Browsing by Author Zatz, Mayana

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 14 to 18 of 18 < previous 
Issue DateTitleAuthor(s)
1-Jan-2010Ringo: Discordance between the molecular and clinical manifestation in a Golden Retriever Muscular Dystrophy dogZucconi, Eder; Valadares, Marcos Costa; Vieira, Natassia M.; Bueno, Carlos R.; Secco, Mariane; Jazedje, Tatiana; Almeida da Silva, Helga Cristina [UNIFESP]; Vainzof, Mariz; Zatz, Mayana; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Oct-2002Rod distribution and muscle fibers type modification in the progression of nemaline myopathyGurgel-Giannetti, Juliana; Zanoteli, Edmar [UNIFESP]; Werneck, Lineu Cesar; Reed, Umbertina Conti; Beggs, Alan H.; Marie, Sueli Kazue Nagahashi; Fireman, Moacir Antonio Tenorio [UNIFESP]; Oliveira, Acary Souza Bulle [UNIFESP]; Zatz, Mayana; Vainzof, Mariz; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP); Div Neurol; Harvard Univ
9-Oct-2002Telethonin protein expression in neuromuscular disordersVainzof, Mariz; Moreira, Eloisa de Sá; Suzuki, Oscar Takeo; Faulkner, Georgine; Valle, Georgio; Beggs, Alan H.; Carpen, Olli; Ribeiro, Alberto F.; Zanoteli, Edmar [UNIFESP]; Gurgel-Gianneti, Juliana; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da [UNIFESP]; Passos-Bueno, Maria Rita; Zatz, Mayana; Universidade de São Paulo (USP); Int Ctr Genet Engn & Biotechnol; Univ Padua; Harvard Univ; Univ Helsinki; Universidade Federal de São Paulo (UNIFESP)
1-Feb-2012Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotypeGurgel-Giannetti, Juliana; Senkevics, Adriano S.; Zilbersztajn-Gotlieb, Dinorah; Yamamoto, Lydia Uraco; Muniz, Viviane Palhares; Pavanello, Rita C. M.; Oliveira, Acary Souza Bulle [UNIFESP]; Zatz, Mayana; Vainzof, Mariz; Universidade de São Paulo (USP); Universidade Federal de Minas Gerais (UFMG); Universidade Federal de São Paulo (UNIFESP)
14-Apr-2009Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriersArashiro, Patricia; Eisenberg, Iris; Kho, Alvin T.; Cerqueira, Antonia M. P.; Canovas, Marta; Silva, Helga Cristina Almeida da [UNIFESP]; Pavanello, Rita C. M.; Verjovski-Almeida, Sergio; Kunkel, Louis M.; Zatz, Mayana; Universidade de São Paulo (USP); Howard Hughes Med Inst; Harvard Univ; Universidade Federal de São Paulo (UNIFESP)