Mostrando 31,221 - 31,240 Resultados de 32,492 Para Buscar '"The Girls"', tiempo de consulta: 0.56s Limitar resultados
  1. 31221
    “…CASE PRESENTATION: This was a case of bilateral isolated congenital ACLD in a 15-year-old girl with chronic bilateral knee instability, bilateral mild genu valgum, and positive Lachman’s tests. …”
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  2. 31222
    “…The next double diagnosis had never been reported before: through exome sequencing, a girl with FXS who was of 7 years of age with macrocephaly and severe psychomotor delay was found to carry a de novo variant in the PPP2R5D gene. …”
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  3. 31223
    “…We report a case of a 3-year-old girl admitted to the hospital for abdominal pain and a low-grade fever, with abdominal ultrasonography revealing a hepatic lesion. …”
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  4. 31224
    “…They contributed to a cumulative asthma prevalence of 12.6% among the sampled population, with a girl-boy percentage of 37.4% to 62.6%. Air-pollution and weedy areas were associated with greater risk for asthma, while a suburban residence showed lesser odds. …”
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  5. 31225
    “…PRESENTATION OF CASE: We report a case of a 16-month-old girl who presented to the emergency department unconscious with a four-day history of a swollen right eyelid. …”
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  6. 31226
  7. 31227
    “…We report a case of a 14-year-old girl known to have end-stage renal disease, secondary to the autosomal recessive polycystic kidney. …”
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  8. 31228
    “…In this case study, we present an 8-year-old girl presenting with HSP-induced myocarditis and thrombus in the right atrium and HSP nephritis. …”
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  9. 31229
    “…OBSERVATIONS: Case 1 was an 8-month-old girl whose bilateral retinoblastoma (group D, OU) was treated by chemotherapy and focal ablation therapy. …”
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  10. 31230
    “…This article presents three paradigmatic cases to exemplify how this translational effort can, at least in some instances, be undertaken today with very positive results: (a) a young girl carrying a chr. 16p11.2 duplication can be screened using targeted exams and undertake therapeutic/preventive interventions related to her genetic diagnosis; (b) a 13-year-old boy with intellectual disability and autism spectrum disorder carries a chr. 11q14.1 deletion, partly spanning the DLG2 gene important for synaptic function, and gained over 20 I.Q. points ostensibly due to carbolithium, prescribed in the absence of affective symptoms, exclusively following the pathophysiology pointed out by the genetic results; (c) a 58-year-old woman carries a COL3A1 gene variant responsible for the vascular form of Ehler–Danlos syndrome with colon rupture. …”
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  11. 31231
  12. 31232
    “…We present a case of a nine-year old girl, which rapidly worsened due to stress and isolation related to the COVID-19 pandemic. …”
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  13. 31233
    “…CASE SUMMARY: A 10-month-old girl accidently aspirated a metallic piece that was dislodged further to the right main bronchus after failed trials to remove it. …”
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  14. 31234
  15. 31235
    “…To explore these questions, 138 5- to 7-year-olds (younger children) and 8- to 10-year-olds (older children) evaluated a series of boy and girl characters who partook in physical or relational aggression with ambiguous or purposeful intent. …”
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  16. 31236
    por Alhalabi, Marouf M., Abbas, Ahmad J.
    Publicado 2022
    “…CASE PRESENTATION: A 10-year-old Syrian girl, anti-TNF naïve, chronically active ulcerative colitis was weighs 25 kg, standing 142 cm tall, body surface area (BSA) of 0.993 m(2), past medications included oral prednisone and mesalamine, no prior surgery. …”
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  17. 31237
    “…CASE PRESENTATION: A 9‐year‐old Asian girl who experienced left hip pain after an injury was diagnosed with Garden IV left femoral neck fracture, which was treated through manipulation reduction and fixed with splints. …”
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  18. 31238
    “…CASE REPORT: We report a case of an otherwise healthy 9-year-old girl who presented with manifestations of Cushing syndrome (easy fatigability, weakness, back pain, easy bruising, hirsutism, acne, skin discoloration [pigmentation], and blurred vision). …”
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  19. 31239
  20. 31240
    “…In this case report, we describe a clinical course of a child with severe autoimmune enteropathy after a heart transplant in infancy and detail a treatment approach with abatacept and alemtuzumab. A 21-month-old girl with a medical history of congenital dilated cardiomyopathy and heart transplantation at 2 months was evaluated for chronic hematochezia. …”
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