Výsledky vyhledávání - "MANISHA MAURYA"

Akademický článek

Clinico-laboratory profile and treatment outcome of persistent diarrhea in under 5-year children of a tertiary care hospital in North India

Autor: Hanshika Srivastava, Manisha Maurya, Shahid Akhtar Siddiqui, Nandita Mishra, Anubha Shrivastava

Publikováno v: Journal of Medical and Allied Sciences, Vol 12, Iss 1, Pp 8-13 (2022)

Persistent diarrhea (PD) accounts for a third of all deaths due to diar-rhea in under 5 children. Its etiology and treatment are poorly under-stood. So, we aimed to study various host and environmental risk fac-tors, clinical profile and treatment ou

Externí odkaz: https://doaj.org/article/7e47d0eafbdc49e081873ff024b9b022

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Akademický článek

TP53 Mutations Identified Using NGS Comprise the Overwhelming Majority of TP53 Disruptions in CLL: Results From a Multicentre Study

Publikováno v: Frontiers in Oncology, Vol 12 (2022)

Limited data exists to show the correlation of (tumour protein 53) TP53 mutation detected by Next generation sequencing (NGS) and the presence/absence of deletions of 17p13 detected by FISH. The study which is the largest series to date includes 2332

Externí odkaz: https://doaj.org/article/f68447793d1e43bead15fecab502e322

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Akademický článek

Systematic evaluation of PAXgene® tissue fixation for the histopathological and molecular study of lung cancer

Autor: Mark Southwood, Tomasz Krenz, Natasha Cant, Manisha Maurya, Jana Gazdova, Perry Maxwell, Claire McGready, Ellen Moseley, Susan Hughes, Peter Stewart, Manuel Salto‐Tellez, Daniel Groelz, Doris Rassl, On behalf of the STRATfix Consortium

Publikováno v: The Journal of Pathology: Clinical Research, Vol 6, Iss 1, Pp 40-54 (2020)

Abstract Whilst adequate for most existing pathological tests, formalin is generally considered a poor DNA preservative and use of alternative fixatives may prove advantageous for molecular testing of tumour material; an increasingly common approach

Externí odkaz: https://doaj.org/article/a9d620a0402d45b48de3ed93c2c95d54

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Akademický článek

Caffey Disease in Infancy: A diagnostic dilemma for primary care physicians

Autor: Shahid A. Siddiqui, Gulnaz F. Siddiqui, Manisha Maurya, Anubha Shrivastava, Mukesh V . Singh

Publikováno v: Sultan Qaboos University Medical Journal, Vol 20, Iss 1, Pp 109-111 (2020)

Caffey disease is a rare and self-limiting condition characterised by cortical hyperostosis with inflammation of adjacent fascia and muscles. It usually presents in infancy and clinical features include hyperirritability, acute inflammation with swel

Externí odkaz: https://doaj.org/article/7d8ea6699ea94f1c80e30ae7cf45be03

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