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Results: 1-15 |
Results: 15
3 NOVEL KCNA1 MUTATIONS IN EPISODIC ATAXIA TYPE-I FAMILIES (VOL 102, PG 464, 1998)
Authors: SCHEFFER H BRUNT ERP MOL GJJ VANDERVLIES P STULP RP VERLIND E MANTEL G AVERYANOV YN HOFSTRA RMW BUYS CHCM
Citation: H. Scheffer et al., 3 NOVEL KCNA1 MUTATIONS IN EPISODIC ATAXIA TYPE-I FAMILIES (VOL 102, PG 464, 1998), Human genetics, 102(6), 1998, pp. 713-713
3 NOVEL KCNA1 MUTATIONS IN EPISODIC ATAXIA TYPE-I FAMILIES
Authors: SCHEFFER H BRUNT ERP MOL GJJ VANDERVLIES P STULP RP VERLIND E MANTEL G AVERYANOV YN HOFSTRA RMW BUYS CHCM
Citation: H. Scheffer et al., 3 NOVEL KCNA1 MUTATIONS IN EPISODIC ATAXIA TYPE-I FAMILIES, Human genetics, 102(4), 1998, pp. 464-466
VISUOSPATIAL ATTENTION AND INTENTION IN ASYMMETRIC PARKINSONS-DISEASE(PD)
Authors: BROUWER WH IETSWAART M BRUNT ERP WIJERS AA
Citation: Wh. Brouwer et al., VISUOSPATIAL ATTENTION AND INTENTION IN ASYMMETRIC PARKINSONS-DISEASE(PD), Brain and cognition, 37(1), 1998, pp. 70-72
BOTULINUM TOXIN VERSUS TRIHEXYPHENIDYL IN CERVICAL DYSTONI - A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND CONTROLLED TRIAL
Authors: BRANS JWM LINDEBOOM R SNOEK JW ZWARTS MJ VANWEERDEN TW BRUNT ERP VANHILTEN JJ VANDERKAMP W PRINS MH SPEELMAN JD
Citation: Jwm. Brans et al., BOTULINUM TOXIN VERSUS TRIHEXYPHENIDYL IN CERVICAL DYSTONI - A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND CONTROLLED TRIAL, Neurology, 46(4), 1996, pp. 1066-1072
CAG REPEAT EXTENSION CORRELATES WITH AGE-OF-ONSET BUT DOES NOT EXPLAIN ANTICIPATION IN DUTCH SCA3 MJD FAMILY/
Authors: BRUNT ERP VERSCHUUREN CC MENSINK RGJ JOOSTEN A STOLTE I SCHEFFER H
Citation: Erp. Brunt et al., CAG REPEAT EXTENSION CORRELATES WITH AGE-OF-ONSET BUT DOES NOT EXPLAIN ANTICIPATION IN DUTCH SCA3 MJD FAMILY/, Neurology, 46(2), 1996, pp. 2100-2100
IDENTIFICATION OF 2 NEW KCNA1 MUTATIONS IN EPISODIC ATAXIA MYOKYMIA FAMILIES
Authors: BROWNE DL BRUNT ERP GRIGGS RC NUTT JG GANCHER ST SMITH EA LITT M
Citation: Dl. Browne et al., IDENTIFICATION OF 2 NEW KCNA1 MUTATIONS IN EPISODIC ATAXIA MYOKYMIA FAMILIES, Human molecular genetics, 4(9), 1995, pp. 1671-1672
UNIQUE MYOCLONIC PATTERN IN CORTICOBASAL DEGENERATION
Authors: BRUNT ERP VANWEERDEN TW PRUIM J LAKKE JWPF
Citation: Erp. Brunt et al., UNIQUE MYOCLONIC PATTERN IN CORTICOBASAL DEGENERATION, Movement disorders, 10(2), 1995, pp. 132-142
REFINEMENT BY LINKAGE ANALYSIS IN 2 LARGE FAMILIES OF THE CANDIDATE REGION OF THE 3RD LOCUS (SCA3) FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIATYPE-I
Authors: VERSCHUURENBEMELMANS CC BRUNT ERP BURTON M MENSINK RGJ VANDERMEULEN MA SMIT NH STOLTEDIJKSTRA I BUYS CHCM SCHEFFER H
Citation: Cc. Verschuurenbemelmans et al., REFINEMENT BY LINKAGE ANALYSIS IN 2 LARGE FAMILIES OF THE CANDIDATE REGION OF THE 3RD LOCUS (SCA3) FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIATYPE-I, Human genetics, 96(6), 1995, pp. 691-694
CONFIRMATION OF SPINOCEREBELLAR ATAXIA (SCA) 3 LOCUS IN A DUTCH FAMILY SHOWING ANTICIPATION IN MALE OFFSPRING
Authors: BRUNT ERP VERSCHUUREN CC JOOSTEN AAJ STOLTE I SCHEFFER H
Citation: Erp. Brunt et al., CONFIRMATION OF SPINOCEREBELLAR ATAXIA (SCA) 3 LOCUS IN A DUTCH FAMILY SHOWING ANTICIPATION IN MALE OFFSPRING, Neurology, 45(4), 1995, pp. 453-453
HEREDITARY MYOKYMIA AND PAROXYSMAL ATAXIA LINKED TO CHROMOSOME-12 IS RESPONSIVE TO ACETAZOLAMIDE
Authors: LUBBERS WJ BRUNT ERP SCHEFFER H LITT M STULP R BROWNE DL VANWEERDEN TW
Citation: Wj. Lubbers et al., HEREDITARY MYOKYMIA AND PAROXYSMAL ATAXIA LINKED TO CHROMOSOME-12 IS RESPONSIVE TO ACETAZOLAMIDE, Journal of Neurology, Neurosurgery and Psychiatry, 59(4), 1995, pp. 400-405
EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE, KCNA1
Authors: BROWNE DL GANCHER ST NUTT TG BRUNT ERP SMITH EA KRAMER P LITT M
Citation: Dl. Browne et al., EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE, KCNA1, Nature genetics, 8(2), 1994, pp. 136-140
AUTOSOMAL-DOMINANT EPISODIC ATAXIA REPRESENTS AT LEAST 2 GENETIC-DISORDERS
Authors: KRAMER P LITT M BROWNE D PROMCHOTIKUL T BRUNT ERP DUBAY C GANCHER S NUTT J
Citation: P. Kramer et al., AUTOSOMAL-DOMINANT EPISODIC ATAXIA REPRESENTS AT LEAST 2 GENETIC-DISORDERS, Annals of neurology, 36(2), 1994, pp. 279-279
DISTAL AXONAL ORIGIN AND MOTOR UNIT INVOLVEMENT IN MYOKYMIA
Authors: BRUNT ERP VANWEERDEN TW
Citation: Erp. Brunt et Tw. Vanweerden, DISTAL AXONAL ORIGIN AND MOTOR UNIT INVOLVEMENT IN MYOKYMIA, Neurology, 44(4), 1994, pp. 10000411-10000411
EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1)
Authors: LITT M BROWNE DL GANCHER ST NUTT JG BRUNT ERP SMITH EA
Citation: M. Litt et al., EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1), The Journal of general physiology, 104(6), 1994, pp. 10000010-10000010
A GENE FOR EPISODIC ATAXIA MYOKYMIA MAPS TO CHROMOSOME 12P13/
Authors: LITT M KRAMER P BROWNE D GANCHER S BRUNT ERP ROOT D PHROMCHOTIKUL T DUBAY CJ NUTT J
Citation: M. Litt et al., A GENE FOR EPISODIC ATAXIA MYOKYMIA MAPS TO CHROMOSOME 12P13/, American journal of human genetics, 55(4), 1994, pp. 702-709
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