Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jayesh C Sardhara"'
Autor:
Suyash Singh, Jayesh C Sardhara, Deepak Khatri, Jeena Joseph, Abhijit N Parab, Kamlesh S Bhaisora, Kuntal Kanti Das, Anant Mehrotra, Arun Kumar Srivastava, Sanjay Behari
Publikováno v:
Journal of Craniovertebral Junction and Spine, Vol 9, Iss 2, Pp 122-129 (2018)
Background: There is growing indications of minimally invasive spine surgery. The inherent attitude and institutive learning curve limit transition from standard open surgery to minimally invasive surgery demanding understanding of new instruments an
Externí odkaz:
https://doaj.org/article/8d3856d29a1141e7bcad0ad16e31a420
Autor:
Ashutosh Kumar, Waseem Ahamed, Kamlesh S. Bhaisora, Jayesh C. Sardhara, Vandan Raiyyani, Arun Srivastava, Anant Mehrotra, Sanjay Behari
Publikováno v:
Indian Journal of Neurosurgery, Vol 13, Iss 02, Pp 095-102 (2024)
Proximal or A1 segment anterior cerebral artery (ACA) aneurysms are rare aneurysms. They have certain unique properties when compared to all other intracranial aneurysms. They are smaller and prone to an early rupture. Thus, they need an aggressive i
Externí odkaz:
https://doaj.org/article/3c759b321ce34a1f9f73dc38702124a9
Autor:
Ashutosh, Kumar, Jayesh C, Sardhara, Guramritpal, Singh, Soumen, Kanjilal, Ved P, Maurya, Sanjay, Behari
Publikováno v:
Neurology India. 69:443
Malignant meningitis (MM) is the diffuse involvement of the leptomeninges by infiltrating cancer cells, most frequently from lung and breast cancers. This review is aimed to discuss the current advances in the diagnosis and management of MM, along wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::758cf6c8e7b2d15530ac277e4dd6f4f8
https://doi.org/10.4103/0028-3886.332278
https://doi.org/10.4103/0028-3886.332278
Publikováno v:
Indian Journal of Neurosurgery, Vol 03, Iss 02, Pp 106-109 (2014)
Acromesomelic dysplasia Maroteaux type (AMDM) is a rare autosomal recessive osteochondrodysplasia. The responsible gene, AMDM gene, in human beings, has been mapped on 9p13-q12 chromosome by homozygous mapping and pathogenic mutation was later identi
Externí odkaz:
https://doaj.org/article/3df6508d7282416ab638668c14774d48