Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Yazdi M. Italia"'
Publikováno v:
PARIPEX INDIAN JOURNAL OF RESEARCH. :1-4
Introduction: Sickle hemoglobin (HbS), an autosomal recessive hemoglobinopathy cause of Sickle cell disease (SCD), is widely sprayed around the globe affecting millions of people . SCD results from single nucleotide polymorphism (SNP) or point mutati
Autor:
Priyanka Khurana, Aastha Aggarwal, Siuli Mitra, Yazdi M Italia, Kallur N Saraswathy, Adimoolam Chandrasekar, Gautam K Kshatriya
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90414 (2014)
The present study was carried out in the Indo-European speaking tribal population groups of Southern Gujarat, India to investigate and reconstruct their paternal population structure and population histories. The role of language, ethnicity and geogr
Externí odkaz:
https://doaj.org/article/b520564c5be14f618e616b9d95a7fe97
Autor:
Yazdi M. Italia, Erik Serrao, Roshan B. Colah, Dipty Jain, Shrey Desai, Nikhil Shinde, Bhavesh Raicha, Malay B. Mukherjee, Kapilkumar Dave, Pallavi Mehta
Publikováno v:
American journal of clinical pathology. 153(1)
Objectives Sickle cell anemia is the commonest genetic disorder in India, and the frequency of the sickle cell gene is very high in the remote tribal areas where facilities are generally limited. Therefore, a rapid and affordable point-of-care test f
Autor:
Pallavi Mehta, Roshan B. Colah, Bhavesh Raicha, Lakshmanan Krishnamurti, Vishal Mehta, Kanjaksha Ghosh, Khushnooma Italia, Yazdi M. Italia
Publikováno v:
Journal of Medical Screening. 22:1-7
Objectives To evaluate the feasibility of a newborn screening and follow-up programme for sickle cell disease (SCD) among tribal populations of south Gujarat, India. Methods A total of 5467 newborn babies were screened over 2 years using High-perform
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
Autor:
Mahrukh Wadia, Kumar S. Ashokan, Yazdi M. Italia, Rajni Kaul, Dipika Mohanty, Vasantha Muthuswamy, Kanjaksha Ghosh, Dipty Jain, Malay B. Mukherjee, Roshan B. Colah, Guru Prasad Chottray, Deepak Kumar Shukla
Publikováno v:
Asia Pacific Journal of Public Health. 27:NP562-NP571
We evaluated the spectrum of hemoglobinopathies among the primitive tribal groups from 4 states in India. A total of 15 200 individuals from 14 primitive tribal groups were studied by automated high-performance liquid chromatography. The hemoglobin S
Autor:
Vandana Pradhan, Yazdi M. Italia, Harshada K. Kangne, Farah Jijina, Dipti L. Jain, Roshan B. Colah, Rati D. Mukesh, Maya Gupta, Kanjaksha Ghosh, Anita Nadkarni
Publikováno v:
BioMed Research International, Vol 2013 (2013)
BioMed Research International
BioMed Research International
Objective. Sickle cell disease has variable clinical manifestations. Activation of neutrophils plays an important role in the initiation and propagation of vaso occlusive crises which can be analysed by determining the expression of neutrophil antige
Publikováno v:
Annals of Human Biology. 38:583-591
Due to its geographic location, Gujarat has played a major role in assimilation of different cultures with those of the subcontinent of India and is home to a number of Indo-European speaking tribes.This study examined the genetic structure and exten
Autor:
Kanjaksha Ghosh, Harshada K. Kangne, Dipti L. Jain, Roshan B. Colah, Yazdi M. Italia, Anita Nadkarni, Farah Jijina
Publikováno v:
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 21(2)
The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reductase (MTHFR; C677T) mutation was determined in 180 patients with sickle cell (SS) disease (126 sickle homozygous and 54 sickle β-thalassaemia—age 1
Publikováno v:
Indian journal of pediatrics. 81(3)
Following impressions that the use of blood transfusion in sickle cell disease may be inappropriately high, transfusion practice at a major blood bank in an area of high prevalence of sickle cell disease was assessed. Retrospective review of blood us