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1
New once‐daily, highly effective rescue triple therapy after multiple Helicobacter pylori treatment failures: a pilot study
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Artigo
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New once‐daily, highly effective rescue triple therapy after multiple Helicobacter pylori treatment failures: a pilot study

Coelho, L. G. V. ; Moretzsohn, L. D. ; Vieira, W. L. S. ; Gallo, M. A. ; Passos, M. C. F. ; Cindr, J. M. ; Cerqueira, M. C. ; Vitiello, L. ; Ribeiro, M. L. ; Mendonça, S. ; Pedrazzoli‐Júnior, J. ; Castro, L. P.

Alimentary pharmacology & therapeutics, 2005-03, Vol.21 (6), p.783-787 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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2
Once‐daily, low‐cost, highly effective Helicobacter pylori treatment to family members of gastric cancer patients
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Artigo
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Once‐daily, low‐cost, highly effective Helicobacter pylori treatment to family members of gastric cancer patients

Coelho, L. G. V. ; Martins, G. M. ; Passos, M. C. F. ; Bueno, M. L. ; Sanches, B. S. F. ; Lopes, L. G. ; Miranda, C. H. D. ; Castro, L. P.

Alimentary pharmacology & therapeutics, 2003-01, Vol.17 (1), p.131-136 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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3
Meanings of quality of care: Perspectives of Portuguese health professionals and patients
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Artigo
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Meanings of quality of care: Perspectives of Portuguese health professionals and patients

Silva, Sílvia A. ; Costa, Patrícia L. ; Costa, Rita ; Tavares, Susana M. ; Leite, Ema S. ; Passos, Ana M.

British journal of health psychology, 2013-11, Vol.18 (4), p.858-873 [Periódico revisado por pares]

London: Blackwell Publishing Ltd

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4
Familial spongiform encephalopathy associated with a novel prion protein gene mutation
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Artigo
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Familial spongiform encephalopathy associated with a novel prion protein gene mutation

Nitrini, Ricardo ; Rosemberg, Sergio ; Passos-Bueno, Maria Rita ; da Silva, Luís S. Teixeira ; Iughetti, Paula ; Papadopoulos, Maria ; Carrilho, Paulo M. ; Caramelli, Paulo ; Albrecht, Steffen ; Zatz, Mayana ; LeBlanc, Andrea

Annals of neurology, 1997-08, Vol.42 (2), p.138-146 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
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Artigo
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Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?

Eggers, Sabine ; Lauriano, Valèria ; Melo, Marcio ; Takata, Reinaldo Issao ; Akiyama, Jeanne ; Passos-Bueno, Maria Rita ; Gentil, Valentim ; Frota-Pessoa, Oswaldo ; Zatz, Mayana

American journal of medical genetics, 1995-02, Vol.60 (1), p.27-32 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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6
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
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Artigo
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Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G

Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S. ; Zatz, Mayana

American journal of medical genetics, 1999-02, Vol.82 (5), p.392-398

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
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Artigo
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Further evidence for a fourth gene causing X-linked pure spastic paraplegia

Starling, A. ; Rocco, P. ; Cambi, F. ; Hobson, G.M. ; Passos Bueno, M.R. ; Zatz, M.

American journal of medical genetics, 2002-08, Vol.111 (2), p.152-156

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation?
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Artigo
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Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno, Maria Rita ; Byth, Barbara C. ; Rosenberg, Sergio ; Takata, Reinaldo I. ; Bakker, Egbert ; Beggs, Alan H. ; Pavanello, Rita C. ; Vainzof, Mariz ; Davies, Kay E. ; Zatz, Mayana

American journal of medical genetics, 1993-04, Vol.46 (2), p.172-175

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
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Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia

Iughetti, Paula ; Alonso, Luis Garcia ; Wilcox, William ; Alonso, Nivaldo ; Passos-Bueno, Maria Rita

American journal of medical genetics, 2000-12, Vol.95 (5), p.482-491

New York: John Wiley & Sons, Inc

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10
Serum I‐FABP as marker for enterocyte damage in coeliac disease and its relation to villous atrophy and circulating autoantibodies
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Artigo
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Serum I‐FABP as marker for enterocyte damage in coeliac disease and its relation to villous atrophy and circulating autoantibodies

Adriaanse, M. P. M. ; Tack, G. J. ; Passos, V. Lima ; Damoiseaux, J. G. M. C. ; Schreurs, M. W. J. ; Wijck, K. ; Riedl, R. G. ; Masclee, A. A. M. ; Buurman, W. A. ; Mulder, C. J. J. ; Vreugdenhil, A. C. E.

Alimentary pharmacology & therapeutics, 2013-02, Vol.37 (4), p.482-490 [Periódico revisado por pares]

Oxford: Blackwell

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