Michelson s j (24 resultados)
Editorial: Nnn, No Date (Looks ca 1930-1950), 1930
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Añadir al carritoPaperback. Metal spiral bound softcover, with 4 heavy cardboard "leaves". Premium present by the Ilion (New York) National Bank & Trust Co. , being a "bank" in the form of a circus themed children's book, illustrated with color drawings, with paper-backed slots provided for inserting coins. Very good. L-shaped 1 inch tear upper corner of front cover, other corners creased, spirals slightly askew, with covers starting to detach, 1 coin holderhas paper backing punched out, otherwise tight, clean and unmarked. Unusual. Children's; economics; thrift; personal finance; ephemera.…

Near Zero: New Frontiers of Physics
J. D. Fairbank & P. F. Michelson & C. W. Everitt & B. S. Deaver, Jr.
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Hardcover. Condición: New. No Jacket. 1st Edition. Not as pictured.
Más imágenesEditorial: Newman Advertising Service, New York, NY, 1946
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Añadir al carritoA Circus themed coin savings book illustrated by George Hollrock and distributed by Coin Books, Inc. for various banks. Good. The boards are creased, tear to lower right-hand corner of rear board, and a tear to the coin slot by elephant's trunk on page 3. 8vo. (7" x 9") Spiral bound with pictorial cardstock boards. Illustrations by George Hollrock. (ilustrador).…

Evaluation of New Antiarrhythmic Drugs : Proceedings of the Symposium on How to Evaluate a New Antiarrhythmic Drug: The Evaluation of New Antiarrhythmic Agents for the Treatment of Ventricular Arrhythmias, held at Philadelphia, Pennsylvania, October 8-9, 1980
Morganroth, J. (EDT); Moore, E. Neil (EDT); Dreifus, L. S. (EDT); Michelson, E. L. (EDT)
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Evaluation of New Antiarrhythmic Drugs : Proceedings of the Symposium on How to Evaluate a New Antiarrhythmic Drug: The Evaluation of New Antiarrhythmic Agents for the Treatment of Ventricular Arrhythmias, held at Philadelphia, Pennsylvania, October 8-9, 1980
Morganroth, J. (EDT); Moore, E. Neil (EDT); Dreifus, L. S. (EDT); Michelson, E. L. (EDT)
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Evaluation of New Antiarrhythmic Drugs : Proceedings of the Symposium on How to Evaluate a New Antiarrhythmic Drug: The Evaluation of New Antiarrhythmic Agents for the Treatment of Ventricular Arrhythmias, held at Philadelphia, Pennsylvania, October 8-9, 1980
Morganroth, J. (EDT); Moore, E. Neil (EDT); Dreifus, L. S. (EDT); Michelson, E. L. (EDT)
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Evaluation of New Antiarrhythmic Drugs : Proceedings of the Symposium on How to Evaluate a New Antiarrhythmic Drug: The Evaluation of New Antiarrhythmic Agents for the Treatment of Ventricular Arrhythmias, held at Philadelphia, Pennsylvania, October 8-9, 1980
Morganroth, J. (EDT); Moore, E. Neil (EDT); Dreifus, L. S. (EDT); Michelson, E. L. (EDT)
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Condición: New. pp. 340.

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Taschenbuch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Thus, there are now several chronic canine myocardial infarction ventricular tachyarrhythmia models which are available for the evaluation of new antiarrhythmic drugs (Table I). The available models fulfill many, but not all of the requirements for an ideal chronic arrhythmia model (Table 11). The sustained arrhythmias initiated in these models using programmed pacing presumably have the same localized reentrant mechanism that characterizes chronic human myocardial infarction and chronic coronary 26 artery disease. However, these models are not suitable for determining whether a new drug will abolish spontaneous ly-occurring PVCs. In addition, these models are of unproven value in the study of acute spontaneously occurring sudden death; although recently initiated, provocative work may shed further light on this subject. Most importantly, the available models do seem well-suited to the evaluation of new drugs intended for use in chronic coronary artery disease patients at risk for sustained reentrant ventricular tachycardia or VF. Notably, the results of preliminary electropharmacologic studies in these canine models parallel closely those findings reported in human patients with sustained life-threatening ventricu lar tachyarrhythmias (Table Ill). Therefore, increased use of these chronic models for new antiarrhythmic drug testing is strongly recommended. TABLE II Ideal vs Available Chronic Canine - Arrhythmia Models Ideal Available 1. (a) Arrhythmia mechanism comparable to Yes patients with chronic CAD: Reentry (b) Pathophysiology similar (e. g. , atherogenic CAD) No 2. Susceptible to: (a) spontaneous PVCs No l No (b) spontaneous VT/VF (c) inducible VT/VF Yes 3.…

The Evaluation of New Antiarrhythmic Drugs: Proceedings of the Symposium on How to Evaluate a New Antiarrhythmic Drug: The Evaluation of New Antiarrhythmic Agents for the Treatment of Ventricular Arrhythmias, held at Philadelphia, Pennsylvania, October 8-9, 1980
Moore, E. Neil (Editor) / Morganroth, J. (Editor) / Dreifus, L.S. (Editor) / Michelson, E.L. (Editor)
Idioma: Inglés
Editorial: Martinus Nijhoff Publishers, 2013
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The Evaluation of New Antiarrhythmic Drugs
Morganroth, J.|Moore, E. Neil|Dreifus, L. S.|Michelson, E. L.
Idioma: Inglés
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Idioma: Inglés
Editorial: Journal of Cellular and Comparative Physiology, 1950
Librería: Robinson Street Books, IOBA, Binghamton, NY, Estados Unidos de AmericaRobinson Street Books, IOBA
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Añadir al carritoPamphlet. Condición: very good clean pages. Prompt Shipment, shipped in Boxes, Tracking PROVIDEDOffprint. collectible, offprint, reprinted from the Journal of Cellular and Comparative Physiology, Vol. 38, Supplement 1, July (1951) Oak Ridge Tennessee April 13, 14, 1950, sponsored by The Biology Division of Oak Ridge National Laboratory, pg. 1-245, sm4to.…
Más imágenesBell: "Upon the Electrical Experiments to determine the location of the Bullet in the body of the late President Garfield; and upon a successful form of Induction Balance for the painless detection of Metallic Masses in the Human Body," found in "American Journal of Science and the Arts" (plus numerous other papers by different contributors).
BELL. Alexander Graham. AND J. Willard Gibbs, and S.P. Langley, and A.A. Michelson.
Editorial: J.D. and E.S. Dana, 1883
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Añadir al carritoHardcover. Condición: Fine. ++BELL. Alexander Graham. AND J. Willard Gibbs, and S.P. Langley, and A.A. Michelson. ++ Bell: "Upon the Electrical Experiments to determine the location of the Bullet in the body of the late President Garfield; and upon a successful form of Induction Balance for the painless detection of Metallic Masses in the Human Body," found in "American Journal of Science and the Arts," New Haven, pp 22-61 (a long article for the AJSA), along with 31 text illustrations, volume 23, 1883. offered in the full volume of 488pp (with 5 folding plates). Newly and very tastefully rebound in calf-backed marbled boards. The text is in VG+ condition. PROVENANCE: there is an interesting collection and rich lineage of ex-libris rubber stamps on the title page, including an ownership stamp of the Carl Zeiss library in Jena (see pic). [++] Also in this volume: A.A. Michelson, "A Method for Determining the Rate of Tuning Forks", pp 61-64. [AND WITH] J. Willard Gibbs, "Notes on the Electromagnetic Theory of Light. No. III, On the General Equations of Monochromatic Light in Media of Every Degree of Transparency", pp 107-114. [AND WITH] S.P. LANGLEY, "The Selective Absorption of Solar Energy", pp 169-196. [++] The first paper here is a long one by Bell on a rather famous attempt/experiment modifying his telephone in attempting to explore for the bullet in the mortally-wounded U.S. President James Garfield (who was shot by an assassin in July 1881). This was a very well-documented and public event that was followed in popular magazines, and yet there are scant references to this paper that I have been able to locate. At the time the paper was submitted, Garfield was still alive, though by the time of publication he would be dead, succumbing 79 days after the assassination attempt. Bell made several attempts to locate the projectile but was unsuccessful. That said, this was a major application of his "telephonic" device to non-invasively locate metal objects in patients in the pre-X-ray period. As a piece of trivia I should note that the device was developed at Bell's Volta Bureau, which was only two blocks away from my store back in my old Georgetown (DC) days. [++] There were earlier treatments on this event, though none that I can find come anywhere close to thorough description (with additions and improvements) that we see here. (For example, there was a one-page summation of the event--"Probing by Electricity"-- that appeared in "Nature, an Illustrated Weekly Journal of Science", London, 10 November 1881, vol 25 no. 628, page 40.).…

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Idioma: Inglés
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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Thus, there are now several chronic canine myocardial infarction ventricular tachyarrhythmia models which are available for the evaluation of new antiarrhythmic drugs (Table I). The available models fulfill many, but not all of the requirements for an ideal chronic arrhythmia model (Table 11). The sustained arrhythmias initiated in these models using programmed pacing presumably have the same localized reentrant mechanism that characterizes chronic human myocardial infarction and chronic coronary 26 artery disease. However, these models are not suitable for determining whether a new drug will abolish spontaneous ly-occurring PVCs. In addition, these models are of unproven value in the study of acute spontaneously occurring sudden death; although recently initiated, provocative work may shed further light on this subject. Most importantly, the available models do seem well-suited to the evaluation of new drugs intended for use in chronic coronary artery disease patients at risk for sustained reentrant ventricular tachycardia or VF. Notably, the results of preliminary electropharmacologic studies in these canine models parallel closely those findings reported in human patients with sustained life-threatening ventricu lar tachyarrhythmias (Table Ill). Therefore, increased use of these chronic models for new antiarrhythmic drug testing is strongly recommended. TABLE II Ideal vs Available Chronic Canine - Arrhythmia Models Ideal Available 1. (a) Arrhythmia mechanism comparable to Yes patients with chronic CAD: Reentry (b) Pathophysiology similar (e. g. , atherogenic CAD) No 2. Susceptible to: (a) spontaneous PVCs No l No (b) spontaneous VT/VF (c) inducible VT/VF Yes 3. 340 pp. Englisch.…

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Condición: New. Print on Demand pp. 340 49:B&W 6.14 x 9.21 in or 234 x 156 mm (Royal 8vo) Perfect Bound on White w/Gloss Lam.

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Kartoniert / Broschiert. Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The springboard for this sixth volume in the Industry and Health Care series was a conference sponsored by the Center for Industry and Health Care of Boston University on June 9 and 10, 1978. That conference had a gradual genesis. Over a year ago we spent s.…

Idioma: Inglés
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Condición: New. PRINT ON DEMAND pp. 340.

Idioma: Inglés
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Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Thus, there are now several chronic canine myocardial infarction ventricular tachyarrhythmia models which are available for the evaluation of new antiarrhythmic drugs (Table I). The available models fulfill many, but not all of the requirements for an ideal chronic arrhythmia model (Table 11). The sustained arrhythmias initiated in these models using programmed pacing presumably have the same localized reentrant mechanism that characterizes chronic human myocardial infarction and chronic coronary 26 artery disease. However, these models are not suitable for determining whether a new drug will abolish spontaneous ly-occurring PVCs. In addition, these models are of unproven value in the study of acute spontaneously occurring sudden death; although recently initiated, provocative work may shed further light on this subject. Most importantly, the available models do seem well-suited to the evaluation of new drugs intended for use in chronic coronary artery disease patients at risk for sustained reentrant ventricular tachycardia or VF. Notably, the results of preliminary electropharmacologic studies in these canine models parallel closely those findings reported in human patients with sustained life-threatening ventricu lar tachyarrhythmias (Table Ill). Therefore, increased use of these chronic models for new antiarrhythmic drug testing is strongly recommended. TABLE II Ideal vs Available Chronic Canine - Arrhythmia Models Ideal Available 1. (a) Arrhythmia mechanism comparable to Yes patients with chronic CAD: Reentry (b) Pathophysiology similar (e. g. , atherogenic CAD) No 2. Susceptible to: (a) spontaneous PVCs No l No (b) spontaneous VT/VF (c) inducible VT/VF Yes 3.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 340 pp. Englisch.…