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Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations. [electronic resource] by
- Melo, U S
- Freua, F
- Lynch, D S
- Ripa, B D
- Tenorio, R B
- Saute, J A M
- de Souza Leite, F
- Kitajima, J
- Houlden, H
- Zatz, M
- Kok, F
Producer: 20191114
In:
Clinical genetics vol. 94
Availability: No items available.
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5.
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SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil. [electronic resource] by
- França, M C
- Dogini, D B
- D'Abreu, A
- Teive, H A G
- Munhoz, R P
- Raskin, S
- Moro, A
- Melo, C C
- Gomes, A P
- Saute, J A M
- Jardim, L B
- Lopes-Cendes, I
Producer: 20150312
In:
Clinical genetics vol. 86
Availability: No items available.
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6.
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Age at onset prediction in spinocerebellar ataxia type 3 changes according to population of origin. [electronic resource] by
- de Mattos, E P
- Leotti, V B
- Soong, B-W
- Raposo, M
- Lima, M
- Vasconcelos, J
- Fussiger, H
- Souza, G N
- Kersting, N
- Furtado, G V
- Saute, J A M
- Camey, S A
- Saraiva-Pereira, M L
- Jardim, L B
Producer: 20190603
In:
European journal of neurology vol. 26
Availability: No items available.
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7.
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Autonomic dysfunction in hereditary spastic paraplegia type 4. [electronic resource] by
- González-Salazar, C
- Takazaki, K A G
- Martinez, A R M
- Pimentel-Silva, L R
- Jacinto-Scudeiro, L A
- Nakagawa, É Y
- Fujiwara Murakami, C E
- Saute, J A M
- Pedroso, J L
- Barsottini, O G P
- Teive, H A G
- França, M C
Producer: 20200727
In:
European journal of neurology vol. 26
Availability: No items available.
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8.
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Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. [electronic resource] by
- Trott, A
- Jardim, L B
- Ludwig, H T
- Saute, J A M
- Artigalás, O
- Kieling, C
- Wanderley, H Y C
- Rieder, C R M
- Monte, T L
- Socal, M
- Alonso, I
- Ferro, A
- Carvalho, T
- do Céu Moreira, M
- Mendonça, P
- Ferreirinha, F
- Silveira, I
- Sequeiros, J
- Giugliani, R
- Saraiva-Pereira, M L
Producer: 20061003
In:
Clinical genetics vol. 70
Availability: No items available.
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9.
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Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil. [electronic resource] by
- Gheno, T C
- Furtado, G V
- Saute, J A M
- Donis, K C
- Fontanari, A M V
- Emmel, V E
- Pedroso, J L
- Barsottini, O
- Godeiro-Junior, C
- van der Linden, H
- Ternes Pereira, E
- Cintra, V P
- Marques, W
- de Castilhos, R M
- Alonso, I
- Sequeiros, J
- Cornejo-Olivas, M
- Mazzetti, P
- Leotti, V B
- Jardim, L B
- Saraiva-Pereira, M L
Producer: 20180228
In:
European journal of neurology vol. 24
Availability: No items available.
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10.
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Genetic profile of Brazilian patients with dystrophinopathies. [electronic resource] by
- de Almeida, P A D
- Machado-Costa, M C
- Manzoli, G N
- Ferreira, L S
- Rodrigues, M C S
- Bueno, L S M
- Saute, J A M
- Pinto Vairo, F
- Matte, U S
- Siebert, M
- Cossio, S L
- Macedo, G S
- Winckler, P B
- Becker, M M
- Magalhães, L V B
- Gonçalves, M V M
- Marrone, C D
- Nucci, A
- França, M C
Producer: 20180418
In:
Clinical genetics vol. 92
Availability: No items available.
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11.
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Huntington disease and Huntington disease-like in a case series from Brazil. [electronic resource] by
- Castilhos, R M
- Souza, A F D
- Furtado, G V
- Gheno, T C
- Silva, A L
- Vargas, F R
- Lima, M-A F D
- Barsottini, O
- Pedroso, J L
- Godeiro, C
- Salarini, D
- Pereira, E T
- Lin, K
- Toralles, M-B
- Saute, J A M
- Rieder, C R
- Quintas, M
- Sequeiros, J
- Alonso, I
- Saraiva-Pereira, M L
- Jardim, L B
Producer: 20150525
In:
Clinical genetics vol. 86
Availability: No items available.
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