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Mayana Zatz

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Disorders

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Brazil

Physiology

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Recessive Genes

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Co-Publications
Name
91
Vainzof, Mariz
85
Passos-Bueno, Maria Rita
33
Pavanello, Rita
27
Marie, Suely
16
Cerqueira, Antonia
15
Moreira, Eloisa
14
Oliveira, João
10
Starling, Alessandra
9
Otto, Paulo
9
Nishimura, Agnes
9
Vieira, Natassia
8
Zucconi, Eder
8
Reed, Umbertina Conti
7
de Paula, Flavia
7
Kok, Fernando

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Publications

TOP 3
Zatz Mayana
Stem cell researches in Brazil: present and future challenges.
Macedo-Souza Lúcia Inês; Kok Fernando; Santos Silvana; Licinio Luciana; Lezirovitz Karina; Cavaçana Natale; Bueno Clarissa; Amorim Simone; Pessoa André; Graciani Zodja; Ferreira Aurea; Prazeres Abdísio; de Melo Aurea Nogueira; Otto Paulo Alberto; Zatz Mayana
Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes.
Arashiro Patricia; Eisenberg Iris; Kho Alvin T; Cerqueira Antonia M P; Canovas Marta; Silva Helga C A; Pavanello Rita C M; Verjovski-Almeida Sergio; Kunkel Louis M; Zatz Mayana
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers.

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All Publications

2009: Zatz Mayana
Stem cell researches in Brazil: present and future challenges.
Stem cell reviews and reports 2009;5(2):123-9.
2009: Macedo-Souza Lúcia Inês; Kok Fernando; Santos Silvana; Licinio Luciana; Lezirovitz Karina; Cavaçana Natale; Bueno Clarissa; Amorim Simone; Pessoa André; Graciani Zodja; Ferreira Aurea; Prazeres Abdísio; de Melo Aurea Nogueira; Otto Paulo Alberto; Zatz Mayana
Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes.
Annals of human genetics 2009;73(Pt 3):382-7.
2009: Arashiro Patricia; Eisenberg Iris; Kho Alvin T; Cerqueira Antonia M P; Canovas Marta; Silva Helga C A; Pavanello Rita C M; Verjovski-Almeida Sergio; Kunkel Louis M; Zatz Mayana
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(15):6220-5.
2009: Jazedje Tatiana; Perin Paulo M; Czeresnia Carlos E; Maluf Mariangela; Halpern Silvio; Secco Mariane; Bueno Daniela F; Vieira Natassia M; Zucconi Eder; Zatz Mayana
Human fallopian tube: a new source of multipotent adult mesenchymal stem cells discarded in surgical procedures.
Journal of translational medicine 2009;7():46.
2009: Jazedje Tatiana; Secco Mariane; Vieira Natássia M; Zucconi Eder; Gollop Thomaz R; Vainzof Mariz; Zatz Mayana
Stem cells from umbilical cord blood do have myogenic potential, with and without differentiation induction in vitro.
Journal of translational medicine 2009;7():6.
2008: Ambrósio C E; Valadares M C; Zucconi E; Cabral R; Pearson P L; Gaiad T P; Canovas M; Vainzof M; Miglino M A; Zatz M
Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength.
Neuromuscular disorders : NMD 2008;18(11):892-3.
2008: Yamamoto Lydia U; Velloso Fernando J; Lima Bruno L; Fogaça Luciana L Q; de Paula Flávia; Vieira Natássia M; Zatz Mayana; Vainzof Mariz
Muscle protein alterations in LGMD2I patients with different mutations in the Fukutin-related protein gene.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2008;56(11):995-1001.
2008: Vieira Natássia M; Bueno Carlos R; Brandalise Vanessa; Moraes Luciana V; Zucconi Eder; Secco Mariane; Suzuki Miriam F; Camargo Maristela M; Bartolini Paolo; Brum Patricia C; Vainzof Mariz; Zatz Mayana
SJL dystrophic mice express a significant amount of human muscle proteins following systemic delivery of human adipose-derived stromal cells without immunosuppression.
Stem cells (Dayton, Ohio) 2008;26(9):2391-8.
2008: Eduardo Fernanda de P; Bueno Daniela F; de Freitas Patricia M; Marques Márcia Martins; Passos-Bueno Maria Rita; Eduardo Carlos de P; Zatz Mayana
Stem cell proliferation under low intensity laser irradiation: a preliminary study.
Lasers in surgery and medicine 2008;40(6):433-8.
2008: Macedo-Souza Lúcia Inês; Kok Fernando; Santos Silvana; Licinio Luciana; Lezirovitz Karina; Nascimento Rafaella M P; Bueno Clarissa; Martyn Marcília; Leão Emília K E A; Zatz Mayana
Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25.
Neurogenetics 2008;9(3):225-6.
2008: Kolski Hanna K; Hawkins Cynthia; Zatz Mayana; de Paula Flavia; Biggar Doug; Alman Ben; Vajsar Jiri
Diagnosis of limb-girdle muscular dystrophy 2A by immunohistochemical techniques.
Neuropathology : official journal of the Japanese Society of Neuropathology 2008;28(3):264-8.
2008: Vieira Natássia M; Brandalise Vanessa; Zucconi Eder; Jazedje Tatiana; Secco Mariane; Nunes Viviane A; Strauss Bryan E; Vainzof Mariz; Zatz Mayana
Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro.
Biology of the cell / under the auspices of the European Cell Biology Organization 2008;100(4):231-41.
2008: Secco Mariane; Zucconi Eder; Vieira Natassia M; Fogaça Luciana L Q; Cerqueira Antonia; Carvalho Maria Denise F; Jazedje Tatiana; Okamoto Oswaldo K; Muotri Alysson R; Zatz Mayana
Mesenchymal stem cells from umbilical cord: do not discard the cord!
Neuromuscular disorders : NMD 2008;18(1):17-8.
2008: Secco Mariane; Zucconi Eder; Vieira Natassia M; Fogaça Luciana L Q; Cerqueira Antonia; Carvalho Maria Denise F; Jazedje Tatiana; Okamoto Oswaldo K; Muotri Alysson R; Zatz Mayana
Multipotent stem cells from umbilical cord: cord is richer than blood!
Stem cells (Dayton, Ohio) 2008;26(1):146-50.
2008: Kerkis Irina; Ambrosio Carlos E; Kerkis Alexandre; Martins Daniele S; Zucconi Eder; Fonseca Simone A S; Cabral Rosa M; Maranduba Carlos M C; Gaiad Thais P; Morini Adriana C; Vieira Natassia M; Brolio Marina P; Sant'Anna Osvaldo A; Miglino Maria A; Zatz Mayana
Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
Journal of translational medicine 2008;6():35.
2007: Mitne-Neto Miguel; Kok Fernando; Beetz Christian; Pessoa André; Bueno Clarissa; Graciani Zodja; Martyn Marcilia; Monteiro Carlos B M; Mitne Guilherme; Hubert Paulo; Nygren Anders O H; Valadares Marcos; Cerqueira Antonia M P; Starling Alessandra; Deufel Thomas; Zatz Mayana
A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree.
European journal of human genetics : EJHG 2007;15(12):1276-9.
2007: Mitne-Neto M; Ramos C R R; Pimenta D C; Luz J S; Nishimura A L; Gonzales F A; Oliveira C C; Zatz M
A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteins.
Protein expression and purification 2007;55(1):139-46.
2007: Schmidt Wolfgang M; Kraus Cornelia; Höger Harald; Hochmeister Sonja; Oberndorfer Felicitas; Branka Manuela; Bingemann Sonja; Lassmann Hans; Müller Markus; Macedo-Souza Lúcia Inês; Vainzof Mariz; Zatz Mayana; Reis André; Bittner Reginald E
Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.
EMBO reports 2007;8(7):691-7.
2007: Costa Marcelo Fernandes; Oliveira Andre Gustavo Fernandes; Feitosa-Santana Claudia; Zatz Mayana; Ventura Dora Fix
Red-green color vision impairment in Duchenne muscular dystrophy.
American journal of human genetics 2007;80(6):1064-75.
2007: Silva Marly Conceição; Meira Zilda Maria Alves; Gurgel Giannetti Juliana; da Silva Marcelo Moreira; Campos Alysson Félix Oliveira; Barbosa Márcia de Melo; Starling Filho Geraldo Moll; Ferreira Rogério de Aguiar; Zatz Mayana; Rochitte Carlos Eduardo
Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy.
Journal of the American College of Cardiology 2007;49(18):1874-9.
2007: Kossugue Patrícia M; Paim Júlia F; Navarro Monica M; Silva Helga C; Pavanello Rita C M; Gurgel-Giannetti Juliana; Zatz Mayana; Vainzof Mariz
Central core disease due to recessive mutations in RYR1 gene: is it more common than described?
Muscle & nerve 2007;35(5):670-4.
2007: Gouveia Telma L F; Kossugue Patrícia M; Paim Julia F; Zatz Mayana; Anderson Louise V B; Nigro Vincenzo; Vainzof Mariz
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG protein.
Journal of molecular medicine (Berlin, Germany) 2007;85(4):415-20.
2007: Nunes Viviane A; Cavaçana Natale; Canovas Martha; Strauss Bryan E; Zatz Mayana
Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment.
Biology of the cell / under the auspices of the European Cell Biology Organization 2007;99(4):185-96.
2007: Valdmanis Paul N; Meijer Inge A; Reynolds Annie; Lei Adrienne; MacLeod Patrick; Schlesinger David; Zatz Mayana; Reid Evan; Dion Patrick A; Drapeau Pierre; Rouleau Guy A
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
American journal of human genetics 2007;80(1):152-61.
2006: Vieira N M; Schlesinger D; de Paula F; Vainzof M; Zatz M
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I.
Neuromuscular disorders : NMD 2006;16(12):870-3.
2006: Gouveia Telma L F; Paim Julia F O; Pavanello Rita C; Zatz Mayana; Vainzof Mariz
Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations.
Diagnostic molecular pathology : the American journal of surgical pathology, part B 2006;15(2):95-100.
2006: Tonini Maria Manuela O; Lemmers Richard J L F; Pavanello Rita C M; Cerqueira Antonia M P; Frants Rune R; van der Maarel Silvere M; Zatz Mayana
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy.
Human genetics 2006;119(1-2):23-8.
2005: Starling A; Schlesinger D; Kok F; Passos-Bueno M Rita; Vainzof M; Zatz M
A family with McLeod syndrome and calpainopathy with clinically overlapping diseases.
Neurology 2005;65(11):1832-3.
2005: Nishimura Agnes L; Al-Chalabi Ammar; Zatz Mayana
A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population.
Human genetics 2005;118(3-4):499-500.
2005: Vainzof Mariz; Richard Pascale; Herrmann Ralf; Jimenez-Mallebrera Cecilia; Talim Beril; Yamamoto Lydia U; Ledeuil Céline; Mein Rachael; Abbs Stephen; Brockington Martin; Romero Norma B; Zatz Mayana; Topaloglu Haluk; Voit Thomas; Sewry Caroline; Muntoni Francesco; Guicheney Pascale; Tomé Fernando M S
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
Neuromuscular disorders : NMD 2005;15(9-10):588-94.
2005: Zatz Mayana; Starling Alessandra
Calpains and disease.
The New England journal of medicine 2005;352(23):2413-23.
2005: Guindalini Camila; Scivoletto Sandra; Ferreira Ricardo G M; Nishimura Agnes; Zilberman Monica L; Peluso Marcoaurélio M; Zatz Mayana
Association of MAO A polymorphism and alcoholism in Brazilian females.
Psychiatric genetics 2005;15(2):141-4.
2005: Guindalini Camila; Scivoletto Sandra; Ferreira Ricardo G M; Breen Gerome; Zilberman Monica; Peluso Marco Aurélio; Zatz Mayana
Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in Brazilian patients.
The American journal of psychiatry 2005;162(5):1005-7.
2005: Macedo-Souza Lucia I; Kok Fernando; Santos Silvana; Amorim Simone C; Starling Alessandra; Nishimura Agnes; Lezirovitz Karina; Lino Angelina M M; Zatz Mayana
Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13.
Annals of neurology 2005;57(5):730-7.
2005: Nishioka Silvana Angelina D'Orio; Martinelli Filho Martino; Marie Suely; Zatz Mayana; Costa Roberto
[Myotonic dystrophy and heart disease: behavior of arrhythmic events and conduction disturbances]
Arquivos brasileiros de cardiologia 2005;84(4):330-6.
2005: Zatz Mayana
Global voices of science. When science is not enough: fighting genetic disease in Brazil.
Science (New York, N.Y.) 2005;308(5718):55-7.
2005: Frosk Patrick; Greenberg Cheryl R; Tennese Alysa A P; Lamont Ryan; Nylen Edward; Hirst Cheryl; Frappier Danielle; Roslin Nicole M; Zaik Michaela; Bushby Kate; Straub Volker; Zatz Mayana; de Paula Flavia; Morgan Kenneth; Fujiwara T Mary; Wrogemann Klaus
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations.
Human mutation 2005;25(1):38-44.
2005: Nishimura Agnes L; Guindalini Camila; Oliveira João R M; Nitrini Ricardo; Bahia Valéria S; de Brito-Marques Paulo R; Otto Paulo A; Zatz Mayana
Monoamine oxidase a polymorphism in Brazilian patients: risk factor for late-onset Alzheimer's disease?
Journal of molecular neuroscience : MN 2005;27(2):213-7.
2004: Starling Alessandra; Kok Fernando; Passos-Bueno Maria Rita; Vainzof Mariz; Zatz Mayana
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
European journal of human genetics : EJHG 2004;12(12):1033-40.
2004: Nishimura Agnes L; Mitne-Neto Miguel; Silva Helga C A; Richieri-Costa Antônio; Middleton Susan; Cascio Duilio; Kok Fernando; Oliveira João R M; Gillingwater Tom; Webb Jeanette; Skehel Paul; Zatz Mayana
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.
American journal of human genetics 2004;75(5):822-31.
2004: Yamamoto Lydia U; Gollop Thomas R; Naccache Nadyr F; Pavanello Rita C M; Zanoteli Edmar; Zatz Mayana; Vainzof Mariz
Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophy.
Diagnostic molecular pathology : the American journal of surgical pathology, part B 2004;13(3):167-71.
2004: Zorick Todd S; Kleimann Suzana; Sertié A; Zatz Mayana; Rosenberg Sérgio; Passos-Bueno Maria Rita
Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction.
American journal of medical genetics. Part A 2004;127A(3):321-3.
2004: Abe K T; Lino A M M; Hirata M T A; Pavanello R C M; Brotto M W I; Marchiori P E; Zatz M
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype.
Neuromuscular disorders : NMD 2004;14(5):313-20.
2004: Nishimura A L; Mitne-Neto M; Silva H C A; Oliveira J R M; Vainzof M; Zatz M
A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13.
Journal of medical genetics 2004;41(4):315-20.
2004: Tonini M M O; Pavanello R C M; Gurgel-Giannetti J; Lemmers R J; van der Maarel S M; Frants R R; Zatz M
Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype.
Journal of medical genetics 2004;41(2):e17.
2004: Tonini M M O; Passos-Bueno M R; Cerqueira A; Matioli S R; Pavanello R; Zatz M
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD).
Neuromuscular disorders : NMD 2004;14(1):33-8.
2004: Nishimura Agnes L; Oliveira João R M; Mitne-Neto Miguel; Guindalini Camila; Nitrini Ricar; Bahia Valéria S; de Brito-Marques Paulo R; Otto Paulo A; Zatz Mayana
Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimer's disease (LOAD) in Brazilian patients.
Journal of molecular neuroscience : MN 2004;22(3):257-60.
2004: Fertuzinhos Sofia M M; Oliveira João R M; Nishimura Agnes L; Pontual Deyse; Carvalho Daniel R; Sougey Everton B; Otto Paulo A; Zatz Mayana
Analysis of IL-1alpha, IL-1beta, and IL-1RA [correction of IL-RA] polymorphisms in dysthymia.
Journal of molecular neuroscience : MN 2004;22(3):251-6.
2003: de Paula Flavia; Vieira Natássia; Starling Alessandra; Yamamoto Lydia Uraco; Lima Bruno; de Cássia Pavanello Rita; Vainzof Mariz; Nigro Vincenzo; Zatz Mayana
Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum.
European journal of human genetics : EJHG 2003;11(12):923-30.
2003: Bernardino Andrea L Ferreira; Guarita Dulce Reis; Mott Carlos Barros; Pedroso Martha Regina Arcon; Machado Marcel Cerqueira Cesar; Laudanna Antonio Atilio; Tani Claudia Megume; Almeida Fatima Lovatti; Zatz Mayana
CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in Brazilian patients.
JOP : Journal of the pancreas 2003;4(5):169-77.
2003: Zatz Mayana; de Paula Flavia; Starling Alessandra; Vainzof Mariz
The 10 autosomal recessive limb-girdle muscular dystrophies.
Neuromuscular disorders : NMD 2003;13(7-8):532-44.
2003: Vainzof M; de Paula F; Tsanaclis A M; Zatz M
The effect of calpain 3 deficiency on the pattern of muscle degeneration in the earliest stages of LGMD2A.
Journal of clinical pathology 2003;56(8):624-6.
2003: Vainzof M; Zatz M
Protein defects in neuromuscular diseases.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2003;36(5):543-55.
2003: Gurgel-Giannetti Juliana; Reed Umbertina C; Marie Sueli K; Zanoteli Edmar; Fireman Moacir A T; Oliveira Acary S B; Werneck Lineu C; Beggs Alan H; Zatz Mayana; Vainzof Mariz
Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.
Journal of child neurology 2003;18(3):235-40.
2003: Zanoteli Edmar; Lotuffo Renato M; Oliveira Acary S B; Beggs Alan H; Canovas Marta; Zatz Mayana; Vainzof Mariz
Deficiency of muscle alpha-actinin-3 is compatible with high muscle performance.
Journal of molecular neuroscience : MN 2003;20(1):39-42.
2003: Moreira E S; Vainzof M; Suzuki O T; Pavanello R C M; Zatz M; Passos-Bueno M R
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations.
Journal of medical genetics 2003;40(2):E12.
2003: Starling Alessandra; de Paula Flavia; Silva Helga; Vainzof Mariz; Zatz Mayana
Calpainopathy: how broad is the spectrum of clinical variability?
Journal of molecular neuroscience : MN 2003;21(3):233-6.
2003: Vainzof Mariz; Passos-Bueno Maria Rita; Zatz Mayana
Immunological methods for the analysis of protein expression in neuromuscular diseases.
Methods in molecular biology (Clifton, N.J.) 2003;217():355-78.
2002: Starling A; Rocco P; Passos-Bueno M R; Hazan J; Marie S K; Zatz M
Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree.
Journal of medical genetics 2002;39(12):e77.
2002: de Paula Flávia; Vainzof Mariz; Passos-Bueno Maria Rita; de Cássia M Pavanello Rita; Matioli Sergio Russo; V B Anderson Louise; Nigro Vincenzo; Zatz Mayana
Clinical variability in calpainopathy: what makes the difference?
European journal of human genetics : EJHG 2002;10(12):825-32.
2002: Vainzof Mariz; Moreira Eloisa S; Suzuki Oscar T; Faulkner Georgine; Valle Georgio; Beggs Alan H; Carpen Olli; Ribeiro Alberto F; Zanoteli Edmar; Gurgel-Gianneti Juliana; Tsanaclis Ana Maria; Silva Helga C A; Passos-Bueno Maria Rita; Zatz Mayana
Telethonin protein expression in neuromuscular disorders.
Biochimica et biophysica acta 2002;1588(1):33-40.
2002: Starling A; Rocco P; Cambi F; Hobson G M; Passos Bueno M R; Zatz M
Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
American journal of medical genetics 2002;111(2):152-6.
2002: Tonini M M O; Passos-Bueno M R; Cerqueira A; Pavanello R; Vainzof M; Dubowitz V; Zatz M
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?
Neuromuscular disorders : NMD 2002;12(6):554-7.
2002: Gurgel-Giannetti J; Bang M-L; Reed U; Marie S; Zatz M; Labeit S; Vainzof M
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy.
Muscle & nerve 2002;25(5):747-52.
2001: Zorick T S; Mustacchi Z; Bando S Y; Zatz M; Moreira-Filho C A; Olsen B; Passos-Bueno M R
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours.
European journal of human genetics : EJHG 2001;9(11):811-4.
2001: Vainzof M; Anderson L V; McNally E M; Davis D B; Faulkner G; Valle G; Moreira E S; Pavanello R C; Passos-Bueno M R; Zatz M
Dysferlin protein analysis in limb-girdle muscular dystrophies.
Journal of molecular neuroscience : MN 2001;17(1):71-80.
2001: Nitrini R; Teixeira da Silva L S; Rosemberg S; Caramelli P; Carrilho P E; Iughetti P; Passos-Bueno M R; Zatz M; Albrecht S; LeBlanc A
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17.
Arquivos de neuro-psiquiatria 2001;59(2-A):161-4.
2001: de Paula F; Vainzof M; Bernardino A L; McNally E; Kunkel L M; Zatz M
Mutations in the caveolin-3 gene: When are they pathogenic?
American journal of medical genetics 2001;99(4):303-7.
2001: Gurgel-Giannetti J; Reed U; Bang M L; Pelin K; Donner K; Marie S K; Carvalho M; Fireman M A; Zanoteli E; Oliveira A S; Zatz M; Wallgren-Pettersson C; Labeit S; Vainzof M
Nebulin expression in patients with nemaline myopathy.
Neuromuscular disorders : NMD 2001;11(2):154-62.
2001: Nishimura A L; Oliveira J R; Otto P A; Matioli S R; Brito-Marques P R; Bahia V S; Nitrini R; Zatz M
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patients.
Journal of neural transmission (Vienna, Austria : 1996) 2001;108(3):305-10.
2000: Zatz M; Vainzof M; Passos-Bueno M R
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes.
Current opinion in neurology 2000;13(5):511-7.
2000: Nishimura A L; Oliveira J R; Matioli S R; Brito-Marques P R; Bahia V S; Nitrini R; Zatz M
Analysis of the disease risk locus DXS1047 polymorphism in Brazilian Alzheimer patients.
Molecular psychiatry 2000;5(5):563-6.
2000: Sertié A L; Sossi V; Camargo A A; Zatz M; Brahe C; Passos-Bueno M R
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome).
Human molecular genetics 2000;9(13):2051-8.
2000: Oliveira J R; Carvalho D R; Pontual D; Gallindo R M; Sougey E B; Gentil V; Lafer B; Maia L G; Morais M A; Matioli S; Vallada H; Moreno R A; Nishimura A; Otto P A; Passos-Bueno M R; Zatz M
Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder.
Molecular psychiatry 2000;5(4):348-9.
2000: Vainzof M; Moreira E S; Canovas M; Anderson L V; Pavanello R C; Passos-Bueno M R; Zatz M
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family.
Muscle & nerve 2000;23(6):984-8.
2000: Rocco P; Vainzof M; Froehner S C; Peters M F; Marie S K; Passos-Bueno M R; Zatz M
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin.
American journal of medical genetics 2000;92(2):122-7.
2000: Reed U C; Marie S K; Vainzof M; Gobbo L F; Gurgel J E; Carvalho M S; Resende M B; Espíndola A A; Zatz M; Diament A
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases.
Journal of child neurology 2000;15(3):172-8.
2000: Moreira E S; Wiltshire T J; Faulkner G; Nilforoushan A; Vainzof M; Suzuki O T; Valle G; Reeves R; Zatz M; Passos-Bueno M R; Jenne D E
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
Nature genetics 2000;24(2):163-6.
1999: Gaspar D A; Pavanello R C; Zatz M; Passos-Bueno M R; André M; Steman S; Wyszynski D F; Matiolli S R
Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in Brazil.
American journal of medical genetics 1999;87(2):197-9.
1999: Eggers S; Pavanello R C; Passos-Bueno M R; Zatz M
Genetic counseling for childless women at risk for Duchenne muscular dystrophy.
American journal of medical genetics 1999;86(5):447-53.
1999: Oliveira J R; Zatz M
The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 1999;32(4):463-7.
1999: Vainzof M; Passos-Bueno M R; Pavanello R C; Marie S K; Oliveira A S; Zatz M
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population.
Journal of the neurological sciences 1999;164(1):44-9.
1999: Vainzof M; Moreira E S; Ferraz G; Passos-Bueno M R; Marie S K; Zatz M
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex.
European journal of human genetics : EJHG 1999;7(2):251-4.
1999: Passos-Bueno M R; Vainzof M; Moreira E S; Zatz M
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
American journal of medical genetics 1999;82(5):392-8.
1999: Oliveira J R; Shimokomaki C M; Brito-Marques P R; Gallindo R M; Okuma M; Maia L G; Otto P A; Passos-Bueno M R; Zatz M
The association of the short variant of the 5-HTTPLR polymorphism and the apoE epsilon4 allele does not increase the risk for late onset Alzheimer's disease.
Molecular psychiatry 1999;4(1):19-20.
1998: Sumita D R; Vainzof M; Campiotto S; Cerqueira A M; Cánovas M; Otto P A; Passos-Bueno M R; Zatz M
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
American journal of medical genetics 1998;80(4):356-61.
1998: Moreira E S; Vainzof M; Marie S K; Nigro V; Zatz M; Passos-Bueno M R
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
Journal of medical genetics 1998;35(11):951-3.
1998: Oliveira J R; Gallindo R M; Maia L G; Brito-Marques P R; Otto P A; Passos-Bueno M R; Morais M A; Zatz M
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease.
Molecular psychiatry 1998;3(5):438-41.
1998: Zatz M; Sumita D; Campiotto S; Canovas M; Cerqueira A; Vainzof M; Passos-Bueno M R
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases.
American journal of medical genetics 1998;78(4):361-5.
1998: Passos-Bueno M R; Sertié A L; Richieri-Costa A; Alonso L G; Zatz M; Alonso N; Brunoni D; Ribeiro S F
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
American journal of medical genetics 1998;78(3):237-41.
1998: Iughetti P; Otto P A; Zatz M; Passos Bueno M R; Marie S K
Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) families.
American journal of medical genetics 1998;77(3):246-8.
1998: Zatz M; Marie S K; Cerqueira A; Vainzof M; Pavanello R C; Passos-Bueno M R
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.
American journal of medical genetics 1998;77(2):155-61.
1998: Mendes de Oliveira J R; Otto P A; Vallada H; Lauriano V; Elkis H; Lafer B; Vasquez L; Gentil V; Passos-Bueno M R; Zatz M
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophrenia.
American journal of medical genetics 1998;81(3):225-7.
1998: Vallada H P; Vasques L; Curtis D; Zatz M; Kirov G; Lauriano V; Gentil V; Murray R M; McGuffin P; Owen M; Gill M; Craddock N; Collier D A
Linkage analysis between bipolar affective disorder and markers on chromosome X.
Psychiatric genetics 1998;8(3):183-6.
1997: Zatz M; Cerqueira A; Vainzof M; Passos-Bueno M R
Segregation distortion of the CTG repeats at the myotonic dystrophy (DM) locus: new data from Brazilian DM families.
Journal of medical genetics 1997;34(9):790-1.
1997: Vainzof M; Costa C S; Marie S K; Moreira E S; Reed U; Passos-Bueno M R; Beggs A H; Zatz M
Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophy.
Neuropediatrics 1997;28(4):223-8.
1997: Nitrini R; Rosemberg S; Passos-Bueno M R; da Silva L S; Iughetti P; Papadopoulos M; Carrilho P M; Caramelli P; Albrecht S; Zatz M; LeBlanc A
Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
Annals of neurology 1997;42(2):138-46.
1997: Passos-Bueno M R; Sertié A L; Zatz M; Richieri-Costa A
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?
American journal of medical genetics 1997;71(2):243-5.
1997: Moreira E S; Vainzof M; Marie S K; Sertié A L; Zatz M; Passos-Bueno M R
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.
American journal of human genetics 1997;61(1):151-9.
1997: Oliveira J R; Lima Filho J L; Shimokomaki C M; Okuma M; Passos-Bueno M R; Zatz M; Brito-Marques P R
The use of apolipoprotein E genotype for preclinical detection of risk's group for Alzheimer's disease.
American journal of medical genetics 1997;74(2):216-7.
1997: Sitnik R; Campiotto S; Vainzof M; Pavanello R C; Takata R I; Zatz M; Passos-Bueno M R
Novel point mutations in the dystrophin gene.
Human mutation 1997;10(3):217-22.
1996: Vallada H; Craddock N; Vasques L; Curtis D; Kirov G; Lauriano V; Gentil V; Passos-Bueno R; Murray R M; Zatz M; McGuffin P; Powell J F; Gill M; Owen M; Collier D A
Linkage studies in bipolar affective disorder with markers on chromosome 21.
Journal of affective disorders 1996;41(3):217-21.
1996: Vainzof M; Passos-Bueno M R; Canovas M; Moreira E S; Pavanello R C; Marie S K; Anderson L V; Bonnemann C G; McNally E M; Nigro V; Kunkel L M; Zatz M
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics 1996;5(12):1963-9.
1996: Bönnemann C G; Passos-Bueno M R; McNally E M; Vainzof M; de Sá Moreira E; Marie S K; Pavanello R C; Noguchi S; Ozawa E; Zatz M; Kunkel L M
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
Human molecular genetics 1996;5(12):1953-61.
1996: McNally E M; Passos-Bueno M R; Bönnemann C G; Vainzof M; de Sá Moreira E; Lidov H G; Othmane K B; Denton P H; Vance J M; Zatz M; Kunkel L M
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
American journal of human genetics 1996;59(5):1040-7.
1996: Nigro V; de Sá Moreira E; Piluso G; Vainzof M; Belsito A; Politano L; Puca A A; Passos-Bueno M R; Zatz M
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
Nature genetics 1996;14(2):195-8.
1996: Sertié A L; Quimby M; Moreira E S; Murray J; Zatz M; Antonarakis S E; Passos-Bueno M R
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3.
Human molecular genetics 1996;5(6):843-7.
1996: Passos-Bueno M R; Moreira E S; Vainzof M; Marie S K; Zatz M
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.
Human molecular genetics 1996;5(6):815-20.
1996: Iughetti P; Zatz M; Bueno M R; Marie S K
Different origins of mutations at the Machado-Joseph locus (MJD1)
Journal of medical genetics 1996;33(5):439.
1996: Zatz M; Passos-Bueno M R; Cerqueira A; Vainzof M
CTG repeat length in muscle from patients affected with myotonic dystrophy (DM)
Journal of medical genetics 1996;33(2):173.
1996: Passos-Bueno M R; Moreira E S; Marie S K; Bashir R; Vasquez L; Love D R; Vainzof M; Iughetti P; Oliveira J R; Bakker E; Strachan T; Bushby K; Zatz M
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
Journal of medical genetics 1996;33(2):97-102.
1996: Reed U C; Marie S K; Vainzof M; Salum P B; Levy J A; Zatz M; Diament A
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency.
Brain & development 1996;18(1):53-8.
1995: Vainzof M; Marie S K; Reed U C; Schwartzman J S; Pavanello R C; Passos-Bueno M R; Zatz M
Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
Neuropediatrics 1995;26(6):293-7.
1995: Bueno M R; Moreira E S; Vainzof M; Chamberlain J; Marie S K; Pereira L; Akiyama J; Roberds S L; Campbell K P; Zatz M
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
Human molecular genetics 1995;4(7):1163-7.
1995: Vainzof M; Passos-Bueno M R; Pavanello R C; Zatz M
Is dystrophin always altered in Becker muscular dystrophy patients?
Journal of the neurological sciences 1995;131(1):99-104.
1995: Zatz M; Passos-Bueno M R; Cerqueira A; Marie S K; Vainzof M; Pavanello R C
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
Human molecular genetics 1995;4(3):401-6.
1995: Eggers S; Lauriano V; Melo M; Takata R I; Akiyama J; Passos-Bueno M R; Gentil V; Frota-Pessoa O; Zatz M
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
American journal of medical genetics 1995;60(1):27-32.
1995: Passos-Bueno M R; Cerqueira A; Vainzof M; Marie S K; Zatz M
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families.
Journal of medical genetics 1995;32(1):14-8.
1995: Zatz M; Marie S K; Passos-Bueno M R; Vainzof M; Campiotto S; Cerqueira A; Wijmenga C; Padberg G; Frants R
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.
American journal of human genetics 1995;56(1):99-105.
1994: Reed U C; Passos-Bueno M R; Nagahashi-Marie S K; Cerqueira A; Mendonça L I; Levy J A; Diament A; Zatz M
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]
Arquivos de neuro-psiquiatria 1994;52(4):545-8.
1994: Passos-Bueno M R; Marie S K; Monteiro M; Neustein I; Whittle M R; Vainzof M; Zatz M
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
American journal of medical genetics 1994;52(2):170-3.
1994: Passos-Bueno M R; Vainzof M; Marie S K; Zatz M
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy.
Human molecular genetics 1994;3(6):919-22.
1994: Zatz M; Matsumura K; Vainzof M; Passos-Bueno M R; Pavanello R C; Marie S K; Campbell K P
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.
Journal of the neurological sciences 1994;123(1-2):122-8.
1993: Passos-Bueno M R; Oliveira J R; Bakker E; Anderson R D; Marie S K; Vainzof M; Roberds S; Campbell K P; Zatz M
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.
Human molecular genetics 1993;2(11):1945-7.
1993: Vainzof M; Passos-Bueno M R; Takata R I; Pavanello R de C; Zatz M
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype.
Journal of the neurological sciences 1993;119(1):38-42.
1993: Eggers S; Passos-Bueno M R; Zatz M
Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness.
Journal of medical genetics 1993;30(7):589-92.
1993: Passos-Bueno M R; Byth B C; Rosenberg S; Takata R I; Bakker E; Beggs A H; Pavanello R C; Vainzof M; Davies K E; Zatz M
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
American journal of medical genetics 1993;46(2):172-5.
1993: Vainzof M; Nicholson L V; Bulman D E; Tsanaclis A M; Passos-Bueno M R; Pavanello R C; Zatz M
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers.
Neuromuscular disorders : NMD 1993;3(2):135-40.
1993: Passos-Bueno M R; Bakker E; Marie S K; Pavanello R C; Vainzof M; Carvalho A A; Cohen D; Beckmann J; Zatz M
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families.
Human molecular genetics 1993;2(2):201-2.
1993: Zatz M; Vallada H; Melo M S; Passos-Bueno M R; Vieira A H; Vainzof M; Gill M; Gentil V
Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?
Journal of medical genetics 1993;30(2):131-4.
1993: Vainzof M; Takata R I; Passos-Bueno M R; Pavanello R C; Zatz M
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
Human molecular genetics 1993;2(1):39-42.
1992: Passos-Bueno M R; Bakker E; Kneppers A L; Takata R I; Rapaport D; den Dunnen J T; Zatz M; van Ommen G J
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.
American journal of human genetics 1992;51(5):1150-5.
1992: Vainzof M; Passos-Bueno M R; Rapaport D; Pavanello R C; Zatz M; Bulman D E
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletion.
American journal of medical genetics 1992;44(3):382-4.
1992: Vainzof M; Passos-Bueno M R; Pavanello R C; Schreiber R; Zatz M
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.
Journal of medical genetics 1992;29(7):476-9.
1992: Rapaport D; Passos-Bueno M R; Takata R I; Campiotto S; Eggers S; Vainzof M; Makover A; Nudel U; Yaffe D; Zatz M
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation.
Neuromuscular disorders : NMD 1992;2(2):117-20.
1992: Zatz M; Pavanello R de C; Vainzof M; Passos-Bueno M R
Steroids in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1992;2(1):59.
1991: Rapaport D; Passos-Bueno M R; Brandão L; Love D; Vainzof M; Zatz M
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.
American journal of medical genetics 1991;39(4):437-41.
1991: Passos-Bueno M R; Vainzof M; Pavanello R de C; Pavanello-Filho I; Lima M A; Zatz M
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
Journal of the neurological sciences 1991;103(1):65-75.
1991: Zatz M; Rapaport D; Vainzof M; Passos-Bueno M R; Bortolini E R; Pavanello R de C; Peres C A
Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy.
Journal of the neurological sciences 1991;102(2):190-6.
1991: Passos-Bueno M R; Byth B; Love D; Terwilliger J; Ott J; Rapaport D; Vainzof M; Zatz M; Davies K E
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27.
Journal of the neurological sciences 1991;102(2):206-8.
1991: Vainzof M; Pavanello R C; Pavanello-Filho I; Rapaport D; Passos-Bueno M R; Zubrzycka-Gaarn E E; Bulman D E; Zatz M
Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.
American journal of medical genetics 1991;39(1):38-41.
1991: Rapaport D; Colletto G M; Vainzof M; Duaik M C; Zatz M
Short stature in Duchenne muscular dystrophy.
Growth regulation 1991;1(1):11-5.
1991: Vainzof M; Zubrzycka-Gaarn E E; Rapaport D; Passos-Bueno M R; Pavanello R C; Pavanello-Filho I; Zatz M
Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein.
Journal of the neurological sciences 1991;101(2):141-7.
1991: Passos-Bueno M R; Terwilliger J; Ott J; Vainzof M; Love D R; Davies K E; Zatz M
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
American journal of medical genetics 1991;38(1):140-6.
1991: Zatz M; Passos-Bueno M R; Rapaport D; Vainzof M
Familial occurrence of Duchenne dystrophy through paternal lines in four families.
American journal of medical genetics 1991;38(1):80-4.
1991: Rapaport D; Colletto G M; Vainzof M; Zatz M
Estimates of genetic and environmental components of serum isocitrate dehydrogenase (ICDH) in normal twins.
Acta geneticae medicae et gemellologiae 1991;40(1):77-82.
1991: Vainzof M; Pavanello R C; Pavanello I; Tsanaclis A M; Levy J A; Passos-Bueno M R; Rapaport D; Zatz M
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages.
Neuromuscular disorders : NMD 1991;1(3):177-83.
1990: Vainzof M; Pavanello R C; Pavanello Filho I; Passos-Bueno M R; Rapaport D; Hsi C T; Zatz M
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study.
Journal of the neurological sciences 1990;98(2-3):221-33.
1990: Passos-Bueno M R; Rapaport D; Love D; Flint T; Bortolini E R; Zatz M; Davies K E
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.
Journal of medical genetics 1990;27(3):145-50.
1989: Zatz M; Rapaport D; Pavanello R C; Rocha J M; Vainzof M; Nicolau W
Nocturnal rhythm of growth hormone in Duchenne patients: effect of different doses of mazindol and/or cyproheptadine.
American journal of medical genetics 1989;33(4):457-67.
1989: Zatz M; Passos-Bueno M R; Vainzof M; Pavanello R C
Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings.
American journal of medical genetics 1989;32(3):438-41.
1989: Zatz M; Passos-Bueno M R; Rapaport D
Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance.
American journal of medical genetics 1989;32(3):407-10.
1988: Zatz M; Rapaport D; Vainzof M; Pavanello R de C; Rocha J M; Betti R T; Otto P A
Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy.
American journal of medical genetics 1988;31(4):821-33.
1988: Rapaport D; Colletto G M; Zatz M
Genetic and environmental components of serum creatine kinase (CK) and pyruvate kinase (PK) in normal twins: implication for genetic risks estimates in Duchenne muscular dystrophy carriers.
American journal of medical genetics 1988;31(2):291-8.
1988: Zatz M; Rapaport D; Vainzof M; Rocha J M; Pavanello R de C; Colletto G M; Peres C A
Relation between height and clinical course in Duchenne muscular dystrophy.
American journal of medical genetics 1988;29(2):405-10.
1987: Zatz M; Vainzof M; Rapaport D; da Rocha J M; Pavanello R de C; Betti R T
Mazindol and growth hormone inhibition in Duchenne muscular dystrophy.
American journal of medical genetics 1987;27(4):993-5.

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