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Sunitha, Balaraju
25
results:
Search for persons
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Format
Online (25)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (17)
Sorted by: Relevance
Sorted by: Year
?
1
Unique genotypic pattern in Indian DPAGT1 congenital myasth..:
Polavarapu, Kiran
;
Sunitha, Balaraju
;
Töpf, Ana
...
Journal of the Neurological Sciences. 455 (2023) - p. 122042 , 2023
Link:
https://doi.org/10.1016/..
?
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
Muscle biopsies from human muscle diseases with myopathic p..:
Sunitha, Balaraju
;
Gayathri, Narayanappa
;
Kumar, Manish
...
Journal of Neurochemistry. 138 (2016) 1 - p. 174-191 , 2016
Link:
https://doi.org/10.1111/..
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4
Mitochondrial Alterations and Oxidative Stress in an Acute ..:
Ramadasan-Nair, Renjini
;
Gayathri, Narayanappa
;
Mishra, Sudha
...
Journal of Biological Chemistry. 289 (2014) 1 - p. 485-509 , 2014
Link:
https://doi.org/10.1074/..
?
5
Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dy..:
Francis, Amirtharaj
;
Sunitha, Balaraju
;
Vinodh, Kandavalli
...
PLoS ONE. 9 (2014) 7 - p. e102763 , 2014
Link:
https://doi.org/10.1371/..
?
6
Autosomal recessive variants in TUBGCP2 alter the γ-tubulin..:
Gungor, Serdal
;
Oktay, Yavuz
;
Hiz, Semra
...
iScience. 24 (2021) 1 - p. 101948 , 2021
Link:
https://doi.org/10.1016/..
?
7
Congenital myasthenic syndrome with mild intellectual disab..:
Balaraju, Sunitha
;
Töpf, Ana
;
McMacken, Grace
...
European Journal of Human Genetics. 28 (2019) 3 - p. 373-377 , 2019
Link:
https://doi.org/10.1038/..
?
8
Severe neurodevelopmental disease caused by a homozygous TL..:
Töpf, Ana
;
Oktay, Yavuz
;
Balaraju, Sunitha
...
European Journal of Human Genetics. 28 (2019) 3 - p. 383-387 , 2019
Link:
https://doi.org/10.1038/..
?
9
Autosomal recessive variants in TUBGCP2 alter the γ-tubulin..:
Serdal Gungor
;
Yavuz Oktay
;
Semra Hiz
...
http://www.sciencedirect.com/science/article/pii/S2589004220311457. , 2021
Link:
https://doi.org/10.1016/..
?
10
Mitochondrial Alterations and Oxidative Stress in an Acute ..:
Ramadasan-Nair, Renjini
;
Gayathri, Narayanappa
;
Mishra, Sudha
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC. , 2014
Link:
http://www.ncbi.nlm.nih...
?
11
Autosomal recessive variants in TUBGCP2 alter the gamma-tub..:
Gungor, Serdal
;
Oktay, Yavuz
;
Hiz, Semra
...
https://aperta.ulakbim.gov.tr/record/233492. , 2021
Link:
https://aperta.ulakbim.g..
?
12
Autosomal recessive variants in TUBGCP2 alter the γ-tubulin..:
Gungor, Serdal
;
Oktay, Yavuz
;
Hiz, Semra
...
https://www.repository.cam.ac.uk/handle/1810/317426. , 2021
Link:
https://www.repository.c..
?
13
Congenital myasthenic syndrome with mild intellectual disab..:
Balaraju, Sunitha
;
Töpf, Ana
;
McMacken, Grace M
...
https://freidok.uni-freiburg.de/data/155183. , 2020
Link:
https://freidok.uni-frei..
?
14
Congenital myasthenic syndrome with mild intellectual disab..:
Balaraju, Sunitha
;
Töpf, Ana
;
McMacken, Grace
...
https://www.repository.cam.ac.uk/handle/1810/297858. , 2020
Link:
https://www.repository.c..
?
15
Severe neurodevelopmental disease caused by a homozygous TL..:
Töpf, Ana
;
Oktay, Yavuz
;
Balaraju, Sunitha
...
https://freidok.uni-freiburg.de/data/155324. , 2020
Link:
https://freidok.uni-frei..
1-15
