skip to main content
Idioma:
Mostrar Somente
Refinado por: idioma: Inglês remover EBSCOhost Academic Search Premier remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Molecular and Cytogenic Analyses on Brazilian Youths with Pervasive Developmental Disorders
Molecular and Cytogenic Analyses on Brazilian Youths with Pervasive Developmental Disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular and Cytogenic Analyses on Brazilian Youths with Pervasive Developmental Disorders

Estecio, Marcos Roberto Higino ; Fett-Conte, Agnes Cristina ; Varella-Garcia, Marileila ; Fridman, Cintia ; Silva, Ana Elizabete

Journal of autism and developmental disorders, 2002, Vol.32 (1), p.35 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
2
Molecular and cytogenetic analyses on brazilian youths with Pervasive Developmental Disorders
Molecular and cytogenetic analyses on brazilian youths with Pervasive Developmental Disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular and cytogenetic analyses on brazilian youths with Pervasive Developmental Disorders

HIGINO ESTECIO, Marcos Roberto ; FETT-CONTE, Agnes Cristina ; VARELLA-GARCIA, Marileila ; FRIDMAN, Cintia ; SILVA, Ana Elizabete

Journal of autism and developmental disorders, 2002-02, Vol.32 (1), p.35-41 [Periódico revisado por pares]

Heidelberg: Springer

Texto completo disponível

Citações Citado por
3
Association of a new polymorphism in ALOX12 gene with bipolar disorder
Association of a new polymorphism in ALOX12 gene with bipolar disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Association of a new polymorphism in ALOX12 gene with bipolar disorder

Fridman, Cintia ; Ojopi, Elida P B ; Gregório, Sheila P ; Ikenaga, Elisa H ; Moreno, Doris H ; Demetrio, Frederico N ; Guimarães, Pedro E M ; Vallada, Homero P ; Gattaz, Wagner F ; Dias Neto, Emmanuel

European archives of psychiatry and clinical neuroscience, 2003-02, Vol.253 (1), p.40-43 [Periódico revisado por pares]

Germany: Springer Nature B.V

Texto completo disponível

Citações Citado por
4
A new duplication in the mitochondrially encoded tRNA proline gene in a patient with dilated cardiomyopathy
A new duplication in the mitochondrially encoded tRNA proline gene in a patient with dilated cardiomyopathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

A new duplication in the mitochondrially encoded tRNA proline gene in a patient with dilated cardiomyopathy

Cardena, Mari Maki Siria Godoy ; Mansur, Alfredo José ; Pereira, Alexandre Da Costa ; Fridman, Cintia

Mitochondrial DNA, 2013-02, Vol.24 (1), p.46-49

England: Informa Healthcare

Texto completo disponível

Citações Citado por
5
Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals. e62005
Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals. e62005
Material Type:
Artigo 		Adicionar ao Meu Espaço

Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals. e62005

Cardena, M SG ; Ribeiro-dos-Santos, Andrea ; Santos, Sidney ; Mansur, Alfredo J ; Pereira, Alexandre C ; Fridman, Cintia

PloS one, 2013-04, Vol.8 (4) [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
6
Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals
Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals
Material Type:
Artigo 		Adicionar ao Meu Espaço

Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals

Cardena, Mari M S G ; Ribeiro-Dos-Santos, Andrea ; Santos, Sidney ; Mansur, Alfredo J ; Pereira, Alexandre C ; Fridman, Cintia Samuels, David C.

PloS one, 2013-04, Vol.8 (4), p.e62005-e62005 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
7
MYH9 and APOL1 Gene Polymorphisms and the Risk of CKD in Patients with Lupus Nephritis from an Admixture Population: e87716
MYH9 and APOL1 Gene Polymorphisms and the Risk of CKD in Patients with Lupus Nephritis from an Admixture Population: e87716
Material Type:
Artigo 		Adicionar ao Meu Espaço

MYH9 and APOL1 Gene Polymorphisms and the Risk of CKD in Patients with Lupus Nephritis from an Admixture Population: e87716

Colares, Vinicius Sardao ; Titan, Maria deOliveira ; Pereira, Alexandre daCosta ; Malafronte, Patricia ; Cardena, Mari M ; Santos, Sidney ; Santos, Paulo C ; Fridman, Cintia ; Barros, Rui Toledo ; Woronik, Viktoria

PloS one, 2014-03, Vol.9 (3) [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
8
MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population
MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population
Material Type:
Artigo 		Adicionar ao Meu Espaço

MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population

Colares, Vinícius Sardão ; Titan, Silvia Maria de Oliveira ; Pereira, Alexandre da Costa ; Malafronte, Patrícia ; Cardena, Mari M ; Santos, Sidney ; Santos, Paulo C ; Fridman, Cíntia ; Barros, Rui Toledo ; Woronik, Viktória Assassi, Shervin

PloS one, 2014-03, Vol.9 (3), p.e87716-e87716 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (7)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.