Suchergebnisse - "Mandal, Kausik"

PubPharm (4)

1

Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene

enthalten in: Pediatric nephrology | 2023

von Deepthi, B. | Sivakumar, R. | Krishnasamy, S. | +3

2

Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience

enthalten in: Pediatric nephrology | 2023

von Krishnasamy, S. | Deepthi, B. | Kamath, N. | +10

3

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13

4

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13

1
[1]