E-LIB Suche - Ergebnisse für: Anjanappa, Ram M.

1

Disease Progression and Mutation Pattern in a Large Cohort ..:

Polavarapu, Kiran ; Ganaraja, Valakunja H. ; Bardhan, Mainak...
Global Medical Genetics. 9 (2021) 1 - p. 034-041 , 2021

Link: https://doi.org/10.1055/..

2

A linkage and exome study implicates rare variants of KANK4..:

Anjanappa, Ram M. ; Nayak, Sourav ; Moily, Nagaraj S....
Bipolar Disorders. 22 (2019) 1 - p. 70-78 , 2019

Link: https://doi.org/10.1111/..

3

Disease Progression and Mutation Pattern in a Large Cohort ..:

Valakunja H. Ganaraja ; Kiran Polavarapu ; Mainak Bardhan...
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0041-1736567. , 2022

Link: https://doi.org/10.1055/..

4

Design and performance of a 24‐station high throughput micr..:

Harms, Peter ; Kostov, Yordan ; French, Joseph A....
Biotechnology and Bioengineering. 93 (2005) 1 - p. 6-13 , 2005

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

5

A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype ..:

Nishadham, Vikas ; Santhoshkumar, Rashmi ; Nashi, Saraswati...
Journal of Neuromuscular Diseases. 11 (2024) 1 - p. 221-232 , 2024

Link: https://doi.org/10.3233/..

6

Clinical and genetic characterisation of a large Indian con..:

Polavarapu, Kiran ; Sunitha, Balaraju ; Töpf, Ana...
Brain. 147 (2023) 1 - p. 281-296 , 2023

Link: https://doi.org/10.1093/..

7

Rare forms of genetically mediated familial and sporadic am..:

Cheriyan, Anoop ; Nashi, Saraswati ; Vengalil, Seena...
Journal of the Neurological Sciences. 455 (2023) - p. 121708 , 2023

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

8

Large Region of Homozygous (ROH) Identified in Indian Patie..:

Manjunath, V. ; Thenral, S. G. ; Lakshmi, B. R....
Human Mutation. 2023 (2023) - p. 1-10 , 2023

Link: https://doi.org/10.1155/..

9

Clinical, genetic profile and disease progression of sarcog..:

Bardhan, Mainak ; Anjanappa, Ram Murthy ; Polavarapu, Kiran...
neurogenetics. 23 (2022) 3 - p. 187-202 , 2022

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

10

Genotype–phenotype correlation and natural history study of..:

Nashi, ‬Saraswati ; Polavarapu, Kiran ; Bardhan, Mainak...
neurogenetics. 24 (2022) 1 - p. 43-53 , 2022

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

11

Correction: Megaconial congenital muscular dystrophy second..:

Bardhan, Mainak ; Polavarapu, Kiran ; Bevinahalli, Nandeesh N....
Journal of Human Genetics. 66 (2021) 8 - p. 841-841 , 2021

Link: https://doi.org/10.1038/..

12

Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Muta..:

Polavarapu, Kiran ; Bardhan, Mainak ; Anjanappa, Ram Murthy...
Journal of Clinical Neurology. 17 (2021) 3 - p. 409 , 2021

Link: https://doi.org/10.3988/..

13

Megaconial congenital muscular dystrophy secondary to novel..:

Bardhan, Mainak ; Polavarapu, Kiran ; Bevinahalli, Nandeesh N....
Journal of Human Genetics. 66 (2021) 8 - p. 813-823 , 2021

Link: https://doi.org/10.1038/..

14

Trinucleotide repeats and haplotypes at the Huntingtin locu..:

Moily, Nagaraj S ; Kota, Lakshmi Narayanan ; Anjanappa, Ram Murthy...
PLoS Currents. , 2014

Link: https://doi.org/10.1371/..

15

Impact of COVID-19 on Management of MIBC: a Quantitative an..:

Kombathula, S.H. ; Anjanappa, M. ; Song, Y.P....
Clinical Oncology. 35 (2023) 2 - p. e240 , 2023

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