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761
Effective and Efficient Correction of Severe Skeletal Class II Division 1 Malocclusion with Intermaxillary Elastics
Published 2021-01-01“…This case report describes a successful management of a 12-year-old young adolescent boy that was presented with a Class II division 1 malocclusion with an underlying skeletal discrepancy in horizontal and vertical dimensions. …”
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762
Microduplication of 3p26.3 Implicated in Cognitive Development
Published 2014-01-01“…We report here a 34-month-old boy with global developmental delay referred for molecular karyotyping and fragile X studies. …”
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763
Pseudoaneurysm of the Common Carotid Artery in an Infant due to Swallowed Fish Bone
Published 2015-01-01“…This paper reports the case of a giant pseudoaneurysm of the left common carotid artery due to swallowed fish bone by an 8-year-old boy. This pseudoaneurysm was 5.5 cm transverse-diameter and resulted in severe respiratory distress. …”
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764
Dziecko w ramach wojny. Przypadek Donbasu
Published 2021-09-01“…Based on the analysis of materials from the Russian media (the case of crucifixion of a boy in Slavyansk) and ethnographic interviews with teachers in Kramatorsk, the author asks questions about the mechanisms of constructing the ontologies of child subjects by institutions of power in the conditions of war and the differentiation of grief after them. …”
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765
Acquired Umbilico-Inguinal Fistula with Persistent Discharge due to Suture Reaction: A Case Report and Review of the Literature
Published 2012-01-01“…The aim of this paper is to stay a very rare umbilico-inguinal fistula (UIF) resulting from a delayed suture reaction after the use of silk suture to repair an inguinal hernia. A 3-year-old boy presented with persistent umbilical discharge. …”
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766
A Two-Species Cooperative Lotka-Volterra System of Degenerate Parabolic Equations
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767
A New Numerical Algorithm for Two-Point Boundary Value Problems
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768
Bladder Wall Telangiectasia in a Patient with Ataxia-Telangiectasia and How to Manage?
Published 2015-01-01“…We aimed to report recurrent hemorrhage from bladder wall telangiectasia in a 9-year-old boy with A-T who had received intravenous cyclophosphamide for non-Hodgkin’s lymphoma. …”
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769
Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
Published 2014-01-01“…We present a case that to our knowledge is the first case in literature of osteomyelitis of the pubic symphysis in a 17-year-old boy with juvenile idiopathic arthritis (JIA), which was initially misdiagnosed and progressed to bilateral adductor abscesses. …”
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770
Prosthodontic Rehabilitation of Hereditary Ectodermal Dysplasia in an 11-Year-Old Patient with Flexible Denture: A Case Report
Published 2012-01-01“…This clinical report describes the prosthetic rehabilitation of an 11-year-old boy with hereditary ectodermal dysplasia. Maxillary flexible removable partial denture and mandibular conventional complete denture were fabricated to establish an acceptable masticatory function, speech, and esthetics for the patient.…”
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771
Case Report of Nonfamilial Cherubism in a Toddler: Description of Clinic-Radiographic Features and Osseous-Dental Treatments
Published 2016-01-01“…Most of the cherubism cases show familial history, but there are some cases without familial histories of disorder. A two-year-old boy with a painless symmetrical progressive swelling of the jaws had visited maxillofacial radiology department. …”
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772
Erythema Multiforme Attributable to Herpes Simplex Virus: Clinical Aspects and Treatment
Published 2021-01-01“…We report a case of recurrent herpes-associated erythema multiforme managed with prophylactic acyclovir for 6 months: a 17-year-old boy had recurrent cutaneous lesions as well as lesions in the oral cavity and lips. …”
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773
The Masquerades of a Childhood Ciliary Body Medulloepithelioma: A Case of Chronic Uveitis, Cataract, and Secondary Glaucoma
Published 2012-01-01“…We report a case where a ciliary body medulloepithelioma in a two-year-old boy presents with chronic uveitis, cataract, and an uncontrolled secondary glaucoma after an innocuous blunt ocular trauma. …”
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774
Early Bifrontal Brain Injury: Disturbances in Cognitive Function Development
Published 2010-01-01“…We describe six psychomotor, language, and neuropsychological sequential developmental evaluations in a boy who sustained a severe bifrontal traumatic brain injury (TBI) at 19 months of age. …”
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775
Hair Coil Penile Tourniquet Syndrome in an Unusual Age
Published 2015-01-01“…Therefore, we aimed to present a boy who is 8 years old diagnosed as PTS because of his mother’s hair coil.…”
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776
Plexiform Neurofibroma of the Submandibular Salivary Gland in a Child
Published 2001-01-01“…In the literature, most reported tumours have been present in the parotid gland region. A three-year-old boy with a family history of neurofibromatosis presented with a rapidly growing left submandibular mass. …”
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777
Management of a Severely Submerged Primary Molar: A Case Report
Published 2013-01-01“…In this case report, a five-year-old boy, who had a retained and submerged left lower second primary molar, was presented. …”
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778
Low-Grade Mucoepidermoid Carcinoma of the Lacrimal Gland in a Teenaged Patient
Published 2017-01-01“…Herein, we report clinical and radiological findings of a mucoepidermoid carcinoma arising from the lacrimal gland in a 15-year-old boy. We suggest that since preoperative imaging findings are not diagnostic for mucoepidermoid carcinoma, histopathologic examination should be performed for definitive diagnosis. …”
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779
Dramatic Improvement of Subcutaneous Calcinosis by Intermittent, High-Dose Etidronate plus Cimetidine in a Patient with Juvenile Dermatomyositis
Published 2015-01-01“…A 17-year-old boy with juvenile dermatomyositis presented with typical skin symptoms, mild myositis, and bilateral lower limb calcinosis. …”
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780
Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature
Published 2025-01-01“…Using the determination of a methylation pattern and comparison with an established episignature, we reveal the first hypomorphic variant in the kinase domain of CDK13, leading to a never before described autosomal recessive form of CHDFIDD in a boy with characteristic features. This highlights the utility of episignatures in variant interpretation, as well as a potential novel diagnostic approach in unsolved cases or for disease prognosis.…”
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