E-LIB Suche - Ergebnisse für: Ramprasad, Vedam L

1

Comprehensive germline profiling of patients with breast ca..:

Pramanik, Raja ; Chitikela, Sindhura ; Deo, SVS...
ecancermedicalscience. 18 (2024) - p. , 2024

Link: https://doi.org/10.3332/..

2

Identification of a shared, common haplotype segregating wi..:

Sanga, Shamita ; Chakraborty, Sudipta ; Bardhan, Mainak...
Scientific Reports. 13 (2023) 1 - p. , 2023

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

3

Comprehensive laboratory diagnosis of Fanconi anaemia: comp..:

Joshi, Gaurav ; Arthur, Nancy Beryl Janet ; Geetha, Thenral S...
Journal of Medical Genetics. 60 (2023) 8 - p. 801-809 , 2023

Link: https://doi.org/10.1136/..

4

Molecular epidemiology of SARS-CoV-2 in healthcare workers ..:

Bhattacharya, Sanjay ; Chatterji, Soumyadip ; Chandy, Mammen...
Indian Journal of Medical Microbiology. 41 (2023) - p. 104-110 , 2023

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

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

Oculogyric Crisis Phenotype of Levodopa‐Induced Ocular Dysk..:

Olszewska, Diana A. ; Shetty, Rajesh ; Geetha, Thenral S....
Movement Disorders Clinical Practice. 9 (2022) 3 - p. 390-393 , 2022

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

7

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/..

8

Genome‐Wide Polygenic Score Predicts Large Number of High R..:

Kukkle, Prashanth Lingappa ; Geetha, Thenral S. ; Chaudhary, Ruchi...
Advanced Biology. 6 (2022) 11 - p. , 2022

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

9

Clinical Study of 668 Indian Subjects with Juvenile, Young,..:

Kukkle, Prashanth L. ; Goyal, Vinay ; Geetha, Thenral S....
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49 (2021) 1 - p. 93-101 , 2021

Link: https://doi.org/10.1017/..

10

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/..

11

Growth and neurodevelopmental disorder with arthrogryposis,..:

Bijarnia-Mahay, Sunita ; Somashekar, Puneeth H. ; Kaur, Parneet...
Journal of Human Genetics. 67 (2021) 3 - p. 133-136 , 2021

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

12

Matrilineal analysis of mutations in the DMD gene in a mult..:

Shastry, Arun ; Aravind, Sankaramoorthy ; Sunil, Meeta...
Molecular Genetics & Genomic Medicine. 9 (2021) 5 - p. , 2021

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

13

Retinoblastoma genetics screening and clinical management:

Gupta, Himika ; Malaichamy, Sivasankar ; Mallipatna, Ashwin...
BMC Medical Genomics. 14 (2021) 1 - p. , 2021

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

14

Reply to: Fatal Familial Insomnia: A Rare Disease with Uniq..:

Kukkle, Prashanth L. ; Geetha, Thenral S. ; Mahadevan, Anita.
Movement Disorders Clinical Practice. 8 (2020) 1 - p. 164-165 , 2020

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

15

A Case of Autosomal Dominant Ataxia with Vocal Cord Palsy A..:

Kukkle, Prashanth L. ; Geetha, Thenral S. ; Mahadevan, Anita.
Movement Disorders Clinical Practice. 7 (2020) 6 - p. 688-692 , 2020

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