Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rahul Bhakat"'
Publikováno v:
Journal of Cleft Lip Palate and Craniofacial Anomalies, Vol 9, Iss 2, Pp 180-183 (2022)
Isolated deficiency of gonadotropin-releasing hormone is a heterogeneous disorder with wide genetic and clinical overlap. It mainly presents as hypogonadotropic hypogonadism (HH). HH associated with anosmia is known as Kallmann syndrome (KS), while i
Externí odkaz:
https://doaj.org/article/c69bf9af788b4d41865733c90f8ac4b1
Autor:
Prateek Kumar Panda, Indar Kumar Sharawat, Vivekanand Natarajan, Rahul Bhakat, Pragnya Panda, Lesa Dawman
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 10, Iss 9, Pp 3292-3302 (2021)
Background: Exact information about the efficacy of various medications proposed by regulatory bodies in children with COVID-19 is limited due to the lack of controlled trials in the existing literature. Methods: Different electronic databases (MEDLI
Externí odkaz:
https://doaj.org/article/6a7f2d43147148d49b90a7133d5cf9ba
Autor:
Swati Umasanker, Rahul Bhakat, Sonalika Mehta, Vyas Kumar Rathaur, Prashant Kumar Verma, N K Bhat, Manisha Naithani, Swathi Chacham
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 9, Pp 4985-4991 (2020)
Background and Aims: Subclinical Vitamin B12 deficiency is a very common entity in the Indian subcontinent with devastating clinical and socio-economic consequences. The objective of this study was to estimate the proportion of vitamin B12 deficient
Externí odkaz:
https://doaj.org/article/6097afa4acf8413ea2def093c3bd001a
Autor:
Swathi Chacham, Yatika Chaudhary, Manisha Naithani, Rahul Bhakat, Swati Rajput, Prashant Kumar Verma, Sriparna Basu, Kriti Mohan
Publikováno v:
Indian Journal of Child Health. 9:183-188
Objectives: This study aimed to estimate the frequency of Glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant (563 C->T) and G6PD Odisha (131 C->G) variants along with the prevalence of G6PD deficiency quantitatively. This study also estim
Publikováno v:
Current Pediatric Reviews. 20
Aim: Electroencephalogram (EEG) is specific, but not sensitive, for the diagnosis of epilepsy. This study aimed to correlate the clinic-electrographic and radiological features of seizure disorders in children attending a tertiary care centre in nort
Autor:
Jaya Chaturvedi, Avinish Singh, Swathi Chacham, Kriti Mohan, Sriparna Basu, Balram Ji Omar, Rahul Bhakat
Publikováno v:
Current Pediatric Reviews. 18:53-58
Background: Malaria is endemic in many states of India. Though there are reports of maternal and congenital malaria from endemic areas, however, there remains a paucity of data from hilly terrains. The present study evaluated the prevalence, clinical
Publikováno v:
Annals of Pediatric Gastroenterology & Hepatology. 3:10-12
Autor:
Vivekanand Natarajan, Pragnya Panda, Rahul Bhakat, Prateek Kumar Panda, Indar Kumar Sharawat, Lesa Dawman
Publikováno v:
Journal of Family Medicine and Primary Care
Journal of Family Medicine and Primary Care, Vol 10, Iss 9, Pp 3292-3302 (2021)
Journal of Family Medicine and Primary Care, Vol 10, Iss 9, Pp 3292-3302 (2021)
Background: Exact information about the efficacy of various medications proposed by regulatory bodies in children with COVID-19 is limited due to the lack of controlled trials in the existing literature. Methods: Different electronic databases (MEDLI
Autor:
Vyas Kumar Rathaur, Nowneet Kumar Bhat, Sonalika Mehta, Rahul Bhakat, Swati Umasanker, Prashant Verma, Manisha Naithani, Swathi Chacham
Publikováno v:
Journal of Family Medicine and Primary Care
Journal of Family Medicine and Primary Care, Vol 9, Iss 9, Pp 4985-4991 (2020)
Journal of Family Medicine and Primary Care, Vol 9, Iss 9, Pp 4985-4991 (2020)
Background and Aims: Subclinical Vitamin B12 deficiency is a very common entity in the Indian subcontinent with devastating clinical and socio-economic consequences. The objective of this study was to estimate the proportion of vitamin B12 deficient
Autor:
Avinish Singh, Rahul Bhakat, Shaik Naseeruddin, Manisha Naithani, Swathi Chacham, Nowneet Kumar Bhat, Najeeb Ahmad, Debdip Mandal
Publikováno v:
Indian Journal of Child Health. 7:320-323
Hyperimmunoglobulin E syndrome (HIES) more commonly referred to as Job’s syndrome, is an infrequent primary immunodeficiency disorder. It can be inherited either by autosomal dominant or recessive mode with each one having distinct varied clinical