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Showing 1 to 12 of 114 entries
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The use of sugammadex for bariatric surgery: analysis of recovery time from neuromuscular blockade and possible economic impact.

ClinicoEconomics and outcomes research : CEOR

De Robertis E, Zito Marinosci G, Romano GM, Piazza O, Iannuzzi M, Cirillo F, De Simone S, Servillo G.
PMID: 27418846
Clinicoecon Outcomes Res. 2016 Jun 29;8:317-22. doi: 10.2147/CEOR.S109951. eCollection 2016.

BACKGROUND: Neuromuscular block (NMB) monitoring and use of reversal agents accelerate the recovery time and improve the workflow in the operating room. We aimed to compare recovery times after sugammadex or neostigmine administration, and estimate the time spent in...

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De Robertis E, Zito Marinosci G, Romano GM, et al. The use of sugammadex for bariatric surgery: analysis of recovery time from neuromuscular blockade and possible economic impact. Clinicoecon Outcomes Res. 2016;8:317-22doi: 10.2147/CEOR.S109951.
De Robertis, E., Zito Marinosci, G., Romano, G. M., Piazza, O., Iannuzzi, M., Cirillo, F., De Simone, S., & Servillo, G. (2016). The use of sugammadex for bariatric surgery: analysis of recovery time from neuromuscular blockade and possible economic impact. ClinicoEconomics and outcomes research : CEOR, 8317-22. https://doi.org/10.2147/CEOR.S109951
De Robertis, Edoardo, et al. "The use of sugammadex for bariatric surgery: analysis of recovery time from neuromuscular blockade and possible economic impact." ClinicoEconomics and outcomes research : CEOR vol. 8 (2016): 317-22. doi: https://doi.org/10.2147/CEOR.S109951
De Robertis E, Zito Marinosci G, Romano GM, Piazza O, Iannuzzi M, Cirillo F, De Simone S, Servillo G. The use of sugammadex for bariatric surgery: analysis of recovery time from neuromuscular blockade and possible economic impact. Clinicoecon Outcomes Res. 2016 Jun 29;8:317-22. doi: 10.2147/CEOR.S109951. eCollection 2016. PMID: 27418846; PMCID: PMC4934482.
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Point mutations in the tumor suppressor Smad4/DPC4 enhance its phosphorylation by GSK3 and reversibly inactivate TGF-β signaling.

Molecular & cellular oncology

Demagny H, De Robertis EM.
PMID: 27308538
Mol Cell Oncol. 2015 Apr 14;3(1):e1025181. doi: 10.1080/23723556.2015.1025181. eCollection 2016 Jan.

The tumor suppressor Smad4/DPC4 is an essential transcription factor in the TGF-β pathway and is frequently mutated or deleted in prostate, colorectal, and pancreatic carcinomas. We recently discovered that Smad4 activity and stability are regulated by the FGF/EGF and...

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Demagny H, De Robertis EM. Point mutations in the tumor suppressor Smad4/DPC4 enhance its phosphorylation by GSK3 and reversibly inactivate TGF-β signaling. Mol Cell Oncol. 2015;3(1):e1025181doi: 10.1080/23723556.2015.1025181.
Demagny, H., & De Robertis, E. M. (2016). Point mutations in the tumor suppressor Smad4/DPC4 enhance its phosphorylation by GSK3 and reversibly inactivate TGF-β signaling. Molecular & cellular oncology, 3(1), e1025181. https://doi.org/10.1080/23723556.2015.1025181
Demagny, Hadrien, and De Robertis, Edward M. "Point mutations in the tumor suppressor Smad4/DPC4 enhance its phosphorylation by GSK3 and reversibly inactivate TGF-β signaling." Molecular & cellular oncology vol. 3,1 (2016): e1025181. doi: https://doi.org/10.1080/23723556.2015.1025181
Demagny H, De Robertis EM. Point mutations in the tumor suppressor Smad4/DPC4 enhance its phosphorylation by GSK3 and reversibly inactivate TGF-β signaling. Mol Cell Oncol. 2015 Apr 14;3(1):e1025181. doi: 10.1080/23723556.2015.1025181. eCollection 2016 Jan. PMID: 27308538; PMCID: PMC4845174.
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The quest for the holy volume therapy.

European journal of anaesthesiology

De Robertis E, Afshari A, Longrois D.
PMID: 27270704
Eur J Anaesthesiol. 2016 Jul;33(7):483-7. doi: 10.1097/EJA.0000000000000441.

No abstract available.

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De Robertis E, Afshari A, Longrois D. The quest for the holy volume therapy. Eur J Anaesthesiol. 2016;33(7):483-7doi: 10.1097/EJA.0000000000000441.
De Robertis, E., Afshari, A., & Longrois, D. (2016). The quest for the holy volume therapy. European journal of anaesthesiology, 33(7), 483-7. https://doi.org/10.1097/EJA.0000000000000441
De Robertis, Edoardo, et al. "The quest for the holy volume therapy." European journal of anaesthesiology vol. 33,7 (2016): 483-7. doi: https://doi.org/10.1097/EJA.0000000000000441
De Robertis E, Afshari A, Longrois D. The quest for the holy volume therapy. Eur J Anaesthesiol. 2016 Jul;33(7):483-7. doi: 10.1097/EJA.0000000000000441. PMID: 27270704.
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Steric strain and reactivity: electrophilic bromination of trans-(1-methyl-2-adamantylidene)-1-methyladamantane.

The Journal of organic chemistry

Chiappe C, De Rubertis A, Lemmen P, Lenoir D.
PMID: 10814086
J Org Chem. 2000 Mar 10;65(5):1273-9. doi: 10.1021/jo9910076.

trans-(1-Methyl-2-adamantylidene)-1-methyladamantane (DMAD, 1b) reacts with Br(2) in chlorinated hydrocarbon solvents to give either a bromonium polybromide ion pair or a substitution product, depending on bromine concentration. The first intermediate is a 1:1 pi-complex having K(f) = 1.85(0.19) x 10(3)...

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Chiappe C, De Rubertis A, Lemmen P, et al. Steric strain and reactivity: electrophilic bromination of trans-(1-methyl-2-adamantylidene)-1-methyladamantane. J Org Chem. 2000;65(5):1273-9doi: 10.1021/jo9910076.
Chiappe, C., De Rubertis A, Lemmen, P., & Lenoir, D. (2000). Steric strain and reactivity: electrophilic bromination of trans-(1-methyl-2-adamantylidene)-1-methyladamantane. The Journal of organic chemistry, 65(5), 1273-9. https://doi.org/10.1021/jo9910076
Chiappe, et al. "Steric strain and reactivity: electrophilic bromination of trans-(1-methyl-2-adamantylidene)-1-methyladamantane." The Journal of organic chemistry vol. 65,5 (2000): 1273-9. doi: https://doi.org/10.1021/jo9910076
Chiappe C, De Rubertis A, Lemmen P, Lenoir D. Steric strain and reactivity: electrophilic bromination of trans-(1-methyl-2-adamantylidene)-1-methyladamantane. J Org Chem. 2000 Mar 10;65(5):1273-9. doi: 10.1021/jo9910076. PMID: 10814086.
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Reactivity of homoallylic substituted adamantylideneadamantanes with bromine. Substituent effects on the stability of the ionic and nonionic intermediates.

The Journal of organic chemistry

Chiappe C, De Rubertis A, Jaber A, Lenoir D, Wattenbach C, Pomelli CS.
PMID: 12354001
J Org Chem. 2002 Oct 04;67(20):7066-74. doi: 10.1021/jo0203490.

Sterically congested adamantylideneadamantanes (1b-g) (X = Br, Cl, F, OH, OEt, OCOCH(3)), homoallylically substituted with equatorial groups (X), react with bromine in 1,2-dichloroethane to give a stable bromonium ion intermediate or a substitution product depending on the nature of...

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Chiappe C, De Rubertis A, Jaber A, et al. Reactivity of homoallylic substituted adamantylideneadamantanes with bromine. Substituent effects on the stability of the ionic and nonionic intermediates. J Org Chem. 2002;67(20):7066-74doi: 10.1021/jo0203490.
Chiappe, C., De Rubertis, A., Jaber, A., Lenoir, D., Wattenbach, C., & Pomelli, C. S. (2002). Reactivity of homoallylic substituted adamantylideneadamantanes with bromine. Substituent effects on the stability of the ionic and nonionic intermediates. The Journal of organic chemistry, 67(20), 7066-74. https://doi.org/10.1021/jo0203490
Chiappe, Cinzia, et al. "Reactivity of homoallylic substituted adamantylideneadamantanes with bromine. Substituent effects on the stability of the ionic and nonionic intermediates." The Journal of organic chemistry vol. 67,20 (2002): 7066-74. doi: https://doi.org/10.1021/jo0203490
Chiappe C, De Rubertis A, Jaber A, Lenoir D, Wattenbach C, Pomelli CS. Reactivity of homoallylic substituted adamantylideneadamantanes with bromine. Substituent effects on the stability of the ionic and nonionic intermediates. J Org Chem. 2002 Oct 04;67(20):7066-74. doi: 10.1021/jo0203490. PMID: 12354001.
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The interaction between atropine sulphate and a proteolipid from cerebral cortex studied by light scattering.

FEBS letters

De Robertis E, Gonzalez-Rodriguez J, Teller DN.
PMID: 11947130
FEBS Lett. 1969 Jul;4(1):4-8. doi: 10.1016/0014-5793(69)80180-8.

No abstract available.

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De Robertis E, Gonzalez-Rodriguez J, Teller DN. The interaction between atropine sulphate and a proteolipid from cerebral cortex studied by light scattering. FEBS Lett. 1969;4(1):4-8doi: 10.1016/0014-5793(69)80180-8.
De Robertis, E., Gonzalez-Rodriguez, J., & Teller, D. N. (1969). The interaction between atropine sulphate and a proteolipid from cerebral cortex studied by light scattering. FEBS letters, 4(1), 4-8. https://doi.org/10.1016/0014-5793(69)80180-8
De Robertis, E, et al. "The interaction between atropine sulphate and a proteolipid from cerebral cortex studied by light scattering." FEBS letters vol. 4,1 (1969): 4-8. doi: https://doi.org/10.1016/0014-5793(69)80180-8
De Robertis E, Gonzalez-Rodriguez J, Teller DN. The interaction between atropine sulphate and a proteolipid from cerebral cortex studied by light scattering. FEBS Lett. 1969 Jul;4(1):4-8. doi: 10.1016/0014-5793(69)80180-8. PMID: 11947130.
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Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations.

Talanta

Crea F, De Robertis A, De Stefano C, Sammartano S, Gianguzza A, Piazzese D.
PMID: 18968218
Talanta. 2001 Mar 16;53(6):1241-8. doi: 10.1016/s0039-9140(00)00617-2.

The interactions between some acrylic and sulphonic polyanions and some protonated amines (diamines NH(2)-(CH(2))(x)-NH(2), x=2,...,10; linear tri-, tetra-, penta- and hexa-amines) were studied potentiometrically in aqueous solution, at 25 degrees C. For both types of polyanions AL(2)H(i) (L(-), monomer...

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Crea F, De Robertis A, De Stefano C, et al. Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations. Talanta. 2001;53(6):1241-8doi: 10.1016/s0039-9140(00)00617-2.
Crea, F., De Robertis, A., De Stefano, C., Sammartano, S., Gianguzza, A., & Piazzese, D. (2001). Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations. Talanta, 53(6), 1241-8. https://doi.org/10.1016/s0039-9140(00)00617-2
Crea, F, et al. "Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations." Talanta vol. 53,6 (2001): 1241-8. doi: https://doi.org/10.1016/s0039-9140(00)00617-2
Crea F, De Robertis A, De Stefano C, Sammartano S, Gianguzza A, Piazzese D. Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations. Talanta. 2001 Mar 16;53(6):1241-8. doi: 10.1016/s0039-9140(00)00617-2. PMID: 18968218.
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The determination of formation constants of weak complexes by potentiometric measurements: experimental procedures and calculation methods.

Talanta

De Robertis A, De Stefano C, Sammartano S, Rigano C.
PMID: 18964435
Talanta. 1987 Nov;34(11):933-8. doi: 10.1016/0039-9140(87)80132-7.

Experimental and calculation procedures for the study of weak complexes by the pH-measurement technique are described. An algorithm for the calculation of formation constants, together with a computer program in FORTRAN and BASIC versions, is reported. The problems of...

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De Robertis A, De Stefano C, Sammartano S, et al. The determination of formation constants of weak complexes by potentiometric measurements: experimental procedures and calculation methods. Talanta. 1987;34(11):933-8doi: 10.1016/0039-9140(87)80132-7.
De Robertis, A., De Stefano, C., Sammartano, S., & Rigano, C. (1987). The determination of formation constants of weak complexes by potentiometric measurements: experimental procedures and calculation methods. Talanta, 34(11), 933-8. https://doi.org/10.1016/0039-9140(87)80132-7
De Robertis, A, et al. "The determination of formation constants of weak complexes by potentiometric measurements: experimental procedures and calculation methods." Talanta vol. 34,11 (1987): 933-8. doi: https://doi.org/10.1016/0039-9140(87)80132-7
De Robertis A, De Stefano C, Sammartano S, Rigano C. The determination of formation constants of weak complexes by potentiometric measurements: experimental procedures and calculation methods. Talanta. 1987 Nov;34(11):933-8. doi: 10.1016/0039-9140(87)80132-7. PMID: 18964435.
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Binding of polyanions by biogenic amines. I. Formation and stability of protonated putrescine and cadaverine complexes with inorganic anions.

Talanta

De Robertis A, De Stefano C, Gianguzza A, Sammartano S.
PMID: 18967233
Talanta. 1998 Aug;46(5):1085-93. doi: 10.1016/s0039-9140(97)00388-3.

The formation and stability of proton diamine-inorganic anion [Cl(-), SO(4)(2-), HPO(4)(2-), P(2)O(7)(4-) and Fe(CN)(6)(4-)] complexes was studied potentiometrically [(H(+))-glass electrode] at 25 degrees C. Several general formula ALH(r) complexes are formed in these various systems. The stability of complexes...

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De Robertis A, De Stefano C, Gianguzza A, et al. Binding of polyanions by biogenic amines. I. Formation and stability of protonated putrescine and cadaverine complexes with inorganic anions. Talanta. 1998;46(5):1085-93doi: 10.1016/s0039-9140(97)00388-3.
De Robertis, A., De Stefano, C., Gianguzza, A., & Sammartano, S. (1998). Binding of polyanions by biogenic amines. I. Formation and stability of protonated putrescine and cadaverine complexes with inorganic anions. Talanta, 46(5), 1085-93. https://doi.org/10.1016/s0039-9140(97)00388-3
De Robertis, A, et al. "Binding of polyanions by biogenic amines. I. Formation and stability of protonated putrescine and cadaverine complexes with inorganic anions." Talanta vol. 46,5 (1998): 1085-93. doi: https://doi.org/10.1016/s0039-9140(97)00388-3
De Robertis A, De Stefano C, Gianguzza A, Sammartano S. Binding of polyanions by biogenic amines. I. Formation and stability of protonated putrescine and cadaverine complexes with inorganic anions. Talanta. 1998 Aug;46(5):1085-93. doi: 10.1016/s0039-9140(97)00388-3. PMID: 18967233.
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Harken caged-disc mitral valve replacement, 1969-1975: analysis of late mortality, thromboembolism, and valve failure.

Texas Heart Institute journal

Gray RJ, Czer LS, Chaux A, Sethna D, DeRobertis M, Raymond M, Matloff JM.
PMID: 15227298
Tex Heart Inst J. 1987 Dec;14(4):411-7.

We evaluated the long-term outcome of mitral valve replacement with a Harken caged-disc prosthesis for up to 11 years (range, 50 to 130 months; mean, 81 months) in 170 patients whose mean age was 55 years. The early (30-day)...

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Gray RJ, Czer LS, Chaux A, et al. Harken caged-disc mitral valve replacement, 1969-1975: analysis of late mortality, thromboembolism, and valve failure. Tex Heart Inst J. 1987;14(4):411-7
Gray, R. J., Czer, L. S., Chaux, A., Sethna, D., DeRobertis, M., Raymond, M., & Matloff, J. M. (1987). Harken caged-disc mitral valve replacement, 1969-1975: analysis of late mortality, thromboembolism, and valve failure. Texas Heart Institute journal, 14(4), 411-7.
Gray, R J, et al. "Harken caged-disc mitral valve replacement, 1969-1975: analysis of late mortality, thromboembolism, and valve failure." Texas Heart Institute journal vol. 14,4 (1987): 411-7.
Gray RJ, Czer LS, Chaux A, Sethna D, DeRobertis M, Raymond M, Matloff JM. Harken caged-disc mitral valve replacement, 1969-1975: analysis of late mortality, thromboembolism, and valve failure. Tex Heart Inst J. 1987 Dec;14(4):411-7. PMID: 15227298; PMCID: PMC324766.
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The Mechanism of the Therapeutic Effect of Iodine on the Thyroid Gland.

Science (New York, N.Y.)

DE Robertis E, Nowinski WW.
PMID: 17751256
Science. 1946 Apr 05;103(2675):421-2. doi: 10.1126/science.103.2675.421.

No abstract available.

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DE Robertis E, Nowinski WW. The Mechanism of the Therapeutic Effect of Iodine on the Thyroid Gland. Science. 1946;103(2675):421-2doi: 10.1126/science.103.2675.421.
DE Robertis, E., & Nowinski, W. W. (1946). The Mechanism of the Therapeutic Effect of Iodine on the Thyroid Gland. Science (New York, N.Y.), 103(2675), 421-2. https://doi.org/10.1126/science.103.2675.421
DE Robertis, E, and Nowinski, W W. "The Mechanism of the Therapeutic Effect of Iodine on the Thyroid Gland." Science (New York, N.Y.) vol. 103,2675 (1946): 421-2. doi: https://doi.org/10.1126/science.103.2675.421
DE Robertis E, Nowinski WW. The Mechanism of the Therapeutic Effect of Iodine on the Thyroid Gland. Science. 1946 Apr 05;103(2675):421-2. doi: 10.1126/science.103.2675.421. PMID: 17751256.
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Antigenic differences between a proteolipid and a proteodetergent from Torpedo electroplax having similar cholinergic binding properties.

Neurochemistry international

Barkas T, De Robertis E, Harrison R, Lunt GG.
PMID: 20487888
Neurochem Int. 1982;4(5):361-5. doi: 10.1016/0197-0186(82)90077-8.

The nicotinic acetylcholine receptor from Torpedo marmorata was extracted and purified from the electroplax membranes by using both aqueous detergent (proteodetergent) or chloroform-methanol (proteolipid). When studied with a highly sensitive radioimmunoassay, it was found that both proteins do not...

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Barkas T, De Robertis E, Harrison R, et al. Antigenic differences between a proteolipid and a proteodetergent from Torpedo electroplax having similar cholinergic binding properties. Neurochem Int. 1982;4(5):361-5doi: 10.1016/0197-0186(82)90077-8.
Barkas, T., De Robertis, E., Harrison, R., & Lunt, G. G. (1982). Antigenic differences between a proteolipid and a proteodetergent from Torpedo electroplax having similar cholinergic binding properties. Neurochemistry international, 4(5), 361-5. https://doi.org/10.1016/0197-0186(82)90077-8
Barkas, T, et al. "Antigenic differences between a proteolipid and a proteodetergent from Torpedo electroplax having similar cholinergic binding properties." Neurochemistry international vol. 4,5 (1982): 361-5. doi: https://doi.org/10.1016/0197-0186(82)90077-8
Barkas T, De Robertis E, Harrison R, Lunt GG. Antigenic differences between a proteolipid and a proteodetergent from Torpedo electroplax having similar cholinergic binding properties. Neurochem Int. 1982;4(5):361-5. doi: 10.1016/0197-0186(82)90077-8. PMID: 20487888.
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Showing 1 to 12 of 114 entries