Spartanburg Surgery Center 391 Serpentine Dr STE 200, Spartanburg, SC 29303 (864)5852002 (phone), (864)2164290 (fax)
Urology Center Of Spartanburg 391 Serpentine Dr STE 500, Spartanburg, SC 29303 (864)5858221 (phone), (864)5853907 (fax)
Education:
Medical School Wright State University Boonshoft School of Medicine Graduated: 1989
Procedures:
Bladder Repair Nephrectomy Cystoscopy Cystourethroscopy Hernia Repair Kidney Stone Lithotripsy Prostate Biopsy Transurethral Resection of Prostate Urinary Flow Tests Vasectomy
Conditions:
Benign Prostatic Hypertrophy Bladder Cancer Breast Disorders Calculus of the Urinary System Cholelethiasis or Cholecystitis
Languages:
English Russian Spanish
Description:
Dr. Ellis graduated from the Wright State University Boonshoft School of Medicine in 1989. He works in Spartanburg, SC and 1 other location and specializes in Urology. Dr. Ellis is affiliated with Mary Black Health System and Spartanburg Regional Medical Center.
Dr. Ellis graduated from the East Tennessee State University College of Medicine in 1993. He works in Johns Creek, GA and specializes in Family Medicine. Dr. Ellis is affiliated with Emory Johns Creek Hospital and Northside Hospital.
Lankford Hand Surgery Associates 3600 Gaston Ave STE 450, Dallas, TX 75246 (214)8235351 (phone), (214)8232825 (fax)
Education:
Medical School University of Texas Southwestern Medical Center at Dallas Graduated: 1982
Procedures:
Arthrocentesis Carpal Tunnel Decompression Occupational Therapy Evaluation Wound Care
Conditions:
Fractures, Dislocations, Derangement, and Sprains Internal Derangement of Knee Cartilage Lateral Epicondylitis Osteoarthritis Retinal Detachments
Languages:
English Spanish
Description:
Dr. Ellis graduated from the University of Texas Southwestern Medical Center at Dallas in 1982. He works in Dallas, TX and specializes in Hand Surgery. Dr. Ellis is affiliated with Baylor University Medical Center.
DuPage Medical GroupDuPage Medical Group Pain Management 120 Spalding Dr STE 400, Naperville, IL 60540 (630)9676000 (phone), (630)4283971 (fax)
DuPage Medical GroupDuPage Medical Group Spine Center 120 Spalding Dr STE 400, Naperville, IL 60540 (630)9672225 (phone), (630)4283971 (fax)
DuPage Medical GroupDuPage Medical Group Spine Center 1801 S Highland Ave STE 220, Lombard, IL 60148 (630)9672225 (phone), (630)4283971 (fax)
Languages:
English
Description:
Mr. Ellis works in Naperville, IL and 2 other locations and specializes in Orthopaedic Surgery Of Spine. Mr. Ellis is affiliated with Advocate Good Samaritan Hospital, Edward Hospital and Elmhurst Memorial Hospital.
Empire Metal Products Phoenix, AZ Sep 2005 to Apr 2014 Sheet Metal WorkerGeneral Metal Company Phoenix, AZ Mar 2005 to Dec 2005 MachinistManpower Skills Training Center Youngstown, OH Sep 1978 to Sep 1979 Machinist
Education:
Grand Canyon University Phoenix, AZ Sep 2010 to Sep 2012 Communications
Skills:
Mathematical and Artistic Ability
Name / Title
Company / Classification
Phones & Addresses
Paul Ellis President
Praise Assembly of God Religious Organization
1004 N Main St, Niles, OH 44446 (330)6529224
Paul Ellis
ELLIS ENTERPRISES LLC
Paul E. Ellis
PAUL E. ELLIS CONSTRUCTION, LLC
Paul E. Ellis
SOUNDZ RIGHTEOUS, LLC
Paul E Ellis
ELLIS REAL ESTATE INVESTMENTS, INC
Paul E. Ellis
ALPHATRONX, LTD
Paul W. Ellis
PAUL W. ELLIS, LLC
Paul Ellis Manager
The Sherwin-Williams Company Ret Paint/Glass/Wallpaper Mfg Paints/Allied Products Whol Paints/Varnishes · Paint & Wallpaper Stores
317 W Lancaster Ave, Wayne, PA 19087 314 E Lancaster Ave, Wayne, PA 19087 (610)9750126, (216)5154825, (216)5661392, (610)9750128
Isbn (Books And Publications)
Trends in Theoretical Physics: Based on the 1989-90 Distinguished-Speaker Colloquium Series of the Theorectical Physics Institute at the University
Manoj V. Bhinde - Boothwyn PA James E. Lyons - Wallingford PA Paul E. Ellis - Downingtown PA
Assignee:
Sun Company, Inc. (R&M) - Philadelphia PA
International Classification:
C07C 2900 C07C 3112 C07C 3514 C07C 3322
US Classification:
568835
Abstract:
Organic hydroperoxides are decomposed by drying a reaction mixture containing the organic hydroperoxide and an organic solvent and contacting the dried reaction mixture with a metal organic ligand catalyst under hydroperoxide decomposition conditions. An organic co-solvent for the hydroperoxide may also be used.
Hydrocarbon Oxidations Catalyzed By Azide-Activated Metal Coordination Complexes
Paul E. Ellis - Downingtown PA James E. Lyons - Wallingford PA Harry K. Myers - Cochranville PA
Assignee:
Sun Refining and Marketing Copany - Philadelphia PA
International Classification:
C07C 6700 C07C 2712 C07C 4532
US Classification:
2604109R
Abstract:
Hydrocarbons, and particularly lower molecular weight alkanes and cycloalkanes, may readily be oxidixed with air or O. sub. 2 to form such products as alcohols, ketones, and the like selectively in high yields when there is employed as the catalyst a highly active azide-activated metal coordination complex having the structure ##STR1## where M is a transition metal; " " is a ligand; and X is azide. The invention is also directed to certain novel azide-activated metal coordination complex catalysts per se.
Paul E. Ellis - Downingtown PA James E. Lyons - Wallingford PA
Assignee:
Sun Company, Inc. (R&M) - Philadelphia PA
International Classification:
C07C 2950 C07C 3112
US Classification:
568910
Abstract:
The invention provides novel methods for the oxidation of hydrocarbons with oxygen-containing gas to form hydroxy-group containing compounds and for the decomposition of hydroperoxides to form hydroxygroup containing compounds. The catalysts used in the methods of the invention comprise transition metal complexes of a porphyrin ring having 1 to 12 halogen substituents on the porphyrin ring, at least one of said halogens being in a meso position and/or the catalyst containing no aryl group in a meso position. The catalyst compositions are prepared by halogenating a transition metal complex of a porphyrin. In one embodiment, a complex of a porphyrin with a metal whose porphyrin complexes are not active for oxidation of alkanes is halogenated, thereby to obtain a haloporphyrin complex of that metal, the metal is removed from the haloporphyrin complex to obtain the free base form of the haloporphyrin, and a metal such as iron whose porphyrin complexes are active for oxidation of alkanes and for the decomposition of alkyl hydroperoxides is complexed with the free base to obtain an active catalyst for oxidation of alkanes and decomposition of alkyl hydroperoxides.
James E. Lyons - Wallingford PA Paul E. Ellis - Downingtown PA Harry K. Myers - Cochranville PA George Suld - Springfield PA Wayne A. Langdale - Milmont Park PA
Assignee:
Sun Refining and Marketing Company - Philadelphia PA
International Classification:
C07G 2712
US Classification:
568399
Abstract:
Alkanes are oxidized in the liquid phase at relatively low temperatures using heteropolyacids or polyoxoanions promoted with azide or certain metals. Such azide catalysts are also part of the invention.
Process For The Production And Purification Of Diethoxymethane By Azeotropic Distillation
Chao-Yang Hsu - Media PA Paul E. Ellis - Downingtown PA
Assignee:
Sun Refining and Marketing Company - Philadelphia PA
International Classification:
B01D 336 C07C 4158
US Classification:
203 67
Abstract:
Diethoxymethane (ethylal), prepared by reacting formaldehyde with ethanol, may be recovered from the product mixture in substantially pure form by first distilling off an azeotrope comprising ethanol and diethoxymethane, adding a selected solvent to the azeotrope which will form an azeotrope with the ethanol, distilling off said latter azeotrope and recovering the substantially pure diethoxymethane.
Chao-Yang Hsu - Media PA Paul E. Ellis - Downingtown PA
Assignee:
Sun Refining and Marketing Company - Philadelphia PA
International Classification:
C07C 4550
US Classification:
568454
Abstract:
Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes. The novel catalyst comprises an organo metallic complex formed from a mixture of: (1) platinum (II) acetylacetonate; (2) a Group IVB metal halide; and (3) a bidentate tertiary ligand of the formula ##STR1## wherein Q is arsenic, antimony, or phosphorus; and R. sub. 1, R. sub. 2, R. sub. 3 and R. sub. 4 are alkyl, alkoxyl, aryl, or aryloxyl groups, and may be the same or different.
Tilak P. Wijesekera - Glens Mills PA James E. Lyons - Wallingford PA Paul E. Ellis - Malvern PA
Assignee:
Sunoco, Inc. (R&M) - Philadelphia PA Rohm and Haas Company - Philadelphia PA
International Classification:
B01J 2714 B01J 2300 B01J 2340 B01J 2372 B01J 2316
US Classification:
502208
Abstract:
Alkanes are converted to unsaturated carboxylic acids by contacting an alkane with an oxidizing agent and a Wells-Dawson type heteropolyacid supported on wide pore polyoxometallate salts.
EuropeInternational Operations Director specialising in business assessments and improvements, process management, risk management and business continuity planning
Hodge Elementary School Savannah GA 1979-1980, White Bluff Elementary School Savannah GA 1980-1981, Pennsylvania Avenue Elementary School Savannah GA 1981-1982, Romana Riley School Savannah GA 1982-1984, Isle of Hope Elementary School Savannah GA 1984-1986, Wilder Middle School Savannah GA 1986-1988, Mercer Middle School Garden City GA 1988-1988, Myers Middle School Savannah GA 1989-1990
Record producer Paul Ellis told TV ONE's Breakfast this morning: "Last night that show went out to over 30 million people around the world so obviously the record sales will spike over the next weeks.
Date: Jan 27, 2014
Category: Entertainment
Source: Google
Recommended: Help scientists decipher 'lost' gospel
Other leaders of the effort include Oxford's William MacFarlane, the lead developer and designer; James Brusuelas, the team's papyrologist; and Paul Ellis, an imaging specialist who helped digitize the texts. "It's with the digital advancements of our own age that we're able to open up this window i