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Farinelli
Edward John Farinelli, Fort Collins, CO US
| Patent application number | Description | Published |
|---|---|---|
| 20080214357 | Exercise intra-repetition assessment system - An intra-repetition exercise system which allows comparison of actual performance of intra-repetition exercise characteristics ( | 09-04-2008 |
Giulia Farinelli, Rome IT
| Patent application number | Description | Published |
|---|---|---|
| 20100057345 | SYSTEM AND METHOD FOR ITEM IDENTIFICATION, LOCATION AND NAVIGATION INSTRUCTION THERETO - A method and system for identifying, locating and providing navigational instructions among distributed items is disclosed. The method includes the steps of designating a plurality of items, identifying each of the items, accessing a data base to obtain at least location information associated with each identified item, providing a map of the location of each item, determining a distance to each item, determining a first item based on a user's position and sorting the list by distance with respect to the first item and providing navigational instructions to each item on the list. | 03-04-2010 |
Laurent Farinelli, Vevey CH
| Patent application number | Description | Published |
|---|---|---|
| 20080286795 | Method of nucleic acid amplification - A nucleic acid molecule can be annealed to an appropriate immobilized primer. The primer can then be extended and the molecule and the primer can be separated from one another. The extended primer can then be annealed to another immobilized primer and the other primer can be extended. Both extended primers can then be separated from one another and can be used to provided further extended primers. The process can be repeated to provide amplified, immobilized nucleic acid molecules. These can be used for many different purposes, including sequencing, screening, diagnosis, in situ nucleic acid synthesis, monitoring gene expression, nucleic acid fingerprinting, etc. | 11-20-2008 |
| 20110045541 | METHOD OF NUCLEIC ACID AMPLIFICATION - A nucleic acid molecule can be annealed to an appropriate immobilised primer. The primer can then be extended and the molecule and the primer can be separated from one another. The extended primer can then be annealed to another immobilised primer and the other primer can be extended. Both extended primers can then be separated from one another and can be used to provide further extended primers. The process can be repeated to provide amplified, immobilised nucleic acid molecules. These can be used for many different purposes, including sequencing, screening, diagnosis, in situ nucleic acid synthesis, monitoring gene expression, nucleic acid fingerprinting, etc. | 02-24-2011 |
Matthew Farinelli, Bronx, NY US
| Patent application number | Description | Published |
|---|---|---|
| 20110290413 | Laser Ablation of Adhesive for Integrated Circuit Fabrication - A method for releasing a handler from a wafer, the wafer comprising an integrated circuit (IC), includes attaching the handler to the wafer using an adhesive comprising a thermoset polymer, the handler comprising a material that is transparent in a wavelength range of about 193 nanometers (nm) to about 400 nm; ablating the adhesive through the handler using a laser, wherein a wavelength of the laser is selected based on the transparency of the handler material; and separating the handler from the wafer. | 12-01-2011 |
Matthew Farinelli, Yorktown Heights, NY US
| Patent application number | Description | Published |
|---|---|---|
| 20110152104 | Superconducting Low Pass Filter for Quantum Computing and Method of Manufacturing the Same - An apparatus and method for manufacturing a superconducting low-pass filter for quantum computing devices. The apparatus includes a plurality of containers and input and output ports connected to opposite ends of the apparatus. A plurality of coils of superconducting wire are wound using a mandrel. An adhesive is applied to the coils for maintaining a wound state. Each of the coils are positioned in each of the containers and electrically connected to each other with at least one coil being connected to the input port and at least one coil being connected to the output port. The coils are released or expanded from their wound state using an adhesive solvent. The containers are then filled with a conductive polymer and the containers are closed with one or more covers. | 06-23-2011 |
Matthew J. Farinelli, Riverdale, NY US
| Patent application number | Description | Published |
|---|---|---|
| 20090032920 | LASER RELEASE PROCESS FOR VERY THIN SI-CARRIER BUILD - A laser release and glass chip removal process for a integrated circuit module avoiding carrier edge cracking is provided. | 02-05-2009 |
| 20090053908 | Metalized Elastomeric Electrical Contacts - Techniques for forming enhanced electrical connections are provided. In one aspect, an electrical connecting device comprises an electrically insulating carrier having one or more contact structures traversing a plane thereof. Each contact structure comprises an elastomeric material having an electrically conductive layer running along at least one surface thereof continuously through the plane of the carrier. | 02-26-2009 |
| 20090300914 | Metallized Elastomeric Electrical Contacts - Techniques for forming enhanced electrical connections are provided. In one aspect, a method of forming an electrical connecting device includes the steps of: depositing an elastomeric material on an electrically insulating carrier; and metallizing the elastomeric material so as to form an electrically conductive layer running continuously through a plane of the carrier and along a surface of the elastomeric material. | 12-10-2009 |
Melissa Farinelli, Basel CH
| Patent application number | Description | Published |
|---|---|---|
| 20100310543 | METHOD OF PREVENTING AND TREATING ACUTE BRAIN PATHOLOGIES - Described are novel means in the treatment of cerebral neurological conditions such as ischemic insult of the brain. Furthermore, a kit for a non-radioactive protein serine/threonine phosphatase activity assay is provided, which is capable of detecting and distinguishing the activity of PP1, PP2A, and calcineurin (PP2B). | 12-09-2010 |
Mélissa Farinelli, Zurich CH
| Patent application number | Description | Published |
|---|---|---|
| 20100048687 | USE OF PHOSPHATASE INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES - Provided are novel a target and drugs in the treatment of neurological disorders related to amyloid beta pathology/amyloidosis. More specifically, the use of phosphatase inhibitors for the treatment of brain impairments mediated by Aβ-oligomers is described. | 02-25-2010 |
| 20110086908 | USE OF PHOSPHATASE INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES - Provided are novel a target and drugs in the treatment of neurological disorders related to amyloid beta pathology/amyloidosis. More specifically, the use of phosphatase inhibitors for the treatment of brain impairments mediated by Aβ-oligomers is described. | 04-14-2011 |
Mélissa Farinelli, Zurich CH
| Patent application number | Description | Published |
|---|---|---|
| 20100048687 | USE OF PHOSPHATASE INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES - Provided are novel a target and drugs in the treatment of neurological disorders related to amyloid beta pathology/amyloidosis. More specifically, the use of phosphatase inhibitors for the treatment of brain impairments mediated by Aβ-oligomers is described. | 02-25-2010 |
| 20110086908 | USE OF PHOSPHATASE INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES - Provided are novel a target and drugs in the treatment of neurological disorders related to amyloid beta pathology/amyloidosis. More specifically, the use of phosphatase inhibitors for the treatment of brain impairments mediated by Aβ-oligomers is described. | 04-14-2011 |
William Farinelli, Denvers, MA US
| Patent application number | Description | Published |
|---|---|---|
| 20110264115 | METHOD AND APPARATUS FOR GRAFTING OF SKIN TISSUE - Methods and apparatus are provided for affecting an appearance of skin by harvesting small portions of tissue from a donor (first) site and applying them at a recipient (second) site. A plurality of micrografts can be formed from a piece of graft tissue and attached to a dressing material. The dressing material can then be expanded to increase a separation distance between the micrografts, and the dressing material having spaced-apart micrografts attached thereto can be applied to a prepared recipient site. An apparatus can be provided that expands the dressing material using a pressurized fluid. A further method can include providing a suspension of small portions of graft tissue in a solution. The solution can be injected into blisters formed at a recipient (second) site and the tissue portions allowed to attach and proliferate. A method and apparatus can also be provided for forming corresponding blisters at a donor site and at a recipient site. The raised (removed) portions of the blisters can be removed and attached to a dressing material, and the portions from the donor (first) site can be placed onto the exposed blister areas at the recipient site. | 10-27-2011 |
William A. Farinelli, Danvers, MA US
| Patent application number | Description | Published |
|---|---|---|
| 20090259167 | METHODS AND COMPOSITIONS FOR DOSE-DEPENDENT PHOTODYNAMIC THERAPY OF DISORDERS - The invention provides methods and compositions for treating a tissue disorder in a subject by parenterally administering a solution of aminolevulinic acid (ALA) or a derivative thereof that is not greater than 1.0 percent by weight into a local subcutaneous or dermal region of the subject; and administering high fluence light to said bodily area to produce a phototoxic species in said local region, thereby treating a tissue disorder in the subject. | 10-15-2009 |
| 20100174223 | METHOD AND APPARATUS FOR OPTICAL INHIBITION OF PHOTODYNAMIC THERAPY - A system and method are provided for preventing damage to the epidermis or other epithelial or non-target tissue during photodynamic therapy treatment. For example, an inhibiting radiation can be used to control formation of a photosensitizer from a precursor photosensitizer in the epidermis or epithelial tissue. Subsequent application of a treatment radiation can activate the photosensitizer to damage or destroy target sites while the non-target tissue remains substantially unaffected. | 07-08-2010 |
| 20100305495 | METHOD AND APPARATUS FOR DERMAL DELIVERY OF A SUBSTANCE - The present invention is directed to a method and apparatus for delivering substances, e.g., therapeutic substances, into openings on or near a skin surface, such as hair follicles, pores and/or into sebaceous glands. This can be achieved by using an apparatus to direct a substance into the openings under pressure via one or more nozzles or slits. A portion of the sebum present in the hair follicle is optionally heated and/or removed, e.g. using low-pressure conduit located on the lower surface of the apparatus, before introducing the therapeutic substance. | 12-02-2010 |
| 20110224656 | METHOD AND APPARATUS FOR SELECTIVE PHOTOTHERMOLYSIS OF VEINS - Exemplary embodiments of the present disclosure provide method and apparatus for providing electromagnetic radiation to a biological tissue that may be selectively absorbed by venous structures as compared to arteries. For example, a wavelength of the electromagnetic radiation can be selected based on absorptivity of the radiation by oxygenated hemoglobin, deoxygenated hemoglobin, and/or met-hemoglobin. The wavelength can be, e.g., between about 685 nm and about 705 nm, or between about 690 nm and about 700 nm, or about 694 nm. The exemplary methods and apparatus can be used, e.g., for photothermolysis treatment of venous structures such as port wine stains or varicose veins, while reducing or avoiding undesirable damage to nearby arteries in the irradiated tissue. | 09-15-2011 |
| 20110251602 | METHOD AND APPARATUS FOR TISSUE EXPANSION - Exemplary embodiments of the present disclosure provide method and apparatus for facilitating stretching of a bio-logical tissue by forming a plurality of micro-slits in the tissue. Each micro-slit can be less than about 2 mm or less than about 1.5 mm long, or even less than about 1 mm, such that small gaps that can heal quickly can be formed when the tissue is stretched. The micro-slits can be formed using a plurality of cutting arrangements or an ablative laser. The micro-slits can be formed in various patterns, including staggered rows, circular or spiral patterns, or random patterns. | 10-13-2011 |