Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Rajpreet, Soni"'
Autor:
Rama Krishna Sanjeev, Lakshmi Narayan Taneja, Ashok Kumar Sharma, Amit Kumar, Sunil Dutt Sharma, Rajpreet Soni
Publikováno v:
Journal of Marine Medical Society, Vol 21, Iss 1, Pp 75-80 (2019)
Background: Indian academy of pediatrics basic life support (IAP BLS) group runs BLS courses both with and without certification through accredited centers. The certification courses test both BLS and choking skills for all ages. This study is about
Externí odkaz:
https://doaj.org/article/55b053b315df4715a0806940ab97f2dc
Autor:
Stalin Ramprakash, Rajat Agarwal, Rakesh Dhanya, Priya Marwah, Rajpreet Soni, Naila Yaqub, Itrat Fatima, Tatheer Zhara, Lallindra Gooneratne, Senani Williams, Sadaf Khalid, Santanu Sen, Vikramjit Kanwar, Lawrence Faulkner
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 4, Pp 107-113 (2017)
Thalassemias are the most common inherited genetic disorder in India and a major public health burden with bone marrow transplant (BMT) considered the only established curative therapy. We describe outcomes for patients (n = 71) with standard-risk th
Externí odkaz:
https://doaj.org/article/579c7bb850c04c9d98384ee4cd01a004
Autor:
Lawrence Faulkner, Cornelio Uderzo, Sadaf Khalid, Priya Marwah, Rajpreet Soni, Naila Yaqub, Samina Amanat, Itrat Fatima, Sarah Khan Gilani, Tatheer Zahra, Stalin Ramprakash, Lallindra Gooneratne, Ruwangi Dissanayake, Senani Williams, Wasantha Rathnayake, Reshma Srinivas, Amit Sedai, Ankita Kumari, Lailith Parmar, Rakesh Dhanya, Rajat Kumar Agarwal
Publikováno v:
Blood Advances, Vol 1, Iss 13, Pp 792-801 (2017)
Abstract: Matched-related bone marrow transplantation (BMT) may cure >80% of low-risk children with severe thalassemia (ST). Very long-term follow-up studies have shown how the standard busulfan-cyclophosphamide (BuCy) regimen may be associated with
Externí odkaz:
https://doaj.org/article/ecbaf71f9a8b422892a284b76a3037a1
Autor:
Stalin Ramprakash, Rajat Agarwal, Rakesh Dhanya, Priya Marwah, Rajpreet Soni, Naila Yaqub, Itrat Fatima, Lallindra Gooneratne, Senani Williams, Sadaf Khalid, Santanu Sen, Lawrence Faulkner
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S22 (2017)
Externí odkaz:
https://doaj.org/article/e338b3bd94114f658f0f68aa7e43957c
Autor:
Lawrence, Faulkner, Marta, Verna, Attilio, Rovelli, Rajat Kumar, Agarwal, Rakesh, Dhanya, Lalith, Parmar, Amit, Sedai, Ankita, Kumari, Stalin, Ramprakash, C P, Raghuram, Pallavi, Mehta, Sandeep, Elizabeth, Sadaf, Khalid, Aliya, Batool, Sarah Khan, Ghilani, Itrat, Fatima, Tatheer, Zara, Priya, Marwah, Rajpreet, Soni, Deepa, Trivedi, Valentino, Conter, Marta, Canesi, Dosti, Othman, Vian, Faeq, Katharina, Kleinschmidt, Akif, Yesillipek, Catherine G, Lam, Scott C, Howard, Selim, Corbacioglu, Jacek, Wachowiak
Publikováno v:
Bone Marrow Transplantation
Publisher Copyright: © 2020, The Author(s). Severe blood disorders and cancer are the leading cause of death and disability from noncommunicable diseases in the global pediatric population and a major financial burden. The most frequent of these con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51974687907bd7d633840caa7bcd7ff2
http://hdl.handle.net/10138/340832
http://hdl.handle.net/10138/340832
Autor:
Mohamed Hamed Hussein, Mohamed El Missiry, Sadaf Khalid, Naila Yaqub, Sarah Khan Gilani, Itrat Fatima, Tatheer Zara, Priya Marwah, Rajpreet Soni, Frederic Bernard, Annunziata Manna, Cornelio Uderzo, Lawrence Faulkner
Publikováno v:
Thalassemia Reports, Vol 3, Iss 1s, Pp e42-e42 (2013)
Even though severe thalassemia is a preventable disease, over 100,000 new cases are born yearly, particularly in the Middle East and South-East Asia. Most of these children may not reach adulthood because long-term appropriate supportive care is eith
Externí odkaz:
https://doaj.org/article/4ed126902e29451092d751d00fccb0b7
Autor:
Lawrence Faulkner, C P Raghuram, Stalin Ramprakash, Sadaf Khalid, Rakesh Dhanya, Rajpreet Soni, Sarah Khan Gilani, Priya Marwah, Rajat Kumar Agarwal, Fatima Itrat, Naila Yaqub, Deepa Trivedi, Tatheer Zahra
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 26(10)
Severe thalassemia syndromes (ST) are highly curable by bone marrow transplant (BMT), but rejection may still occur. We retrospectively analyzed our fully matched related donor transplants to establish if isolated splenomegaly is an independent risk
Autor:
Lawrence Faulkner, Priya Marwah, Rakesh Dhanya, Naila Yaqub, Tatheer Zhara, Stalin Ramprakash, Santanu Sen, Sadaf Khalid, Senani Williams, Itrat Fatima, Rajpreet Soni, Vikramjit Kanwar, Lallindra Gooneratne, Rajat Kumar Agarwal
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 4, Pp 107-113 (2017)
Thalassemias are the most common inherited genetic disorder in India and a major public health burden with bone marrow transplant (BMT) considered the only established curative therapy. We describe outcomes for patients (n = 71) with standard-risk th
Autor:
Amit Sedai, Sarah Khan Gilani, Ankita Kumari, Rajpreet Soni, Wasantha Rathnayake, Sadaf Khalid, Senani Williams, Lailith Parmar, Lawrence Faulkner, Naila Yaqub, Lallindra Gooneratne, Ruwangi Dissanayake, Tatheer Zahra, Rakesh Dhanya, Cornelio Uderzo, Stalin Ramprakash, Samina Amanat, Priya Marwah, Rajat Kumar Agarwal, Itrat Fatima, Reshma Srinivas
Publikováno v:
Blood Advances. 1:792-801
Matched-related bone marrow transplantation (BMT) may cure >80% of low-risk children with severe thalassemia (ST). Very long-term follow-up studies have shown how the standard busulfan-cyclophosphamide (BuCy) regimen may be associated with normalizat
Autor:
Lalith Parmar, Rajat Kumar Agarwal, Deepa Trivedi, Rakesh Dhanya, Priya Marwah, Lawrence Faulkner, Amit Sedai, Ankita Kumari, C P Raghuram, Rajpreet Soni, Stalin Ramprakash
Publikováno v:
Bone Marrow Transplantation