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Clinical Utility of Gallium-68 PSMA PET/CT Scan for Prostate Cancer.

Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India

Kallur KG, Ramachandra PG, Rajkumar K, Swamy SS, Desai I, Rao RM, Patil SG, Sridhar PS, Madhusudhan N, Krishnappa RS, Bhadrasetty V, Kumara HM, Santhosh SD, Ajaikumar BS.
PMID: 28533638
Indian J Nucl Med. 2017 Apr-Jun;32(2):110-117. doi: 10.4103/0972-3919.202255.

BACKGROUND: Prostate cancer is biologically and clinically a heterogeneous disease that makes imaging evaluation challenging. One of the important challenges in this cancer is to detect recurrent disease. Biochemical response using Prostate Specific Antigen (PSA) and Imaging using several...

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Kallur KG, Ramachandra PG, Rajkumar K, et al. Clinical Utility of Gallium-68 PSMA PET/CT Scan for Prostate Cancer. Indian J Nucl Med. 2017;32(2):110-117doi: 10.4103/0972-3919.202255.
Kallur, K. G., Ramachandra, P. G., Rajkumar, K., Swamy, S. S., Desai, I., Rao, R. M., Patil, S. G., Sridhar, P. S., Madhusudhan, N., Krishnappa, R. S., Bhadrasetty, V., Kumara, H. M., Santhosh, S. D., & Ajaikumar, B. S. (2017). Clinical Utility of Gallium-68 PSMA PET/CT Scan for Prostate Cancer. Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India, 32(2), 110-117. https://doi.org/10.4103/0972-3919.202255
Kallur, Kumaraswamy G, et al. "Clinical Utility of Gallium-68 PSMA PET/CT Scan for Prostate Cancer." Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India vol. 32,2 (2017): 110-117. doi: https://doi.org/10.4103/0972-3919.202255
Kallur KG, Ramachandra PG, Rajkumar K, Swamy SS, Desai I, Rao RM, Patil SG, Sridhar PS, Madhusudhan N, Krishnappa RS, Bhadrasetty V, Kumara HM, Santhosh SD, Ajaikumar BS. Clinical Utility of Gallium-68 PSMA PET/CT Scan for Prostate Cancer. Indian J Nucl Med. 2017 Apr-Jun;32(2):110-117. doi: 10.4103/0972-3919.202255. PMID: 28533638; PMCID: PMC5439210.
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Synthesis of Nanoparticle Assemblies: general discussion.

Faraday discussions

Som M, Majumdar S, Bachhar N, Kumaraswamy G, Pavan Kumar GV, Manoharan VN, Kumar S, Basavaraj MG, Kulkarni S, Bandyopadhyay R, Punnathanam S, Medhi H, Srivastav A, Frenkel D, Tripathy M, Eiser E, Gonzalez-Garcia L, Roy Chowdhury P, Singh J, Sridurai V, Edwards A, Prasad BL, Singh AK, Bockstaller M, John NS, Seth J, Misra M, Chakravarty C, Shinde V, Bandyopadhyaya R, Jestin J, Poojari R, Kotov N, Gang O, Karim A, Ju-Nam Y, Granick S, Chervinskii S, Tao A.
PMID: 27042810
Faraday Discuss. 2016;186:123-52. doi: 10.1039/C6FD90001A.

No abstract available.

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Som M, Majumdar S, Bachhar N, et al. Synthesis of Nanoparticle Assemblies: general discussion. Faraday Discuss. 2016;186:123-52doi: 10.1039/C6FD90001A.
Som, M., Majumdar, S., Bachhar, N., Kumaraswamy, G., Pavan Kumar, G. V., Manoharan, V. N., Kumar, S., Basavaraj, M. G., Kulkarni, S., Bandyopadhyay, R., Punnathanam, S., Medhi, H., Srivastav, A., Frenkel, D., Tripathy, M., Eiser, E., Gonzalez-Garcia, L., Roy Chowdhury, P., Singh, J., Sridurai, V., Edwards, A., Prasad, B. L., Singh, A. K., Bockstaller, M., John, N. S., Seth, J., Misra, M., Chakravarty, C., Shinde, V., Bandyopadhyaya, R., Jestin, J., Poojari, R., Kotov, N., Gang, O., Karim, A., Ju-Nam, Y., Granick, S., Chervinskii, S., & Tao, A. (2016). Synthesis of Nanoparticle Assemblies: general discussion. Faraday discussions, 186123-52. https://doi.org/10.1039/C6FD90001A
Som, Madhura, et al. "Synthesis of Nanoparticle Assemblies: general discussion." Faraday discussions vol. 186 (2016): 123-52. doi: https://doi.org/10.1039/C6FD90001A
Som M, Majumdar S, Bachhar N, Kumaraswamy G, Pavan Kumar GV, Manoharan VN, Kumar S, Basavaraj MG, Kulkarni S, Bandyopadhyay R, Punnathanam S, Medhi H, Srivastav A, Frenkel D, Tripathy M, Eiser E, Gonzalez-Garcia L, Roy Chowdhury P, Singh J, Sridurai V, Edwards A, Prasad BL, Singh AK, Bockstaller M, John NS, Seth J, Misra M, Chakravarty C, Shinde V, Bandyopadhyaya R, Jestin J, Poojari R, Kotov N, Gang O, Karim A, Ju-Nam Y, Granick S, Chervinskii S, Tao A. Synthesis of Nanoparticle Assemblies: general discussion. Faraday Discuss. 2016;186:123-52. doi: 10.1039/C6FD90001A. PMID: 27042810.
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Evaluation of dosimetric effect caused by slowing with multi-leaf collimator (MLC) leaves for volumetric modulated arc therapy (VMAT).

Radiology and oncology

Xu Z, Wang IZ, Kumaraswamy LK, Podgorsak MB.
PMID: 27069458
Radiol Oncol. 2016 Feb 16;50(1):121-8. doi: 10.1515/raon-2016-0008. eCollection 2016 Mar 01.

BACKGROUND: This study is to report 1) the sensitivity of intensity modulated radiation therapy (IMRT) QA method for clinical volumetric modulated arc therapy (VMAT) plans with multi-leaf collimator (MLC) leaf errors that will not trigger MLC interlock during beam...

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Xu Z, Wang IZ, Kumaraswamy LK, et al. Evaluation of dosimetric effect caused by slowing with multi-leaf collimator (MLC) leaves for volumetric modulated arc therapy (VMAT). Radiol Oncol. 2016;50(1):121-8doi: 10.1515/raon-2016-0008.
Xu, Z., Wang, I. Z., Kumaraswamy, L. K., & Podgorsak, M. B. (2016). Evaluation of dosimetric effect caused by slowing with multi-leaf collimator (MLC) leaves for volumetric modulated arc therapy (VMAT). Radiology and oncology, 50(1), 121-8. https://doi.org/10.1515/raon-2016-0008
Xu, Zhengzheng, et al. "Evaluation of dosimetric effect caused by slowing with multi-leaf collimator (MLC) leaves for volumetric modulated arc therapy (VMAT)." Radiology and oncology vol. 50,1 (2016): 121-8. doi: https://doi.org/10.1515/raon-2016-0008
Xu Z, Wang IZ, Kumaraswamy LK, Podgorsak MB. Evaluation of dosimetric effect caused by slowing with multi-leaf collimator (MLC) leaves for volumetric modulated arc therapy (VMAT). Radiol Oncol. 2016 Feb 16;50(1):121-8. doi: 10.1515/raon-2016-0008. eCollection 2016 Mar 01. PMID: 27069458; PMCID: PMC4825334.
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Traumatic brain injury: Does gender influence outcomes?.

International journal of critical illness and injury science

Munivenkatappa A, Agrawal A, Shukla DP, Kumaraswamy D, Devi BI.
PMID: 27308254
Int J Crit Illn Inj Sci. 2016 Apr-Jun;6(2):70-3. doi: 10.4103/2229-5151.183024.

BACKGROUND: Traumatic brain injury (TBI) is a major public health problem. Both genders are affected, but little is known about female TBI. The present study exclusively explores epidemiological, clinical, imaging, and death aspects of female TBI, and how it...

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Munivenkatappa A, Agrawal A, Shukla DP, et al. Traumatic brain injury: Does gender influence outcomes?. Int J Crit Illn Inj Sci. 2016;6(2):70-3doi: 10.4103/2229-5151.183024.
Munivenkatappa, A., Agrawal, A., Shukla, D. P., Kumaraswamy, D., & Devi, B. I. (2016). Traumatic brain injury: Does gender influence outcomes?. International journal of critical illness and injury science, 6(2), 70-3. https://doi.org/10.4103/2229-5151.183024
Munivenkatappa, Ashok, et al. "Traumatic brain injury: Does gender influence outcomes?." International journal of critical illness and injury science vol. 6,2 (2016): 70-3. doi: https://doi.org/10.4103/2229-5151.183024
Munivenkatappa A, Agrawal A, Shukla DP, Kumaraswamy D, Devi BI. Traumatic brain injury: Does gender influence outcomes?. Int J Crit Illn Inj Sci. 2016 Apr-Jun;6(2):70-3. doi: 10.4103/2229-5151.183024. PMID: 27308254; PMCID: PMC4901830.
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Dinuclear and Tetranuclear Cages of Oxodiphenylantimony Phosphinates: Synthesis and Structures.

Inorganic chemistry

Said MA, Kumara Swamy KC, Poojary DM, Clearfield A, Veith M, Huch V.
PMID: 11666523
Inorg Chem. 1996 May 22;35(11):3235-3241. doi: 10.1021/ic950713w.

The novel dimeric compounds [Ph(2)Sb(O(2)PR(2))O](2).2CH(2)Cl(2) [R = cycl-C(6)H(11) (2) and cycl-C(8)H(15) (3)] have been synthesized by reacting diphenylantimony trichloride (1) with 3 mol equiv of silver acetate followed by 1 mol equiv of the phosphinic acid. By the same...

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Said MA, Kumara Swamy KC, Poojary DM, et al. Dinuclear and Tetranuclear Cages of Oxodiphenylantimony Phosphinates: Synthesis and Structures. Inorg Chem. 1996;35(11):3235-3241doi: 10.1021/ic950713w.
Said, M. A., Kumara Swamy, K. C., Poojary, D. M., Clearfield, A., Veith, M., & Huch, V. (1996). Dinuclear and Tetranuclear Cages of Oxodiphenylantimony Phosphinates: Synthesis and Structures. Inorganic chemistry, 35(11), 3235-3241. https://doi.org/10.1021/ic950713w
Said, Musa A., et al. "Dinuclear and Tetranuclear Cages of Oxodiphenylantimony Phosphinates: Synthesis and Structures." Inorganic chemistry vol. 35,11 (1996): 3235-3241. doi: https://doi.org/10.1021/ic950713w
Said MA, Kumara Swamy KC, Poojary DM, Clearfield A, Veith M, Huch V. Dinuclear and Tetranuclear Cages of Oxodiphenylantimony Phosphinates: Synthesis and Structures. Inorg Chem. 1996 May 22;35(11):3235-3241. doi: 10.1021/ic950713w. PMID: 11666523.
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Apical versus equatorial disposition of substituents in tetraoxyphosphoranes bearing a 1,3,2-dioxaphosphocin ring: implications on apicophilicity in trigonal bipyramidal phosphorus.

Inorganic chemistry

Kommana P, Kumaraswamy S, Vittal JJ, Kumara Swamy KC.
PMID: 11978098
Inorg Chem. 2002 May 06;41(9):2356-63. doi: 10.1021/ic010935w.

New spirocyclic (amino/amido)tetraoxyphosphoranes CH(2)(6-t-Bu-4-Me-C(6)H(2)O)(2)P(NRR')(O(2)C(6)Cl(4)) [R = Me, R' = Ph (1), R = R' = i-Pr (2); R = R' = H (3); R = H, R' = Ph (4)] and the isothiocyanatotetraoxyphosphorane CH(2)(6-t-Bu-4-Me-C(6)H(2)O)(2)P(NCS)(O(2)C(6)Cl(4)) (5) have been synthesized. X-ray...

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Kommana P, Kumaraswamy S, Vittal JJ, et al. Apical versus equatorial disposition of substituents in tetraoxyphosphoranes bearing a 1,3,2-dioxaphosphocin ring: implications on apicophilicity in trigonal bipyramidal phosphorus. Inorg Chem. 2002;41(9):2356-63doi: 10.1021/ic010935w.
Kommana, P., Kumaraswamy, S., Vittal, J. J., & Kumara Swamy, K. C. (2002). Apical versus equatorial disposition of substituents in tetraoxyphosphoranes bearing a 1,3,2-dioxaphosphocin ring: implications on apicophilicity in trigonal bipyramidal phosphorus. Inorganic chemistry, 41(9), 2356-63. https://doi.org/10.1021/ic010935w
Kommana, Praveen, et al. "Apical versus equatorial disposition of substituents in tetraoxyphosphoranes bearing a 1,3,2-dioxaphosphocin ring: implications on apicophilicity in trigonal bipyramidal phosphorus." Inorganic chemistry vol. 41,9 (2002): 2356-63. doi: https://doi.org/10.1021/ic010935w
Kommana P, Kumaraswamy S, Vittal JJ, Kumara Swamy KC. Apical versus equatorial disposition of substituents in tetraoxyphosphoranes bearing a 1,3,2-dioxaphosphocin ring: implications on apicophilicity in trigonal bipyramidal phosphorus. Inorg Chem. 2002 May 06;41(9):2356-63. doi: 10.1021/ic010935w. PMID: 11978098.
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Pentacoordinate phosphoranes with reversed apicophilicity as stable intermediates in a mitsunobu-type reaction.

The Journal of organic chemistry

Satish Kumar N, Kommana P, Vittal JJ, Kumara Swamy KC.
PMID: 12227794
J Org Chem. 2002 Sep 20;67(19):6653-8. doi: 10.1021/jo011150a.

Diisopropyl azodicarboxylate (DIAD) undergoes a cycloaddition reaction with the cyclic phosphites CH(2)(6-t-Bu-4-Me-C(6)H(2)O)(2)PX (1) [X = NCS (a), N(3) (b), Cl (c), NHMe (d) and Ph (e)] to afford the novel pentacoordinate phosphoranes 2a-e as crystalline solids. This result is...

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Satish Kumar N, Kommana P, Vittal JJ, et al. Pentacoordinate phosphoranes with reversed apicophilicity as stable intermediates in a mitsunobu-type reaction. J Org Chem. 2002;67(19):6653-8doi: 10.1021/jo011150a.
Satish Kumar, N., Kommana, P., Vittal, J. J., & Kumara Swamy, K. C. (2002). Pentacoordinate phosphoranes with reversed apicophilicity as stable intermediates in a mitsunobu-type reaction. The Journal of organic chemistry, 67(19), 6653-8. https://doi.org/10.1021/jo011150a
Satish Kumar, N, et al. "Pentacoordinate phosphoranes with reversed apicophilicity as stable intermediates in a mitsunobu-type reaction." The Journal of organic chemistry vol. 67,19 (2002): 6653-8. doi: https://doi.org/10.1021/jo011150a
Satish Kumar N, Kommana P, Vittal JJ, Kumara Swamy KC. Pentacoordinate phosphoranes with reversed apicophilicity as stable intermediates in a mitsunobu-type reaction. J Org Chem. 2002 Sep 20;67(19):6653-8. doi: 10.1021/jo011150a. PMID: 12227794.
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Anatomy of a cyclohexatriene: chemical dissection of the pi and sigma frame of angular [3]phenylene.

Angewandte Chemie (International ed. in English)

Kumaraswamy S, Jalisatgi SS, Matzger AJ, Miljanić OS, Vollhardt KP.
PMID: 15248280
Angew Chem Int Ed Engl. 2004 Jul 12;43(28):3711-5. doi: 10.1002/anie.200454126.

No abstract available.

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Kumaraswamy S, Jalisatgi SS, Matzger AJ, et al. Anatomy of a cyclohexatriene: chemical dissection of the pi and sigma frame of angular [3]phenylene. Angew Chem Int Ed Engl. 2004;43(28):3711-5doi: 10.1002/anie.200454126.
Kumaraswamy, S., Jalisatgi, S. S., Matzger, A. J., Miljanić, O. S., & Vollhardt, K. P. (2004). Anatomy of a cyclohexatriene: chemical dissection of the pi and sigma frame of angular [3]phenylene. Angewandte Chemie (International ed. in English), 43(28), 3711-5. https://doi.org/10.1002/anie.200454126
Kumaraswamy, Sriram, et al. "Anatomy of a cyclohexatriene: chemical dissection of the pi and sigma frame of angular [3]phenylene." Angewandte Chemie (International ed. in English) vol. 43,28 (2004): 3711-5. doi: https://doi.org/10.1002/anie.200454126
Kumaraswamy S, Jalisatgi SS, Matzger AJ, Miljanić OS, Vollhardt KP. Anatomy of a cyclohexatriene: chemical dissection of the pi and sigma frame of angular [3]phenylene. Angew Chem Int Ed Engl. 2004 Jul 12;43(28):3711-5. doi: 10.1002/anie.200454126. PMID: 15248280.
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Reparative granuloma following stapes surgery.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Mahadevaiah A, Parikh B, Kumaraswamy K.
PMID: 23120470
Indian J Otolaryngol Head Neck Surg. 2007 Dec;59(4):346-8. doi: 10.1007/s12070-007-0098-y. Epub 2007 Dec 11.

Reparative granuloma of the oval window is an uncommon complication of stapes surgery, which usually develops within one to six weeks after operation and causes a sudden hearing loss and disturbance of balance. We report 2 cases of post-stapedectomy...

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Mahadevaiah A, Parikh B, Kumaraswamy K. Reparative granuloma following stapes surgery. Indian J Otolaryngol Head Neck Surg. 2007;59(4):346-8doi: 10.1007/s12070-007-0098-y.
Mahadevaiah, A., Parikh, B., & Kumaraswamy, K. (2007). Reparative granuloma following stapes surgery. Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India, 59(4), 346-8. https://doi.org/10.1007/s12070-007-0098-y
Mahadevaiah, A, et al. "Reparative granuloma following stapes surgery." Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India vol. 59,4 (2007): 346-8. doi: https://doi.org/10.1007/s12070-007-0098-y
Mahadevaiah A, Parikh B, Kumaraswamy K. Reparative granuloma following stapes surgery. Indian J Otolaryngol Head Neck Surg. 2007 Dec;59(4):346-8. doi: 10.1007/s12070-007-0098-y. Epub 2007 Dec 11. PMID: 23120470; PMCID: PMC3452263.
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Bicentric bipolar hip prosthesis: A radiological study of movement at the interprosthetic joint.

Indian journal of orthopaedics

Rai AK, Singh S, Kumaraswamy V, Khare G, Yadav V, Agarwal R.
PMID: 22144743
Indian J Orthop. 2011 Nov;45(6):508-13. doi: 10.4103/0019-5413.87120.

BACKGROUND: The bipolar hip prostheses after some time functions as a unipolar device. There is a need to change the design of bipolar hip prostheses to make it function as a bipolar device over a prolonged period of time....

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Rai AK, Singh S, Kumaraswamy V, et al. Bicentric bipolar hip prosthesis: A radiological study of movement at the interprosthetic joint. Indian J Orthop. 2011;45(6):508-13doi: 10.4103/0019-5413.87120.
Rai, A. K., Singh, S., Kumaraswamy, V., Khare, G., Yadav, V., & Agarwal, R. (2011). Bicentric bipolar hip prosthesis: A radiological study of movement at the interprosthetic joint. Indian journal of orthopaedics, 45(6), 508-13. https://doi.org/10.4103/0019-5413.87120
Rai, Anil Kumar, et al. "Bicentric bipolar hip prosthesis: A radiological study of movement at the interprosthetic joint." Indian journal of orthopaedics vol. 45,6 (2011): 508-13. doi: https://doi.org/10.4103/0019-5413.87120
Rai AK, Singh S, Kumaraswamy V, Khare G, Yadav V, Agarwal R. Bicentric bipolar hip prosthesis: A radiological study of movement at the interprosthetic joint. Indian J Orthop. 2011 Nov;45(6):508-13. doi: 10.4103/0019-5413.87120. PMID: 22144743; PMCID: PMC3227354.
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Synthesis of functional hybrid silica scaffolds with controllable hierarchical porosity by dynamic templating.

Chemical communications (Cambridge, England)

Ganai AK, Kumari S, Sharma KP, Panda C, Kumaraswamy G, Gupta SS.
PMID: 22466999
Chem Commun (Camb). 2012 May 28;48(43):5292-4. doi: 10.1039/c2cc30885a. Epub 2012 Mar 30.

We report a facile one-pot synthesis of hierarchically porous scaffolds, with independent control over nanoparticle mesoporosity and scaffold macroporosity. Our technique combines the chemistry of mesoporous silica nanoparticles with the control afforded by dynamic templating of surfactant mesophases. These...

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Ganai AK, Kumari S, Sharma KP, et al. Synthesis of functional hybrid silica scaffolds with controllable hierarchical porosity by dynamic templating. Chem Commun (Camb). 2012;48(43):5292-4doi: 10.1039/c2cc30885a.
Ganai, A. K., Kumari, S., Sharma, K. P., Panda, C., Kumaraswamy, G., & Gupta, S. S. (2012). Synthesis of functional hybrid silica scaffolds with controllable hierarchical porosity by dynamic templating. Chemical communications (Cambridge, England), 48(43), 5292-4. https://doi.org/10.1039/c2cc30885a
Ganai, Anal Kr, et al. "Synthesis of functional hybrid silica scaffolds with controllable hierarchical porosity by dynamic templating." Chemical communications (Cambridge, England) vol. 48,43 (2012): 5292-4. doi: https://doi.org/10.1039/c2cc30885a
Ganai AK, Kumari S, Sharma KP, Panda C, Kumaraswamy G, Gupta SS. Synthesis of functional hybrid silica scaffolds with controllable hierarchical porosity by dynamic templating. Chem Commun (Camb). 2012 May 28;48(43):5292-4. doi: 10.1039/c2cc30885a. Epub 2012 Mar 30. PMID: 22466999.
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Sequential allylic substitution/Pauson-Khand reaction: a strategy to bicyclic fused cyclopentenones from MBH-acetates of acetylenic aldehydes.

The Journal of organic chemistry

Raji Reddy C, Kumaraswamy P, Singarapu KK.
PMID: 25105763
J Org Chem. 2014 Sep 05;79(17):7880-8. doi: 10.1021/jo500962d. Epub 2014 Aug 19.

An efficient approach for the construction of novel bicyclic fused cyclopentenones starting from Morita-Baylis-Hillman (MBH) acetates of acetylenic aldehydes with flexible scaffold diversity has been achieved using a two-step reaction sequence involving allylic substitution and the Pauson-Khand reaction. This...

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Raji Reddy C, Kumaraswamy P, Singarapu KK. Sequential allylic substitution/Pauson-Khand reaction: a strategy to bicyclic fused cyclopentenones from MBH-acetates of acetylenic aldehydes. J Org Chem. 2014;79(17):7880-8doi: 10.1021/jo500962d.
Raji Reddy, C., Kumaraswamy, P., & Singarapu, K. K. (2014). Sequential allylic substitution/Pauson-Khand reaction: a strategy to bicyclic fused cyclopentenones from MBH-acetates of acetylenic aldehydes. The Journal of organic chemistry, 79(17), 7880-8. https://doi.org/10.1021/jo500962d
Raji Reddy, Chada, et al. "Sequential allylic substitution/Pauson-Khand reaction: a strategy to bicyclic fused cyclopentenones from MBH-acetates of acetylenic aldehydes." The Journal of organic chemistry vol. 79,17 (2014): 7880-8. doi: https://doi.org/10.1021/jo500962d
Raji Reddy C, Kumaraswamy P, Singarapu KK. Sequential allylic substitution/Pauson-Khand reaction: a strategy to bicyclic fused cyclopentenones from MBH-acetates of acetylenic aldehydes. J Org Chem. 2014 Sep 05;79(17):7880-8. doi: 10.1021/jo500962d. Epub 2014 Aug 19. PMID: 25105763.
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