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Radha Rama Devi, Akella
37  Ergebnisse:
Personensuche X
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1

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/..
 
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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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

SLC25A13 c.1610_1612delinsAT mutation in an Indian patient ..:

Radha Rama Devi, Akella ; Naushad, Shaik Mohammad
Gene.  668 (2018)  - p. 190-195 , 2018
Link: https://doi.org/10.1016/..
 
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8

Neuro-fuzzy model of homocysteine metabolism:

Naushad, Shaik Mohammad ; Radha Rama Devi, Akella ; Nivetha, Sriraman...
Journal of Genetics.  96 (2017)  6 - p. 919-926 , 2017
Link: https://doi.org/10.1007/..
 
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9

FOXN1 Italian founder mutation in Indian family: Implicatio..:

Radha Rama Devi, Akella ; Panday, Nagesh Narayan ; Naushad, Shaik Mohammad
Gene.  627 (2017)  - p. 222-225 , 2017
Link: https://doi.org/10.1016/..
 
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10

Application of adaptive neuro-fuzzy inference systems (ANFI..:

Mohan, Iyyapu Krishna ; Khan, Siraj Ahmed ; Jacob, Rachel...
Clinical Nutrition ESPEN.  20 (2017)  - p. 41-46 , 2017
Link: https://doi.org/10.1016/..
 
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11

Association of parental hyperhomocysteinemia and C677T Meth..:

Govindaiah, Vinukonda ; Naushad, Shaik Mohammad ; Prabhakara, Krishnamurthy..
Clinical Biochemistry.  42 (2009)  4-5 - p. 380-386 , 2009
Link: https://doi.org/10.1016/..
 
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12

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/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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