Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M. R. Lokeshwar"'
Autor:
Amruta Dhawale, Pallavi Gaikwad, Ramya Uppuluri, Snehal Shabrish, Swati Kanakia, Meena Sivasankaran, Ambreen Pandrowala, Dharani Jayaraman, Pranoti Kini, Abhilasha Sampagar, Deenadayalan Munirathnam, Sneha Sawant-Desai, Mukesh Desai, Aparna Dalvi, Shweta Shinde, Brijesh Arora, Pandiarajan Vignesh, Aaqib Zaffar Banday, Madhura Kelkar, Meenakshi Girish, Manisha Madkaikar, Jahnavi Aluri, Santanu Sen, Amit Rawat, Gouri Hule, Narendra K Chaudhary, Ramprasad Vedam, R Yadav, Nayana Nambiar, Umair Ahmed Bargir, Revathi Raj, Vijaya Gowri, Farah Jijina, Priyanka Setia, Neha Jodhawat, Manasi Kulkarni, M. R. Lokeshwar, Abhijit Chaudhary, S. Chandrakla, Priyanka Kambli, Ratna Sharma, Nitin Shah, Prasad Taur, Maya Gupta, Ujjal Poddar, Amita Aggarwal
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology
Frontiers in Immunology
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of immune dysregulation characterized by hyperactivation of the immune system, excessive cytokine secretion and severe systemic inflammation. HLH is classified as familial (FHL) when associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4e0d2955b6a99b8a804cf5a0922dd11
https://doi.org/10.3389/fimmu.2021.612583
https://doi.org/10.3389/fimmu.2021.612583
Autor:
M. R. Lokeshwar, Mukesh Desai, Aparna Dalvi, Priyanka Kambli, Jahnavi Aluri, Prasad Taur, Maya Gupta, Jenna R.E. Bergerson, Michael J. Lenardo, Manasi Kulkarni, Manisha Madkaikar, Snehal Mhatre
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 9 (2018)
Frontiers in Immunology, Vol 9 (2018)
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder caused by mutations in the CARD11 gene and results in constitutive NF-κB activation in B and T cells. Affected patients present with polyclonal expans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7875bc37c1cfec49b2bc3d68208ca5fe
https://doi.org/10.3389/fimmu.2018.01049
https://doi.org/10.3389/fimmu.2018.01049
Autor:
M. R. Lokeshwar, Meghana Phadke, Chandralekha Tampi, Renu Saxena, Shraddha Bhutada, Ketki Shah, Sudha Kohli
Publikováno v:
The Indian Journal of Pediatrics. 79:650-654
Kearns-Sayre Syndrome is form of rare mitochondrial cytopathy, first described by Thomas P. Kearns and George Pomeroy Sayre in 1958 and is characterized by progressive external opthalmoplegia, cardiac conduction block, pigmentary retinal degeneration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47b15d9448739736215002a4e54062f1
https://doi.org/10.1007/s12098-011-0618-3
https://doi.org/10.1007/s12098-011-0618-3
Publikováno v:
The Indian Journal of Pediatrics. 70:893-902
In neonatal period anemia is a complex problem owing to the unique blood picture. The erythrocytic system undergoes serial adaptation to meet progressively changing demands of oxygen in the embryo, the fetus and neonate. This leads to rapid change in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::637aa9172982a9bdf7181fd9455bd957
https://doi.org/10.1007/bf02730596
https://doi.org/10.1007/bf02730596
Publikováno v:
The Indian Journal of Pediatrics. 65:651-661
Various blood indices vary in a newborn as compared to older child or adult. It depends on the gestational age, day of life, maternal factors, mode of delivery and site of blood collection. Hemoglobin, HCT & MCV tend to be higher in newborns. They fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9986c51a549c89084350863145c0818e
https://doi.org/10.1007/bf02731037
https://doi.org/10.1007/bf02731037
Autor:
Meghana, Phadke, M R, Lokeshwar, Shraddha, Bhutada, Chandralekha, Tampi, Renu, Saxena, Sudha, Kohli, K N, Shah
Publikováno v:
Indian journal of pediatrics. 79(5)
Kearns-Sayre Syndrome is form of rare mitochondrial cytopathy, first described by Thomas P. Kearns and George Pomeroy Sayre in 1958 and is characterized by progressive external opthalmoplegia, cardiac conduction block, pigmentary retinal degeneration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::36a404312e6efd87aed44d8e03c2b9d2
https://pubmed.ncbi.nlm.nih.gov/23853060
https://pubmed.ncbi.nlm.nih.gov/23853060
Publikováno v:
Indian journal of pediatrics. 79(11)
Normally, there is no obvious communication between the intracranial and extra cranial venous drainages in the head. In Sinus Pericranii, there is an abnormal communication, either from the extra cranial system to the intracranial venous sinuses or f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df7f260e6c8372cd3158eb1ba3fc2c3c
https://pubmed.ncbi.nlm.nih.gov/22415496
https://pubmed.ncbi.nlm.nih.gov/22415496
Publikováno v:
Indian journal of pediatrics. 78(5)
Anemia is a global problem of immense public health significance. Iron deficiency anemia is the most common nutritional disorder seen all over the world, more in the developing countries, particularly, affecting young children of 6-24 months of age,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d7da5b7fac368b40b4ba5f86617733c
https://pubmed.ncbi.nlm.nih.gov/21191672
https://pubmed.ncbi.nlm.nih.gov/21191672
Publikováno v:
Indian pediatrics. 43(6)
Infectious purpura fulminans is associated with high mortality and morbidity despite standard antimicrobial therapy. We report satisfactory clinical outcome in two children with sepsis associated purpura fulminans who were treated with activated prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::514ff74150c6ea8a219428f0f0057cb8
https://pubmed.ncbi.nlm.nih.gov/16820663
https://pubmed.ncbi.nlm.nih.gov/16820663
Publikováno v:
Indian pediatrics. 40(4)
Diamond-Blackfan anemia is a rare congenital hypoplastic anemia. We report 6 children diagnosed as Diamond-Blackfan anemia at our clinic. All had severe pallor at presentation, with mild hepatomegaly and just palpable spleen in one child. Thumb anoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93a18207a89b2fd4f8e0a1f1ab05e8c6
https://pubmed.ncbi.nlm.nih.gov/12736411
https://pubmed.ncbi.nlm.nih.gov/12736411