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A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability
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A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability

Figueiredo, T ; Melo, U S ; Pessoa, A L S ; Nobrega, P R ; Kitajima, J P ; Rusch, H ; Vaz, F ; Lucato, L T ; Zatz, M ; Kok, F ; Santos, S

Molecular psychiatry, 2016-08, Vol.21 (8), p.1125-1129 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin
Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin
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Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin

Vieira, N. M. ; Valadares, M. ; Zucconi, E. ; Secco, M. ; Junior, C. R. Bueno ; Brandalise, V. ; Assoni, A. ; Gomes, J. ; Landini, V. ; Andrade, T. ; Caetano, H. V. A. ; Vainzof, M. ; Zatz, M.

Cell transplantation, 2012-01, Vol.21 (7), p.1407-1417 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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3
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
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Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin

Zatz, M ; Pavanello, R.C.M ; Lazar, M ; Yamamoto, G.L ; Lourenço, N.C.V ; Cerqueira, A ; Nogueira, L ; Vainzof, M

Neuromuscular disorders : NMD, 2014-11, Vol.24 (11), p.986-989 [Periódico revisado por pares]

England: Elsevier B.V

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4
African ancestry protects against Alzheimer's disease-related neuropathology
African ancestry protects against Alzheimer's disease-related neuropathology
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African ancestry protects against Alzheimer's disease-related neuropathology

SCHLESINGER, D ; GRINBERG, L. T ; DOS SANTOS, Acf ; BRENTANI, H ; PASQUALUCCI, C. A ; NITRINI, R ; JACOB-FILHO, W ; ZATZ, M ; ALBA, J. G ; NASLAVSKY, M. S ; LICINIO, L ; FARFEL, J. M ; SUEMOTO, C. K ; DE LUCENA FERRETTI, R. E ; LEITE, Rep ; DE ANDRADE, M. P

Molecular psychiatry, 2013-01, Vol.18 (1), p.79-85 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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5
Human Endometrial-Derived Mesenchymal Stem Cells Suppress Inflammation in the Central Nervous System of EAE Mice
Human Endometrial-Derived Mesenchymal Stem Cells Suppress Inflammation in the Central Nervous System of EAE Mice
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Human Endometrial-Derived Mesenchymal Stem Cells Suppress Inflammation in the Central Nervous System of EAE Mice

Peron, J. P. S. ; Jazedje, T. ; Brandão, W. N. ; Perin, P. M. ; Maluf, M. ; Evangelista, L. P. ; Halpern, S. ; Nisenbaum, M. G. ; Czeresnia, C. E. ; Zatz, M. ; Câmara, N. O. S. ; Rizzo, L. V.

Stem cell reviews, 2012-09, Vol.8 (3), p.940-952 [Periódico revisado por pares]

New York: Humana Press Inc

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6
The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case
The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case
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The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

Funke, AD ; Esser, M ; Krüttgen, A ; Weis, J ; Mitne-Neto, M ; Lazar, M ; Nishimura, AL ; Sperfeld, AD ; Trillenberg, P ; Senderek, J ; Krasnianski, M ; Zatz, M ; Zierz, S ; Deschauer, M

Clinical genetics, 2010-03, Vol.77 (3), p.302-303 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

Nigro, V ; de Sá Moreira, E ; Piluso, G ; Vainzof, M ; Belsito, A ; Politano, L ; Puca, A A ; Passos-Bueno, M R ; Zatz, M

Nature genetics, 1996-10, Vol.14 (2), p.195-198 [Periódico revisado por pares]

United States

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8
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J mice
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J mice
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Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J mice

Valadares, M C ; Gomes, J P ; Castello, G ; Assoni, A ; Pellati, M ; Bueno, C ; Corselli, M ; Silva, H ; Bartolini, P ; Vainzof, M ; Margarido, P F ; Baracat, E ; Péault, B ; Zatz, M

Stem cell reviews and reports, 2014-12, Vol.10 (6), p.830-840 [Periódico revisado por pares]

United States

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9
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)
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Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)

Tonini, M.M.O ; Passos-Bueno, M.R ; Cerqueira, A ; Matioli, S.R ; Pavanello, R ; Zatz, M

Neuromuscular disorders : NMD, 2004, Vol.14 (1), p.33-38 [Periódico revisado por pares]

England: Elsevier B.V

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10
A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13
A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13
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A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13

Nishimura, A L ; Mitne-Neto, M ; Silva, H C A ; Oliveira, J R M ; Vainzof, M ; Zatz, M

Journal of medical genetics, 2004-04, Vol.41 (4), p.315-320 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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