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Unraveling the expression of the oncogene YAP1, a Wnt/beta-catenin target, in adrenocortical tumors and its association with poor outcome in pediatric patients
Unraveling the expression of the oncogene YAP1, a Wnt/beta-catenin target, in adrenocortical tumors and its association with poor outcome in pediatric patients
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Unraveling the expression of the oncogene YAP1, a Wnt/beta-catenin target, in adrenocortical tumors and its association with poor outcome in pediatric patients

Abduch, Rafael H ; Carolina Bueno, Ana ; Leal, Leticia F ; Cavalcanti, Marcelo M ; Gomes, Débora C ; Brandalise, Silvia R ; Masterallo, Maria J ; Yunes, José A ; Martinelli, Jr, Carlos E ; Tone, Luiz G ; Tucci, Silvio ; Molina, Carlos A F ; Ramalho, Fernando S ; Moreira, Ayrton C ; Cardinalli, Izilda A ; Scrideli, Carlos A ; Ramalho, Leandra N Z ; de Castro, Margaret ; Antonini, Sonir R

Oncotarget, 2016-12, Vol.7 (51), p.84634-84644

United States: Impact Journals LLC

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2
Enterocytozoon bieneusi (microsporidia) in clinical samples from immunocompetent individuals in Tenerife, Canary Islands, Spain
Enterocytozoon bieneusi (microsporidia) in clinical samples from immunocompetent individuals in Tenerife, Canary Islands, Spain
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Enterocytozoon bieneusi (microsporidia) in clinical samples from immunocompetent individuals in Tenerife, Canary Islands, Spain

Abreu-Acosta, Néstor ; Lorenzo-Morales, Jacob ; Leal-Guio, Yaiza ; Coronado-Álvarez, Nieves ; Foronda, Pilar ; Alcoba-Florez, Julia ; Izquierdo, Fernando ; Batista-Díaz, Ninive ; Águila, Carmen Del ; Valladares, Basilio

Transactions of the Royal Society of Tropical Medicine and Hygiene, 2005-11, Vol.99 (11), p.848-855 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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3
A psychopathological study of a group of schizophrenic patients after attempting suicide. Are there two different clinical subtypes?
A psychopathological study of a group of schizophrenic patients after attempting suicide. Are there two different clinical subtypes?
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A psychopathological study of a group of schizophrenic patients after attempting suicide. Are there two different clinical subtypes?

Aguilar, E.J. ; Leal, C. ; Acosta, F.J. ; Cejas, M.R. ; Fernández, L. ; Gracia, R.

European psychiatry, 2003-06, Vol.18 (4), p.190-192 [Periódico revisado por pares]

Paris: Elsevier SAS

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4
Menstrual and hormonal alterations in juvenile dermatomyositis
Menstrual and hormonal alterations in juvenile dermatomyositis
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Menstrual and hormonal alterations in juvenile dermatomyositis

AIKAWA, N. E ; SALLUM, A. M. E ; LEAL, M. M ; BONFA, E ; PEREIRA, R. M. R ; SILVA, C. A. A

Clinical and experimental rheumatology, 2010-07, Vol.28 (4), p.571-575 [Periódico revisado por pares]

Pisa: Clinical and Experimental Rheumatology

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5
Thoracic endovascular aortic repair - a Brazilian experience in 255 patients over a period of 112 months
Thoracic endovascular aortic repair - a Brazilian experience in 255 patients over a period of 112 months
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Thoracic endovascular aortic repair - a Brazilian experience in 255 patients over a period of 112 months

Almeida, Rui M.S ; Leal, Joao C ; Saadi, Eduardo K ; Braile, Domingo M ; Rocha, Antonio S.T ; Volpiani, Giuliano ; Centola, Crescencio ; Zago, Alcides

Interactive cardiovascular and thoracic surgery, 2009-05, Vol.8 (5), p.524-528 [Periódico revisado por pares]

England: Eur Assoc Cardio Surg

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6
Relations between delayed diagnosis and forms of onset in Duchenne muscular dystrophy
Relations between delayed diagnosis and forms of onset in Duchenne muscular dystrophy
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Relations between delayed diagnosis and forms of onset in Duchenne muscular dystrophy

Alvarez Leal, M ; Morales Aguilera, A ; Pérez Zuno, J A ; Segura Romero, S ; Quiroz Góngora, M C ; Paredes García, A

Gaceta médica de México, 1994-11, Vol.130 (6), p.459-464 [Periódico revisado por pares]

Mexico

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7
The BRAzil MAGnesium (BRAMAG) trial: a randomized clinical trial of oral magnesium supplementation in pregnancy for the prevention of preterm birth and perinatal and maternal morbidity
The BRAzil MAGnesium (BRAMAG) trial: a randomized clinical trial of oral magnesium supplementation in pregnancy for the prevention of preterm birth and perinatal and maternal morbidity
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The BRAzil MAGnesium (BRAMAG) trial: a randomized clinical trial of oral magnesium supplementation in pregnancy for the prevention of preterm birth and perinatal and maternal morbidity

Alves, Joao Guilherme B ; de Araújo, Carla Adriane Fonseca Leal ; Pontes, Isabelle E A ; Guimarães, Angélica C ; Ray, Joel G

BMC pregnancy and childbirth, 2014-07, Vol.14 (1), p.222-222, Article 222 [Periódico revisado por pares]

England: BioMed Central

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8
Contrast echocardiography during cardiac catheterization in patients with congenital heart diseases
Contrast echocardiography during cardiac catheterization in patients with congenital heart diseases
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Contrast echocardiography during cardiac catheterization in patients with congenital heart diseases

Andrade, Jose L. ; Leal, Samira M. Borges ; Filho, Orlando Campos ; Carvalho, Antonio C. ; Tebexreni, Antonio S. ; Lima, Valter C.

Catheterization and cardiovascular diagnosis, 1993-06, Vol.29 (2), p.117-121

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
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Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability

Ansar, Muhammad ; Jan, Abid ; Santos-Cortez, Regie Lyn P ; Wang, Xin ; Suliman, Muhammad ; Acharya, Anushree ; Habib, Rabia ; Abbe, Izoduwa ; Ali, Ghazanfar ; Lee, Kwanghyuk ; Smith, Joshua D ; Nickerson, Deborah A ; Shendure, Jay ; Bamshad, Michael J ; Ahmad, Wasim ; Leal, Suzanne M

European journal of human genetics : EJHG, 2016-08, Vol.24 (8), p.1223-1227 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Mutation of ATF6 causes autosomal recessive achromatopsia
Mutation of ATF6 causes autosomal recessive achromatopsia
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Mutation of ATF6 causes autosomal recessive achromatopsia

Ansar, Muhammad ; Santos-Cortez, Regie Lyn P. ; Saqib, Muhammad Arif Nadeem ; Zulfiqar, Fareeha ; Lee, Kwanghyuk ; Ashraf, Naeem Mahmood ; Ullah, Ehsan ; Wang, Xin ; Sajid, Sundus ; Khan, Falak Sher ; Amin-ud-Din, Muhammad ; Smith, Joshua D. ; Shendure, Jay ; Bamshad, Michael J. ; Nickerson, Deborah A. ; Hameed, Abdul ; Riazuddin, Saima ; Ahmed, Zubair M. ; Ahmad, Wasim ; Leal, Suzanne M.

Human genetics, 2015-09, Vol.134 (9), p.941-950 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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Deste Autor:

  1. Leite, A
  2. Leal, C
  3. Universidade Estadual De Campinas
  4. Oliveira, F
  5. Oliveira, C

Neste Assunto:

  1. Adolescent
  2. Adolescent
  3. Humans
  4. Female
  5. Science & Technology

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

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