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  1. 32301
    “…INTRODUCTION: This is the case of a girl, aged 13, starting on 2021 with a first psychotic episode. …”
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    Early-onset schizophrenia: an adolescent case report
  2. 32302
    por Unzue, L., Royo, J., Llovera, L., Corrales, A.
    Publicado 2023
    “…INTRODUCTION: This is a case aboout a 12-year-old girl, lives with her mother, father and younger brother. …”
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    ¿What do we know about Very Early Onset Schizophrenia? - A case report
  3. 32303
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    A Medical Research Council phase II trial of alternating chemotherapy and radiotherapy in small-cell lung cancer. The Medical Research Council Lung Cancer Working Party.
  4. 32304
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    Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
  5. 32305
    “…I spend most of the time thinking, crying and struggling within myself asking God why He really had to do such a thing and saying to myself that: "God, help me overcome these problems!" Girl, 15.…”
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    "They don't care what happens to us." The situation of double orphans heading households in Rakai District, Uganda
  6. 32306
    “…Owing to the widely known inverse relationship between maternal education and infant mortality, there is need for concerted efforts to promote girl child education. Owing to the important role played by the short preceding birth interval to the upsurge in infant mortality, there is need to promote family planning methods in Kenya.…”
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    In search for an explanation to the upsurge in infant mortality in Kenya during the 1988–2003 period
  7. 32307
    “…Additionally, we applied direct Sanger sequencing for all exons and exon/intron boundaries of the PHEX gene for an affected girl from an independent second Indian family. RESULTS: WES revealed a novel PHEX splice acceptor mutation in intron 9 (c.1080-3C>A) in a family with 3 affected individuals with HR. …”
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    Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets
  8. 32308
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    Information and Risk Modification Trial (INFORM): design of a randomised controlled trial of communicating different types of information about coronary heart disease risk, alongside lifestyle advice, to achieve change in health-related behaviour
  9. 32309
    por Stenzel, Martin
    Publicado 2013
    “…There was one incident recorded that fit the criteria of a possible adverse effect. In an 8-year-old girl nausea was noted, that started 15 minutes after the end of the examination and resolved spontaneously. …”
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    Intravenous contrast-enhanced sonography in children and adolescents – a single center experience
  10. 32310
    por Peng, Qian, Deng, Yan, Yang, Yuan, Liu, Hanmin
    Publicado 2016
    “…CASE PRESENTATION: An 8-month-old Han Chinese girl presented with the classic nMFS phenotype, including prominent manifestations of bone overgrowth, aortic root dilatation, and multiple cardiac valve dysfunctions. …”
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    A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum
  11. 32311
    “…CASE PRESENTATION: A 10- year-old girl with consanguineous parents suffered from congenital camptodactyly and progressive swollen and painful joints. …”
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    Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
  12. 32312
    “…Using a comparative genomic hybridization (CGH) array, we identified a 1.24 Mb heterozygous deletion at 1q21 resulting in the loss of 9 genes in a girl with learning disability, hypothyroidism, short stature, sensory integration disorder, and soft dysmorphic features including cupped ears and a unilateral ear pit. …”
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    The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability
  13. 32313
    “…CONCLUSIONS: Our findings strengthen the need to lay emphasis on improving girl child education and removing financial barriers to their access to MHS. …”
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    Factors influencing utilisation of maternal health services by adolescent mothers in Low-and middle-income countries: a systematic review
  14. 32314
    “…CASE PRESENTATION: A 19-year-old girl presented at our hospital with a 7-day history of fever and headache since a one day’s exertion, accompanied by 2 days of weakness. …”
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    A case of neuropsychiatric lupus Erythematosus characterized by the Owl’s eye sign: a case report
  15. 32315
    “…RESULTS: Hip dysplasia was diagnosed in 8 hips of 5 patients (4 boys, 1 girl; age at diagnosis ranged between 3 wk and 27 mo old). …”
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    Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide Mutations
  16. 32316
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    Improving outcomes after pediatric cardiac arrest – the ICU-Resuscitation Project: study protocol for a randomized controlled trial
  17. 32317
    “…CASE PRESENTATION: We report a 1½ year old girl, only child of a non-consanguinous couple who presented with delayed developmental milestones and delayed dentition. …”
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    A novel homozygous mutation in POLR3A gene causing 4H syndrome: a case report
  18. 32318
    “…CASE PRESENTATION: A 6-year-old girl was born to healthy third degree consanguineous parents. …”
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    A case of Raine syndrome presenting with facial dysmorphy and review of literature
  19. 32319
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    Using Normalization Process Theory in feasibility studies and process evaluations of complex healthcare interventions: a systematic review
  20. 32320
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    Improving the normalization of complex interventions: part 1 - development of the NoMAD instrument for assessing implementation work based on normalization process theory (NPT)
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