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Refinado por: autor: Zeni, C remover
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1
LPHN3 and attention-deficit/hyperactivity disorder a susceptibility and pharmacogenetic study
LPHN3 and attention-deficit/hyperactivity disorder a susceptibility and pharmacogenetic study
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LPHN3 and attention-deficit/hyperactivity disorder a susceptibility and pharmacogenetic study

E. M. Bruxel A Salatino-Oliveira; G. C Akutagava-Martins; L Tovo-Rodrigues; J. P Genro; C. P Zeni; G. V Polanczyk; R Chazan; M Schmitz; M Arcos-Burgos; L. A Rohde; M. H Hutz

Genes, Brain and Behavior Oxford v. 14, n. 5, p. 419-427, 2015

Oxford 2015

Localização: FM - Fac. Medicina    (BCSEP 331 2015 )(Acessar)

2
Lack of association between the GRM7 gene and attention deficit hyperactivity disorder
Lack of association between the GRM7 gene and attention deficit hyperactivity disorder
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Lack of association between the GRM7 gene and attention deficit hyperactivity disorder

Glaucia Chiyoko Akutagava-Martins Angélica Salatino-Oliveira; Estela M Bruxel; Julia P Genro; Nina R Mota; Guilherme V Polanczyk; Christian P Zeni; Eugênio H Grevet; Claiton H. D Bau; Luis A Rohde; Mara H Hutz

Psychiatrics Genetics London v. 24, p. 281-282, 2014

London 2014

Localização: FM - Fac. Medicina    (BCSEP 548 2014 )(Acessar)

3
Attention-based classification pattern, a research domain criteria framework, in youths with bipolar disorder and attention-deficit/hyperactivity disorder
Attention-based classification pattern, a research domain criteria framework, in youths with bipolar disorder and attention-deficit/hyperactivity disorder
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Attention-based classification pattern, a research domain criteria framework, in youths with bipolar disorder and attention-deficit/hyperactivity disorder

Ana Kleinman Sheila Cavalcante Caetano; Helena Brentani; Cristiana C. de Almeida Rocca; Bernardo dos Santos; Enio Roberto Andrade; Cristian Patrick Zeni; Silzá Tramontina; Luis Augusto P Rohde; Beny Lafer

The Australian and New Zealand journal of psychiatry Carlton South/Austrália v. 49, n. 3, p. 255-265, 2015

Carlton South 2015

Localização: FM - Fac. Medicina    (BCSEP 073 2015 )(Acessar)

4
Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder
Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder
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Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder

Angélica Salatino-Oliveira Julia P Genro; Cristian Zeni; Guilherme V Polanczyk; Rodrigo Chazan; Ana P Guimarães; Sidia M Callegari-Jacques; Luis A Rohde; Mara H Hutz

Biological Psychiatry Philadelphia v. 70, n. 3, p. 216-221, 2011

Philadelphia 2011

Localização: FM - Fac. Medicina    (BCSEP 077 2011 )(Acessar)

5
Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder
Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder
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Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder

Angélica Salatino-Oliveira Julia Pasqualini Genro; Guilherme Polanczyk; Cristian Zeni; Marcelo Schmitz; Christian Kieling; Luciana Anselmi; Ana Maria Baptista Menezes; Fernando C. de Barros; Evelise Regina Polina; Nina R Mota; Eugênio Horácio Grevet; Claiton Henrique Dotto Bau; Luis Augusto Rohde; Mara Helena Hutz

American Journal of Medical Genetics Part B - neuropsychiatric genetics Hoboken VOL. 168B, n. 3, p. 162-169, 2015

Hoboken 2015

Localização: FM - Fac. Medicina    (BCSEP 201 2015 )(Acessar)

6
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children
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NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children

Angélica Salatino-Oliveira Glaucia C Akutagava-Martins; Estela M Bruxel; Julia P Genro; Guilherme V Polanczyk; Cristian Zeni; Christian Kieling; Rafael G Karam; Diego Luiz Rovaris; Verônica Contini; Renata B Cupertino; Nina R Mota; Eugenio H Grevet; Claiton H Bau; Luis A Rohde; Mara H Hutz

Journal of Psychiatric Research Oxford v. 75, p. 75-81, 2016

Oxford 2016

Localização: FM - Fac. Medicina    (BCSEP 141 2016 )(Acessar)

7
Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder
Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder
Material Type:
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Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder

Glaucia Chiyoko Akutagava-Martins Angelica Salatino-Oliveira; Julia P Genro; Verônica Contini; Guilherme Polanczyk; Cristian Zeni; Rodrigo Chazan; Christian Kieling; Luciana Anselmi; Ana M. B Menezes; Eugênio H Grevet; Claiton H. D Bau; Luis A Rohde; Mara H Hutz

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Hoboken v. 165B, n. 6, p. 502-509, 2014

Hoboken 2014

Localização: FM - Fac. Medicina    (BCSEP 426 2014 )(Acessar)

8
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD

Angélica Salatino-Oliveira Julia P Genro; Ana P Guimarães; Rodrigo Chazan; Cristian Zeni; Marcelo Schmitz; Guilherme Polanczyk; Tatiana Roman; Luis A Rohde; Mara H Hutz

Journal of Neural Transmission Wien v. 119, n. 6, p. 729-733, 2012

Wien 2012

Acesso online. A biblioteca também possui exemplares impressos.

9
CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD) further evidence linking sleep and circadian disturbances and ADHD
CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD) further evidence linking sleep and circadian disturbances and ADHD
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CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD) further evidence linking sleep and circadian disturbances and ADHD

Marina Xavier Carpena Mara H Hutz; Angelica Salatino-Oliveira; Guilherme V Polanczyk; Cristian Zeni; Marcelo Schmitz; Rodrigo Chazan; Julia P Genro; Luis Augusto Rohde; Luciana Tovo-Rodrigues

Genes v. 10, n. 2, article ID 88, 13p, 2019

Basel 2019

Acesso online. A biblioteca também possui exemplares impressos.

10
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD

Angélica Salatino-Oliveira Julia P Genro; Ana P Guimarães; Rodrigo Chazan; Cristian Zeni; Marcelo Schmitz; Guilherme Polanczyk; Tatiana Roman; Luis A Rohde; Mara H Hutz

Journal of Neural Transmission Wien v. 119, n. 6, p. 729-733, 2012

Wien 2012

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Zeni, C
  2. Rohde, L
  3. Salatino-Oliveira, A
  4. Hutz, M
  5. Polanczyk, G

Neste Assunto:

  1. Hiperatividade
  2. Crianças
  3. Polimorfismo
  4. Adolescentes
  5. Sinais E Sintomas

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

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