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Foreword for the special section on power and energy education

Undergraduate training programs stem

Butler-Purry KL, Pahwa A.
GSID: ZhZa36G1aqcJ
A Pahwa, KL Butler-Purry… - IEEE Transactions on …, 2014 - researchgate.net

… students feel they could be successful in STEM fields. … -on experiments for undergraduate and graduate level students … a simulation platform for ongoing training and education of power …

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Pahwa, A., Butler-Purry, K. L., & Zareipour, H. (2014). Foreword for the special section on power and energy education. IEEE Transactions on Power Systems, 29(4), 1871-1873.
Pahwa, Anil, Karen L. Butler-Purry, and Hamidreza Zareipour. "Foreword for the special section on power and energy education." IEEE Transactions on Power Systems 29.4 (2014): 1871-1873.
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Robot assisted adrenalectomy: a handy tool or glorified obsession?.

Gland surgery

Pahwa M.
PMID: 26312212
Gland Surg. 2015 Aug;4(4):279-82. doi: 10.3978/j.issn.2227-684X.2015.05.01.

Robotic surgery has recently expanded its horizon in urology apart from radical prostatectomy, one of them being adrenalectomy. Till now, laparoscopic adrenalectomy has established itself as the procedure of choice for benign adrenal disorders. Brandao et al. have recently...

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Pahwa M. Robot assisted adrenalectomy: a handy tool or glorified obsession?. Gland Surg. 2015;4(4):279-82doi: 10.3978/j.issn.2227-684X.2015.05.01.
Pahwa, M. (2015). Robot assisted adrenalectomy: a handy tool or glorified obsession?. Gland surgery, 4(4), 279-82. https://doi.org/10.3978/j.issn.2227-684X.2015.05.01
Pahwa, Mrinal. "Robot assisted adrenalectomy: a handy tool or glorified obsession?." Gland surgery vol. 4,4 (2015): 279-82. doi: https://doi.org/10.3978/j.issn.2227-684X.2015.05.01
Pahwa M. Robot assisted adrenalectomy: a handy tool or glorified obsession?. Gland Surg. 2015 Aug;4(4):279-82. doi: 10.3978/j.issn.2227-684X.2015.05.01. PMID: 26312212; PMCID: PMC4523626.
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Cutaneous alternariosis in a renal transplant patient successfully treated with posaconazole: Case report and literature review.

Medical mycology case reports

Bajwa R, Wojciechowski AL, Hsiao CB.
PMID: 28180057
Med Mycol Case Rep. 2017 Jan 21;15:16-20. doi: 10.1016/j.mmcr.2017.01.003. eCollection 2017 Mar.

Cutaneous alternariosis is an uncommon fungal infection that most commonly presents in organ transplant patients on immunosuppressive therapy. There are no clinical trials or guidelines to guide treatment of this condition, however itraconazole is the most commonly used antifungal...

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Bajwa R, Wojciechowski AL, Hsiao CB. Cutaneous alternariosis in a renal transplant patient successfully treated with posaconazole: Case report and literature review. Med Mycol Case Rep. 2017;15:16-20doi: 10.1016/j.mmcr.2017.01.003.
Bajwa, R., Wojciechowski, A. L., & Hsiao, C. B. (2017). Cutaneous alternariosis in a renal transplant patient successfully treated with posaconazole: Case report and literature review. Medical mycology case reports, 1516-20. https://doi.org/10.1016/j.mmcr.2017.01.003
Bajwa, Rajinder, et al. "Cutaneous alternariosis in a renal transplant patient successfully treated with posaconazole: Case report and literature review." Medical mycology case reports vol. 15 (2017): 16-20. doi: https://doi.org/10.1016/j.mmcr.2017.01.003
Bajwa R, Wojciechowski AL, Hsiao CB. Cutaneous alternariosis in a renal transplant patient successfully treated with posaconazole: Case report and literature review. Med Mycol Case Rep. 2017 Jan 21;15:16-20. doi: 10.1016/j.mmcr.2017.01.003. eCollection 2017 Mar. PMID: 28180057; PMCID: PMC5279863.
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The influence of graft placement on clinical outcome in anterior cruciate ligament reconstruction.

Joints

Padua R, Alviti F, Venosa M, Mazzola C, Padua L.
PMID: 27386442
Joints. 2016 Jun 13;4(1):12-6. doi: 10.11138/jts/2016.4.1.012. eCollection 2016.

PURPOSE: the aim of the present study was to investigate the influence of graft tunnel position on both clinical outcome and instrumental knee stability in patients submitted to arthroscopic ACL reconstruction using a bone-patellar tendon-bone (BPTB) graft.METHODS: thirty patients...

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Padua R, Alviti F, Venosa M, et al. The influence of graft placement on clinical outcome in anterior cruciate ligament reconstruction. Joints. 2016;4(1):12-6doi: 10.11138/jts/2016.4.1.012.
Padua, R., Alviti, F., Venosa, M., Mazzola, C., & Padua, L. (2016). The influence of graft placement on clinical outcome in anterior cruciate ligament reconstruction. Joints, 4(1), 12-6. https://doi.org/10.11138/jts/2016.4.1.012
Padua, Roberto, et al. "The influence of graft placement on clinical outcome in anterior cruciate ligament reconstruction." Joints vol. 4,1 (2016): 12-6. doi: https://doi.org/10.11138/jts/2016.4.1.012
Padua R, Alviti F, Venosa M, Mazzola C, Padua L. The influence of graft placement on clinical outcome in anterior cruciate ligament reconstruction. Joints. 2016 Jun 13;4(1):12-6. doi: 10.11138/jts/2016.4.1.012. eCollection 2016. PMID: 27386442; PMCID: PMC4914368.
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Scalp Seeding Post Craniotomy and Radiosurgery for Solitary Brain Metastasis: A Case Report and Systematic Review.

Cureus

Sharieff W, Mulroy L, Weeks A, Mansoor S, Pahil R, Islam MU.
PMID: 28405533
Cureus. 2017 Mar 07;9(3):e1083. doi: 10.7759/cureus.1083.

BACKGROUND  : Radiosurgery is being increasingly used post craniotomy for brain metastasis, instead of whole-brain radiation. We report a case of scalp metastasis following craniotomy and radiosurgery, along with a systematic review of the literature.METHODS        : Our patient was...

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Sharieff W, Mulroy L, Weeks A, et al. Scalp Seeding Post Craniotomy and Radiosurgery for Solitary Brain Metastasis: A Case Report and Systematic Review. Cureus. 2017;9(3):e1083doi: 10.7759/cureus.1083.
Sharieff, W., Mulroy, L., Weeks, A., Mansoor, S., Pahil, R., & Islam, M. U. (2017). Scalp Seeding Post Craniotomy and Radiosurgery for Solitary Brain Metastasis: A Case Report and Systematic Review. Cureus, 9(3), e1083. https://doi.org/10.7759/cureus.1083
Sharieff, Waseem, et al. "Scalp Seeding Post Craniotomy and Radiosurgery for Solitary Brain Metastasis: A Case Report and Systematic Review." Cureus vol. 9,3 (2017): e1083. doi: https://doi.org/10.7759/cureus.1083
Sharieff W, Mulroy L, Weeks A, Mansoor S, Pahil R, Islam MU. Scalp Seeding Post Craniotomy and Radiosurgery for Solitary Brain Metastasis: A Case Report and Systematic Review. Cureus. 2017 Mar 07;9(3):e1083. doi: 10.7759/cureus.1083. PMID: 28405533; PMCID: PMC5384848.
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Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines.

Optics express

Pahwa K, Mudarikwa L, Goldwin J.
PMID: 23038298
Opt Express. 2012 Jul 30;20(16):17456-66. doi: 10.1364/OE.20.017456.

We study modulation-free methods for producing sub-Doppler, dispersive line shapes for laser stabilization near the potassium D(2) transitions at 767 nm. Polarization spectroscopy is performed and a comparison is made between the use of a mirror or beam splitter...

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Pahwa K, Mudarikwa L, Goldwin J. Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines. Opt Express. 2012;20(16):17456-66doi: 10.1364/OE.20.017456.
Pahwa, K., Mudarikwa, L., & Goldwin, J. (2012). Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines. Optics express, 20(16), 17456-66. https://doi.org/10.1364/OE.20.017456
Pahwa, K, et al. "Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines." Optics express vol. 20,16 (2012): 17456-66. doi: https://doi.org/10.1364/OE.20.017456
Pahwa K, Mudarikwa L, Goldwin J. Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines. Opt Express. 2012 Jul 30;20(16):17456-66. doi: 10.1364/OE.20.017456. PMID: 23038298.
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A Facile and Efficient Synthesis of Thieno[2,3-c]furans and Furo[3,4-b]indoles via a Pummerer-Induced Cyclization Reaction.

The Journal of organic chemistry

Kappe CO, Padwa A.
PMID: 11667451
J Org Chem. 1996 Sep 06;61(18):6166-6174. doi: 10.1021/jo9607929.

The alpha-thiocarbocation generated from the Pummerer reaction of an o-heteroaroyl-substituted sulfoxide is intercepted by the adjacent keto group to produce an alpha-thio-substituted heteroaromatic isobenzofuran. In the presence of a suitable dienophile, the reactive o-xylylene undergoes a Diels-Alder cycloaddition followed...

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Kappe CO, Padwa A. A Facile and Efficient Synthesis of Thieno[2,3-c]furans and Furo[3,4-b]indoles via a Pummerer-Induced Cyclization Reaction. J Org Chem. 1996;61(18):6166-6174doi: 10.1021/jo9607929.
Kappe, C. O., & Padwa, A. (1996). A Facile and Efficient Synthesis of Thieno[2,3-c]furans and Furo[3,4-b]indoles via a Pummerer-Induced Cyclization Reaction. The Journal of organic chemistry, 61(18), 6166-6174. https://doi.org/10.1021/jo9607929
Kappe, C. Oliver, and Padwa, Albert. "A Facile and Efficient Synthesis of Thieno[2,3-c]furans and Furo[3,4-b]indoles via a Pummerer-Induced Cyclization Reaction." The Journal of organic chemistry vol. 61,18 (1996): 6166-6174. doi: https://doi.org/10.1021/jo9607929
Kappe CO, Padwa A. A Facile and Efficient Synthesis of Thieno[2,3-c]furans and Furo[3,4-b]indoles via a Pummerer-Induced Cyclization Reaction. J Org Chem. 1996 Sep 06;61(18):6166-6174. doi: 10.1021/jo9607929. PMID: 11667451.
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A Cycloaddition Approach toward the Synthesis of Substituted Indolines and Tetrahydroquinolines.

The Journal of organic chemistry

Padwa A, Brodney MA, Liu B, Satake K, Wu T.
PMID: 11674487
J Org Chem. 1999 May 14;64(10):3595-3607. doi: 10.1021/jo982453g.

The intramolecular Diels-Alder reaction of 2-substituted aminofurans (IMDAF) results in the formation of various indolines and tetrahydroquinolines. The isolation of these ring systems from the IMDAF reaction can be rationalized in terms of an initial [4 + 2]-cycloaddition that...

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Padwa A, Brodney MA, Liu B, et al. A Cycloaddition Approach toward the Synthesis of Substituted Indolines and Tetrahydroquinolines. J Org Chem. 1999;64(10):3595-3607doi: 10.1021/jo982453g.
Padwa, A., Brodney, M. A., Liu, B., Satake, K., & Wu, T. (1999). A Cycloaddition Approach toward the Synthesis of Substituted Indolines and Tetrahydroquinolines. The Journal of organic chemistry, 64(10), 3595-3607. https://doi.org/10.1021/jo982453g
Padwa, Albert, et al. "A Cycloaddition Approach toward the Synthesis of Substituted Indolines and Tetrahydroquinolines." The Journal of organic chemistry vol. 64,10 (1999): 3595-3607. doi: https://doi.org/10.1021/jo982453g
Padwa A, Brodney MA, Liu B, Satake K, Wu T. A Cycloaddition Approach toward the Synthesis of Substituted Indolines and Tetrahydroquinolines. J Org Chem. 1999 May 14;64(10):3595-3607. doi: 10.1021/jo982453g. PMID: 11674487.
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Theoretical Insights Regarding the Cycloaddition Behavior of Push-Pull Stabilized Carbonyl Ylides.

The Journal of organic chemistry

Weingarten MD, Prein M, Price AT, Snyder JP, Padwa A.
PMID: 11671503
J Org Chem. 1997 Apr 04;62(7):2001-2010. doi: 10.1021/jo962184z.

A series of diazoamido keto esters were prepared by the reaction of N-substituted 3-carbethoxy-2-piperidone with n-butylmagnesium chloride followed by the addition of ethyl 2-diazomalonyl chloride. Treatment of these diazo amides with rhodium(II) acetate afforded transient push-pull carbonyl ylide dipoles...

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Weingarten MD, Prein M, Price AT, et al. Theoretical Insights Regarding the Cycloaddition Behavior of Push-Pull Stabilized Carbonyl Ylides. J Org Chem. 1997;62(7):2001-2010doi: 10.1021/jo962184z.
Weingarten, M. D., Prein, M., Price, A. T., Snyder, J. P., & Padwa, A. (1997). Theoretical Insights Regarding the Cycloaddition Behavior of Push-Pull Stabilized Carbonyl Ylides. The Journal of organic chemistry, 62(7), 2001-2010. https://doi.org/10.1021/jo962184z
Weingarten, M. David, et al. "Theoretical Insights Regarding the Cycloaddition Behavior of Push-Pull Stabilized Carbonyl Ylides." The Journal of organic chemistry vol. 62,7 (1997): 2001-2010. doi: https://doi.org/10.1021/jo962184z
Weingarten MD, Prein M, Price AT, Snyder JP, Padwa A. Theoretical Insights Regarding the Cycloaddition Behavior of Push-Pull Stabilized Carbonyl Ylides. J Org Chem. 1997 Apr 04;62(7):2001-2010. doi: 10.1021/jo962184z. PMID: 11671503.
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Studies Dealing with the Cycloaddition/Ring Opening/Elimination Sequence of 2-Amino-Substituted Isobenzofurans.

The Journal of organic chemistry

Padwa A, Kappe CO, Cochran JE, Snyder JP.
PMID: 11671641
J Org Chem. 1997 May 02;62(9):2786-2797. doi: 10.1021/jo962358c.

The alpha-thiocarbocation generated from the Pummerer reaction of an o-amido-substituted sulfoxide is intercepted by the adjacent amido carbonyl group to produce a 2-amino-substituted isobenzofuran as a transient intermediate. In the presence of an electron-deficient dienophile, the reactive isobenzofuran undergoes...

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Padwa A, Kappe CO, Cochran JE, et al. Studies Dealing with the Cycloaddition/Ring Opening/Elimination Sequence of 2-Amino-Substituted Isobenzofurans. J Org Chem. 1997;62(9):2786-2797doi: 10.1021/jo962358c.
Padwa, A., Kappe, C. O., Cochran, J. E., & Snyder, J. P. (1997). Studies Dealing with the Cycloaddition/Ring Opening/Elimination Sequence of 2-Amino-Substituted Isobenzofurans. The Journal of organic chemistry, 62(9), 2786-2797. https://doi.org/10.1021/jo962358c
Padwa, Albert, et al. "Studies Dealing with the Cycloaddition/Ring Opening/Elimination Sequence of 2-Amino-Substituted Isobenzofurans." The Journal of organic chemistry vol. 62,9 (1997): 2786-2797. doi: https://doi.org/10.1021/jo962358c
Padwa A, Kappe CO, Cochran JE, Snyder JP. Studies Dealing with the Cycloaddition/Ring Opening/Elimination Sequence of 2-Amino-Substituted Isobenzofurans. J Org Chem. 1997 May 02;62(9):2786-2797. doi: 10.1021/jo962358c. PMID: 11671641.
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Criteria for the diagnosis of essential tremor.

Neurology

Bain P, Brin M, Deuschl G, Elble R, Jankovic J, Findley L, Koller WC, Pahwa R.
PMID: 10854345
Neurology. 2000;54(11):S7.

No abstract available.

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Bain P, Brin M, Deuschl G, et al. Criteria for the diagnosis of essential tremor. Neurology. 2000;54(11):S7
Bain, P., Brin, M., Deuschl, G., Elble, R., Jankovic, J., Findley, L., Koller, W. C., & Pahwa, R. (2000). Criteria for the diagnosis of essential tremor. Neurology, 54(11), S7.
Bain, P, et al. "Criteria for the diagnosis of essential tremor." Neurology vol. 54,11 (2000): S7.
Bain P, Brin M, Deuschl G, Elble R, Jankovic J, Findley L, Koller WC, Pahwa R. Criteria for the diagnosis of essential tremor. Neurology. 2000;54(11):S7. PMID: 10854345.
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Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones.

Organic letters

Rashatasakhon P, Ozdemir AD, Willis J, Padwa A.
PMID: 15012064
Org Lett. 2004 Mar 18;6(6):917-20. doi: 10.1021/ol036347z.

[reaction: see text] Radical cyclization of N-allyl-7-bromo-3a-methyl-hexahydroindol-2-one affords a six-membered ring product that prevails over the isomeric five-membered compound. The former product is generated through two reaction pathways: (a) 6-endo-trig ring closure and (b) rearrangement of an intermediate methylenecyclopentyl...

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Rashatasakhon P, Ozdemir AD, Willis J, et al. Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones. Org Lett. 2004;6(6):917-20doi: 10.1021/ol036347z.
Rashatasakhon, P., Ozdemir, A. D., Willis, J., & Padwa, A. (2004). Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones. Organic letters, 6(6), 917-20. https://doi.org/10.1021/ol036347z
Rashatasakhon, Paitoon, et al. "Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones." Organic letters vol. 6,6 (2004): 917-20. doi: https://doi.org/10.1021/ol036347z
Rashatasakhon P, Ozdemir AD, Willis J, Padwa A. Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones. Org Lett. 2004 Mar 18;6(6):917-20. doi: 10.1021/ol036347z. PMID: 15012064.
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Showing 1 to 12 of 402 entries