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1.
Indian Pediatr ; 2018 Nov; 55(11): 1006-1007
Article | IMSEAR | ID: sea-199101
3.
Indian Pediatr ; 2018 Jun; 55(6): 489-494
Article | IMSEAR | ID: sea-198986

Résumé

Justification: Practitioners and people need information about the therapeutic potential of umbilical cord blood stem cells and pros andcons of storing cord blood in public versus private banks.Process: Indian Academy of Pediatrics conducted a consultative meeting on umbilical cord blood banking on 25th June 2016 in Pune,attended by experts in the field of hematopoietic stem cell transplantation working across India. Review of scientific literature was alsoperformed. All expert committee members reviewed the final manuscript.Objective: To bring out consensus guidelines for umbilical cord banking in India.Recommendations: Umbilical cord blood stem cell transplantation has been used to cure many malignant disorders, hematologicalconditions, immune deficiency disorders and inherited metabolic disorders, even when it’s partially HLA mismatched. Collectionprocedure is safe for mother and baby in an otherwise uncomplicated delivery. Public cord blood banking should be promoted over privatebanking. Private cord blood banking is highly recommended when an existing family member (sibling or biological parent) is sufferingfrom diseases approved to be cured by allogenic stem cell transplantation. Otherwise, private cord blood banking is not a ‘biologicalinsurance’, and should be discouraged. At present, autologous cord stem cells cannot be used for treating diseases of genetic origin,metabolic disorders and hematological cancers. Advertisements for private banking are often misleading. Legislative measures arerequired to regularize the marketing strategies of cord blood banking.

4.
Indian Pediatr ; 2016 Mar; 53(3): 199-200
Article Dans Anglais | IMSEAR | ID: sea-178901
5.
Indian Pediatr ; 2014 May; 51(5): 397-398
Article Dans Anglais | IMSEAR | ID: sea-170620

Résumé

Background: Isolated mediastinal involvement in Langerhans cell histiocytosis (LCH) has been rarely reported. Case characteristics: A 3-month-old boy presented with history of low grade intermittent fever, cough and noisy breathing for 2 weeks. Observation: A chest X-ray showed massive mediastinal widening. Biopsy of the mass confirmed LCH. Outcome: Patient is doing well after one year of treatment with LCH III protocol. Message: Langerhans cell histiocytosis should be considered in differential diagnosis of mediastinal mass in infants.

6.
Indian Pediatr ; 2013 October; 50(10): 974
Article Dans Anglais | IMSEAR | ID: sea-170026
7.
Indian Pediatr ; 2013 September; 50(9): 886
Article Dans Anglais | IMSEAR | ID: sea-169983
8.
Indian Pediatr ; 2013 July; 50(7): 659-662
Article Dans Anglais | IMSEAR | ID: sea-169883

Résumé

Objective: To evaluate serum vascular endothelial growth factor (VEGF) levels in children with acute lymphoblastic leukemia (ALL) during the induction phase of chemotherapy. Design: Prospective sudy. Setting: Hospital-based study over 18 months. Patients: 30 children with ALL and 17 healthy age- and sexmatched controls. Intervention: Serum concentration of VEGF-A–165 isoform (s- VEGF) was measured by enzyme-linked immunoabsorbant assay at diagnosis and at the end of induction chemotherapy. Main outcome measures: s-VEGF was compared with markers of tumor burden. Kinetics of s-VEGF was assessed in response to induction chemotherapy. Results: Median VEGF was significantly lower in untreated patients than in controls (17.0 vs. 42.6 pg/mL, P=0.004). s-VEGF levels were fairly correlated with WBC count (r=-0.56, P=0.004) and LDH (r=-0.52, P=0.02) at diagnosis. All patients but one were in morphologic remission at the end of induction. Median s-VEGF concentration on day 29/33 was significantly higher than on day 1 (44.2 pg/mL, P=0.009). Conclusion: Untreated children with ALL have significantly lower s-VEGF concentration than controls. At the end of the induction therapy, s-VEGF increased to levels similar to controls. The role of ligand-receptor interaction between VEGF and VEGF receptors on leukemia cells needs to be further delineated.

9.
Indian Pediatr ; 2013 March; 50(3): 345
Article Dans Anglais | IMSEAR | ID: sea-169741
10.
Indian Pediatr ; 2012 April; 49(4): 335-336
Article Dans Anglais | IMSEAR | ID: sea-169314
11.
Indian Pediatr ; 2012 March; 49(3): 250
Article Dans Anglais | IMSEAR | ID: sea-169268
12.
Indian Pediatr ; 2012 March; 49(3): 248
Article Dans Anglais | IMSEAR | ID: sea-169266
13.
Indian Pediatr ; 2011 Jan; 48(1): 79-80
Article Dans Anglais | IMSEAR | ID: sea-168761
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