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1
GP109 Documentation of neurological examination when determining eligibility for therapeutic hypothermia
GP109 Documentation of neurological examination when determining eligibility for therapeutic hypothermia
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GP109 Documentation of neurological examination when determining eligibility for therapeutic hypothermia

Foley, DJ ; Filan, PM ; Walsh, BH

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A74 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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2
Cardiovascular autonomic tone in rats with heart failure treated with allogeneic mesenchymal stem cells
Cardiovascular autonomic tone in rats with heart failure treated with allogeneic mesenchymal stem cells
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Cardiovascular autonomic tone in rats with heart failure treated with allogeneic mesenchymal stem cells

Sharon D. B. V. Morais Renata Maria Lataro; Carlos Alberto Aguiar Silva; Lindolfo S Meirelles; Rubens Fazan Júnior; Hélio César Salgado; Annual Meeting at Experimental Biology (2016 San Diego)

Abstracts San Diego, 2016

San Diego 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2808029 Estantes Deslizantes )(Acessar)

3
GP69 Cerebral vascular accident association post primary varicella infection
GP69 Cerebral vascular accident association post primary varicella infection
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GP69 Cerebral vascular accident association post primary varicella infection

Elbishari, Zaineb ; Barrett, Michael

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A57 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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4
Decreased expression of BATF2 is significantly associatedwith poor prognosis in childhood medulloblastoma
Decreased expression of BATF2 is significantly associatedwith poor prognosis in childhood medulloblastoma
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Decreased expression of BATF2 is significantly associatedwith poor prognosis in childhood medulloblastoma

A. F. Andrade K. S Borges; V. K Suazo; E. J. R Vasconcelos; C. A. P Corrêa; K. B Salomão; L Geron; Carlos Alberto Scrideli; Luiz Gonzaga Tone; Annual Congress of the International Society of Paediatric Oncology (48. 2016 Dublin)

Abstracts Dublin, 2016

Dublin 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2829561 Estantes Deslizantes )(Acessar)

5
Modulation of the CTNNB1(B-CATENIN) by the aurora kinases inhibitor AMG900 in paediatric medulloblastoma cell lines
Modulation of the CTNNB1(B-CATENIN) by the aurora kinases inhibitor AMG900 in paediatric medulloblastoma cell lines
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Modulation of the CTNNB1(B-CATENIN) by the aurora kinases inhibitor AMG900 in paediatric medulloblastoma cell lines

L. Geron K. B Salomão; A. F Andrade; K. S Borges; Carlos Alberto Scrideli; Luiz Gonzaga Tone; Annual Congress of the International Society of Paediatric Oncology (48. 2016 Dublin)

Abstracts Dublin, 2016

Dublin 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2829565 Estantes Deslizantes )(Acessar)

6
P101 Intractable seizures in a neonate-case report
P101 Intractable seizures in a neonate-case report
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P101 Intractable seizures in a neonate-case report

Mallappa, Anupama ; Bali, Sanjeev

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A196 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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7
GP111 Incident reporting and the non-consultant hospital doctor in a general hospital
GP111 Incident reporting and the non-consultant hospital doctor in a general hospital
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GP111 Incident reporting and the non-consultant hospital doctor in a general hospital

Canty, Niofa ; Elbadry, M ; Reidy, B ; Stokes, H ; O’Neill, Michael B

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A75 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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8
P496 X- linked infantile spinal muscular atrophy (smax2) caused by novel c.1681g>a substitution in the uba1 gene, expanding the phenotype
P496 X- linked infantile spinal muscular atrophy (smax2) caused by novel c.1681g>a substitution in the uba1 gene, expanding the phenotype
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P496 X- linked infantile spinal muscular atrophy (smax2) caused by novel c.1681g>a substitution in the uba1 gene, expanding the phenotype

Shaughnessy, Niamh ; Forman, Eva B ; Rourke, Declan O’ ; Lynch, Sally Ann ; Bryan, Lynch

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A351 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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9
GP237 The use of massage therapy for treatment of neonatal hyperbilirubinemia: a systematic review and network meta-analysis
GP237 The use of massage therapy for treatment of neonatal hyperbilirubinemia: a systematic review and network meta-analysis
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GP237 The use of massage therapy for treatment of neonatal hyperbilirubinemia: a systematic review and network meta-analysis

Abdelrahman, Mohammed ; Vuong, Nguyen Lam ; Tawfik, Gehad ; Nguyen, Do Phuc Nhu ; Thanh, Le Van ; Elfaituri, Muhammed ; Mansour, Marwa ; Thoa Le, TB ; Zaki, Marwa ; Hirayama, Kenji ; Huy, Nguyen Tien

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A127 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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10
333 Age-related disorders in children
333 Age-related disorders in children
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333 Age-related disorders in children

Harutyunyan, Eline ; Aghajanyan, A ; Shahumyan, L ; Asatryan, A ; Shahumyan, H ; Khachatryan, S ; Atoyan, I ; Sahakyan, A ; Manukyan, G ; Esoyan, K ; Mirabyan, S ; Grigoryan, M ; Baveyan, B ; Asoyan, V ; Apresyan, H

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A140-A140 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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