Koshy B - Search Results

1

Morphometric analysis of Corpus Callosum in autistic and typically developing Indian children.

Berkins S, Koshy B, Livingstone RS, Jasper A, Grace H, Ravibabu P, Rai E. Berkins S, et al. Among authors: koshy b. Psychiatry Res Neuroimaging. 2023 Jan;328:111580. doi: 10.1016/j.pscychresns.2022.111580. Epub 2022 Dec 1. Psychiatry Res Neuroimaging. 2023. PMID: 36481591

2

Relationship between growth and illness, enteropathogens and dietary intakes in the first 2 years of life: findings from the MAL-ED birth cohort study.

MAL-ED Network Investigators. MAL-ED Network Investigators. BMJ Glob Health. 2017 Dec 28;2(4):e000370. doi: 10.1136/bmjgh-2017-000370. eCollection 2017. BMJ Glob Health. 2017. PMID: 29333282 Free PMC article.

3

Correction: Impact of early-onset persistent stunting on cognitive development at 5 years of age: Results from a multi-country cohort study.

Alam MA, Richard SA, Fahim SM, Mahfuz M, Nahar B, Das S, Shrestha B, Koshy B, Mduma E, Seidman JC, Murray-Kolb LE, Caulfield LE, Lima AAM, Bessong P, Ahmed T. Alam MA, et al. Among authors: koshy b. PLoS One. 2020 Feb 20;15(2):e0229663. doi: 10.1371/journal.pone.0229663. eCollection 2020. PLoS One. 2020. PMID: 32078654 Free PMC article.

4

Development and dysmorphism in Joubert syndrome--short case series from India.

Koshy B, Oommen SP, Jasper S, Danda S, Surendrababu NR. Koshy B, et al. J Trop Pediatr. 2010 Jun;56(3):209-12. doi: 10.1093/tropej/fmp084. Epub 2009 Sep 15. J Trop Pediatr. 2010. PMID: 19755534

5

Co-occurrence of Aicardi-Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1: a case series from India.

Sathishkumar D, Muthusamy K, Gupta A, Malhotra M, Thomas M, Koshy B, Jasper A, Danda S, George R. Sathishkumar D, et al. Among authors: koshy b. Clin Exp Dermatol. 2021 Jun;46(4):704-709. doi: 10.1111/ced.14531. Epub 2021 Jan 4. Clin Exp Dermatol. 2021. PMID: 33289110

6

Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent.

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Abraham SSC, et al. Among authors: koshy b. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. Eur J Med Genet. 2021. PMID: 34303877

7

The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study.

Varala S, George R, Mathew L, Russell P, Koshy B, Oommen SP, Thomas M, Muthusamy K, Yoganathan S, Jeyaseelan L, Muliyil J. Varala S, et al. Among authors: koshy b. Indian Dermatol Online J. 2021 Jan 16;12(1):84-89. doi: 10.4103/idoj.IDOJ_275_20. eCollection 2021 Jan-Feb. Indian Dermatol Online J. 2021. PMID: 33768027 Free PMC article.

8

The Impact of Autism Spectrum Disorder in Comparison with Other Neuro-Developmental Disorders in Children on the Family: Single Centre Experience.

Srinivasaraghavan R, Koshy B, Devarajan C, Beulah R, Glory L, Manoharan M. Srinivasaraghavan R, et al. Among authors: koshy b. Indian J Psychol Med. 2020 Apr 25;42(3):233-237. doi: 10.4103/IJPSYM.IJPSYM_376_19. eCollection 2020 May-Jun. Indian J Psychol Med. 2020. PMID: 32612327 Free PMC article.

9

Methyl-CpG-binding protein 2 gene mutations and its association with epilepsy: a single centre study from the Indian subcontinent.

Kamdar P, Thomas M, Yoganathan S, Muthusamy K, Koshy B, Philip Oommen S, Aaron R, Barney A, Susan C Abraham S, Danda S. Kamdar P, et al. Among authors: koshy b. J Genet. 2020;99:79. J Genet. 2020. PMID: 33168794 Free article. Clinical Trial.

10

Developmental trends in early childhood and their predictors from an Indian birth cohort.

Koshy B, Srinivasan M, Bose A, John S, Mohan VR, Roshan R, Ramanujam K, Kang G. Koshy B, et al. BMC Public Health. 2021 Jun 6;21(1):1083. doi: 10.1186/s12889-021-11147-3. BMC Public Health. 2021. PMID: 34090391 Free PMC article.

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