Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Dipti Upadhye"'
Publikováno v:
Indian Journal of Medical Research, Vol 151, Iss 4, Pp 326-332 (2020)
The Indian Journal of Medical Research
The Indian Journal of Medical Research
Background & objectives: Homozygous sickle cell (SS) disease in Central India runs a more severe clinical course than reports from other areas of India. The current study was undertaken to compare the disease in Central India (Nagpur) with that in Ja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05e56e14e0e57be8526017bf8a3bb408
http://www.ijmr.org.in/article.asp?issn=0971-5916
http://www.ijmr.org.in/article.asp?issn=0971-5916
Autor:
Pratibha Sawant, Pallavi Mehta, Kanjaksha Ghosh, Manju Gorivale, Dipti Upadhye, Roshan B. Colah, Ajit Gorakshakar, Priya Hariharan, Khushnooma Italia, Anita Nadkarni
Publikováno v:
International Journal of Laboratory Hematology. 41:218-226
Introduction The hemoglobinopathies pose a significant health burden in India. Apart from the β thalassemias and sickle cell disorders, α thalassemias and structural hemoglobin variants are also common. Here we have reviewed the phenotypic and mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::600efbafb2b2ff496ba63584223b591c
https://doi.org/10.1111/ijlh.12948
https://doi.org/10.1111/ijlh.12948
Autor:
G. Subramanian, Priya Hariharan, Dipti Upadhye, Khushnooma Italia, Pratibha Sawant, Pallavi Mehta, Anita Nadkarni, Malay B. Mukherjee
Publikováno v:
International Journal of Laboratory Hematology. 39:e51-e54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22c791215109f743fdad0ea07aedbd0c
https://doi.org/10.1111/ijlh.12608
https://doi.org/10.1111/ijlh.12608
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 35(1)
This study evaluated the effect of alpha thalassemia on the red cell indices and hemoglobin profiles of normal, sickle heterozygous and sickle homozygous newborn babies in central India where the sickle gene is linked to the Arab-Indian haplotype. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30a28dd0aa069cf875d5b5edfa97ddf
https://pubmed.ncbi.nlm.nih.gov/30828156
https://pubmed.ncbi.nlm.nih.gov/30828156
Autor:
Dipti Upadhye, Anita Nadkarni, Manju Gorivale, Pratibha Sawant, Pallavi Mehta, Roshan B. Colah, Kanjaksha Ghosh, Chandrakala Shanmukhaiah
Publikováno v:
Annals of Hematology. 94:1953-1958
Co-inheritance of triplicated α-genes can alter the clinical and hematological phenotypes of β-thalassemias. We evaluated the phenotypic diversity and transfusion requirements in β-thalassemia heterozygotes, homozygotes, and normal individuals wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2b4fcdb31c8733f0a5c0606d83c4c35
https://doi.org/10.1007/s00277-015-2479-8
https://doi.org/10.1007/s00277-015-2479-8
Publikováno v:
Annals of Hematology. 95:1201-1203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aabf1c27d53cf5d39b4222406818071
https://doi.org/10.1007/s00277-016-2675-1
https://doi.org/10.1007/s00277-016-2675-1
Autor:
Harshali Gaikwad, Kanjaksha Ghosh, Dipti Upadhye, Pratibha Sawant, Ajit Gorakshakar, Khushnooma Italia, Anita Nadkarni, Roshan B. Colah
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 34(3)
The clinical presentation of HbE-β-thalassemia is extremely variable, however, many cases are severe and transfusion dependent. We offered prenatal diagnosis to 108 couples, 20 of whom came prospectively. CVS was done in 93 cases (9.5–13 weeks of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f43d4b31b86c4fbf46f136f5642be02
https://pubmed.ncbi.nlm.nih.gov/30127556
https://pubmed.ncbi.nlm.nih.gov/30127556
Autor:
S. Tarakeshwari, P. Koduri, Roshan B. Colah, Dipti Upadhye, Prabhakar Kedar, Prashant Warang, Reema Surve, Pallavi Mehta, K. Ghosh, Anita Nadkarni
Publikováno v:
International Journal of Laboratory Hematology. 37:e40-e43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9202cb3a71730bc6750a8bf0c0b9e921
https://doi.org/10.1111/ijlh.12281
https://doi.org/10.1111/ijlh.12281
Autor:
Roshan B. Colah, Dipti Upadhye, Pratibha Sawant, Dipty Jain, Pooja Dabke, Ajit Gorakshakar, Yazdi M. Italia, Harshada Kangane, Stacy Colaco, Kanjaksha Ghosh, Khushnooma Italia, Anita Nadkarni
Publikováno v:
Clinica Chimica Acta. 431:46-51
Background Co-inheritance of structural hemoglobin variants like HbS, HbD Punjab and HbE can lead to a variable clinical presentation and only few cases have been described so far in the Indian population. Methods We present the varied clinical and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052f9f0ad287d0701521397710adffde
https://doi.org/10.1016/j.cca.2014.01.028
https://doi.org/10.1016/j.cca.2014.01.028
Autor:
Kanjaksha Ghosh, Yogesh L. Trivedi, Dipti Upadhye, Dipty Jain, Anita Nadkarni, Roshan B. Colah
Publikováno v:
Clinical chemistry and laboratory medicine. 52(12)
Sickle cell disease is a major health burden in India. The aim of the study was to compare the diagnostic utility of two different approaches on automated high performance liquid chromatography (HPLC) for newborn screening for sickle cell disorders a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a22bca4fc8d7241d930f8164dd2db301
https://pubmed.ncbi.nlm.nih.gov/24978900
https://pubmed.ncbi.nlm.nih.gov/24978900