Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Devdeep, Mukherjee"'
Autor:
Sunetra Mondal, Lakshmi Nagendra, Amarta S. Chowdhury, Rajan Palui, Soumyadeep Biswas, Devdeep Mukherjee, Krishnendu Khan, Aritra Sengupta, Anupama Pandey
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 145-152 (2024)
Introduction: Infants born preterm, with low birth weight (LBW), or with perinatal stress are at high risk for neonatal hypoglycemia. Low cortisol levels have also been demonstrated in this group of neonates, which is often transient. We report a ser
Externí odkaz:
https://doaj.org/article/e250726c808f464b84090f444120d332
Autor:
Ishita Majumdar, Hemant Kumar Nayak, Rajarshi Ghosh, Srirup Chatterjee, Prithwish Roy, Devdeep Mukherjee
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 1, Pp 71-73 (2023)
Primary chylopericardium (PC) is a rare entity in the pediatric population with very few reported cases. Most cases of chylopericardium manifest after trauma or following cardiac surgery. The other etiologies which may lead to chylopericardium are ma
Externí odkaz:
https://doaj.org/article/7267ec24e74c4bd0931a05342341e930
Autor:
Satyajit Das, Gopikrishna Kursa, Sukalyan Purkayastha, Subrata Nag, Ashok Bharati, Devdeep Mukherjee
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 5, Iss 2, Pp e1722023-e1722023 (2023)
Background: Spinal vascular malformations (SVM) are a complex entity and rarely noted in children. They are commonly seen in the elderly with a predilection for the thoraco-lumbar region. The incidence varies from 3-11% and varies across all age grou
Externí odkaz:
https://doaj.org/article/977ee6795228422f945b3157ba75284b
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 10, Iss 2, Pp e100201-e100201 (2021)
Factor XIII deficiency is an autosomal recessive disorder with an incidence of 1 in 1-5 million. On activation factor XIII stabilizes clot formation by cross-linking fibrin strands. Deficiency is characterized by severe bleeding due to impairment in
Externí odkaz:
https://doaj.org/article/90a2afea658a474b96138a039a21b16b
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 18, Iss 4, Pp 338-340 (2017)
Henoch–Schonlein purpura (HSP) with facial involvement with bullous rashes are extremely rare. A 12-year-old boy presented with abdominal pain and features of arthritis. He also had multiple purpuric rashes over his lower limbs. Gradually, he devel
Externí odkaz:
https://doaj.org/article/23cca1b6899b4b41b833b94f4f939804
Autor:
Laura W Dillon, Gege Gui, Niveditha Ravindra, Zoë Wong, Georgia Andrew, Devdeep Mukherjee, Scott L. Zeger, Firas El Chaer, Stephen Spellman, Alan Howard, Karen Chen, Jeffery Auletta, Steven M. Devine, Antonio Martin Jimenez Jimenez, Marcos J.G. De Lima, Mark Robert Litzow, Partow Kebriaei, Wael Saber, Daniel Jordan Weisdorf, Kristin M. Page, Christopher S. Hourigan
BackgroundPrevention of relapse for adults with Acute Myeloid Leukemia (AML) in first remission (CR1) is the most common indication for allogeneic hematopoietic cell transplantation (alloHCT). Measurable residual disease (MRD) detection has been asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcf1835c4431e09c1b3c24206be3a102
https://doi.org/10.1101/2022.10.21.22281322
https://doi.org/10.1101/2022.10.21.22281322
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 1, Pp 45-47 (2016)
Central nervous system involvement in segmental nevus depigmentosus (SND) is rare. A 7-month-old boy having convulsion and segmental hypopigmented patch in the right inguinal region. Magnetic resonance imaging of brain showed bilateral periventricula
Externí odkaz:
https://doaj.org/article/04d9adb141b045f8af24fe3ae296f9aa
Publikováno v:
Journal of Pediatric Critical Care, Vol 3, Iss 2, Pp 52-54 (2016)
Staphylococcal toxic shock syndrome (TSS) is a rare and potentially fatal multi system dysfunction. The syndrome occurs primarily due to TSS Toxin-1 (TSS-1) liberated by Staphylococcus aureus (SA). Fever with rash followed by multi organ dysfunction
Externí odkaz:
https://doaj.org/article/7d33d2305dd4406da6d56c4d88a925ec
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 6, Iss 2, Pp e060216-e060216 (2017)
Ascariasis is endemic in India and is common in areas of poor sanitation. The most common complications are intestinal and biliary ascariasis, which are associated with significant morbidity. We report a 7-month-old child who presented with obstructi
Externí odkaz:
https://doaj.org/article/964fea0006c2413686c924af4cb889e1
Autor:
Rialnat A. Lawal, Devdeep Mukherjee, Emily M. Limerick, Wynona Coles, Matthew M. Hsieh, Laura W. Dillon, Christopher S. Hourigan, Courtney D. Fitzhugh
Publikováno v:
Blood. 140(23)
Lawal et al report on a 45-fold increase in secondary hematologic malignancy in 120 patients following hematopoietic stem cell transplantation (HSCT) for sickle cell disease (SCD), comparable to what has been reported following gene therapy. Notably,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f229950bbc95a81cdd6cbddfe0e8cc10
https://pubmed.ncbi.nlm.nih.gov/36044658
https://pubmed.ncbi.nlm.nih.gov/36044658