Zobrazeno 1 - 10
of 4 679
pro vyhledávání: '"B Mukherjee"'
Publikováno v:
BMC Medical Education, Vol 24, Iss 1, Pp 1-20 (2024)
Abstract Background Coaching in academic medicine may help learners develop lifelong learning skills. Studies typically evaluate the impact on coachees and program outcomes. Limited information is available about educating faculty to integrate the ro
Externí odkaz:
https://doaj.org/article/e23f8948c2494e69b231dd0e166bd732
Publikováno v:
Indian Journal of Urology, Vol 18, Iss 2, Pp 148-150 (2002)
A 38-year-old male presented with right hypochon-dralgia and backache for two rears. Plain X-ray KUB showed a radio-opaque calculus in the left renal area. Urinalysis and culture were negative. IVU (after a nor-mal serum urea and creatinine report) s
Externí odkaz:
https://doaj.org/article/37a87c679fe645fea3dd22dc9c1ba984
Publikováno v:
Thalassemia Reports, Vol 12, Iss 3, Pp 73-84 (2022)
Alpha thalassemia is an autosomal recessive disorder caused by large deletions and/or point mutations in the α- globin genes. Hemoglobin H (Hb H) disease is most frequently due to deletion of three of the four α globin genes associated with variabl
Externí odkaz:
https://doaj.org/article/f0695a5b481e44908cc3737494d23770
Autor:
Ranjana Mishra, Meenakshi Bothra Gupta, Sharmila B Mukherjee, Avinash Lomash, Sangeeta Gupta, Seema Kapoor
Publikováno v:
Indian Pediatrics Case Reports, Vol 2, Iss 1, Pp 12-16 (2022)
Background: Biotin is the coenzyme of multiple carboxylases involved in gluconeogenesis, fatty acid synthesis, and amino acid catabolism. Biotinidase (BTD) deficiency is an autosomal recessive disorder affecting the biotin cycle. It disrupts endogeno
Externí odkaz:
https://doaj.org/article/9f5d2279a3e3415fadad0b1981120860
Autor:
Aishwarya Madaan, Vidya Yadav, Sumit Kataria, Vibhu Mendiratta, Shailaja Shukla, P Lalita Jyotsna, Sharmila B Mukherjee
Publikováno v:
Indian Pediatrics Case Reports, Vol 2, Iss 4, Pp 221-225 (2022)
Background: Mastocytosis is a heterogeneous group of disorders that is characterized by excessive proliferation and pathologic accumulation of mast cells in various body tissues. The mast cells also have abnormal morphology and aberrant expression of
Externí odkaz:
https://doaj.org/article/66885c5398fc40dbb290e20bf9225265
Publikováno v:
National Journal of Laboratory Medicine, Vol 11, Iss 3, Pp 1-3 (2022)
Langerhans Cell Histiocytosis (LCH) is a disease of abnormal clonal proliferation of langerhans cell of the bone marrow derived monocyte-macrophage lineage. Cells with characteristic coffee bean/grooved/indented nuclei with a background of histiocyt
Externí odkaz:
https://doaj.org/article/5c5586b3a85a4947b98f5a55ef9714a4
Publikováno v:
Indian Pediatrics Case Reports, Vol 1, Iss 1, Pp 57-61 (2021)
Background: Congenital long QT syndrome (cLQTS) are heritable disorders due to genetic mutations causing prolonged corrected QT (QTc) interval that may result in fatal arrhythmias. Clinical Description: A well 20-day-old, exclusively breastfed boy ha
Externí odkaz:
https://doaj.org/article/a775aaf373934b4ea7b58bd2b1cd8b2c
Autor:
Rati Devendra, Vinod Gupta, Somashekhar S. Biradar, Pradeep Bhat, Shantharam Hegde, S. L. Hoti, Malay B. Mukherjee, Harsha V. Hegde
Publikováno v:
Annals of Human Biology, Vol 47, Iss 1, Pp 55-58 (2020)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human erythroenzymopathy affecting more than 400 million people worldwide. G6PD deficiency was reported in India more than 50 years ago and the prevalence rate varies
Externí odkaz:
https://doaj.org/article/7a4c8b00f81b454d9a3b770eda22dc96
Autor:
Aakanksha Choudhary, Divyani Garg, Sharmila B Mukherjee, Rama Anand, Partap Yadav, Anita Nangia, Suvasini Sharma
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 307-309 (2021)
Externí odkaz:
https://doaj.org/article/30dd6c5cab534057832fbd8bac719df2
Publikováno v:
Indian Pediatrics. 60:187-192