Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Kapil, Bhalla"'
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 13, Iss 11, Pp 5367-5369 (2024)
Cough is a protective reflex that allows clearance of secretions from upper respiratory tract. It is not a disease by itself but a symptom of underlying disease. In a majority of cases, it is self-limiting and requires only supportive care. But over-
Externí odkaz:
https://doaj.org/article/091a466ae5b5409d9ad8208e01aaca87
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 13, Iss 9, Pp 4030-4034 (2024)
Background: Constipation is one of the most common gastrointestinal symptoms in patients with cerebral palsy. This study was conducted with the aim to compare the efficacy of a high fiber diet and polyethylene glycol in the management of chronic cons
Externí odkaz:
https://doaj.org/article/33b688df7f224be09e3ad51ea5aaa3da
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 10, Pp 01-03 (2024)
Infantile Tremor Syndrome (ITS) is a complex neurological syndrome that affects exclusively breastfed infants, typically seen between 9 to 12 months of age. However, in the present case, it started at the ages of three months and four months, respect
Externí odkaz:
https://doaj.org/article/e2acbbb7b2fa44acba113f1e12bd17e9
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 12, Pp 01-02 (2024)
Congenital Adrenal Hyperplasia (CAH) is a group of autosomal recessive disorders that occur due to defects in steroid synthesis. It is characterised by a deficiency of adrenocortical hormones and an excess of steroid precursors. A deficiency of 21-hy
Externí odkaz:
https://doaj.org/article/01773319874b4f119657d133bf9b4fa6
Autor:
Alok Khanna, Nancy P. Kharkongor, Anjali Verma, Kapil Bhalla, Paramjeet S. Gill, Surender Verma, Gulshan Prakash
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 17, Iss Suppl 1, Pp S121-S125 (2024)
Introduction Nephrotic syndrome (NS) is a common chronic kidney disease in children characterized by the leakage of protein through a pathologically altered glomerular filtration membrane. There is not much literature on a clear association between I
Externí odkaz:
https://doaj.org/article/83729b3b2fd249d6afa12507cae0a722
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 03, Pp 01-03 (2024)
Juvenile Dermatomyositis (JDM) is a rare autoimmune disorder which mainly affects the skin and skeletal muscles. Characteristic features of this rare disorder include Gottron papules, heliotrope rashes and proximal muscle weakness. MDA5 positive JDM
Externí odkaz:
https://doaj.org/article/581065be00d74e859797deb0c3af1301
Autor:
Alok khanna, Mukesh saini, Ashuma sachdeva, Jyotsna sen, kapil bhalla, Animesh debbarma, Yogesh verma, Preet lamba
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 10, Pp 15-19 (2023)
Introduction: Nephrotic Syndrome (NS) is characterised by proteinuria, oedema, hypoalbuminaemia, and hypercholesterolemia. The latter is a risk factor for atherosclerosis, suggesting a higher risk of cardiovascular disease in children with NS. Ath
Externí odkaz:
https://doaj.org/article/eb377c3ca871447f9b786e2c498b8d2a
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 12, Pp 3412-3414 (2023)
Tuberculosis (TB) is an infectious disease of which congenital TB is a rare form even in TB-endemic countries such as India. There are very few case reports of the same in the literature. Though the incidence rate of congenital TB is low, mortality r
Externí odkaz:
https://doaj.org/article/20cce10f32e8498bb1a91c4477bc16ab
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 7, Pp 1336-1341 (2023)
Background: Asthma is a common childhood disease that leads to impairment of quality of life (QOL) of both the children affected by the disease and their caregivers. Management of asthma includes pharmacotherapy along with education about asthma and
Externí odkaz:
https://doaj.org/article/02a89edf8e17438f86f508eece176205
Autor:
Yannan Jia, Lina Han, Cassandra L. Ramage, Zhe Wang, Connie C. Weng, Lei Yang, Simona Colla, Helen Ma, Weiguo Zhang, Michael Andreeff, Naval Daver, Nitin Jain, Naveen Pemmaraju, Kapil Bhalla, Satu Mustjoki, Peiyi Zhang, Guangrong Zheng, Daohong Zhou, Qi Zhang, Marina Konopleva
Publikováno v:
Haematologica, Vol 108, Iss 10 (2023)
BCL-XL and BCL-2 are key anti-apoptotic proteins and validated cancer targets. 753B is a novel BCL-XL/BCL-2 proteolysis targeting chimera (PROTAC) that targets both BCL-XL and BCL-2 to the von Hippel-Lindau (VHL) E3 ligase, leading to BCLX L/BCL-2 ub
Externí odkaz:
https://doaj.org/article/44723b7d8a04476c9f09a39b30c15fb8