WPRIM Management System> DCMS> Journal of Clinical Pediatrics> 2016> 34

Volume: 34

1. Research progress in hereditary multiple exostoses Page:232—236
2. Physiological changes and implications during the fetal-neonatal transition Page:223—226
3. Clinical analysis of 408 children with positive blood culture of Escherichia coli Page:220—222
4. Clinical analysis of the microangiopathic hemolytic anemia and renal impairment secondary to methylmalonic ;academia in children Page:217—219
5. A pedigree of a rare Cb1X type X-linked methylmalonic acidemia due to transcriptional co-regulator HCFC1 ;mutation Page:212—216
6. Neonatal congenital hyperinsulinism:one case report and literature review Page:188—191
7. The role of retinoic acid receptor and its signal pathway in the renal disease Page:227—231
8. Methylmalonic aciduria combined with congenital adrenal hyperplasia:a case report Page:208—211
9. The analysis of clinical manifestations and genetic mutations in childhood chronic granulomatous disease Page:204—207
10. Analysis of the quality of life of 230 very low birth weight infants followed up to 6 months of corrected age Page:176—180
11. The value of transesophageal atrial pacing in assessing the mechanism of paroxysmal supraventricular tachycardia ;in children Page:201—203
12. Relationship between plasminogen activator inhibitor-1 gene polymorphism and gastrointestinal bleeding in ;Henoch-Sch?nlein purpura Page:197—200
13. Analysis of the factors related to recurrent vasovagal syncope in children Page:192—196
14. The gene mutation in one neonate with Finnish type congenital nephrotic syndrome Page:185—187
15. Clinical and prognostic analysis of sepsis caused by Streptococcus agalactiae combined with purulent meningitis in 12 ;neonates Page:181—184
16. Analysis of clinical manifestations and drug resistance in purulent meningitis caused by Escherichia coli in ;neonates Page:172—175
17. Application value of plasma N-terminal pro-B-type natriuretic peptide in diagnosis and treatment of symptomatic ;patent ductus arteriosus in preterm infants Page:166—171
18. The impact of prenatal diagnosis on treatment and prognosis of neonatal pulmonary atresia with intact ventricular ;septum and critical pulmonary stenosis with intact ventricular septum Page:161—165
19. A case report of enzyme replacement therapy for glycogen storage disease typeⅡ Page:363—365
20. A case report of paroxysmal kinesigenic dyskinesia and literature review Page:354—356
21. Analysis of pathogen in bronchoalveolar lavage lfuid and its clinical features in 80 children with lobar pneumonia Page:348—350
22. Mixed infection of bacteria and viruses in community-acquired pneumonia in children Page:342—347
23. Improvement of life quality of children with atopic dermatitis by therapeutic patient education Page:338—341
24. Pediatric inherited cancer predisposition syndromes and TP53 germ-line mutation Page:333—337
25. Study on clinical prognosis among ETV6/RUNX1 positive childhood B-precursor acute lymphocyte leukemia Page:321—325
26. Progress on neonatal diabetes mellitus Page:393—398
27. Recent advances of diagnostic approaches in primary ciliary dyskinesia Page:388—392
28. Effect of erythropoietin on expression of MMP-2 in hippocampus of neonatal rats with hypoxic-ischemic brain ;damage Page:366—370
29. One case of chromosome 4q21/22 deletion syndrome Page:360—362
30. Analysis of intervals of pulse oximetry in congenital heart disease screening Page:357—359
31. Paroxysmal sympathetic hyperactivity in a child with tuberculous meningitis:a case study Page:351—353
32. Evaluation of clinical features in predicting relapse of childhood acute lymphoblastic leukemia treated with CCLG-2008 protocol Page:326—331
33. Expression of bFGF and TGF-β1 in different stages of myocardial ifbrosis Page:371—374
34. Clinical features of congenital hepatic ifbrosis in children Page:444—448
35. Epidemiologic and clinical features of hand, foot, and mouth disease caused by Coxsackie virus A16 infection in Suzhou and analysis of polymorphisms ofOAS1 Page:434—438
36. Diagnosis and treatment of 6 cases of Dent’s disease Page:418—420
37. The clinical and pathological features of capillary proliferative purpura nephritis in 19 children Page:414—417
38. The role of zinc ifnger protein A20 in immune regulation of dendritic cells and in the pathogenesis of inlfammatory bowel disease Page:470—474
39. Effect of mibefradil on proliferation of human pulmonary artery smooth muscle cells induced by platelet-derived growth factor Page:465—469
40. Clinical diagnosis, treatment, and prognosis of pulmonary artery sling in 38 children Page:461—464
41. Drug-induced hypersensitivity syndrome in children:a case report Page:457—460
42. Deep venous thrombosis in preterm infants:3 cases report Page:453—456
43. Lissencephaly:a case report and literature review Page:449—452
44. Analysis of related risk factors of neonatal resuscitation dififculty Page:439—443
45. Clinical characteristics of pleural effusion in children withMycoplasma pneumoniae Page:430—433
46. The distribution of pathogens and prognosis in ninety-five children with etiology confirmed bacterial meningitis Page:425—429
47. The value of targeted surveillance in control of nosocomial infection in neonatal intensive care unit Page:421—424
48. The relationships of hyperuricemia with clinical and Oxford classiifcations in children with IgA nephropathy Page:411—413
49. Renal vascular damage and the expression of miR-145 in lupus nephritis Page:406—410
50. The strategy of diagnosis and treatment of anti-neutrophil cytoplasm antibody-associated vasculitis Page:401—405
51. The difference of airway malformation between double aortic arch and pulmonary artery sling in children Page:503—505
52. The signiifcance of heart rate variability analysis in children with congenital heart disease combined with paroxysmal ;supraventricular tachycardia Page:486—488
53. Clinical research of heart rate variability and deceleration capacity in children with idiopathic ventricular premature ;contraction Page:481—485
54. “Vascular hypothesis”and angiogenic therapy in bronchopulmonary dysplasia Page:555—559
55. The protective effect of Clostridium butyricum on intestinal injure in newborn rats with necrotizing enterocolitis Page:549—554
56. Exploration of the regulation site of HIF-1α in Notch signaling pathway in the hippocampus of rats with status ;epilepticus Page:544—548
57. Effect of miR-200b on intestinal epithelial tight junction via MLCK/P-MLC signaling pathway Page:540—543
58. Pathogens distribution and drug resistance from cerebrospinal lfuid culture from 2007 to 2014 Page:535—539
59. Analysis of the non-bacteria pathogens of acute laryngitis in children Page:531—534
60. Clinical features and follow-up of 35 children with post-infectious bronchiolitis obliterans Page:526—528
61. The NROB 1 gene missense mutation causes congenital adrenal dysplasia:a case report Page:522—525
62. Variation and clinical signiifcance of serum galectin-3 in children with chronic heart failure Page:499—502
63. The investigation of urine iodine and blood TSH levels in 695 neonates and urine iodine level in their mothers in ;Yunnan province Page:519—521
64. The value of fecal high mobility group box-1 in early diagnosis and prediction of severity of neonatal necrotizing ;enterocolitis Page:515—518
65. Analysis of sterile pyuria in patients with Kawasaki disease Page:494—498
66. The correlation between mutations in the promoter region of TBX 1 gene and conotruncal heart defects Page:489—493
67. The progress of the mechanism on brain protection of remote ischemic preconditioning Page:634—636
68. Analysis on correlation between dietary fatty acid intake of pregnant women and neonateal anthropometry at birth Page:623—627
69. Chronic granulomatous disease and Mcleod syndrome caused by continuous X chromosome deletion:a report of two cases and literature review Page:614—617
70. Infant with both alpha 1 antitrypsin deifciency and biliary atresia:acase report and literature review Page:610—613
71. Congenital nephrogenic diabetes insipidus:2 cases report of brothers and review Page:606—609
72. Analysis of screening and therapeutic effect of congenital hypothyroidism Page:602—605
73. Aggrecan type spondylometaphyseal dysplasia:one rare case report Page:589—591
74. Association betweenADAM10 polymorphism and clinical characteristics in children with asthma Page:580—583
75. Clinical features and treatment of protracted bacterial bronchitis in children Page:575—579
76. Serum vancomycin concentration distribution and its clinical therapeutic effect on children with severe Gram-positive cocci pneumonia Page:570—574
77. Diagnostic signiifcance of ifbrin related markers for pre-disseminated intravascular coagulation state in children with severe pneumonia Page:566—569
78. The effect of different dosages of low molecular weight heparin on acute pulmonary embolism and inhibition of pulmonary intimal hyperplasiain immature rats Page:628—633
79. Genotype-phenotype analysis in Apert syndrome Page:618—622
80. Mutation spectrum of thePAH gene in phenylketonuria children in Ningxia Page:596—601
81. LMNA- associated congenital muscular dystrophy:a case report and literature review Page:592—595
82. Genetic diagnosis of spondyloenchondrodysplasia with immune dysregulation:a case report and literature review Page:584—588
83. Expression and clinical signiifcance of sB7-H3 and cytokines in the bronchoalveolar lavage lfuid in children with refractory Mycoplasma pneumoniae pneumonia Page:561—565
84. The biological advance in acute lymphoblastic leukemia of t (4;11) in infants Page:787—791
85. CTNS gene mutation leads to cysteine nephropathy combined with corneal crystal in young child Page:783—786
86. Clinical features of Marfan syndrome and analysis ofFBN1 gene mutation Page:775—778
87. NR5A1 gene mutation in child with 46, XY disorders of sex development:a case report and literature review Page:771—774
88. Risk factors of primary nephrotic syndrome complicated with thrombosis in children Page:767—770
89. The clinical features and identification of autonomic nervous mediated syncope and pseudo psychogenic syncope in children Page:755—760
90. The analysis of common mutation in deafness-associated gene in 111 neonates who failed to pass newborn hearing screening Page:750—752
91. Analysis of pathogenic bacteria distribution and drug resistance of otitis media in preschool children Page:747—749
92. Clinical analysis of typhoid fever complicated with hemophagocytic syndrome in one case Page:737—739
93. Hemolytic anemia as the first manifestation in hepatolenticular degeneration combined with ichthyosis:a case report Page:734—736
94. Clinical features of biliary pancreatitis in children Page:730—733
95. Detection of biomarkers and its clinical signiifcance in the inlfammatory bowel disease in Children Page:721—725
96. Early identiifcation, diagnosis, and treatment ofMycoplasma pneumoniae pneumonia complicated with thrombus in children Page:792—795
97. Tyk2 gene mutations in primary immunodeficiency disease:a case report and literature review Page:779—782
98. Correlation between vascular damage and blood myocardin in children with lupus nephritis Page:761—766
99. The clinical features and treatment ofBrucellosis disease in 24 children Page:744—746
100. The relationship between the vitamin A level andMycoplasma pneumonia in children Page:740—743
101. Research progress in pediatric intravenous fluid tension Page:710—713
102. Basic and clinical research of lymphocytic variant hypereosinophilic Page:705—709
103. Glucocorticoid versus intravenous injection of human immunoglobulin in treatment of primary immune ;thrombocytopenia in children:a meta-analysis Page:696—704
104. Clinical analysis of 14 cases of Pseudomonas aeruginosa sepsis in children Page:674—676
105. The clinical characteristics and etiological analysis of diffuse alveolar hemorrhage in 138 children Page:670—673
106. Neonatal dengue fever:four cases report Page:661—663
107. The relationship between the doses in parenteral nutrition and short term outcomes in very low birth weight ;infants Page:657—660
108. The changes in protein and energy intakes and weight in 2 weeks after birth in appropriate for gestational age ;and small for gestational age preterm infants with gestational age less than 34 weeks Page:651—656
109. Analysis of causes of extrauterine growth restriction in premature infants and the status of nutritional ;intake Page:714—717
110. Congenital insensitivity to pain with anhidrosis in a family:2 cases report Page:691—695
111. Application of single nucleotide polymorphism microarray technology in diagnosis of Rubinstein-Taybi syndrome:one case report Page:688—690
112. Lemierre syndrome caused by Staphylococcus aureus:one case report Page:685—687
113. IgA nephropathy combined with hemangioma of bladder in children:a case report Page:680—682
114. The value of clinical features combined with 3-D reconstruction of multi-slice spiral CT in diagnosis of foreign body ;in trachea or bronchus in children Page:677—679
115. Clinical characteristics of pertussis in 17 neonates Page:667—669
116. Congenital hypothyroidism characterized by hydrops fetalis:one case report Page:664—666
117. Analysis of correlation of the mutation of pulmonary surfactant protein B and C gene with respiratory distress ;syndrome in premature infants in Mongolian Page:645—650
118. Logistic regression analysis of risk factors of multiple drug-resistant infections in neonatal intensive care unit Page:641—644
119. The clinical outcomes of nutritional support in children with high nutritional risk Page:919—923
120. Neonatal-onset carbamoyl phosphate synthetaseⅠdeficiency:a case report and literature review Page:903—906
121. The correlation between phenotype and genotype of 5α-reductase 2 deficiency in 5 children Page:886—890
122. Study of endothelial cell toxicity of low dosage of extracellular histones Page:942—948
123. The effect of Quercetin on the long-term memory and PARP-1/AIF signal path in neonatal rats with hypoxic-ischemic brain damage Page:936—941
124. The clinical features of hereditary nephrotic syndrome caused by NPHS 2 mutation in two pediatric patients Page:933—935
125. Clinical features and treatment of autoimmune hemolytic anemia in 29 children Page:930—932
126. Correlation of asthma with ADAM 33 SNP in Uygur and Han children in Urumqi Page:926—929
127. The analysis of bacteriological changes and susceptible factor of nosocomial infection in neonatal intensive care unit Page:922—925
128. Clinical study on the efficacy and safety of Dextromethorphan Hydrochloride, Chlorphenamine Malente, and Ammonium Chloride Syrup on eliminating or relieving the symptoms of acute upper respiratory infection in children Page:910—916
129. Clinical feature and gene detection in one case of Wiskott-Aldrich syndrome Page:907—909
130. MECP 2 duplication syndrome:a pedigree report and literature review Page:898—902
131. Methylmalonic acidemia:3 cases report and literature review Page:894—897
132. Utilization of furosemide/hydrochlorothiazide load test in differential diagnosis of Bartter syndrome from Gitelman syndrome in children Page:891—893
133. Changes of adrenal cortical function in children with growth hormone deficiency before and after treatment with recombinant human growth hormone Page:881—885
134. Five episodes of Kawasaki disease within 2 years:a case report Page:753—754,760
135. Comparison of the quality of life before and after treatment of eczema in infants with or without food allergies Page:726—729,733
136. Neonatal intrahepatic cholestasis caused by citrin deficiency:updated understanding Page:949—953,955