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Isabel Conceição Moreira Pereira Alonso

AuthID: R-000-678

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Confirmed Publications: 33

21

TITLE: Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population Full Text
AUTHORS: Sequeiros, J ; Ramos, EM; Cerqueira, J; Costa, MC; Sousa, A ; Pinto Basto, J; Alonso, I ;
PUBLISHED: 2010, SOURCE: CLINICAL GENETICS, VOLUME: 78, ISSUE: 4

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22

TITLE: Sensory neuronopathy in ataxia with oculomotor apraxia type 2 Full Text
AUTHORS: Jose Gazulla; Isabel Benavente; Isabel P Perez Lopez Fraile; Carlos Tordesillas; Pedro Modrego; Isabel Alonso ; Jorge Pinto Basto;
PUBLISHED: 2010, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 298, ISSUE: 1-2

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23

TITLE: Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10) Full Text
AUTHORS: Teresa Almeida; Isabel Alonso ; Sandra Martins ; Eliana Marisa Ramos; Luisa Azevedo ; Kinji Ohno; Amorim, Antonio ; Maria Luiza Saraiva Pereira; Laura Bannach Jardim; Tohru Matsuura; Jorge Sequeiros ; Isabel Silveira ;
PUBLISHED: 2009, SOURCE: PLOS ONE, VOLUME: 4, ISSUE: 2

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24

TITLE: The Spatial Learning Phenotype of Heterozygous Leaner Mice is Robust to Systematic Variation of the Housing Environment
AUTHORS: Joana M Marques; Isabel Alonso ; Cristina Santos ; Isabel Silveira ; Anna A S Olsson ;
PUBLISHED: 2009, SOURCE: COMPARATIVE MEDICINE, VOLUME: 59, ISSUE: 2

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25

TITLE: Motor and cognitive deficits in the heterozygous leaner mouse, a Ca(v)2.1 voltage-gated Ca2+ channel mutant Full Text
AUTHORS: Isabel Alonso ; Joana M Marques; Nuno Sousa ; Jorge Sequeiros ; Anna A S Olsson ; Isabel Silveira ;
PUBLISHED: 2008, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 29, ISSUE: 11

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26

TITLE: Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10
AUTHORS: Alonso, I ; Jardim, LB; Artigalas, O; Saraiva Pereira, ML; Matsuura, T; Ashizawa, T; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2006, SOURCE: NEUROLOGY, VOLUME: 66, ISSUE: 10

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27

TITLE: Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings Full Text
AUTHORS: Trott, A; Jardim, LB; Ludwig, HT; Saute, JAM; Artigalas, O; Kieling, C; Wanderley, HYC; Rieder, CRM; Monte, TL; Socal, M; Alonso, I ; Ferro, A; Carvalho, T; do Ceu Moreira, M; Mendonca, P; Ferreirinha, F ; Silveira, I ; Sequeiros, J ; Giugliani, R; Saraiva Pereira, ML;
PUBLISHED: 2006, SOURCE: CLINICAL GENETICS, VOLUME: 70, ISSUE: 2

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28

TITLE: A novel H101Q mutation causes PKC gamma loss in spinocerebellar ataxia type 14 Full Text
AUTHORS: Alonso, I ; Costa, C; Gomes, A; Ferro, A; Seixas, AI; Silva, S; Cruz, VT ; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2005, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 50, ISSUE: 10

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29

TITLE: A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha(1A)-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine. Letter to the Editor Full Text
AUTHORS: Alonso, I ; Barros, José ; Tuna, A; Seixas, A; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2004, SOURCE: CLINICAL GENETICS, VOLUME: 65, ISSUE: 1

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30

TITLE: Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family
AUTHORS: Alonso, I ; Barros, José ; Tuna, A; Coelho, J; Sequeiros, J ; Silveira, I ; Coutinho, P ;
PUBLISHED: 2003, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 60, ISSUE: 4

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