Mariz Vainzof

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Zatz MUniversidade de S. PauloVerified email at usp.br
Maria Rita Passos-BuenoDepartamento de Genetica e Biologia Evolutiva, Instituto de Biociências, Universidade de São PauloVerified email at ib.usp.br
Natássia VieiraPostdoc FellowVerified email at enders.tch.harvard.edu
Vincenzo NigroUniversità della Campania "Luigi Vanvitelli" Dipartimento di Medicina di Precisione, and TIGEMVerified email at unicampania.it
Camila F AlmeidaPost-doctoral Scientist at Nationwide Children's HospitalVerified email at nationwidechildrens.org
Georgine FaulknerGuest Scientist, CRIBI, University of Padova, ItalyVerified email at cribi.unipd.it
Carlos Roberto Bueno JúniorProfessor Adjunto Substituto em Fisiologia na Universidade Federal de São PauloVerified email at usp.br
Giorgio ValleProfessor of Molecular Biology, University of Padua, ItalyVerified email at unipd.it
Paolo BartoliniIPENVerified email at ipen.br
Alan H. Beggs, PhDProfessor of Pediatrics, Harvard Medical School, Director The Manton CenterVerified email at enders.tch.harvard.edu
Fernando KokProfessor Titular, Departamento de Neurologia da FMUSPVerified email at mendelics.com.br
Clarissa M. ComimProfessor do Programa de Pós-graduação em Ciências da Saúde, Universidade do Sul de Santa CatarinaVerified email at unisul.br
Miriam Fussae SuzukiInstituto de Pesquisas Energéticas e Nucleares, IPEN - CNEN/SPVerified email at ipen.br
SANTOS, A.L.FVerified email at alumni.usp.br
JOÃO LUCIANO DE QUEVEDOThe University of Texas Health Science Center at HoustonVerified email at uth.tmc.edu
Viviane Abreu NunesUniversidade de São PauloVerified email at ib.usp.br
Donald R. LoveDivision Chief, Pathology Genetics, Sidra MedicineVerified email at sidra.org
ANDRADE, Telma GCSProfessora do Departamento de Ciências Biológicas da Universidade Estadual Paulista - UNESP, Câmpus de AssisVerified email at assis.unesp.br
Giulio PilusoDip. di Medicina di Precisione, Università degli Studi della Campania "LuigiVerified email at unicampania.it
Carlos Eduardo AmbrósioProfessor Anatomia Animal, FZEA, Universidade de São PauloVerified email at usp.br

Mariz Vainzof

Centro de Estudos do Genoma Humano e Células Tronco, IBUSP

Verified email at usp.br


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Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene V Nigro, ES Moreira, G Piluso, M Vainzof, A Belsito, L Politano, AA Puca, ... Nature genetics 14 (2), 195-198, 1996	552	1996
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin ES Moreira, TJ Wiltshire, G Faulkner, A Nilforoushan, M Vainzof, ... Nature genetics 24 (2), 163-166, 2000	433	2000
Approach to the diagnosis of congenital myopathies KN North, CH Wang, N Clarke, H Jungbluth, M Vainzof, JJ Dowling, ... Neuromuscular disorders 24 (2), 97-116, 2014	341	2014
Caveolin-3 in muscular dystrophy EM McNally, E de Sá Moreira, DJ Duggan, CG Bönnemann, MP Lisanti, ... Human molecular genetics 7 (5), 871-877, 1998	293	1998
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ... Human molecular genetics 5 (12), 1963-1969, 1996	232	1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. EM McNally, MR Passos-Bueno, CG Bönnemann, M Vainzof, ... American journal of human genetics 59 (5), 1040, 1996	216	1996
Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy M Zatz, D Rapaport, M Vainzof, MR Passos-Bueno, ER Bortolini, ... Journal of the neurological sciences 102 (2), 190-196, 1991	210	1991
The 10 autosomal recessive limb-girdle muscular dystrophies M Zatz, F De Paula, A Starling, M Vainzof Neuromuscular disorders 13 (7-8), 532-544, 2003	204	2003
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females M Zatz, SK Marie, A Cerqueira, M Vainzof, RCM Pavanello, ... American journal of medical genetics 77 (2), 155-161, 1998	191	1998
Consensus statement on standard of care for congenital myopathies CH Wang, JJ Dowling, K North, MK Schroth, T Sejersen, F Shapiro, ... Journal of child neurology 27 (3), 363-382, 2012	190	2012
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12 ES Moreira, M Vainzof, SK Marie, AL Sertie, M Zatz, MR Passos-Bueno The American Journal of Human Genetics 61 (1), 151-159, 1997	163	1997
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes M Zatz, M Vainzof, MR Passos-Bueno Current opinion in neurology 13 (5), 511-517, 2000	160	2000
Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E) CG Bönnemann, MR Passos-Bueno, EM McNally, M Vainzof, ES Moreira, ... Human molecular genetics 5 (12), 1953-1961, 1996	156	1996
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families. M Zatz, SK Marie, MR Passos-Bueno, M Vainzof, S Campiotto, ... American journal of human genetics 56 (1), 99, 1995	155	1995
Animal models for genetic neuromuscular diseases M Vainzof, D Ayub-Guerrieri, PCG Onofre, PCM Martins, VF Lopes, ... Journal of Molecular Neuroscience 34, 241-248, 2008	145	2008
Human multipotent adipose‐derived stem cells restore dystrophin expression of Duchenne skeletal‐muscle cells in vitro NM Vieira, V Brandalise, E Zucconi, T Jazedje, M Secco, VA Nunes, ... Biology of the Cell 100 (4), 231-241, 2008	144	2008
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G) NM Vieira, MS Naslavsky, L Licinio, F Kok, D Schlesinger, M Vainzof, ... Human molecular genetics 23 (15), 4103-4110, 2014	137	2014
Seven autosomal recessive limb‐girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G MR Passos‐Bueno, M Vainzof, ES Moreira, M Zatz American journal of medical genetics 82 (5), 392-398, 1999	135	1999
Linkage Analysis in Autosomal Recessive Limb-Girdle Muscular Dystrophy (AR LGMD) Maps a Sixth Form to 5q33–34 ( LGMD2F ) and Indicates That … MR Passos-Bueno, ES Moreira, M Vainzof, SK Marie, M Zatz Human molecular genetics 5 (6), 815-820, 1996	135	1996
Clinical variability in calpainopathy: what makes the difference? F de Paula, M Vainzof, MR Passos-Bueno, R de Cássia M Pavanello, ... European Journal of Human Genetics 10 (12), 825-832, 2002	125	2002

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