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P B Agrawal

Showing results (1-10 of 6) with videos related to

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Indian Journal of Pediatrics|November 1, 1996
FluconazoleP B Agrawal, A Narang, P Kumar
Journal of the Indian Medical Association|July 1, 1995
Host factors and pneumonia in hospitalised childrenP B Agrawal, N Shendurnikar, N J Shastri
Journal of Tropical Pediatrics|May 30, 1998
Epidemiology of systemic candidiasis in a tertiary care neonatal unitA Narang, P B Agrawal, A Chakrabarti, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|April 30, 2014
NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblingsK T Leeman, L Dobson, M Towne, et al.
Journal of Neonatal-Perinatal Medicine|May 2, 2026
Relationship between placental oxygen transport, fetal birth weight, and umbilical cord transcriptome in monochorionic twinsS S Ali, Q Li, E A Turk, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Indian Journal of Pediatrics|November 1, 1996
FluconazoleP B Agrawal, A Narang, P Kumar
Journal of the Indian Medical Association|July 1, 1995
Host factors and pneumonia in hospitalised childrenP B Agrawal, N Shendurnikar, N J Shastri
Journal of Tropical Pediatrics|May 30, 1998
Epidemiology of systemic candidiasis in a tertiary care neonatal unitA Narang, P B Agrawal, A Chakrabarti, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|April 30, 2014
NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblingsK T Leeman, L Dobson, M Towne, et al.
Journal of Neonatal-Perinatal Medicine|May 2, 2026
Relationship between placental oxygen transport, fetal birth weight, and umbilical cord transcriptome in monochorionic twinsS S Ali, Q Li, E A Turk, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
Pageof 1