Suchergebnisse - "Srinivasan, Varunvenkat M"

PubPharm (128)

61

Neuronal Ceroid Lipofuscinosis : Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India

enthalten in: Journal of pediatric genetics | 2021

von Gowda, V. | Vegda, H. | Sugumar, K. | +6

62

Childhood Myocerebrohepatopathy Spectrum Disorder due to Polymerase Gamma Pathogenic Variant

enthalten in: Annals of Indian Academy of Neurology | 2021

von Gowda, V. | Srinivasan, V. | Shivappa, S.

63

Homocystinuria Due to MTHFR Variant Presenting As Infantile Tremor Syndrome

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Srinivasan, V. | Shivappa, S.

64

A Treatable Cause of Global Developmental Delay with Epileptic Spasm and Delayed Myelination Due to Cobalamin-Related Remethylation Disorder

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Srinivasan, V. | Reddy, V. | +2

65

Infantile Tremor Syndrome Presenting as Stroke

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Umesh, N. | Srinivasan, V. | +1

66

Infantile Tremor Syndrome Presenting as Stroke

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Umesh, N. | Srinivasan, V. | +1

67

Infantile Tremor Syndrome Presenting as Stroke

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Umesh, N. | Srinivasan, V. | +1

68

Treatable Neurodegenerative Disorder : Cerebral Folate Transport Deficiency--Two Children from Southern India

enthalten in: Journal of pediatric neurosciences | 2021

von Gowda, V. | Natarajan, B. | Srinivasan, V. | +1

69

Krabbe Disease with Normal Enzyme Assay with a Pathogenic Variant in GALC Gene-A Report of Two Indian Cases

enthalten in: Annals of Indian Academy of Neurology | 2021

von Gowda, V. | Srinivasan, V. | Bhat, M. | +1

70

Homocystinuria Due to MTHFR Variant Presenting As Infantile Tremor Syndrome

enthalten in: Indian journal of pediatrics | 2021

von Gowda, V. | Srinivasan, V. | Shivappa, S.