Search Results - "Yao, TC"
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1
Serum 25-hydroxyvitamin D in relation to lung function and exhaled nitric oxide in children
Published in Archives of disease in childhood (01-10-2014)Get full text
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2
PS-172 Serum 25-hydroxyvitamin D In Relation To Lung Function And Exhaled Nitric Oxide In Children
Published in Archives of disease in childhood (01-10-2014)“…Abstract only…”
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3
Evolution of pulmonary function in preterm infants: a prospective birth cohort
Published in Archives of disease in childhood (01-10-2014)Get full text
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4
PO-0999 Suboptimal Vitamin D Status In A Population-based Study Of Asian Children: Prevalence And Relation To Allergic Diseases And Atopy
Published in Archives of disease in childhood (01-10-2014)“…Abstract only…”
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5
Pediatric lupus in Asia
Published in Lupus (01-10-2010)“…Of all patients with systemic lupus erythematosus (SLE), 15—20% are diagnosed during childhood, with disease onset prior to the age of 16 years. Because…”
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Book Review Journal Article -
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PS-178 Evolution Of Pulmonary Function In Preterm Infants: A Prospective Birth Cohort
Published in Archives of disease in childhood (01-10-2014)“…Abstract only…”
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7
Acute pancreatitis in pediatric and adult-onset systemic lupus erythematosus: A comparison and review of the literature
Published in Lupus (01-04-2011)“…This study aimed to compare differences of acute pancreatitis between adult- and pediatric-onset systemic lupus erythematosus (SLE) patients and to clarify the…”
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Prevalence of pediatric systemic lupus erythematosus and juvenile chronic arthritis in a Chinese population: A nation-wide prospective population-based study in Taiwan
Published in Clinical and experimental rheumatology (01-11-2004)“…To estimate the national prevalence of systemic lupus erythematosus (SLE) and juvenile chronic arthritis (JCA) in Chinese children in Taiwan. A nationwide…”
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Sequence variants of the gene encoding chemoattractant receptor expressed on Th2 cells (CRTH2) are associated with asthma and differentially influence mRNA stability
Published in Human molecular genetics (01-11-2004)“…The gene, CRTH2, encoding a receptor for prostaglandin D2 (PGD2), is located within the peak linkage region for asthma on chromosome (Chr.) 11q reported in…”
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10
The RANTES promoter polymorphism: A genetic risk factor for near-fatal asthma in Chinese children
Published in Journal of allergy and clinical immunology (01-06-2003)“…Background: RANTES promoter polymorphisms were found associated with asthma/atopy in some studies but not others, possibly reflecting the genetic heterogeneity…”
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Polymorphisms in the promoter region of RANTES and the regulatory region of monocyte chemoattractant protein-1 among Chinese children with systemic lupus erythematosus
Published in Journal of rheumatology (01-10-2004)“…OBJECTIVE: Chemokines play an important role in the physiology and pathophysiology of acute and chronic inflammatory processes. We investigated whether…”
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12
Lack of association of mannose-binding lectin gene polymorphisms with development and clinical manifestations of systemic lupus erythematosus in Chinese children
Published in Lupus (01-04-2009)“…Mannose-binding lectin (MBL) gene polymorphisms may be associated with adult-onset systemic lupus erythematosus (SLE), but studies in children with SLE are…”
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13
Osteomyelitis in patients with systemic lupus erythematosus
Published in Journal of rheumatology (01-07-2004)“…OBJECTIVE: To investigate the clinical profile of and the risk factors for osteomyelitis in patients with systemic lupus erythematosus (SLE). METHODS: We…”
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14
Failure to thrive caused by the coexistence of vallecular cyst, laryngomalacia and gastroesophageal reflux in an infant
Published in International journal of pediatric otorhinolaryngology (01-11-2004)“…Vallecular cyst is a rare but dangerous cause of stridor in neonates and young infants. Without recognition and proper therapy, the resulting airway…”
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15
MCP-1 gene regulatory region polymorphism in Chinese children with mild, moderate and near-fatal asthma
Published in Journal of allergy and clinical immunology (01-02-2004)“…A polymorphism in the MCP-1 gene regulatory region has been associated with asthma in the Caucasians. This polymorphism is possibly endemic to the Asian…”
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16
Pitfalls in the diagnosis of idiopathic pulmonary haemosiderosis
Published in Archives of disease in childhood (01-06-2002)“…Idiopathic pulmonary haemosiderosis is a very rare but devastating disorder. Diagnosis is sometimes difficult and the clinical course exceedingly variable, as…”
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17
MCP‐1 gene regulatory region polymorphism in Chinese children with mild, moderate and near‐fatal asthma
Published in Allergy (Copenhagen) (01-04-2004)“…Background: A polymorphism in the monocyte chemoattractant protein 1 (MCP‐1) gene regulatory region has been associated with asthma in Caucasians. This…”
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Asthmatic versus non-asthmatic spontaneous pneumomediastinum in children
Published in Asian Pacific journal of allergy and immunology (01-03-2005)“…The aim of this study was to analyze the clinical spectrum and seek potential curable causes of spontaneous pneumomediastinum (SPM) in children in order to…”
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Staphylococcal endocarditis and multiple emboli in a patient with systemic lupus erythematosus
Published in Journal of rheumatology (01-11-2004)“…We describe a patient with systemic lupus erythematosus who developed Staphylococcus aureus endocarditis following dental work. Multiple brain and cutaneous…”
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Idiopathic pulmonary haemosiderosis: An Oriental experience
Published in Journal of paediatrics and child health (01-01-2003)“…Objectives: Idiopathic pulmonary haemosiderosis (IPH) is a rare but potentially lethal disorder. A retrospective analysis of documented cases of IPH in our…”
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