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Cintia Fridman

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Disorders

Anatomy

Chromosomes, Human, Pair 15

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Mari Maki Siria Godoy Cardena; Alfredo José Mansur; Alexandre Da Costa Pereira; Cintia Fridman
A new duplication in the mitochondrially encoded tRNA proline gene in a patient with dilated cardiomyopathy.
Mari M S G Cardena; Alfredo José Mansur; Alexandre C Pereira; Andrea Ribeiro-Dos-Santos; Sidney Santos; Cintia Fridman
Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals.
Camila B Piantino; Juliana M Sousa-Canavez; Marta Bellodi-Privato; Miguel Srougi; Luiz Heraldo Camara-Lopes; Gilka Jorge Figaro Gattás; Fernanda de Toledo Gonçalves; Cintia Fridman; KR Leite
Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3.

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All Publications

2013: Mari Maki Siria Godoy Cardena; Alfredo José Mansur; Alexandre Da Costa Pereira; Cintia Fridman
A new duplication in the mitochondrially encoded tRNA proline gene in a patient with dilated cardiomyopathy.
Mitochondrial DNA 2013;24(1):46-9.
2013: Mari M S G Cardena; Alfredo José Mansur; Alexandre C Pereira; Andrea Ribeiro-Dos-Santos; Sidney Santos; Cintia Fridman
Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals.
PloS one 2013;8(4):e62005.
2010: Camila B Piantino; Juliana M Sousa-Canavez; Marta Bellodi-Privato; Miguel Srougi; Luiz Heraldo Camara-Lopes; Gilka Jorge Figaro Gattás; Fernanda de Toledo Gonçalves; Cintia Fridman; KR Leite
Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3.
In vitro cellular & developmental biology. Animal 2010;46(2):123-30.
2010: Camila B Piantino; Juliana M Sousa-Canavez; Victor Srougi; Fernanda Salvadori; Raphael Kato; Pedro Paulo R Ayres; Miguel Srougi; Luiz Heraldo Camara-Lopes; Gilka Jorge Figaro Gattás; Cintia Fridman; Fernanda de Toledo; Isaque Santana; KR Leite
Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4.
In vitro cellular & developmental biology. Animal 2010;46(2):131-9.
2009: P E M Guimarães; Cintia Fridman; Sheila P Gregório; E M Kalil; A F Cristante; W G J Teixeira; C J Rodrigues; M C R Costa; Wagner F Gattaz; T E P Barros; P S L Oliveira; Emmanuel Dias-Neto
DNA polymorphisms as tools for spinal cord injury research.
Spinal cord 2009;47(2):171-5.
2006: Kette D Valente; Alessandra Freitas; Cintia Fridman; Mônica Varela; Ana Elizabete Silva; Agnes C Fett; Célia P Koiffmann
Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2006;117(4):803-9.
2006: Kette D Valente; Célia P Koiffmann; Cintia Fridman; Mônica Varella; Fernando Kok; Joaquina Q Andrade; Rosi M Grossmann; Maria Joaquina Marques-Dias
Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.
Archives of neurology 2006;63(1):122-8.
2005: Kette D Valente; Cintia Fridman; Monica C Varela; Célia P Koiffmann; Joaquina Q Andrade; Rosi M Grossmann; Fernando Kok; Maria Joaquina Marques-Dias
Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patterns.
Epilepsy research 2005;67(3):163-8.
2003: Kette D Valente; Joaquina Q Andrade; Rosi M Grossmann; Fernando Kok; Cintia Fridman; Célia P Koiffmann; Maria Joaquina Marques-Dias
Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations.
Epilepsia 2003;44(8):1051-63.
2003: Cintia Fridman; N Hosomi; Monica C Varela; A H Souza; K Fukai; Célia P Koiffmann
Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene.
American journal of medical genetics. Part A 2003;119A(2):180-3.
2002: MarcosRobertoHigino Estécio; Agnes Cristina Fett-Conte; Marileila Varella-Garcia; Cintia Fridman; Ana Elizabete Silva
Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.
Journal of autism and developmental disorders 2002;32(1):35-41.
2000: Cintia Fridman; Célia P Koiffmann
Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.
American journal of medical genetics 2000;94(3):249-53.
2000: Cintia Fridman; Monica C Varela; Fernando Kok; Aron Diament; Célia P Koiffmann
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients.
American journal of medical genetics 2000;92(5):322-7.
2000: Cintia Fridman; Monica C Varela; Fernando Kok; N Setian; Célia P Koiffmann
Prader-Willi syndrome: genetic tests and clinical findings.
Genetic testing 2000;4(4):387-92.
2000: Cintia Fridman; M Santos; I Ferrari; Célia P Koiffmann
A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction.
Clinical genetics 2000;57(1):86-7.
1999: J Salomão Schwartzman; M Zatz; L dos Reis Vasquez; R Ribeiro Gomes; Célia P Koiffmann; Cintia Fridman; P Guimarães Otto
Rett syndrome in a boy with a 47,XXY karyotype.
American journal of human genetics 1999;64(6):1781-5.
1998: Cintia Fridman; Monica C Varela; R D Nicholls; Célia P Koiffmann
Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15q.
Clinical genetics 1998;54(4):303-8.
1997: Cintia Fridman; Fernando Kok; Aron Diament; Célia P Koiffmann
[Angelman syndrome: a frequently undiagnosed cause of mental retardation and epilepsy. Case report].
Arquivos de neuro-psiquiatria 1997;55(2):329-33.