Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Vivi M Srivastava"'
Autor:
Priscilla Babu, Vivi M Srivastava
Publikováno v:
Asian Journal of Medical Sciences, Vol 13, Iss 3, Pp 143-151 (2022)
Background: With advances in assisted reproductive techniques management of infertility is changing at a very fast pace. Although minimally invasive techniques such as testicular sperm aspiration and micro-dissection testicular sperm extraction (micr
Externí odkaz:
https://doaj.org/article/889207a8ed6341d993bb8878b0b2c16b
Autor:
Vandana Kamath, Vivi M Srivastava, S Yuvarani, Mary Purna Chacko, Saurabh Kumar Bhattacharya, Samuel Phillip Oommen, Sumita Danda, George Korula
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 1, Pp GC01-GC04 (2019)
Introduction: The balanced translocation t(11;22) is one of the most common constitutional genetic abnormality detected in humans. Carriers of the t(11;22) are usually phenotypically normal and their carrier status is ascertained only if they present
Externí odkaz:
https://doaj.org/article/3cd83fb4195e45f4b36d48c103e90427
Autor:
Mariano Mascarenhas, Sumi Thomas, Mohan S Kamath, Ramya Ramalingam, Ann Marie Kongari, S Yuvarani, Vivi M Srivastava, Korula George
Publikováno v:
Journal of Human Reproductive Sciences, Vol 9, Iss 3, Pp 187-193 (2016)
AIM: To estimate the prevalence of chromosomal abnormalities and Y chromosome microdeletion among men with azoospermia and severe oligozoospermia and its correlation with successful surgical sperm retrieval. SETTING AND DESIGN: A prospective study in
Externí odkaz:
https://doaj.org/article/0dea4e517e514f4dab6795066699f41c
Incontinentia pigmenti, an x-linked dominant disorder, in a 2-year-old boy with Klinefelter syndrome
Autor:
Abhilasha Williams, Laxmisha Chandrashekar, Vivi M Srivastava, Meera Thomas, Saban Horo, Renu George
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 3, Pp 424-426 (2017)
Incontinentia pigmenti (IP) is a rare X-linked dominant disorder, in which skin lesions distributed along Blaschko's lines appear shortly after birth. Early lesions which are erythematous/bullous evolve over time into warty lesions, hyperpigmented sw
Externí odkaz:
https://doaj.org/article/ae89561a98cc45b7a4270fc4ffb43b3c
Autor:
Kiruthiga Kala Gnanasekaran, Mary P Chacko, Marie Therese Manipadam, M S Bindra, Biju George, Vivi M Srivastava
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 59, Iss 1, Pp 104-106 (2016)
Acute myeloid leukemia (AML) is a malignant hematopoietic stem cell disorder which is sub-classified based on bone marrow morphology and the presence of specific genetic abnormalities. One such cytogenetic abnormality is the pericentric inversion (in
Externí odkaz:
https://doaj.org/article/f99b6ac967ed43958fed120183caa661
Autor:
Harsha M Dangare, Samuel P Oommen, Amisha N Sheth, Beena Koshy, Reeba Roshan, Maya M Thomas, Sumita Danda, Vivi M Srivastava
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 55, Iss 4, Pp 501-505 (2012)
The cri du chat syndrome (CdCS) is a chromosomal deletion syndrome associated with a partial deletion of the short (p) arm of chromosome 5. We describe five children who were diagnosed to have CdCS by conventional cytogenetic analysis. The deletion w
Externí odkaz:
https://doaj.org/article/66f685088ef84a6faa53dcdd04846e10
Autor:
Poonam P Jain, Mayur Parihar, Rayaz Ahmed, Aby Abraham, Auro Vishwabandya, Biju George, Vikram Mathews, Alok Srivastava, Vivi M Srivastava
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 55, Iss 3, Pp 347-351 (2012)
Background : Chronic myelogenous leukemia (CML) is characterised by the t(9;22)(q34;q11.2) which results in the formation of the BCR/ABL1 fusion gene. Occasionally, the t(9;22) may be associated with submicroscopic deletions of chromosomes 9 and/or 2
Externí odkaz:
https://doaj.org/article/f1828f906956439cb7268053677e6d8b
Publikováno v:
Haematologica, Vol 92, Iss 7 (2007)
Ninety-eight newly diagnosed cases of PML-RARαpositive APL were treated with a regimen of single agent ATO. FLT3 activating mutations were seen in 33% and an additional cytogenetic finding was noted in 23.2%. FLT3 activating mutations were significa
Externí odkaz:
https://doaj.org/article/18fffab84bc9411db8e95bbc5545bc93
Autor:
Vivi M. Srivastava, Samuel Philip Oommen, Vandana Kamath, S Yuvarani, Beena Koshy, Mary Purna Chacko
Publikováno v:
International Journal of Infertility & Fetal Medicine. 12:60-65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3a1b80baafb12b54100b0df3d5ae79b
https://doi.org/10.5005/jp-journals-10016-1228
https://doi.org/10.5005/jp-journals-10016-1228
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis
Autor:
Gaurav Joshi, Nancy Beryl Janet Arthur, Thenral S Geetha, Phaneendra Venkateswara Rao Datari, Kirti Modak, Debanjan Roy, Anurag Dutta Chaudhury, Prasanth Sundaraganesan, Sweety Priyanka, Fouzia NA, Vedam Ramprasad, Aby Abraham, Vivi M Srivastava, Alok Srivastava, Uday Prakash Kulkarni, Biju George, Shaji R Velayudhan
Publikováno v:
Journal of Medical Genetics. :jmedgenet-2022
BackgroundFanconi anaemia (FA) is a rare inherited bone marrow failure disease caused by germline pathogenic variants in any of the 22 genes involved in the FA-DNA interstrand crosslink (ICL) repair pathway. Accurate laboratory investigations are req
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d399affcaf9c4c279b9ddacc56890cf2
https://doi.org/10.1136/jmg-2022-108714
https://doi.org/10.1136/jmg-2022-108714