A. Radha Rama Devi

发表

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders

T. Hussain, S. Alrokayan, C. Krishna Prasad, 2016, Psychiatric genetics.

1q42.12q42.2 Deletion in a Child with Midline Defects and Hypoplasia of the Corpus Callosum

S. Naushad, A. Mannan, A. Radha Rama Devi, 2019, Molecular Syndromology.

Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders.

L. Lingappa, S. Naushad, A. Radha Rama Devi, 2020, Pediatric neurology.

Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patients

M. Kabra, S. Phadke, K. Mandal, 2020, JIMD reports.

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

F. Benfenati, A. E. Sousa, G. Giardino, 2021, Journal of Clinical Immunology.

FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis.

S. Naushad, A. Radha Rama Devi, Nagesh Narayan Panday, 2017, Gene.

Biochemical, machine learning and molecular approaches for the differential diagnosis of Mucopolysaccharidoses

S. Naushad, A. Radha Rama Devi, V. Bodiga, 2019, Molecular and Cellular Biochemistry.

Association of parental hyperhomocysteinemia and C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss.

S. Naushad, A. Radha Rama Devi, K. Prabhakara, 2009, Clinical biochemistry.

A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype

L. Lingappa, S. Naushad, A. Radha Rama Devi, 2020, Clinical Genetics.

Challenges and Opportunities in Establishing and Maintaining Newborn Screening in a Rural Area of Andhra Pradesh – Task Force Study by Indian Council of Medical Research

A. Radha Rama Devi, Y. Ananthalakshmi, K. Srimannarayana Rao, 2018, The Indian Journal of Pediatrics.

Acute Gaucher Disease-Like Condition in an Indian Infant with a Novel Biallelic Mutation in the Prosaposin Gene

Vineeta Singh, S. Naushad, A. Radha Rama Devi, 2018, Journal of Pediatric Genetics.

Biochemical, machine learning and molecular approaches for the differential diagnosis of Mucopolysaccharidoses

S. Naushad, A. Radha Rama Devi, V. Bodiga, 2019, Molecular and Cellular Biochemistry.

Identification of Two Novel Mutations in Aminomethyltransferase Gene in Cases of Glycine Encephalopathy

L. Lingappa, S. Naushad, A. Radha Rama Devi, 2018, Journal of Pediatric Genetics.

Molecular diagnosis of asparagine synthetase (ASNS) deficiency in two Indian families and literature review of 29 ASNS deficient cases.

S. Naushad, A. Radha Rama Devi, 2019, Gene.

Novel mutations in SERAC1 gene in two Indian patients presenting with dystonia and intellectual disability.

L. Lingappa, A. Radha Rama Devi, 2017, European journal of medical genetics.

Application of adaptive neuro-fuzzy inference systems (ANFIS) to delineate estradiol, glutathione and homocysteine interactions.

S. Naushad, T. Hussain, S. Alrokayan, 2017, Clinical nutrition ESPEN.

Neuro-fuzzy model of homocysteine metabolism

V. Kutala, S. Naushad, T. Hussain, 2017, Journal of Genetics.

SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations.

S. Naushad, A. Radha Rama Devi, 2018, Gene.