Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sreelatha, Komatireddy"'
Autor:
Maurizio Del Poeta, Brian J. Ward, Benjamin Greenberg, Bernhard Hemmer, Bruce A.C. Cree, Sreelatha Komatireddy, Jitendriya Mishra, Roseanne Sullivan, Ajay Kilaru, Alan Moore, Thomas Hach, Joseph R. Berger
Publikováno v:
Neurology(R) neuroimmunology & neuroinflammation, vol 9, iss 3
Background and ObjectivesTo describe the characteristics of patients with MS reporting cryptococcal meningitis (CM) while treated with fingolimod.MethodsThe Novartis safety database was searched for cases with CM between January 26, 2006, and Februar
Glaucoma-associated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes
Autor:
Garudadri Chandrasekhar, Anil K Mandal, Koilkonda R. Devi, Sreelatha Komatireddy, Ravi Thomas, Rajul S Parikh, Kiranpreet Kaur, Subhabrata Chakrabarti
Publikováno v:
Investigative ophthalmologyvisual science. 48(12)
Purpose To understand the involvement of the CYP1B1 gene in cases of primary open-angle (POAG) and primary angle-closure (PACG) glaucomas and obtain the haplotype background of these mutations. Methods The entire coding region of CYP1B1 was screened
Publikováno v:
Foundations in Vitreoretinal Diseases: Diabetic Eye Diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab3c56695c7500a98c80fb40e3e2d389
https://doi.org/10.5005/jp/books/10310_2
https://doi.org/10.5005/jp/books/10310_2
Autor:
Arijit, Mukhopadhyay, Sreelatha, Komatireddy, Moulinath, Acharya, Ashima, Bhattacharjee, Anil Kumar, Mandal, Sanjay K D, Thakur, Garudadri, Chandrasekhar, Arun, Banerjee, Ravi, Thomas, Subhabrata, Chakrabarti, Kunal, Ray
Publikováno v:
Molecular vision. 11
To evaluate the role of the optineurin gene (OPTN) in Indian primary open angle glaucoma (POAG) patients from different parts of the country.Two hundred patients with POAG and 200 ethnically matched normal controls were recruited from various parts o
Autor:
Mitali Mukerji, Ramesh C. Juyal, Sangeeta Sharma, Sreelatha Komatireddy, Shashi Chaudhary, Subhabrata Chakrabarti, Vishwamohini Khare, B.K. Thelma, Uday B. Muthane, Uma Mittal, Nagaraja Sarangmath, Mona Ragothaman
Publikováno v:
Annals of neurology. 55(1)
We describe a consanguineous Indian family having spinocerebellar ataxia type 2 (SCA2) expansions with complex phenotypes (early-onset, dopa-responsive parkinsonism, ataxia and retinitis pigmentosa). The two probands having homozygous SCA2 mutations
Autor:
Subhabrata, Chakrabarti, Sreelatha, Komatireddy, Anil Kumar, Mandal, Dorairajan, Balasubramanian
Publikováno v:
Human genetics. 113(6)
Autor:
Sreelatha, Komatireddy, Subhabrata, Chakrabarti, Anil Kumar, Mandal, Aramati Bindu Madhava, Reddy, Srirangan, Sampath, Shirly George, Panicker, Dorairajan, Balasubramanian
Publikováno v:
Molecular vision. 9
Axenfeld-Rieger anomaly (ARA) is a form of anterior segment dysgenesis of the eye, mainly caused by mutations in the FOXC1 gene. We had earlier reported a novel mutation in the wing region of FOXC1 in an autosomal dominant family. The present study w
Autor:
Mona Ragothaman, Nagaraja Sarangmath, Shashi Chaudhary, Vishwamohini Khare, Uma Mittal, Sangeeta Sharma, Sreelatha Komatireddy, Subhabrata Chakrabarti, Mitali Mukerji, Ramesh C. Juyal, B. K. Thelma, Uday B. Muthane
Publikováno v:
Annals of Neurology; Jan2004, Vol. 55 Issue 1, p130-133, 4p