Search Results - "Gomathi, Mohan" :: K.UTB vyhledávací portál

Drug Studies on Rett Syndrome: From Bench to Bedside

by Gomathi, Mohan, Padmapriya, Subramanian, Balachandar, Vellingiri
Published in Journal of autism and developmental disorders (01.08.2020)

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Recent advances in radiotherapy and its associated side effects in cancer—a review

by Mohan, Gomathi, T P, Ayisha Hamna, A J, Jijo, K M, Saradha Devi, Narayanasamy, Arul, Vellingiri, Balachandar
Published in Journal of basic & applied zoology (27.02.2019)

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The intronic variant of SATB2 gene observed in an Indian Glass syndrome family

by Murugasamy, Pradeepkumar, Mohan, Gomathi, Kaviya Mohandass
Published in Neurology Asia (01.03.2024)

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Highlighting novel genes associated with the classical Rett syndrome patient from India

by Mohan, Gomathi, Sarma, Ranjan Jyoti, Iyer, Mahalaxmi, Kumar, Nachimuthu Senthil, Vellingiri, Balachandar
Published in Genes & diseases (01.11.2022)

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Rett syndrome - a diagnostic odessey

by Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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Association of LAMC3 mutation cortical malformations in Rett syndrome – a familial case study

by Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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Screening of chromosomal instability and inheritance of Rett syndrome

by Zubair, Mohamed, Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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Biochemical profiling of Rett syndrome patients from South Indian population

by Aara, Husne, Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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Asiaticoside A, promising agent to revert Rett Syndrome – Preliminary study results

by Mohan, Gomathi, Vellingiri, Balachandar
Published in Journal of the neurological sciences (01.12.2023)

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Neuroprotective assessment of Bacopa monnieri leaves extract against oxidative-stress-induced cytotoxicity in SHSY5Y neuroblastoma cells

by Karikazi, Adilmehadi, Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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A novel missense mutation identified in a rare skeletal disorder acromesomelic dysplasia in India

by Mohandass, Kaviya, Murugasamy, Pradeepkumar, Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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A case series on citrullinemia in Indian families

by Mohandass, Kaviya, Mohan, Gomathi, Murugasamy, Pradeepkumar
Published in Journal of the neurological sciences (01.12.2023)

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A novel intronic variant causing osteogenesis imperfecta – A rare case study

by Mohandass, Kaviya, Murugasamy, Pradeepkumar, Mohan, Gomathi
Published in Journal of the neurological sciences (01.12.2023)

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A rare Seckel syndrome prenatal diagnosis and genetic counseling: A familial case series

by Mohan, Gomathi, Mohandass, Kaviya, Murugasamy, Pradeepkumar
Published in Journal of the neurological sciences (01.12.2023)

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A coalescence of two syndromes in a boy with interstitial deletion of chromosome 5P and 18Q

by Mohan, Gomathi, Mohandass, Kaviya, Murugasamy, Pradeepkumar
Published in Journal of the neurological sciences (01.12.2023)

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Etiological identification of hermansky Pudlak syndrome using whole exome sequencing

by Mohandass, Kaviya, Mohan, Gomathi, Murugasamy, Pradeepkumar
Published in Journal of the neurological sciences (01.12.2023)

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A Middle-aged Woman With Severe Scoliosis and Encephalopathy

by Mohan, Gomathi, Bharathi, Geetha, Vellingiri, Balachandar
Published in Archives of neurology (Chicago) (01.02.2021)

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3D organoid models for the study of drug permeability

by Mohan, Gomathi, Varghese Deevetha Varghese, Anu, Gokul, Kalaivanan
Published in Journal of the neurological sciences (01.12.2023)

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Sleep disorders in Rett syndrome patients from Indian population

by Mohan, Gomathi, Thanyalakshmi, Balasriabiram Venu Gopal, Varatharaju, Gayathri, Raju, Mathavan
Published in Journal of the neurological sciences (01.12.2023)

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Novel therapeutic approaches: Rett syndrome and human induced pluripotent stem cell technology

by Gomathi, Mohan, Balachandar, Vellingiri
Published in Stem cell investigation (2017)

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