T. Matilla - Concepedia

Author

T. Matilla

Duran i Reynals Hospital

Also Known As

J. Uilchez, T Matilla, T. Matilla, Toni Matilla

Publications

Citations

H-Index

Concepts

All Affiliations

Duran i Reynals Hospital Universidad de Oviedo Baylor College of Medicine

About

T. Matilla is an author at Duran i Reynals Hospital specializing in cell biology, medicine, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	668
2	Cell Biology	3	3	668
3	Molecular Genetics	2	2	75
4	Developmental Biology	1	1	593
5	Epigenetics	1	1	25

T. Matilla

Publications

Citations

H-Index

Page 1

	Year	Citations
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat Eric N. Burright, H. Brent Clark, Antonio Servadio, Cell Knockout MouseNeurodegenerative DiseasesDevelopmental BiologyTransgenic Mouse ModelsGenetics	1995	593
Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred D. E. Genis, T. Matilla, V. Volpini, Neurology	1995	139
Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado‐Joseph disease T. Matilla, Alanna E. McCall, S. H. Subramony, Annals of Neurology	1995	99
Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the <i>SCA1</i> CAG-repeat in a large pedigree displaying anticipation and parental male bias T. Matilla, V. Volpinl, D. E. Genis, Human Molecular Genetics	1993	84
The human collagenase-3 (CLG3) gene is located on chromosome 11q22.3 clustered to other members of the matrix metalloproteinase gene family Alberto M. Pendás, T. Matilla, Xavier Estivill, Genomics ChromatinHuman Collagenase-3Genetic DisorderMedicineGenetics	1995	50
Mapping of the human Zn-α<sub>2</sub>-glycoprotein gene (AZGP1) to chromosome 7q22 by in situ hybridization Alberto M. Pendás, T. Matilla, JA. Uría, Cytogenetic and Genome Research HistocompatibilityCytogeneticsGeneticsMolecular GeneticsGenomics	1994	25
Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1). Sergi Castellvı́-Bel, T. Matilla, M I Banchs, Journal of Medical Genetics	1994	11

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