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MINOTTI S
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DURHAM HD
Citation: J. Roy et al., MECHANISM OF MOTOR-NEURON VULNERABILITY IN AMYOTROPHIC-LATERAL-SCLEROSIS - GLUTAMATE POTENTIATES THE TOXICITY OF MUTANT SUPEROXIDE DISMUTASE-1 IN MOTOR-NEURONS BY POSTSYNAPTIC CALCIUM-DEPENDENT MECHANISMS, Annals of neurology, 44(3), 1998, pp. 115-115
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Citation: R. Tawil et al., FACIOSCAPULOHUMERAL DYSTROPHY - A DISTINCT REGIONAL MYOPATHY WITH A NOVEL MOLECULAR PATHOGENESIS, Annals of neurology, 43(3), 1998, pp. 279-282
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ROY J
MINOTTI S
DONG LC
FIGLEWICZ DA
DURHAM HD
Citation: J. Roy et al., GLUTAMATE POTENTIATES THE TOXICITY OF MUTANT CU ZN-SUPEROXIDE DISMUTASE IN MOTOR-NEURONS BY POSTSYNAPTIC CALCIUM-DEPENDENT MECHANISMS/, The Journal of neuroscience, 18(23), 1998, pp. 9673-9684
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Citation: H. Haravuori et al., TIBIAL MUSCULAR-DYSTROPHY AND LATE-ONSET DISTAL MYOPATHY ARE LINKED TO THE SAME LOCUS ON CHROMOSOME 2Q, Neurology, 50(4), 1998, pp. 15001-15001
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CHANG YN
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BOHN MC
Citation: Mh. Mohajeri et al., MYOBLAST-MEDIATED EX-VIVO GDNF GENE-THERAPY IN A MOUSE MODEL OF AMYOTROPHIC-LATERAL-SCLEROSIS (ALS), Experimental neurology, 153(2), 1998, pp. 384-384
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ORRELL RW
FORRESTER JD
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Citation: Rw. Orrell et al., APPLICATION OF DEFINITIVE MOLECULAR DIAGNOSTIC-CRITERIA IN FACIOSCAPULOHUMERAL DYSTROPHY - CLINICAL IMPLICATIONS OF POSITION EFFECT VARIEGATION, Annals of neurology, 42(6), 1997, pp. 3-3
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PARBOOSINGH JS
FIGLEWICZ DA
KRIZUS A
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ROULEAU GA
Citation: Js. Parboosingh et al., SPINOBULBAR MUSCULAR-ATROPHY CAN MIMIC ALS - THE IMPORTANCE OF GENETIC TESTING IN MALE-PATIENTS WITH ATYPICAL ALS, Neurology, 49(2), 1997, pp. 568-572
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Citation: Mp. Dube et al., A NEW PURE HEREDITARY SPASTIC PARAPLEGIA KINDRED MAPS TO THE PROTEOLIPID PROTEIN GENE LOCUS, American journal of human genetics, 61(4), 1997, pp. 973-973
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Citation: Mp. Dube et al., HEREDITARY SPASTIC PARAPLEGIA - LOD-SCORE CONSIDERATIONS FOR CONFIRMATION OF LINKAGE IN A HETEROGENEOUS TRAIT, American journal of human genetics, 60(3), 1997, pp. 625-629
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HEIMANPATTERSON T
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FIGLEWICZ DA
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Citation: Jk. Fink et al., HEREDITARY SPASTIC PARAPLEGIA - ADVANCES IN GENETIC RESEARCH, Neurology, 46(6), 1996, pp. 1507-1514
Citation: K. Rooke et al., ANALYSIS OF THE KSP REPEAT OF THE NEUROFILAMENT HEAVY SUBUNIT IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Neurology, 46(3), 1996, pp. 789-790
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Citation: A. Rubio et al., COEXISTENCE OF HUNTINGTONS-DISEASE AND FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS - CASE PRESENTATION, Acta Neuropathologica, 92(4), 1996, pp. 421-427
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BROWN RH
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Citation: Js. Parboosingh et al., ABSENCE OF MUTATIONS IN THE MN SUPEROXIDE-DISMUTASE OR CATALASE GENESIN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Neuromuscular disorders, 5(1), 1995, pp. 7-10
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NALBANTOGLU J
FIGLEWICZ DA
Citation: Hp. Durham et al., USE OF TISSUE-CULTURE MODELS TO STUDY ENVIRONMENTAL-GENETIC INTERACTIONS RELEVANT TO NEURODEGENERATIVE DISEASES, Clinical and experimental pharmacology and physiology, 22(5), 1995, pp. 366-367
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FIGLEWICZ DA
THOMAS SM
BUTLER R
LEBUIS L
ROULEAU G
MEININGER V
LEIGHT PN
Citation: O. Garofalo et al., SUPEROXIDE-DISMUTASE ACTIVITY IN LYMPHOBLASTOID-CELLS FROM MOTOR-NEURON DISEASE AMYOTROPHIC-LATERAL-SCLEROSIS (MND ALS) PATIENTS/, Journal of the neurological sciences, 129, 1995, pp. 90-92
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ROULEAU GA
KIBAR Z
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FIGLEWICZ DA
Citation: Mp. Dube et al., AUTOSOMAL-DOMINANT HEREDITARY SPASTIC PARAPLEGIA - LINKAGE ANALYSIS OF A HETEROGENEOUS TRAIT, American journal of human genetics, 57(4), 1995, pp. 1093-1093
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FORRESTER J
MCDERMOTT MP
MENDELL JR
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TAWIL R
Citation: Da. Figlewicz et al., ANALYSIS OF GENOTYPE-PHENOTYPE CORRELATION IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), American journal of human genetics, 57(4), 1995, pp. 1382-1382
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FIGLEWICZ DA
KRIZUS A
HAN FY
CEBALLOSPICOT I
NICOLE A
DIB M
MEININGER V
BROWN RH
ROULEAU GA
Citation: A. Pramatarova et al., IDENTIFICATION OF NEW MUTATIONS IN THE CU ZN SUPEROXIDE-DISMUTASE GENE OF PATIENTS WITH FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS/, American journal of human genetics, 56(3), 1995, pp. 592-596
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HENTATI A
BEJAOUI K
PERICAKVANCE MA
HENTATI F
SPEER MC
HUNG WY
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HAINES J
RIMMLER J
BENHAMIDA C
BENHAMIDA M
BROWN RH
SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF RECESSIVE FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 2Q33-Q35, Nature genetics, 7(3), 1994, pp. 425-428
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PRAMATAROVA A
GOTO J
NANBA E
NAKASHIMA K
TAKAHASHI K
TAKAGI A
KANAZAWA I
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ROULEAU GA
Citation: A. Pramatarova et al., A 2-BASEPAIR DELETION IN THE SOD-1 GENE CAUSES FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Human molecular genetics, 3(11), 1994, pp. 2061-2062
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KRIZUS A
MARTINOLI MG
MEININGER V
DIB M
ROULEAU GA
JULIEN JP
Citation: Da. Figlewicz et al., VARIANTS OF THE HEAVY NEUROFILAMENT SUBUNIT ARE ASSOCIATED WITH THE DEVELOPMENT OF AMYOTROPHIC-LATERAL-SCLEROSIS, Human molecular genetics, 3(10), 1994, pp. 1757-1761
Authors:
FIGLEWICZ DA
MCINNIS MG
GOTO J
HAINES JL
WARREN AC
KRIZUS A
KHODR N
BROWN RH
MCKENNAYASEK D
ANTONARAKIS SE
ROULEAU GA
Citation: Da. Figlewicz et al., IDENTIFICATION OF FLANKING MARKERS FOR THE FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS GENE ALS1 ON CHROMOSOME-21, Journal of the neurological sciences, 124, 1994, pp. 90-95