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1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
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1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis

Murch, Oliver ; Jezkova, Jana ; Halstead, Joseph ; Burke, Katherine ; Oruganti, Siva ; Calvert, Jennifer ; Evans, Jennifer ; Williams, Hywel ; Sansbury, Francis ; Corrin, Sian ; Sloper, Emily

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A256-A256 [Periódico revisado por pares]

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

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2
101 Inherited autoinflammatory encephalopathy in the differential diagnosis of conatal viral infections- newborn with Aicardi-Goutières syndrome
101 Inherited autoinflammatory encephalopathy in the differential diagnosis of conatal viral infections- newborn with Aicardi-Goutières syndrome
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101 Inherited autoinflammatory encephalopathy in the differential diagnosis of conatal viral infections- newborn with Aicardi-Goutières syndrome

Bulić, Dora ; Škorić, Tea ; Žigman, Tamara ; Krnjak, Goran ; Tešović, Goran ; Barišić, Nina ; Barić, Ivo ; Ramadža, Danijela Petković

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A43-A43 [Periódico revisado por pares]

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

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3
1435 Rapid exome sequencing in acutely unwell children – providing new diagnostic options in intensive care settings
1435 Rapid exome sequencing in acutely unwell children – providing new diagnostic options in intensive care settings
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1435 Rapid exome sequencing in acutely unwell children – providing new diagnostic options in intensive care settings

McDermott, Helen ; Baple, Emma ; Ellard, Sian ; Naik, Swati

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A368-A369 [Periódico revisado por pares]

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

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4
442 The influence of HMGB1 gene (RS41369348) polymorphism on the susceptibility and clinical features of patients with IgAV
442 The influence of HMGB1 gene (RS41369348) polymorphism on the susceptibility and clinical features of patients with IgAV
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442 The influence of HMGB1 gene (RS41369348) polymorphism on the susceptibility and clinical features of patients with IgAV

Varga, Mateja Batnozic ; Sestan, Mario ; Wagner, Jasenka ; Crkvenac, Kristina ; Kifer, Nastasia ; Frkovic, Marijan ; Stefinovec, Laura ; Grguric, Danica ; Puseljic, Silvija ; Jelusic, Marija

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A185-A185 [Periódico revisado por pares]

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

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5
423 Genetic predictors of a new form of bronchopulmonary dysplasia
423 Genetic predictors of a new form of bronchopulmonary dysplasia
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423 Genetic predictors of a new form of bronchopulmonary dysplasia

Bondar, VA ; Davydova, IV ; Basargina, MA ; Savostyanov, KV ; Pushkov, AA ; Zhanin, IS ; Nikitin, AG

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A176-A177 [Periódico revisado por pares]

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

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6
1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service
1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service
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1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service

Lerou, Dimitra-Ilektra ; Meng Yin Chen, Jasmine ; Redman, Melody ; Lam, Zena ; Hartill, Verity ; Campbell, Jennifer

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A343-A344 [Periódico revisado por pares]

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

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7
287 Frequency of factor ii, factor v leiden and mthfr mutations in children with cancer
287 Frequency of factor ii, factor v leiden and mthfr mutations in children with cancer
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287 Frequency of factor ii, factor v leiden and mthfr mutations in children with cancer

Roganovic, Jelena Roganovic ; Djordjevic, Ana ; Grahovac, Blazenka ; Zulle, Lidija Bilic ; Roganovic, Jelena

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A121-A122 [Periódico revisado por pares]

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

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8
726 A state of the art: using 3D models to allow better planning of complex vascular surgeries and enhancing safety in children
726 A state of the art: using 3D models to allow better planning of complex vascular surgeries and enhancing safety in children
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726 A state of the art: using 3D models to allow better planning of complex vascular surgeries and enhancing safety in children

Assia-Zamora, Sergio ; Kessaris, Nicos ; Smith, Luke ; Minhas, Kishora ; Forman, Colin ; Stojanovic, Jelena

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A95-A96 [Periódico revisado por pares]

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

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9
1735 Experience of childhood stroke management in a tertiary paediatric neurology unit
1735 Experience of childhood stroke management in a tertiary paediatric neurology unit
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1735 Experience of childhood stroke management in a tertiary paediatric neurology unit

Sheikh, Hajera ; Silwal, Arpana ; Hartley, Louise ; Yoong, Michael Yoong ; Awadalla, Maha

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A471-A471 [Periódico revisado por pares]

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

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10
705 Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic literature review
705 Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic literature review
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705 Calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene mutations: a systematic literature review

Malakasioti, Georgia ; Iancu, Daniela ; Tullus, Kjell

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A89-A89 [Periódico revisado por pares]

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

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