Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Niranjan, Chavan"'
Autor:
Snehal Shabrish, Madhura Kelkar, Niranjan Chavan, Mukesh Desai, Umair Bargir, Maya Gupta, Priti Mehta, Akanksha Chichra, Chandrakala S, Prasad Taur, Vinay Saxena, Babu Rao Vundinti, Manisha Madkaikar
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Fanconi anemia (FA) is a rare inherited syndrome characterized by progressive bone marrow failure (BMF), abnormal skin pigmentation, short stature, and increased cancer risk. BMF in FA is multifactorial and largely results from the death of hematopoi
Externí odkaz:
https://doaj.org/article/5380a41d41c14bcca8714135f40d8eb0
Publikováno v:
Indian Journal of Gynecologic Oncology. 20
Publikováno v:
The Journal of Obstetrics and Gynecology of India. 72:539-541
Publikováno v:
Springer Series on Bio-and Neurosystems ISBN: 9783031100307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6c02f3b2983807954ecda0e908758e4
https://doi.org/10.1007/978-3-031-10031-4_14
https://doi.org/10.1007/978-3-031-10031-4_14
Autor:
Priya Ranjan, Hiren Kumar Deva Sarma, Niranjan Chavan, Uday Kumar, Kumar Dron Shrivastav, Rajiv Janardhanan
Publikováno v:
Lecture Notes in Networks and Systems ISBN: 9789811642432
Lecture Notes in Networks and Systems
Lecture Notes in Networks and Systems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87b614486d167c000b5dc0c0565b6e32
https://doi.org/10.1007/978-981-16-4244-9_36
https://doi.org/10.1007/978-981-16-4244-9_36
Autor:
Chandrakala Shanmukhaiah, Revathi Raj, Sowmyashree Ramesh, Sunil Bhat, Merin George, Shailesh Kanvinde, Nita Radhakrishnan, Avani Solanki, Niranjan Chavan, Sheila Mohan, Aruna Rajendran, Deendayalan Munirathnam, Pritesh Junagade, Sandeep Nemani, Anchu Anna Cherian, Mamta Manglani, Harsha Prasada Lashkari, Radha Gulati Ghildhiyal, Sudha Rao, Babu Rao Vundinti
Publikováno v:
Human mutationREFERENCES. 42(12)
Fanconi anemia (FA) is a rare autosomal or X-linked genetic disorder characterized by chromosomal breakages, congenital abnormalities, bone marrow failure (BMF), and cancer. There has been a discovery of 22 FANC genes known to be involved in the FA p
Publikováno v:
Metaheuristic Algorithms in Industry 4.0 ISBN: 9781003143505
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f0202f37d768c5b8811fd0dc3aa5a7
https://doi.org/10.1201/9781003143505-8
https://doi.org/10.1201/9781003143505-8
Publikováno v:
Indian Journal of Obstetrics and Gynecology Research. 7:608-610
Caesarean section is one of the common treatment offered in modern obstetrics. Despite being common, it can get complicated by life threatening complications like uterine scar rupture. It’s spectrum of manifestation can be from subtle symptoms of a
Autor:
Frank X. Donovan, Kenichi Yoshida, Minoru Takata, Agata Smogorzewska, Babu Rao Vundinti, Avani Solanki, Akifumi Takaori-Kondo, Niranjan Chavan, Yusuke Okuno, Selvaa Kumar C, Minako Mori, Settara C. Chandrasekharappa, Seiji Kojima, Merin George, Hiromasa Yabe, Seishi Ogawa, Sheila Mohan, Arleen D. Auerbach, Aruna Rajendran, Miharu Yabe, Hideki Muramastsu, Ramanagouda Ramanagoudr-Bhojappa, Akira Shimamoto
Publikováno v:
Hum Mutat
Fanconi anemia (FA) is a rare genetic disorder characterized by bone marrow failure, predisposition to cancer, and congenital abnormalities. FA is caused by pathogenic variants in any of 22 genes involved in the DNA repair pathway responsible for rem
Publikováno v:
International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 11:1795
Rectus sheath hematoma is a rare but potentially life-threatening complication following any major abdominal surgery. The nonspecific nature and lower incidence of this disorder may cause a delay in the diagnosis, and can often be misdiagnosed as a c