E-LIB Suche - Ergebnisse für: Anjanappa, Ram Murthy

1

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/..

2

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/..

3

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/..

4

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/..

5

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/..

6

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/..

7

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/..

8

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/..

9

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/..

10

Phenotype genotype characterization of FKRP mutations in an..:

Unnikrishnan, Gopikrishnan ; Bardhan, Mainak ; Huddar, Akshata...
Journal of the Neurological Sciences. 429 (2021) - p. 119768 , 2021

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

11

Clinical and mutational spectrum of sarcoglycanopathies in ..:

Bardhan, Mainak ; Murthy Anjanappa, Ram ; Polavarapu, Kiran...
Journal of the Neurological Sciences. 429 (2021) - p. 119767 , 2021

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

12

Mutational spectrum of dysferlinopathies in a large Indian ..:

Nashi, Saraswati ; Polavarapu, Kiran ; Murthy Anjanappa, Ram...
Journal of the Neurological Sciences. 429 (2021) - p. 119764 , 2021

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

13

Gender-specific association of TSNAX/DISC1 locus for schizo..:

Ram Murthy, Anjanappa ; Purushottam, Meera ; Kiran Kumar, Halagur Bhoge Gowda...
Journal of Human Genetics. 57 (2012) 8 - p. 523-530 , 2012

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

14

Clinical, Biochemical, Radiological, and Genetic Profile of..:

Padmanabha, Hansashree ; Mahale, Rohan ; Christopher, Rita...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965914/. , 2021

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

15

Trinucleotide Repeats and Haplotypes at the Huntingtin Locu..:

Moily, Nagaraj S ; Kota, Lakshmi Narayanan ; Anjanappa, Ram Murthy...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC. , 2014

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