Recent advances in radiotherapy and its associated side effects in cancer—a review von Mohan, Gomathi, T P, Ayisha Hamna, A J, Jijo, K M, Saradha Devi, Narayanasamy, Arul, Vellingiri, Balachandar

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Goldberg–Shprintzen syndrome—A rare case from India von Pradeepkumar, Murugasamy, Kaviya, Mohandass, Gomathi, Mohan

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The intronic variant of SATB2 gene observed in an Indian Glass syndrome family von Murugasamy, Pradeepkumar, Mohan, Gomathi, Kaviya Mohandass

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Drug Studies on Rett Syndrome: From Bench to Bedside von Gomathi, Mohan, Padmapriya, Subramanian, Balachandar, Vellingiri

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Rett syndrome - a diagnostic odessey von Mohan, Gomathi

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Association of LAMC3 mutation cortical malformations in Rett syndrome – a familial case study von Mohan, Gomathi

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Highlighting novel genes associated with the classical Rett syndrome patient from India von Mohan, Gomathi, Sarma, Ranjan Jyoti, Iyer, Mahalaxmi, Kumar, Nachimuthu Senthil, Vellingiri, Balachandar

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Screening of chromosomal instability and inheritance of Rett syndrome von Zubair, Mohamed, Mohan, Gomathi

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Biochemical profiling of Rett syndrome patients from South Indian population von Aara, Husne, Mohan, Gomathi

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Neuroprotective assessment of Bacopa monnieri leaves extract against oxidative-stress-induced cytotoxicity in SHSY5Y neuroblastoma cells von Karikazi, Adilmehadi, Mohan, Gomathi

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Asiaticoside A, promising agent to revert Rett Syndrome – Preliminary study results von Mohan, Gomathi, Vellingiri, Balachandar

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A case series on citrullinemia in Indian families von Mohandass, Kaviya, Mohan, Gomathi, Murugasamy, Pradeepkumar

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A coalescence of two syndromes in a boy with interstitial deletion of chromosome 5P and 18Q von Mohan, Gomathi, Mohandass, Kaviya, Murugasamy, Pradeepkumar

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A novel intronic variant causing osteogenesis imperfecta – A rare case study von Mohandass, Kaviya, Murugasamy, Pradeepkumar, Mohan, Gomathi

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A rare Seckel syndrome prenatal diagnosis and genetic counseling: A familial case series von Mohan, Gomathi, Mohandass, Kaviya, Murugasamy, Pradeepkumar

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Etiological identification of hermansky Pudlak syndrome using whole exome sequencing von Mohandass, Kaviya, Mohan, Gomathi, Murugasamy, Pradeepkumar

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A novel missense mutation identified in a rare skeletal disorder acromesomelic dysplasia in India von Mohandass, Kaviya, Murugasamy, Pradeepkumar, Mohan, Gomathi

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A Middle-aged Woman With Severe Scoliosis and Encephalopathy von Mohan, Gomathi, Bharathi, Geetha, Vellingiri, Balachandar

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Sleep disorders in Rett syndrome patients from Indian population von Mohan, Gomathi, Thanyalakshmi, Balasriabiram Venu Gopal, Varatharaju, Gayathri, Raju, Mathavan

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3D organoid models for the study of drug permeability von Mohan, Gomathi, Varghese Deevetha Varghese, Anu, Gokul, Kalaivanan

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