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[Not Available].

Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie

Champy C, Semprez F, El Sayed I, Maille P, Soyeux P, Allory Y, Vacherot F, De La Taille A, Firlej V.
PMID: 26544219
Prog Urol. 2015 Nov;25(13):727. doi: 10.1016/j.purol.2015.08.024.

No abstract available.

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Champy C, Semprez F, El Sayed I, et al. Implication de la molécule X dans la récidive du cancer de prostate (CaP) localisé. [Not Available]. Prog Urol. 2015;25(13):727doi: 10.1016/j.purol.2015.08.024.
Champy, C., Semprez, F., El Sayed, I., Maille, P., Soyeux, P., Allory, Y., Vacherot, F., De La Taille, A., & Firlej, V. (2015). Implication de la molécule X dans la récidive du cancer de prostate (CaP) localisé. [Not Available]. Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie, 25(13), 727. https://doi.org/10.1016/j.purol.2015.08.024
Champy, C, et al. "Implication de la molécule X dans la récidive du cancer de prostate (CaP) localisé." [Not Available]. Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie vol. 25,13 (2015): 727. doi: https://doi.org/10.1016/j.purol.2015.08.024
Champy C, Semprez F, El Sayed I, Maille P, Soyeux P, Allory Y, Vacherot F, De La Taille A, Firlej V. Implication de la molécule X dans la récidive du cancer de prostate (CaP) localisé. [Not Available]. Prog Urol. 2015 Nov;25(13):727. doi: 10.1016/j.purol.2015.08.024. French. PMID: 26544219.
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A new antibacterial lupane ester from the seeds of Acokanthera oppositifolia Lam.

Natural product research

El Sayed AM, Ezzat SM, Sabry OM.
PMID: 27046822
Nat Prod Res. 2016 Dec;30(24):2813-2818. doi: 10.1080/14786419.2016.1166494. Epub 2016 Apr 04.

As a part of ongoing investigation of Acokanthera oppositifolia (Lam.) Codd., four compounds were isolated from its seeds, a new compound; lup-20(29)-en-3β-O-(3'-β-hydroxy) palmitate (1), three known compounds; a triterpene; lupeol (2), a cardiac glycoside; acovenoside A (3) and a...

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El Sayed AM, Ezzat SM, Sabry OM. A new antibacterial lupane ester from the seeds of Acokanthera oppositifolia Lam. Nat Prod Res. 2016;30(24):2813-2818doi: 10.1080/14786419.2016.1166494.
El Sayed, A. M., Ezzat, S. M., & Sabry, O. M. (2016). A new antibacterial lupane ester from the seeds of Acokanthera oppositifolia Lam. Natural product research, 30(24), 2813-2818. https://doi.org/10.1080/14786419.2016.1166494
El Sayed, Abeer M, et al. "A new antibacterial lupane ester from the seeds of Acokanthera oppositifolia Lam." Natural product research vol. 30,24 (2016): 2813-2818. doi: https://doi.org/10.1080/14786419.2016.1166494
El Sayed AM, Ezzat SM, Sabry OM. A new antibacterial lupane ester from the seeds of Acokanthera oppositifolia Lam. Nat Prod Res. 2016 Dec;30(24):2813-2818. doi: 10.1080/14786419.2016.1166494. Epub 2016 Apr 04. PMID: 27046822.
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Antimicrobial activities of Saudi honey against Pseudomonas aeruginosa.

Saudi journal of biological sciences

Al-Nahari AA, Almasaudi SB, Abd El-Ghany el SM, Barbour E, Al Jaouni SK, Harakeh S.
PMID: 26288553
Saudi J Biol Sci. 2015 Sep;22(5):521-5. doi: 10.1016/j.sjbs.2015.04.006. Epub 2015 Apr 08.

UNLABELLED: Five types of imported and local honey were screened for both their bacteriocidal/bacteriostatic activities against both Imipenem resistant and sensitive Pseudomonas aeruginosa in both Brain Heart infusion broth and Mueller-Hinton agar. The results indicated that the effect was...

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Al-Nahari AA, Almasaudi SB, Abd El-Ghany el SM, et al. Antimicrobial activities of Saudi honey against Pseudomonas aeruginosa. Saudi J Biol Sci. 2015;22(5):521-5doi: 10.1016/j.sjbs.2015.04.006.
Al-Nahari, A. A., Almasaudi, S. B., Abd El-Ghany, e. l. . S. M., Barbour, E., Al Jaouni, S. K., & Harakeh, S. (2015). Antimicrobial activities of Saudi honey against Pseudomonas aeruginosa. Saudi journal of biological sciences, 22(5), 521-5. https://doi.org/10.1016/j.sjbs.2015.04.006
Al-Nahari, Alaa A M, et al. "Antimicrobial activities of Saudi honey against Pseudomonas aeruginosa." Saudi journal of biological sciences vol. 22,5 (2015): 521-5. doi: https://doi.org/10.1016/j.sjbs.2015.04.006
Al-Nahari AA, Almasaudi SB, Abd El-Ghany el SM, Barbour E, Al Jaouni SK, Harakeh S. Antimicrobial activities of Saudi honey against Pseudomonas aeruginosa. Saudi J Biol Sci. 2015 Sep;22(5):521-5. doi: 10.1016/j.sjbs.2015.04.006. Epub 2015 Apr 08. PMID: 26288553; PMCID: PMC4537880.
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The role of plasmapheresis in the treatment of severe lupus nephritis: a case report.

Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

Hussein M, Mooij J, Roujouleh H, El Sayed H.
PMID: 18583750
Saudi J Kidney Dis Transpl. 1995 Oct-Dec;6(4):412-6.

There is still controversy about the efficacy of plasma exchange in the treatment of severe lupus nephritis. Some studies have reported no beneficial effect with plasma exchange, while others claim its usefulness when used in combination ("synchronization") with immunosuppressive...

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Hussein M, Mooij J, Roujouleh H, et al. The role of plasmapheresis in the treatment of severe lupus nephritis: a case report. Saudi J Kidney Dis Transpl. 1995;6(4):412-6
Hussein, M., Mooij, J., Roujouleh, H., & El Sayed, H. (1995). The role of plasmapheresis in the treatment of severe lupus nephritis: a case report. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 6(4), 412-6.
Hussein, M, et al. "The role of plasmapheresis in the treatment of severe lupus nephritis: a case report." Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia vol. 6,4 (1995): 412-6.
Hussein M, Mooij J, Roujouleh H, El Sayed H. The role of plasmapheresis in the treatment of severe lupus nephritis: a case report. Saudi J Kidney Dis Transpl. 1995 Oct-Dec;6(4):412-6. PMID: 18583750.
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Benzyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxo-cyclo-hex-1-enecarbodithio-ate: second triclinic polymorph.

Acta crystallographica. Section E, Structure reports online

El Ashry el SH, Amer MR, Shah MR, Ng SW.
PMID: 21582252
Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o598. doi: 10.1107/S1600536809006151.

The title structure, C(22)H(22)BrNOS(2), is a triclinic modification. Whereas the other reported modification crystallizes with just one mol-ecule in the asymmetric unit, the present modification has Z' = 2. The six-membered cyclo-hexene ring adopts an envelope conformation, with the...

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El Ashry el SH, Amer MR, Shah MR, et al. Benzyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxo-cyclo-hex-1-enecarbodithio-ate: second triclinic polymorph. Acta Crystallogr Sect E Struct Rep Online. 2009;65:o598doi: 10.1107/S1600536809006151.
El Ashry, e. l. . S. H., Amer, M. R., Shah, M. R., & Ng, S. W. (2009). Benzyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxo-cyclo-hex-1-enecarbodithio-ate: second triclinic polymorph. Acta crystallographica. Section E, Structure reports online, 65o598. https://doi.org/10.1107/S1600536809006151
El Ashry, El Sayed H, et al. "Benzyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxo-cyclo-hex-1-enecarbodithio-ate: second triclinic polymorph." Acta crystallographica. Section E, Structure reports online vol. 65 (2009): o598. doi: https://doi.org/10.1107/S1600536809006151
El Ashry el SH, Amer MR, Shah MR, Ng SW. Benzyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxo-cyclo-hex-1-enecarbodithio-ate: second triclinic polymorph. Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o598. doi: 10.1107/S1600536809006151. PMID: 21582252; PMCID: PMC2968632.
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n-Undeca-nyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbodithio-ate.

Acta crystallographica. Section E, Structure reports online

El Ashry el SH, Amer MR, Shah MR, Ng SW.
PMID: 21582254
Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o600. doi: 10.1107/S1600536809006175.

The six-membered cyclo-hexene ring in the title compound, C(26)H(38)BrNOS(2), adopts an envelope conformation, with the C atom bearing the two methyl groups representing the flap. This atom deviates by 0.651 (3) Å from the plane passing through the other...

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El Ashry el SH, Amer MR, Shah MR, et al. n-Undeca-nyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbodithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009;65:o600doi: 10.1107/S1600536809006175.
El Ashry, e. l. . S. H., Amer, M. R., Shah, M. R., & Ng, S. W. (2009). n-Undeca-nyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbodithio-ate. Acta crystallographica. Section E, Structure reports online, 65o600. https://doi.org/10.1107/S1600536809006175
El Ashry, El Sayed H, et al. "n-Undeca-nyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbodithio-ate." Acta crystallographica. Section E, Structure reports online vol. 65 (2009): o600. doi: https://doi.org/10.1107/S1600536809006175
El Ashry el SH, Amer MR, Shah MR, Ng SW. n-Undeca-nyl 2-(4-bromo-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbodithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o600. doi: 10.1107/S1600536809006175. PMID: 21582254; PMCID: PMC2968570.
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2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate.

Acta crystallographica. Section E, Structure reports online

El Ashry el SH, Amer MR, Shah MR, Ng SW.
PMID: 21582256
Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o602. doi: 10.1107/S1600536809006199.

The six-membered cyclo-hexene ring in the title compound, C(17)H(19)Cl(2)NOS(2), adopts an envelope conformation, with the C atom bearing the two methyl groups representing the flap. This atom deviates by 0.716 (3) Å from the plane passing through the other...

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El Ashry el SH, Amer MR, Shah MR, et al. 2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009;65:o602doi: 10.1107/S1600536809006199.
El Ashry, e. l. . S. H., Amer, M. R., Shah, M. R., & Ng, S. W. (2009). 2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate. Acta crystallographica. Section E, Structure reports online, 65o602. https://doi.org/10.1107/S1600536809006199
El Ashry, El Sayed H, et al. "2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate." Acta crystallographica. Section E, Structure reports online vol. 65 (2009): o602. doi: https://doi.org/10.1107/S1600536809006199
El Ashry el SH, Amer MR, Shah MR, Ng SW. 2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009 Feb 25;65:o602. doi: 10.1107/S1600536809006199. PMID: 21582256; PMCID: PMC2968539.
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n-Butyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-enecarbo-dithio-ate.

Acta crystallographica. Section E, Structure reports online

El Ashry el SH, Amer MR, Raza Shah M, Ng SW.
PMID: 21577914
Acta Crystallogr Sect E Struct Rep Online. 2009 Sep 12;65:o2459. doi: 10.1107/S1600536809036320.

The cyclo-hexene ring in the title compound, C(19)H(23)Cl(2)NOS(2), adopts an envelope conformation, with the C atom bearing the two methyl groups representing the flap. This atom deviates by 0.630 (2) Å from the plane passing through the other five...

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El Ashry el SH, Amer MR, Raza Shah M, et al. n-Butyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-enecarbo-dithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009;65:o2459doi: 10.1107/S1600536809036320.
El Ashry, e. l. . S. H., Amer, M. R., Raza Shah, M., & Ng, S. W. (2009). n-Butyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-enecarbo-dithio-ate. Acta crystallographica. Section E, Structure reports online, 65o2459. https://doi.org/10.1107/S1600536809036320
El Ashry, El Sayed H, et al. "n-Butyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-enecarbo-dithio-ate." Acta crystallographica. Section E, Structure reports online vol. 65 (2009): o2459. doi: https://doi.org/10.1107/S1600536809036320
El Ashry el SH, Amer MR, Raza Shah M, Ng SW. n-Butyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-enecarbo-dithio-ate. Acta Crystallogr Sect E Struct Rep Online. 2009 Sep 12;65:o2459. doi: 10.1107/S1600536809036320. PMID: 21577914; PMCID: PMC2970403.
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A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors.

Beilstein journal of organic chemistry

El Ashry el SH, El Tamany el SH, Fattah Mel D, Aly MR, Boraei AT, Duerkop A.
PMID: 23400104
Beilstein J Org Chem. 2013;9:135-46. doi: 10.3762/bjoc.9.16. Epub 2013 Jan 21.

Glycosylations of 5-(1H-indol-2-yl)-1,3,4-oxadiazoline-2(3H)-thione delivered various degrees of S- and/or N-glycosides depending on the reaction conditions. S-Glycosides were obtained regiospecifically by grinding oxadiazolinethiones with acylated α-D-glycosyl halides in basic alumina, whereas 3-N-(glycosyl)oxadiazolinethiones were selectively obtained by reaction with HgCl(2) followed...

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El Ashry el SH, El Tamany el SH, Fattah Mel D, et al. A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors. Beilstein J Org Chem. 2013;9:135-46doi: 10.3762/bjoc.9.16.
El Ashry, e. l. . S. H., El Tamany, e. l. . S. H., Fattah, M. e. l. . D., Aly, M. R., Boraei, A. T., & Duerkop, A. (2013). A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors. Beilstein journal of organic chemistry, 9135-46. https://doi.org/10.3762/bjoc.9.16
El Ashry, El Sayed H, et al. "A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors." Beilstein journal of organic chemistry vol. 9 (2013): 135-46. doi: https://doi.org/10.3762/bjoc.9.16
El Ashry el SH, El Tamany el SH, Fattah Mel D, Aly MR, Boraei AT, Duerkop A. A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors. Beilstein J Org Chem. 2013;9:135-46. doi: 10.3762/bjoc.9.16. Epub 2013 Jan 21. PMID: 23400104; PMCID: PMC3566832.
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Recent advances of hemorrhage management in severe trauma.

Emergency medicine international

El Sayad M, Noureddine H.
PMID: 24627809
Emerg Med Int. 2014;2014:638956. doi: 10.1155/2014/638956. Epub 2014 Jan 30.

Trauma is one of the most common causes of mortality worldwide with a substantial percentage of deaths resulting secondary to haemorrhages, which are preventable and treatable when adequately managed. This paper offers a review of the current literature on...

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El Sayad M, Noureddine H. Recent advances of hemorrhage management in severe trauma. Emerg Med Int. 2014;2014:638956doi: 10.1155/2014/638956.
El Sayad, M., & Noureddine, H. (2014). Recent advances of hemorrhage management in severe trauma. Emergency medicine international, 2014638956. https://doi.org/10.1155/2014/638956
El Sayad, Mohamed, and Noureddine, Hussein. "Recent advances of hemorrhage management in severe trauma." Emergency medicine international vol. 2014 (2014): 638956. doi: https://doi.org/10.1155/2014/638956
El Sayad M, Noureddine H. Recent advances of hemorrhage management in severe trauma. Emerg Med Int. 2014;2014:638956. doi: 10.1155/2014/638956. Epub 2014 Jan 30. PMID: 24627809; PMCID: PMC3929186.
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TREATMENT OF ERYSIPELAS BY INJECTIONS OF MILK.

British medical journal

El Sayed IA.
PMID: 20776673
Br Med J. 1932 Feb 13;1(3710):281-2. doi: 10.1136/bmj.1.3710.281-a.

No abstract available.

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El Sayed IA. TREATMENT OF ERYSIPELAS BY INJECTIONS OF MILK. Br Med J. 1932;1(3710):281-2doi: 10.1136/bmj.1.3710.281-a.
El Sayed, I. A. (1932). TREATMENT OF ERYSIPELAS BY INJECTIONS OF MILK. British medical journal, 1(3710), 281-2. https://doi.org/10.1136/bmj.1.3710.281-a
El Sayed, I A. "TREATMENT OF ERYSIPELAS BY INJECTIONS OF MILK." British medical journal vol. 1,3710 (1932): 281-2. doi: https://doi.org/10.1136/bmj.1.3710.281-a
El Sayed IA. TREATMENT OF ERYSIPELAS BY INJECTIONS OF MILK. Br Med J. 1932 Feb 13;1(3710):281-2. doi: 10.1136/bmj.1.3710.281-a. PMID: 20776673; PMCID: PMC2520119.
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Carrier Dynamics in the Quantum Kinetic Regime.

Physical review letters

Bar-Ad S, Chemla DS, El Sayed K, Kner P, Marquezini MV.
PMID: 10062153
Phys Rev Lett. 1996 Oct 07;77(15):3177-3180. doi: 10.1103/PhysRevLett.77.3177.

No abstract available.

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Bar-Ad S, Chemla DS, El Sayed K, et al. Carrier Dynamics in the Quantum Kinetic Regime. Phys Rev Lett. 1996;77(15):3177-3180doi: 10.1103/PhysRevLett.77.3177.
Bar-Ad, S., Chemla, D. S., El Sayed K, Kner, P., & Marquezini, M. V. (1996). Carrier Dynamics in the Quantum Kinetic Regime. Physical review letters, 77(15), 3177-3180. https://doi.org/10.1103/PhysRevLett.77.3177
Bar-Ad, et al. "Carrier Dynamics in the Quantum Kinetic Regime." Physical review letters vol. 77,15 (1996): 3177-3180. doi: https://doi.org/10.1103/PhysRevLett.77.3177
Bar-Ad S, Chemla DS, El Sayed K, Kner P, Marquezini MV. Carrier Dynamics in the Quantum Kinetic Regime. Phys Rev Lett. 1996 Oct 07;77(15):3177-3180. doi: 10.1103/PhysRevLett.77.3177. PMID: 10062153.
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Showing 1 to 12 of 270 entries