Paper Search Console

Home Search Page About Contact

Journal Title

Title of Journal: Eur J Pediatr

Search In Journal Title:

Abbravation: European Journal of Pediatrics

Search In Journal Abbravation:

Publisher

Springer-Verlag

Search In Publisher:

DOI

10.1016/0020-711x(90)90339-5

Search In DOI:

ISSN

1432-1076

Search In ISSN:
Search In Title Of Papers:

Reply to the correspondence letter by Meyer et al

Authors: M Singendonk A Vlieger
Publish Date: 2013/01/08
Volume: 172, Issue: 3, Pages: 421-421
PDF Link

Abstract

We appreciate the interest shown in our paper 1 by Dr Meyer and colleagues The authors describe in their letter an interesting analysis of all Cochrane reviews in the field of complementary and alternative medicine CAM use in children We agree with the authors that there is a great need for highquality research in the field of CAM in the pediatric population The results of this systematic review give insight to the current recommendations on CAM therapy which is the first step in providing adequate information to parents who would like to visit a CAM therapist with their child or initiate an overthecounter CAM therapyThe authors mentioned they found 7 reviews that recommended a certain intervention as well as 14 reviews which concluded that certain interventions should not be performed We would like to encourage the authors to describe these 21 reviews in more detail in order to help pediatricians and pediatric oncologists provide more specific and evidencebased information to parents The large number of inconclusive reviews based on the quality of the studies is striking This underlines our conclusion that adequately conducted and highquality research of CAM interventions in the pediatric population is highly needed

Keywords:

References

.
Search In Abstract Of Papers:
Other Papers In This Journal:
  1. Massive gastrointestinal haemorrhage in isolated intestinal Henoch-Schonlein purpura with response to intravenous immunoglobulin infusion
  2. Reversible posterior encephalopathy syndrome associated with micronodular adrenocortical disease and Cushing syndrome
  3. Auto-immune pancytopenia in a child with DiGeorge syndrome
  4. Effective parenteral clodronate treatment of a child with severe juvenile idiopathic osteoporosis
  5. Evaluation of the Omron MX3 Plus monitor for blood pressure measurement in adolescents
  6. Analysis of the interleukin-12/interferon-γ pathway in children with non-tuberculous mycobacterial cervical lymphadenitis
  7. The effectiveness of octreotide in the treatment of post-operative chylothorax
  8. Persistence of anti-HBs antibody in children whom vaccinated during infantile period and need to booster needs more discussion
  9. Is 99m Tc-HMPAO granulocyte scan an alternative to endoscopy in pediatric chronic inflammatory bowel disease (IBD)?
  10. Paroxetine during breast-feeding: infant weight gain and maternal adherence to counsel
  11. Characteristics of the menstrual cycle in 13-year-old Flemish girls and the impact of menstrual symptoms on social life
  12. Proportional assist versus assist control ventilation in premature infants
  13. Thrombus obstructing the right ventricle outflow tract in a neonate with methylenetetrahydrofolate reductase 677TT genotype
  14. Evidence of Bordetella pertussis infection in vaccinated 1-year-old Danish children
  15. BTNL2 gene polymorphisms may be associated with susceptibility to Kawasaki disease and formation of coronary artery lesions in Taiwanese children
  16. Eosinophilic tubulointerstitial nephritis on treatment with isotretinoin
  17. A European Society of Paediatric and Neonatal Intensive Care (ESPNIC) survey of European critical care management of young people
  18. Kawasaki disease after burns
  19. Clinical practice
  20. de Quervain thyroiditis in a young boy following hand–foot–mouth disease
  21. Über Wesen und Entstehung der interstitiellen Pneumonie
  22. What’s new in autism?
  23. Parameters affecting length of stay in a pediatric emergency department: a retrospective observational study
  24. Health-related quality of life and symptom reporting: similarities and differences between children and their parents
  25. Clustering of (auto)immune diseases with early-onset and complicated inflammatory bowel disease
  26. Risk factors for ventilator-associated pneumonia in the neonatal intensive care unit: a meta-analysis of observational studies
  27. Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia
  28. Immunisation status of children in Germany: temporal trends and regional differences
  29. Onset of acquired autoimmune hypothyroidism in infancy: a presentation of delayed gross-motor development and rhabdomyolysis
  30. Unusual clinical presentation of primary hypothyroidism in a very young infant caused by autoimmune thyroiditis: case report and update of the literature
  31. Burkholderia gladioli sepsis in newborns
  32. A quality improvement initiative to reduce central line infection in neonates using checklists
  33. Cognition and the risk of eating disorders in Spanish adolescents: the AVENA and AFINOS studies
  34. Transient antiphospholipid antibodies associated with acute infections in children: a report of three cases and a review of the literature
  35. Changes in the perfusion waveform of the internal cerebral vein and intraventricular hemorrhage in the acute management of extremely low-birth-weight infants
  36. Barth syndrome diagnosed in the subclinical stage of heart failure based on the presence of lipid storage myopathy and isolated noncompaction of the ventricular myocardium
  37. Asthma and atopic dermatitis in children born moderately and late preterm
  38. Acute renal failure after treatment with non-steroidal anti-inflammatory drugs
  39. Clinical application of wireless capsule endoscopy in pediatric patients for suspected small bowel diseases
  40. Relationship among the Manual Ability Classification System (MACS), the Gross Motor Function Classification System (GMFCS), and the functional status (WeeFIM) in children with spastic cerebral palsy
  41. Pain and musculoskeletal pain syndromes related to computer and video game use in adolescents
  42. Purpura fulminans in a newborn infant with galactosemia
  43. Hospital-based surveillance of congenital rubella syndrome in Indonesia
  44. Eponym
  45. Outcome of three cases of untreated maternal glutaric aciduria type I
  46. Early intravenous immunoglobin (two-dose regimen) in the management of severe Rh hemolytic disease of newborn—a prospective randomized controlled trial
  47. Genealogy of breastfeeding
  48. Magicplex TM Sepsis Real-Time test to improve bloodstream infection diagnostics in children
  49. Pressure-induced angioedema associated with endotracheal tube: successful treatment with epinephrine in two cases
  50. CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature—a rare case with a novel mutation
  51. Adolescent medicine in Europe: integration and cooperation are needed
  52. Expert consensus statement ‘Neonatologist-performed Echocardiography (NoPE)’—training and accreditation in UK
  53. Primary care-based surveillance to estimate the burden of rotavirus gastroenteritis among children aged less than 5 years in six European countries
  54. Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease
  55. Congenital diaphragmatic hernia: current status and review of the literature
  56. Intravenous paracetamol for PDA closure in the preterm: a single-center experience
  57. Volvulus as a complication of chronic intestinal pseudo-obstruction syndrome
  58. Disseminated nontuberculous mycobacterial infection in a child with interferon-γ receptor 1 deficiency
  59. Clinical manifestations and enzymatic activities of mitochondrial respiratory chain complexes in Pearson marrow-pancreas syndrome with 3-methylglutaconic aciduria: a case report and literature review
  60. Medullary sponge kidney associated with distal renal tubular acidosis in a 5-year-old girl
  61. Non-accidental chlorpyrifos poisoning—an unusual cause of profound unconsciousness
  62. Desferrioxamine treatment of iron overload secondary to RH isoimmunization and intrauterine transfusion in a newborn infant
  63. Clinical and diagnostic relevance of Meckel’s diverticulum in children
  64. Radical trapping in glycogen storage disease 1a
  65. Recommended clinical evaluation of infants with an apparent life-threatening event. Consensus document of the European Society for the Study and Prevention of Infant Death, 2003
  66. A late presenter and long-term survivor of alveolar capillary dysplasia with misalignment of the pulmonary veins
  67. A case of Mondini dysplasia with recurrent Streptococcus pneumoniae meningitis
  68. Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2 gene
  69. Comparison of the developmental tests Bayley-III and Bayley-II in 7-month-old infants born preterm
  70. A previously healthy 15-year-old girl with high fever and progressive dyspnoea
  71. Lack of CD4 + CD25 + FOXP3 + regulatory T cells is associated with resistance to intravenous immunoglobulin therapy in patients with Kawasaki disease
  72. Tendency toward atopy in Kawasaki disease
  73. Sweat test practice in pediatric pulmonology after introduction of cystic fibrosis newborn screening
  74. The effects of estradiol on mood and behavior in human female adolescents: a systematic review
  75. Your diagnosis? Congenital foot drop
  76. Exocrine pancreatic insufficiency and its consequences on physical development and metabolism in children and adolescents with type 1 diabetes mellitus
  77. Pediatric complicated pneumonia and pneumococcal serotype replacement: trends in hospitalized children pre and post introduction of routine vaccination with Pneumococcal Conjugate Vaccine (PCV7)
  78. Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome
  79. Acute hemorrhagic edema of young children: a concise narrative review
  80. Is procalcitonin a good marker of renal lesion in febrile urinary tract infection?
  81. An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (aire)
  82. Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents
Search Result: