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Akella, Radha Rama Devi
31
results:
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Online (31)
Mediatypes
Articles (Online) (27)
OpenAccess-fulltext (4)
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1
Molecular insights into the role of genetic determinants of..:
Kollati, Yedukondalu
;
Akella, Radha Rama Devi
;
Naushad, Shaik Mohammad
...
Genomics & Informatics. 19 (2021) 3 - p. e29 , 2021
Link:
https://doi.org/10.5808/..
?
2
Mitochondrial carbonic anhydrase VA deficiency in three Ind..:
Konanki, Ramesh
;
Akella, Radha Rama Devi
;
Panigrahy, Nalinikanta
...
Brain and Development. 42 (2020) 7 - p. 534-538 , 2020
Link:
https://doi.org/10.1016/..
?
3
The rs1991517 polymorphism is a genetic risk factor for con..:
Kollati, Yedukondalu
;
Akella, Radha Rama Devi
;
Naushad, Shaik Mohammad
...
3 Biotech. 10 (2020) 6 - p. , 2020
Link:
https://doi.org/10.1007/..
?
4
Newborn screening and single nucleotide variation profiling..:
Kollati, Yedukondalu
;
Akella, Radha Rama Devi
;
Naushad, Shaik Mohammad
...
Molecular Biology Reports. 47 (2020) 10 - p. 7467-7475 , 2020
Link:
https://doi.org/10.1007/..
?
5
Amniotic fluid glycosaminoglycans in the prenatal diagnosis..:
Akella, Radha Rama Devi
;
Kadali, Srilatha
Clinica Chimica Acta. 460 (2016) - p. 63-66 , 2016
Link:
https://doi.org/10.1016/..
?
6
Metabolic encephalopathy in beta-ketothiolase deficiency: T..:
Akella, Radha Rama Devi
;
Aoyama, Yuka
;
Mori, Chihiro
...
Brain and Development. 36 (2014) 6 - p. 537-540 , 2014
Link:
https://doi.org/10.1016/..
?
7
Neonatal Screening for Inborn Errors of Metabolism Using Ta..:
Sahai, Inderneel
;
Zytkowicz, Thomas
;
Rao Kotthuri, Srimannarayna
...
The Indian Journal of Pediatrics. 78 (2011) 8 - p. 953-960 , 2011
Link:
https://doi.org/10.1007/..
?
8
Cerebral creatine deficiency disorders – A clinical, geneti..:
Passi, Gouri Rao
;
Pandey, Swati
;
Devi, Akella Radha Rama
...
Brain and Development. 44 (2022) 4 - p. 271-280 , 2022
Link:
https://doi.org/10.1016/..
?
9
Expanding the Nude SCID/CID Phenotype Associated with FOXN1..:
Giardino, Giuliana
;
Sharapova, Svetlana O.
;
Ciznar, Peter
...
Journal of Clinical Immunology. 41 (2021) 4 - p. 756-768 , 2021
Link:
https://doi.org/10.1007/..
?
10
A rare case of fatty acyl‐CoA reductase 1 deficiency in an ..:
Radha Rama Devi, Akella
;
Naushad, Shaik Mohammad
;
Jain, Romit
.
Clinical Genetics. 99 (2021) 5 - p. 744-745 , 2021
Link:
https://doi.org/10.1111/..
?
11
Clinical and Molecular Diagnosis of Joubert Syndrome and Re..:
Radha Rama Devi, Akella
;
Naushad, Shaik Mohammad
;
Lingappa, Lokesh
Pediatric Neurology. 106 (2020) - p. 43-49 , 2020
Link:
https://doi.org/10.1016/..
?
12
Fabry disease in India: A multicenter study of the clinical..:
Nampoothiri, Sheela
;
Yesodharan, Dhanya
;
Bhattacherjee, Amrita
...
JIMD Reports. 56 (2020) 1 - p. 82-94 , 2020
Link:
https://doi.org/10.1002/..
?
13
Molecular diagnosis of asparagine synthetase (ASNS) deficie..:
Radha Rama Devi, Akella
;
Naushad, Shaik Mohammad
Gene. 704 (2019) - p. 97-102 , 2019
Link:
https://doi.org/10.1016/..
?
14
In silico analysis of the structural and functional implica..:
Naushad, Shaik Mohammad
;
Devi, Akella Radha Rama
;
Hussain, Tajamul
...
Journal of Genetics. 98 (2019) 3 - p. , 2019
Link:
https://doi.org/10.1007/..
?
15
Biochemical, machine learning and molecular approaches for ..:
Kadali, Srilatha
;
Naushad, Shaik Mohammad
;
Radha Rama Devi, Akella
.
Molecular and Cellular Biochemistry. 458 (2019) 1-2 - p. 27-37 , 2019
Link:
https://doi.org/10.1007/..
1-15