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WPRIM Management System>
DCMS
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Chinese Journal of Pediatrics
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2014
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52
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7
Volume:
52
Issue:
7
1. Construction of human milk bank is one of the important tasks of pediatrics-briefing of the 2nd International Congress of the European Milk Bank Association.
Page:555—557
2. Two case of neonatal facial spasms associated with fourth ventricular mass.
Page:553—554
3. Left ventricular-right atrium communicarion and cardiac vegetations induced by infective endocarditis: a case report.
Page:552—552
4. Rare combination of dystrophinopathy and Klinefelter's syndrome in one patient.
Page:548—551
5. Genetics and pedigree analysis of primary carnitine deficiency cardiomyopathy in 6 cases.
Page:544—547
6. Comprehensive treatment of neuroblastoma in children associated with opsoclonus-myoclonus-ataxia syndrome.
Page:540—543
7. Balloon angioplasty for native coarctation in children: one year follow-up results.
Page:535—539
8. Negative pressure pulmonary edema with upper airway obstruction: analysis of 3 patients.
Page:531—534
9. Lung function measurements using body plethysmography in young children with acute lower respiratory tract infection.
Page:525—530
10. Treatment of children with steroid-dependent nephrotic syndrome with rituximab.
Page:521—524
11. Function of CD4(+) CD25(+) regulatory T cells in Henoch-Schonlein purpura nephritis in children.
Page:516—520
12. Assay of adiponectin, leptin, true insulin and ghrelin levels in preterm human milk, and its relationship with infants growth.
Page:510—515
13. Changes of intestinal microecology during early infancy and subsequent risk of obesity.
Page:506—509
14. Progress in mitochondrial nephropathy.
Page:503—505
15. Rational application of blood purification therapy in edema of children with nephrotic syndrome.
Page:500—502
16. Effects of response gene to complement 32 as a new biomarker in children with acute kidney injury.
Page:494—499
17. Mutational analysis of MYO1E in children with sporadic steroid-resistant nephrotic syndrome in Chinese Han ethnic group.
Page:488—493
18. Enlightenment on diagnosing and treating hereditary renal diseases.
Page:481—482