
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Prudhomme, JF
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Penet, C
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Mas, JL
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Burgunder, JM
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Hazan, J
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Weissenbach, J
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Brice, A
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE

Fontaine, B
论文数: 0 引用数: 0
h-index: 0
机构: HOP LA PITIE SALPETRIERE,FED NEUROL,F-75651 PARIS 13,FRANCE
[2]
Hereditary spastic paraplegia: Advances in genetic research
[J].
Fink, JK
;
HeimanPatterson, T
;
Bird, T
;
Cambi, F
;
Dube, MP
;
Figlewicz, DA
;
Fink, JK
;
Haines, JL
;
HeimanPatterson, T
;
Hentati, A
;
PericakVance, MA
;
Raskind, W
;
Rouleau, GA
;
Siddique, T
.
NEUROLOGY,
1996, 46 (06)
:1507-1514

Fink, JK
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

HeimanPatterson, T
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Bird, T
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Cambi, F
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Dube, MP
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Figlewicz, DA
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Fink, JK
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Haines, JL
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

HeimanPatterson, T
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Hentati, A
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

PericakVance, MA
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Raskind, W
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Rouleau, GA
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI

Siddique, T
论文数: 0 引用数: 0
h-index: 0
机构: VET AFFAIRS MED CTR,GERIATR RES & EDUC CTR,ANN ARBOR,MI
[3]
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
[J].
Fonknechten, N
;
Mavel, D
;
Byrne, P
;
Davoine, CS
;
Cruaud, C
;
Boentsch, D
;
Samson, D
;
Coutinho, P
;
Hutchinson, M
;
McMonagle, P
;
Burgunder, JM
;
Tartaglione, A
;
Heinzlef, O
;
Feki, I
;
Deufel, T
;
Parfrey, N
;
Brice, A
;
Fontaine, B
;
Prud'homme, JF
;
Weissenbach, J
;
Dürr, A
;
Hazan, J
.
HUMAN MOLECULAR GENETICS,
2000, 9 (04)
:637-644

Fonknechten, N
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Mavel, D
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Byrne, P
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Davoine, CS
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Cruaud, C
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Boentsch, D
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Samson, D
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Coutinho, P
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Hutchinson, M
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

McMonagle, P
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Burgunder, JM
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Tartaglione, A
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Heinzlef, O
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Feki, I
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Deufel, T
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Parfrey, N
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Brice, A
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Fontaine, B
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Prud'homme, JF
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Weissenbach, J
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Dürr, A
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France

Hazan, J
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, F-91000 Evry, France
[4]
LINKAGE OF A NEW LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME 2P
[J].
HAZAN, J
;
FONTAINE, B
;
BRUYN, RPM
;
LAMY, C
;
VANDEUTEKOM, JCT
;
RIME, CS
;
DURR, A
;
MELKI, J
;
LYONCAEN, O
;
AGID, Y
;
MUNNICH, A
;
PADBERG, GW
;
DERECONDO, J
;
FRANTS, RR
;
BRICE, A
;
WEISSENBACH, J
.
HUMAN MOLECULAR GENETICS,
1994, 3 (09)
:1569-1573

HAZAN, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

FONTAINE, B
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

BRUYN, RPM
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

LAMY, C
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

VANDEUTEKOM, JCT
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

RIME, CS
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

DURR, A
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

MELKI, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

LYONCAEN, O
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

AGID, Y
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

MUNNICH, A
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

PADBERG, GW
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

DERECONDO, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

FRANTS, RR
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

BRICE, A
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE

WEISSENBACH, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR,CNRS,URA 1445,UNITE GENET MOLEC HUMAINE,F-75724 PARIS 15,FRANCE
[5]
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
[J].
Hazan, J
;
Fonknechten, N
;
Mavel, D
;
Paternotte, C
;
Samson, D
;
Artiguenave, F
;
Davoine, CS
;
Cruaud, C
;
Dürr, A
;
Wincker, P
;
Brottier, P
;
Cattolico, L
;
Barbe, V
;
Burgunder, JM
;
Prud'homme, JF
;
Brice, A
;
Fontaine, B
;
Heilig, R
;
Weissenbach, J
.
NATURE GENETICS,
1999, 23 (03)
:296-303

Hazan, J
论文数: 0 引用数: 0
h-index: 0
机构:
Genoscope, Evry, France Genoscope, Evry, France

Fonknechten, N
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Mavel, D
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Paternotte, C
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Samson, D
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Artiguenave, F
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Davoine, CS
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Cruaud, C
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Dürr, A
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Wincker, P
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Brottier, P
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Cattolico, L
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Barbe, V
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Burgunder, JM
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Prud'homme, JF
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Brice, A
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Fontaine, B
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Heilig, R
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France

Weissenbach, J
论文数: 0 引用数: 0
h-index: 0
机构: Genoscope, Evry, France
[6]
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
[J].
Hentati, A
;
Deng, HX
;
Zhai, H
;
Chen, W
;
Yang, Y
;
Hung, WY
;
Azim, AC
;
Bohlega, S
;
Tandan, R
;
Warner, C
;
Laing, NG
;
Cambi, F
;
Mitsumoto, H
;
Roos, RP
;
Boustany, RM
;
Ben Hamida, M
;
Hentati, F
;
Siddique, T
.
NEUROLOGY,
2000, 55 (09)
:1388-1390

Hentati, A
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Deng, HX
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Zhai, H
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Chen, W
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Yang, Y
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Hung, WY
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Azim, AC
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Bohlega, S
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Tandan, R
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Warner, C
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Laing, NG
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Cambi, F
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Mitsumoto, H
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Roos, RP
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Boustany, RM
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Ben Hamida, M
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Hentati, F
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA

Siddique, T
论文数: 0 引用数: 0
h-index: 0
机构: Northwestern Univ, Sch Med, Dept Neurol, Chicago, IL 60611 USA
[7]
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
[J].
Lindsey, JC
;
Lusher, ME
;
McDermott, CJ
;
White, KD
;
Reid, E
;
Rubinsztein, DC
;
Bashir, R
;
Hazan, J
;
Shaw, PJ
;
Bushby, KMD
.
JOURNAL OF MEDICAL GENETICS,
2000, 37 (10)
:759-765

Lindsey, JC
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Lusher, ME
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

McDermott, CJ
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

White, KD
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Reid, E
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Rubinsztein, DC
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Bashir, R
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Hazan, J
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Shaw, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

Bushby, KMD
论文数: 0 引用数: 0
h-index: 0
机构:
Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England Newcastle Univ, Sch Biochem & Genet, Human Mol Genet Unit, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
[8]
The AAA team: related ATPases with diverse functions
[J].
Patel, S
;
Latterich, M
.
TRENDS IN CELL BIOLOGY,
1998, 8 (02)
:65-71

Patel, S
论文数: 0 引用数: 0
h-index: 0
机构: Salk Inst Biol Studies, La Jolla, CA 92037 USA

Latterich, M
论文数: 0 引用数: 0
h-index: 0
机构: Salk Inst Biol Studies, La Jolla, CA 92037 USA
[9]
Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation
[J].
White, KD
;
Ince, PG
;
Lusher, M
;
Lindsey, J
;
Cookson, M
;
Bashir, R
;
Shaw, PJ
;
Bushby, KMD
.
NEUROLOGY,
2000, 55 (01)
:89-94

White, KD
论文数: 0 引用数: 0
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Ince, PG
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Lusher, M
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Lindsey, J
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Cookson, M
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Bashir, R
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机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Shaw, PJ
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h-index: 0
机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

Bushby, KMD
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h-index: 0
机构: Newcastle Univ, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England