Vaina CL - Search Results

1

Folded stomach mimicking pneumoperitoneum in an asthmatic child.

Vaina CL, James JA, Paul SP. Vaina CL, et al. Br J Hosp Med (Lond). 2020 Apr 2;81(4):1-2. doi: 10.12968/hmed.2020.0039. Epub 2020 Apr 21. Br J Hosp Med (Lond). 2020. PMID: 32339015 No abstract available.

2

Children and young people with diabetes: recognition and management.

Hamilton H, Knudsen G, Vaina CL, Smith M, Paul SP. Hamilton H, et al. Among authors: vaina cl. Br J Nurs. 2017 Mar 23;26(6):340-347. doi: 10.12968/bjon.2017.26.6.340. Br J Nurs. 2017. PMID: 28345986

3

HLA-DQ2/DQ8 typing for non-biopsy diagnosis of coeliac disease: is it necessary?

Paul SP, Chopra J, Vaina CL, Mallikarjuna A, Basude D. Paul SP, et al. Among authors: vaina cl. Arch Dis Child. 2019 Nov;104(11):1119-1120. doi: 10.1136/archdischild-2019-317297. Epub 2019 Aug 2. Arch Dis Child. 2019. PMID: 31375474 No abstract available.

4

Accessory scrotum with perineal lipoma/hamartoma mimicking penoscrotal pseudoduplication.

Heaton PA, Shalaby MS, Vaina CL, Brown SE, Gradhand E, Paul SP. Heaton PA, et al. Among authors: vaina cl. Sudan J Paediatr. 2021;21(2):219-223. doi: 10.24911/SJP.106-1597356690. Sudan J Paediatr. 2021. PMID: 35221438 Free PMC article.

5

How Useful are Re-feeding Bloods for Paediatric Inpatients with Anorexia Nervosa?

Murdeshwar A, Heaton PA, Vaina CL, Paul SP. Murdeshwar A, et al. Among authors: vaina cl. Mymensingh Med J. 2022 Jan;31(1):258-262. Mymensingh Med J. 2022. PMID: 34999712

6

Diagnosing and managing invasive meningococcal disease in children.

Vaina CL, Paul SP, Heaton PA, Routley C, Mazhar H. Vaina CL, et al. Emerg Nurse. 2013 May;21(2):24-7. doi: 10.7748/en2013.05.21.2.24.e1168. Emerg Nurse. 2013. PMID: 23795539

7

Expanding the phenotypic spectrum of IFT81: Associated ciliopathy syndrome.

Ashraf T, Vaina C, Giri D, Burren CP, James M, Offiah AC, Overton T, Baptista J, Ellard S, Smithson SF. Ashraf T, et al. Am J Med Genet A. 2020 Oct;182(10):2403-2408. doi: 10.1002/ajmg.a.61781. Epub 2020 Aug 11. Am J Med Genet A. 2020. PMID: 32783357

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