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1دورية أكاديمية
المؤلفون: Babu, Aishwarya, Jayan, Achanya S., Sethumadhavan, Anjali, Mandagini, Geetha, Raghavan, Cibin T.Aff1, Aff2, Gopala, SrinivasAff1, Aff2, Krishnan, SyamAff3, IDs12291024012348_cor7, Urulangodi, MadhusoodananAff1, Aff2, IDs12291024012348_cor8
المصدر: Indian Journal of Clinical Biochemistry. :1-10
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2دورية أكاديمية
المؤلفون: Chandran, Deepthy, Krishnan, Syam, Urulangodi, MadhusoodananAff1, IDs10072024074392_cor3, Gopala, SrinivasAff1, IDs10072024074392_cor4
المصدر: Neurological Sciences. 45(8):3625-3639
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3دورية أكاديمية
المؤلفون: Babu, Aishwarya, Urulangodi, MadhusoodananAff1, IDs42764023001108_cor2
المصدر: Genome Instability & Disease. 4(6):315-332
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4دورية أكاديمية
المؤلفون: Harikrishnan, Sivadasanpillai, Koshy, Linda, Ganapathi, Sanjay, Jeemon, Panniyammakal, Ramya Das, N.K., Urulangodi, Madhusoodanan, Madhuma, M., Vysakh, Y., Subran, Anjana, Lakshmikanth, L.R.
المصدر: In International Journal of Cardiology 15 September 2024 411
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5دورية أكاديمية
المؤلفون: Vasu, Mahesh Mundalil, Koshy, Linda, Ganapathi, Sanjay, Jeemon, Panniyammakal, Urulangodi, Madhusoodanan, Gopala, Srinivas, Greeva, Philip, Anitha, Ayyappan, Reethu, Salim, Divya, Prasad, Shamla, Shajahan, Sumitha, Kumar, Madhavan, Madhuma, Vineeth, C. Purushothaman, Kochumoni, Rajamoni, Harikrishnan, Sivadasanpillai
المصدر: In International Journal of Biological Macromolecules March 2024 261 Part 2
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6دورية أكاديمية
المؤلفون: Kishore, AshaAff1, Aff2, Sturm, Marc, Soman Pillai, Kanchana, Hakkaart, Christopher, Kalikavil Puthanveedu, Divya, Urulangodi, Madhusoodanan, Krishnan, Syam, Ashok Kumar Sreelatha, Ashwin, Rajan, Roopa, Pal, Pramod Kumar, Yadav, Ravi, Sarma, Gangadhara, Casadei, Nicolas, Gasser, ThomasAff7, Aff8, Bauer, PeterAff3, Aff9, Aff10, Riess, Olaf, Sharma, ManuAff4, IDs41531024006764_cor17
المصدر: npj Parkinson's Disease. 10(1)
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7دورية أكاديمية
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8دورية أكاديميةC12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child
المؤلفون: Alfiya, F., Jose, Manna, Chandrasekharan, Soumya V., Sundaram, Soumya, Urulangodi, Madhusoodanan, Thomas, Bejoy, Radhakrishnan, Ashalatha, Banerjee, Moinak, Menon, Ramshekhar N.Aff1, IDs12041022013710_cor9
المصدر: Journal of Genetics: Published by the Indian Academy of Sciences. 101(2)
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9دورية أكاديمية
المؤلفون: Rudrabhatla, Pavan Kumar, Divya, K. P., Fasaludeen, Alfiya, Menon, Ramshekhar N., Cherian, Ajith, Urulangodi, Madhusoodanan, Sundaram, Soumya
المصدر: Clinical Pediatrics; Jul2024, Vol. 63 Issue 7, p885-888, 4p
مصطلحات موضوعية: NEUROLOGICAL disorders -- Genetic aspects, CRYING, PHYSICAL diagnosis, NEUROLOGIC examination, PIPERIDINE, RARE diseases, APNEA, ELECTROENCEPHALOGRAPHY, NEUROLOGICAL disorders, GENETIC variation, STARTLE reaction, GENETIC mutation, MUSCARINIC antagonists, CLONAZEPAM, CYANOSIS, SEQUENCE analysis
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10دورية أكاديمية
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