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 |