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Inherited p40phox deficiency differs from classic chronic granulomatous disease.
J Clin Invest. 2018 Aug 31;128(9):3957-3975. doi: 10.1172/JCI97116. Epub 2018 Aug 6.
J Clin Invest. 2018.
PMID: 29969437
Free PMC article.
Very early onset IBD: novel genetic aetiologies.
Batura V, Muise AM.
Batura V, et al.
Curr Opin Allergy Clin Immunol. 2018 Dec;18(6):470-480. doi: 10.1097/ACI.0000000000000486.
Curr Opin Allergy Clin Immunol. 2018.
PMID: 30299396
Review.
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Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease.
Bosa L, Batura V, Colavito D, Fiedler K, Gaio P, Guo C, Li Q, Marzollo A, Mescoli C, Nambu R, Pan J, Perilongo G, Warner N, Zhang S, Kotlarz D, Klein C, Snapper SB, Walters TD, Leon A, Griffiths AM, Cananzi M, Muise AM.
Bosa L, et al. Among authors: batura v.
Sci Rep. 2021 Mar 15;11(1):5945. doi: 10.1038/s41598-021-85399-9.
Sci Rep. 2021.
PMID: 33723309
Free PMC article.
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Diaphragmatic hernia with strangulated loop of bowel presenting after colonoscopy: case report.
Sodhi SS, Zech LA Jr, Batura V, Kulasekhar S.
Sodhi SS, et al. Among authors: batura v.
Int Arch Med. 2009 Dec 11;2(1):38. doi: 10.1186/1755-7682-2-38.
Int Arch Med. 2009.
PMID: 20003353
Free PMC article.
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Temporomandibular ankylosis. A report of 15 cases.
Rajgopal A, Banerji PK, Batura V, Sural A.
Rajgopal A, et al. Among authors: batura v.
J Maxillofac Surg. 1983 Feb;11(1):37-41. doi: 10.1016/s0301-0503(83)80009-5.
J Maxillofac Surg. 1983.
PMID: 6572687
No abstract available.
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