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期刊名:Pediatric health medicine and therapeutics

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e-ISSN:1179-9927

IF/分区:1.8/Q2

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共收录本刊相关文章索引389
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Abayneh Girma Demisse,Fentahun Alemu,Mahlet Abayneh Gizaw et al. Abayneh Girma Demisse et al.
Introduction: The neonatal period is a highly vulnerable time for an infant completing many of the physiologic adjustments required for life outside the uterus. As a result, there are high rates of morbidity and mortality...
Markus Pääkkönen Markus Pääkkönen
Acute septic arthritis in children is usually hematogenous. It is more common in boys, and it most often affects the large joints of the lower limb. Diagnosis is based on cultures obtained from the infected joint and is supported by C-react...
Júlio César Rocha,Anita MacDonald Júlio César Rocha
Phenylketonuria (PKU) is a well-described inborn error of amino acid metabolism that has been treated for >60 years. Enzyme deficiency causes accumulation of phenylalanine (Phe) and if left untreated will lead to profound and irreversible i...
Farida F Negm,Doaa R Soliman,Enas S Ahmed et al. Farida F Negm et al.
Background: In critically ill patients, there are reduced stores of antioxidants, which are associated with increased organ failure and even higher mortality. Trace elements, especially zinc and selenium, are the cornerst...
Elvira Ingrid Levy,Roel Lemmens,Yvan Vandenplas et al. Elvira Ingrid Levy et al.
This review intends to update what is known about and what is still a challenge in functional constipation (FC) in children regarding epidemiology, pathophysiology, diagnosis, and management. Although FC is a common childhood problem, its g...
Noureddin Nourbakhsh,Robert H Mak Noureddin Nourbakhsh
Patients with steroid-resistant nephrotic syndrome (SRNS) represent a challenging subset of patients with nephrotic syndrome who often fail standard immunosuppression and have a higher likelihood of progressing to end-stage renal disease. A...
Filippo Parolini,Anna Lavinia Bulotta,Sonia Battaglia et al. Filippo Parolini et al.
Esophageal atresia remains one of the most challenging congenital anomalies of the newborn. In recent years, because of the advances in prenatal diagnosis, neonatal critical care, and surgical procedures, overall outcomes have improved subs...
Fawzia Elgharbawy,Khalil Salameh,Talal Al Rayes et al. Fawzia Elgharbawy et al.
Omental infarction (OI) is a rare cause of acute abdominal pain occurring in 0.1% of children, which is typically diagnosed during surgery for suspected appendicitis. We present the case of a 7-year-old Pakistani girl. She presented with ac...
Ajay S Kasi,Iris A Perez,Sheila S Kun et al. Ajay S Kasi et al.
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder with failure of central control of breathing and of the autonomic nervous system function due to a mutation in the paired-like homeobox 2B (PHOX2B) gene. Affected...
Marsha L Campbell-Yeo,Timothy C Disher,Britney L Benoit et al. Marsha L Campbell-Yeo et al.
The holding of an infant with ventral skin-to-skin contact typically in an upright position with the swaddled infant on the chest of the parent, is commonly referred to as kangaroo care (KC), due to its simulation of marsupial care. It is r...