Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hesarghatta S Asha"'
Autor:
Jeyashanth Riju, Nihal Thomas, Thomas V Paul, Deepak Thomas Abraham, Rekha Pai, Anne J Prabhu, Paul Mazhuvanchary Jacob, Remya Rajan, Rajiv C Michael, Amit Jiwan Tirkey, Natarajan Ramalingam, Hesarghatta S Asha, Nitin Kapoor
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 1, Pp 3-10 (2024)
The increased detection of thyroid nodules in the human population has led to an increase in the number of thyroid surgeries without an improvement in survival outcomes. Though the choice for surgery is straightforward in malignant thyroid nodules, t
Externí odkaz:
https://doaj.org/article/a3ee2d8099294f53a2bb570d136e8043
Autor:
Basavaraj G Sooragonda, Kalyani Sridharan, Rohit Ninan Benjamin, A T Prabhakar, Ajith Sivadasan, Nitin Kapoor, Kripa Elizabeth Cherian, Felix K Jebasingh, Sanjith Aaron, Vivek Mathew, Hesarghatta S Asha, Nihal Thomas, Thomas V Paul
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 4, Pp 496-501 (2023)
Objective: Parkinson's disease (PD) is a neurodegenerative condition that is characterized by bradykinesia, rigidity, and gait instability. Inherent to this condition is an increased predisposition to falls and fractures. Bone health in Parkinson's d
Externí odkaz:
https://doaj.org/article/352acda7fdc24979893d4a5b5ad288eb
Autor:
Basavaraj G Sooragonda, Sandeep Agarwal, Rohit Ninan Benjamin, A T Prabhakar, Ajith Sivadasan, Nitin Kapoor, Kripa E Cherian, Felix K Jebasingh, Sanjith Aaron, Nihal Thomas, Vivek Mathew, Hesarghatta S Asha, Thomas V Paul
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 211-216 (2021)
Background: Osteoporosis and sarcopenia are important aspects of motor neuron disease (MND). Individuals with amyotrophic lateral sclerosis (MND-ALS) have an increased risk of falls and fractures. Currently, the standard of care does not involve a ro
Externí odkaz:
https://doaj.org/article/f285d61e38d14e0ba436fbd853759dfc
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 10, Iss 4, Pp 1687-1693 (2021)
Objectives: The purpose of this study was to establish the prevalence of diabetes-specific psychological distress (DSPD) among patients with type 2 diabetes mellitus (T2DM) using the “Problem areas in diabetes” (PAID) scale at a teaching hospital
Externí odkaz:
https://doaj.org/article/d8f45c689af74858b7a92a047a651794
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 25, Iss 4, Pp 299-304 (2021)
The occurrence of endocrine tumors in pregnancy poses several diagnostic and therapeutic challenges. Although rare, functioning tumors involving the pituitary, thyroid, adrenal, and pancreas are reported in the literature. Timely diagnosis and manage
Externí odkaz:
https://doaj.org/article/e435089f35ac45b9a7c6b222efa38c14
Autor:
Aneez Joseph, Kripa Elizabeth Cherian, Nitin Kapoor, Vinoo Mathew Cherian, Hesarghatta S. Asha, Thomas V. Paul
Publikováno v:
AACE clinical case reports. 8(4)
Autor:
Geethu Antony, Hirenkumar Kamleshkumar, Shivendra Verma, Nitin Kapoor, Hesarghatta S. Asha, Dincy Peter, Thomas V. Paul
Publikováno v:
Endocrine Practice. 25:293
Publikováno v:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 14(8)
Autor:
Devraj Lath, Venkata S. Nandipati, Felix Jebasingh, Kripa E. Cherian, Nitin Kapoor, Hesarghatta S. Asha, Thomas V. Paul, Nihal Thomas
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 3, Pp 302-307 (2024)
Introduction: Thyroid storm is an uncommon but life-threatening presentation of thyrotoxicosis with a mortality rate of 10%. Our objective was to study the demographics, clinical and biochemical characteristics, and outcomes of inpatients diagnosed w
Externí odkaz:
https://doaj.org/article/813433c33bd4404aa65b6f742114b6ad
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 117-128 (2024)
Congenital adrenal hyperplasia (CAH) comprises a heterogeneous group of autosomal recessive disorders impairing adrenal steroidogenesis. Most cases are caused by mutations in the CYP21A2 gene resulting in 21-hydroxylase (21-OH) deficiency (21-OHD). T
Externí odkaz:
https://doaj.org/article/c687944936c74803b16032173c5a05e6