Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gousia Mukhtar"'
Autor:
Gousia Mukhtar, Bijulal Sasidharan, Kavassery Mahadevan Krishnamoorthy, Harikrishnan K. N. Kurup, Arun Gopalakrishnan, Deepa SasiKumar, Sankara Sarma P, Ajit Kumar Valaparambil, Sivasankaran Sivasubramonian, Harikrishnan Sivadasanpillai
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Introduction Although much research has been done on adult hypertrophic cardiomyopathy, data on pediatric hypertrophic cardiomyopathy is still limited. Methods and results The study enrolled all patients with cardiomyopathy who presented to
Externí odkaz:
https://doaj.org/article/6cf7f8767fee4160a63c4806dd284f48
Autor:
Gousia Mukhtar, Bijulal Sasidharan, Kavassery Mahadevan Krishnamoorthy, Harikrishnan K N. Kurup, Arun Gopalakrishnan, Deepa Sasikumar, Sankara Sarma, Ajit Kumar Valaparambil, Sivasankaran Sivasubramonian
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 3, Pp 175-181 (2023)
Introduction and Aims : Dilated cardiomyopathy (DCM) is an important cause of heart failure (HF) among children. Research on pediatric DCM remains surprisingly scarce. The primary objective of the study was to evaluate the clinical profile and outcom
Externí odkaz:
https://doaj.org/article/1633cfc246e643d99477b31a78aad302
Publikováno v:
IHJ Cardiovascular Case Reports, Vol 6, Iss 4, Pp 182-183 (2022)
Externí odkaz:
https://doaj.org/article/6702693bb4c04c05828236921387bece
Autor:
Gousia Mukhtar Kawoos, Krishna Kumar Mohanan Nair, Bijulal Sasidharan, Ajit Kumar Valaparambil
Publikováno v:
Acta Cardiologica. 77:972-973
Autor:
Aamir Rashid, Imran Hafiz, Nisar A. Tramboo, Hilal A. Rather, Syed Wajid Ali, Bashir Ahmad Charoo, Gousia Mukhtar
Publikováno v:
JMS SKIMS. 22
Background: Congenital Heart disease accounts for 10% of infant deaths in developed countries.Very scarce data exits about the prevalence and patterns of CHD in our local high altitude population .AIMS : To analyse the pattern and prevalence of conge
Publikováno v:
Indian pediatrics. 52(1)
Anemia is a common accompaniment of cerebral palsy, mental retardation and neurodegenerative disorders. A 4-year-old boy with chronic megaloblastic anemia, global developmental delay, seizures, intracranial calcification and new onset neuro-regressio
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