E-LIB Suche - Ergebnisse für: Bellad, Anikha

1

Identification of a rare [Gγ(Aγδβ)0] ‐thalassemia using tan..:

Bellad, Anikha ; Rangiah, Kannan ; Sathe, Gajanan...
PROTEOMICS. , 2024

Link: https://doi.org/10.1002/..

2

Loss of function variants in L2HGDH gene causing l-2-hydrox..:

Bellad, Anikha ; Holla, Vikram V. ; Kumari, Riyanka...
Acta Neurologica Belgica. 123 (2023) 6 - p. 2315-2323 , 2023

Link: https://doi.org/10.1007/..

3

PLA2G6-associated neurodegeneration in four different popul..:

Hanna Al-Shaikh, Rana ; Milanowski, Lukasz M. ; Holla, Vikram V....
Parkinsonism & Related Disorders. 101 (2022) - p. 66-74 , 2022

Link: https://doi.org/10.1016/..

4

Shukla-Vernon Syndrome: A Second Family with a Novel Varian..:

Muthusamy, Babylakshmi ; Bellad, Anikha ; Girimaji, Satish Chandra.
Genes. 12 (2021) 3 - p. 452 , 2021

Link: https://doi.org/10.3390/..

5

Applications of quantitative metabolomics to revolutionize ..:

Chandran, Jisha ; Bellad, Anikha ; Ramarajan, Madan Gopal.
Analytical Science Advances. 2 (2021) 11-12 - p. 546-563 , 2021

Link: https://doi.org/10.1002/..

6

A novel loss of function mutation in adaptor protein comple..:

Bellad, Anikha ; Girimaji, Satish Chandra ; Muthusamy, Babylakshmi
Neurological Sciences. 42 (2021) 12 - p. 5311-5319 , 2021

Link: https://doi.org/10.1007/..

7

A Novel LINS1 Truncating Mutation in Autosomal Recessive No..:

Muthusamy, Babylakshmi ; Bellad, Anikha ; Prasad, Pramada...
Frontiers in Psychiatry. 11 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

8

A Novel Missense Variant in PHF6 Gene Causing Börjeson-Fors..:

Bellad, Anikha ; Bandari, Aravind K. ; Pandey, Akhilesh..
Journal of Molecular Neuroscience. 70 (2020) 9 - p. 1403-1409 , 2020

Link: https://doi.org/10.1007/..

9

KIAA1109 gene mutation in surviving patients with Alkuraya-..:

Kumar, Kishore ; Bellad, Anikha ; Prasad, Pramada..
BMC Medical Genetics. 21 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

10

Shukla-Vernon Syndrome: A Second Family with a Novel Varian..:

Muthusamy, Babylakshmi ; Bellad, Anikha ; Girimaji, Satish Chandra.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8005212/. , 2021

Link: http://www.ncbi.nlm.nih...

11

A Novel LINS1 Truncating Mutation in Autosomal Recessive No..:

Muthusamy, Babylakshmi ; Bellad, Anikha ; Prasad, Pramada...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247441/. , 2020

Link: http://www.ncbi.nlm.nih...

12

KIAA1109 gene mutation in surviving patients with Alkuraya-..:

Kumar, Kishore ; Bellad, Anikha ; Prasad, Pramada..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318400/. , 2020

Link: http://www.ncbi.nlm.nih...

13

Shukla-Vernon Syndrome: A Second Family with a Novel Varian..:

Babylakshmi Muthusamy ; Anikha Bellad ; Satish Chandra Girimaji.
Molecular Genetics and Genomics. , 2021

Link: https://doi.org/10.3390/..

14

Shukla-Vernon Syndrome: A Second Family with a Novel Varian..:

Babylakshmi Muthusamy ; Anikha Bellad ; Satish Chandra Girimaji.
https://www.mdpi.com/2073-4425/12/3/452. , 2021

Link: https://doi.org/10.3390/..

15

A Novel LINS1 Truncating Mutation in Autosomal Recessive No..:

Babylakshmi Muthusamy ; Anikha Bellad ; Pramada Prasad...
https://www.frontiersin.org/article/10.3389/fpsyt.2020.00354/full. , 2020

Link: https://doi.org/10.3389/..