D Fee | AMiner学者主页

1Mutations In The Voltage-Gated Potassium Channel Kcnc3 Cause Degenerative And Developmental Cns Phenotypes

Mf Waters,Na Minassian,G Stevanin,Kp Figueroa,Jpa Bannister,D Nolte,Af Mock, Vgg Evidente,D Fee,U Muller,A Durr,A Brice,

2006NEUROLOGY（2006）引用：8

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2Potassium Channels And Neurodegeneration: Mutations In The Kcnc3 Voltage-Cated K-Channel Cause Spinocerebellar Ataxia Type 13 (Sca13)

Mf Waters,Na Minassian,G Stevanin,Kp Figueroa,D Nolte,Jpa Bannister, A Mock,Vg Evidente,D Fee,U Muller,A Durr,A Brice,

2005ANNALS OF NEUROLOGY（2005）

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3An Autosomal Dominant Ataxia Maps to 19q13: Allelic Heterogeneity of SCA13 or Novel Locus?

MF Waters,D Fee,KP Figueroa,D Nolte,U Muller,J Advincula,H Coon,VG Evidente, SM Pulst

The autosomal dominant spinocerebellar ataxias (ADCAs) represent a growing and heterogeneous disease phenotype. Clinical characterization of a three-generation Filipino family segregating a dominant ataxia revealed cerebellar signs and symptoms. After elimination of known spinocerebellar ataxia (SCA) loci, a genome-wide linkage scan revealed a disease locus in a 4-cM region of 19q13, with a 3.89 lod score. This region overlaps and reduces the SCA13 locus. However, this ADCA is clinically distinguishable from SCA13.

2005Neurology（2005）引用：41

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4SCA13 in a Filipino kindred

VG Evidente, J Advincula,D Fee,M Waters,D Nolte,U Muller,S Pulst

2005JOURNAL OF THE NEUROLOGICAL SCIENCES（2005）

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5Novel autosomal-dominant cerebellar ataxia syndrome in a Filipino kindred

V. G. H. Evidente,D. Fee, J. Advincula,D. Nolte, U. Mueller,S. M. Pulst

2004EUROPEAN JOURNAL OF NEUROLOGY（2004）

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