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  1. 30501
    “…SEIR was diagnosed in an adolescent girl with facial dysmorphism, exuberant scalp and body hair, severe acanthosis, lipoatrophy, dental abnormalities, and short stature (Rabson-Mendenhall phenotype). …”
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    Syndrome of Extreme Insulin Resistance (Rabson-Mendenhall Phenotype) with Atrial Septal Defect: Clinical Presentation and Treatment Outcomes
  2. 30502
    “…The patients were 4.0 years of mean age (4 months-12 years) and consisted of 8 boys and 1 girl. Totally, 11 endoscopic procedures were performed. …”
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    The Usefulness of Electromagnetic Neuronavigation in the Pediatric Neuroendoscopic Surgery
  3. 30503
    “…Participants were instructed to deceive a witch and to tell the truth to a girl. Under the social-context conditions, participants were asked to consider what they inferred about protagonists' preferences from their facial expressions when responding to questions. …”
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    Neural correlates of deception in social contexts in normally developing children
  4. 30504
    “…CASE PRESENTATION: A 12-year-old Japanese girl presented with normal birth and developmental history. …”
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    Recurrent knee arthritis diagnosed as juvenile idiopathic arthritis with a 10-year asymptomatic period after arthroscopic synovectomy: a case report
  5. 30505
    “…In the further clinical course the girl developed marked obesity. By initiating physical activities twice a week, therapeutic control of both diabetes and OTC deficiency improved, but obesity persisted. …”
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    Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management
  6. 30506
    “…CASE PRESENTATION: A previously healthy 7-year-old Thai girl presented with back pain and progressive paraparesis and was unable to walk for 1 month. …”
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    Unusual presentation of giant cell tumor originating from a facet joint of the thoracic spine in a child: a case report and review of the literature
  7. 30507
    “…She later underwent a Cesarean section in the 38(th) week of gestation and the newborn was a healthy girl weighing 2480g with an Apgar score of 8 at the time of birth. …”
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    Successful Pregnancies in Two Orthotopic Liver Transplant (OLT) Recipients in Iran; Two Case Reports
  8. 30508
    “…Herein we report an Iranian girl with a missed diagnosis of osteogenesis imperfecta. …”
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    Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature
  9. 30509
    “…A high AFP level in a pre-pubic girl with an adnexal mass is indicative of a malignant ovarian tumor. …”
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    Ovarian masses in children and adolescents in China: analysis of 203 cases
  10. 30510
    “…Here, we investigated a de novo synonymous variant c.48C>T (p.Gly16Gly) identified in a girl presenting with a typical RTT phenotype. METHODS: In silico analyses to predict the effects of sequence variation on mRNA splicing were employed, followed by sequencing and quantification of lymphocyte mRNAs from the subject for splice variants MECP2_E1 and MECP2_E2. …”
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    A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient
  11. 30511
    “…Three months after ablation, a healthy girl was delivered without any complications. During twelve-month follow-up there was no recurrence of ventricular tachycardia or ICD interventions. …”
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    “Rescue” ablation of electrical storm in arrhythmogenic right ventricular cardiomyopathy in pregnancy
  12. 30512
    “…CASE PRESENTATION: A 16-year-old girl had Peters’ anomaly in both eyes. Corneal opacity was severe in the left eye due to high-grade dysgenesis of the anterior segment. …”
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    Cataract Surgery for Tilted Lens in Peters’ Anomaly Type 2
  13. 30513
    “…DESCRIPTION OF THE CASE: A 13-year-old girl presented to our emergency department with features of disorientation, weakness of left sided extremities. …”
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    Ischemic stroke as a presenting feature of VIPoma due to MEN 1 syndrome
  14. 30514
    “…The pregnancy was continued and a healthy girl was delivered after 41 weeks of gestation. CONCLUSIONS: This is the first report to indicate a mosaic pregnancy after transfer of a “euploid” blastocyst that was screened by DNA microarray, and the case further confirms that mosaicism is present in human blastocysts produced by in vitro fertilization.…”
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    Mosaic pregnancy after transfer of a “euploid” blastocyst screened by DNA microarray
  15. 30515
    “…We report a case of abdominal pregnancy at 32 weeks, which is most likely to have been a tubal abortion with secondary implantation, leading to delivery of a healthy baby girl weighing 1.7 kg. CASE PRESENTATION: A 22-year-old woman, gravid 3 para 2 was referred to our centre from a district hospital with complaint of generalized abdominal pain and reduced fetal movements. …”
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    Hemoperitoneum in advanced abdominal pregnancy with a live baby: a case report
  16. 30516
    “…CASE PRESENTATION: We report our experience in the management and treatment of an infected urachal cyst that occurred in a 12-year-old Caucasian girl who presented to our Department of Paediatric Surgery with a 30-day history of evening fever. …”
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    Clinical considerations, management and treatment of fever of unknown origin caused by urachal cyst: a case report
  17. 30517
    por Wood, Grant
    Publicado 2014
    “…DESIGN AND METHODS: This report reviewed the case of an 11-year-old girl diagnosed with IS, focusing on the in and out-of-brace x-rays, as well as the fit and function of the braces. …”
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    Brace modifications that can result in improved curve correction in idiopathic scoliosis
  18. 30518
    “…In this case report we present a longitudinal perspective of sleep abnormalities in a nine-year-old Caucasian girl with Prader-Willi syndrome from age two to age nine, and detail the response to treatment with the central nervous system stimulant modafinil. …”
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    Prader-Willi syndrome, excessive daytime sleepiness, and narcoleptic symptoms: a case report
  19. 30519
    “…CASE PRESENTATION: We report a case of a 13-year-old Caucasian girl who came to the emergency room with a history of intermittent fever, weight loss and night sweating for at least 1 month. …”
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    Non-neoplastic bulky mediastinal mass presentation in an adolescent patient: a case report
  20. 30520
    “…RESULTS: We detected the concomitant occurrence of partial trisomy 15q and 16p, due to a complex sSMC, in a 6-year-old girl with clinical phenotypic. The karyotype was analyzed by G and C banding, NOR staining, FISH and SNP array and defined as 47,XX,+der(15)t(15;16)(q13;p13.2)mat. …”
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    Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications
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