Suchergebnisse - "Muranjan, Mamta N"

PubPharm (18)

1

Glycogen Storage Disease Type IXb in a 3-y-old Child

enthalten in: Indian journal of pediatrics | 2024

von Jain, S. | Tullu, M. | Muranjan, M. | +1

2

Glycogen Storage Disease Type IXb in a 3-y-old Child

enthalten in: Indian journal of pediatrics | 2023

von Jain, S. | Tullu, M. | Muranjan, M. | +1

3

Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities

enthalten in: Clinical genetics | 2021

von Kaur, P. | do Rosario, M. | Hebbar, M. | +29

4

Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities

enthalten in: Clinical Genetics | 2021

von Kaur, P. | Rosario, M. | Hebbar, M. | +29

5

Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI

enthalten in: The Indian journal of medical research | 2015

von Uttarilli, A. | Ranganath, P. | Jain, S. | +10

6

Neonatal diabetes mellitus due to a novel ABCC8 gene mutation mimicking an organic acidemia

enthalten in: Indian journal of pediatrics | 2014

von Thakkar, A. | Muranjan, M. | Karande, S. | +1

7

Are Indian parents of children with Down syndrome engaged in the blame game?

enthalten in: Indian journal of pediatrics | 2013

von Muranjan, M. | Budyal, S. | Shah, H.

8

Neonatal Diabetes Mellitus Due to a Novel ABCC8 Gene Mutation Mimicking an Organic Acidemia

enthalten in: Indian journal of pediatrics | 2013

von Thakkar, A. | Muranjan, M. | Karande, S. | +1

9

Are Indian Parents of Children with Down Syndrome Engaged in the Blame Game?

enthalten in: Indian journal of pediatrics | 2012

von Muranjan, M. | Budyal, S. | Shah, H.

10

Left ventricular failure due to a rare variant of congenital adrenal hyperplasia

enthalten in: Indian journal of pediatrics | 2012

von Bhatia, S. | Muranjan, M. | Lahiri, K.