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Toplam kayıt 103, listelenen: 41-50
A Rare Case of Pediatric Bullous Spontaneous Acute Urticaria
(Karger, 2018)
Objective: Acute spontaneous bullous urticaria is an extremely rare entity, and there are few reports with blister formation in acute urticaria patients. Clinical Presentation and Intervention: We present a 2-year-old girl ...
Somatic Mutations In Cerebral Cortical Malformations
(Massachusetts Medical Soc, 2014)
BACKGROUND Although there is increasing recognition of the role of somatic mutations in genetic disorders, the prevalence of somatic mutations in neurodevelopmental disease and the optimal techniques to detect somatic ...
The Effect of Swimming and Type of Stroke on Bone Metabolism in Competitive Adolescent Swimmers: A Pilot Study
(Tubitak Scientific & Technical Research Council Turkey, 2015)
Background/aim: Physical activity plays a key role in increasing and preserving bone mineral density (BMD). Effects on bone development associated with various nonweight-bearing sporting activities, such as swimming, are ...
The Effects of Conscious Sedation with Nitrous Oxide/Oxygen on Cognitive Functions
(Tubitak Scientific & Technical Research Council Turkey, 2016)
Background/aim: The aim of this study was to investigate the effects of conscious sedation with 40% nitrous oxide/oxygen ( N 2 O/O 2) on cognitive functions. Materials and methods: Forty dental patients referred to the ...
The Use Of The Midas Questionnaire To Assess Migraine And Tension Type Headache In Adolescents
(Ortadogu Ad Pres & Publ Co, 2012)
Objective: Headache is the most common type of pain that children and adolescents complain as well as being the most common neurological symptom. Among all school-age children, 15-20% experience headache and 3-5% of these ...
Maxillofacial Osteosarcoma Successfully Treated with Surgery and Adjuvant Chemotherapy in a Child
(Comenius Univ, 2012)
Maxillofacial osteosarcoma constitutes a minor percentage of all the head and neck tumors. We describe a 10 year-old girl presenting with swelling and pain in left maxillary region and diagnosed as low grade osteosarcoma. ...
Myo1E Mutations And Childhood Familial Focal Segmental Glomerulosclerosis
(Massachusetts Medical Soc, 2011)
BACKGROUND Focal segmental glomerulosclerosis is a kidney disease that is manifested as the nephrotic syndrome. It is often resistant to glucocorticoid therapy and progresses to end-stage renal disease in 50 to 70% of ...
Nusinersen Versus Sham Control In Infantile-Onset Spinal Muscular Atrophy
(Massachusetts Medical Soc, 2017)
BACKGROUND & para;& para;Spinal muscular atrophy is an autosomal recessive neuromuscular disorder that is caused by an insufficient level of survival motor neuron (SMN) protein. Nusinersen is an antisense oligonucleotide ...
Prediction of Central Lymph Node Metastasis in Patients with Thyroid Papillary Microcarcinoma
(Tubitak Scientific & Technical Research Council Turkey, 2017)
Background/aim: The purpose of this study was to analyze the clinicopathological characteristics of patients with papillary thyroid carcinoma (PTC) and papillary thyroid microcarcinoma (PTMC) and predictive factors for ...
Proteinuria in Frasier Syndrome
(Srpsko Lekarsko Drustvo, 2013)
Introduction Frasier syndrome (FS) is a genetic form of glomerulopathy, which results from mutations in the Wilms' tumour suppressor gene (WT1). Proteinuria in FS has been traditionally considered unresponsive to any ...