Search results for "ROM"

showing 10 items of 37506 documents

Prevention of venous thromboembolism in patients with cancer: guidelines of the Italian Society for Haemostasis and Thrombosis

2012

thrombosis guidelines
researchProduct

Relapsing or refractory idiopathic thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: the role of rituximab.

2010

thrombotic thrombocytopenic purpura rituximab
researchProduct

Editorial: Thymic Epithelial Cells: New Insights Into the Essential Driving Force of T-Cell Differentiation.

2021

thymic stromal cellsT-LymphocytesImmunologyThymus GlandBiology03 medical and health sciences0302 clinical medicinethymusmedicineImmunology and AllergyAnimalsHumansImmunodeficiency030304 developmental biologycentral tolerance0303 health sciencesCell DifferentiationEpithelial CellsRC581-607medicine.diseaseCell biologyEditorialT cell differentiationthymic epithelial cellsCentral toleranceImmunologic diseases. Allergyimmunodeficiency030215 immunologyFrontiers in immunology
researchProduct

Variants of human CLDN9 cause mild to profound hearing loss

2021

Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent onset. Exome sequencing of probands identified a homozygous c.475G>A;p.(Glu159Lys) variant of CLDN9 (NM_020982.4) in one family and a homozygous c.370_372dupATC;p.(Ile124dup) CLDN9 variant in an affected individual of a second family. Claudin 9 (CLDN9) is an integral membrane protein and constituent of epithelial bicellular tight junctions that form semi-permeable, paracellular barriers between inner ear perilymphatic and endolymphatic compartment…

tight junctionsAdolescentclaudin 9In situ hybridizationDeafnessBiologyArticleFrameshift mutationMiceotorhinolaryngologic diseasesGeneticsmedicineAnimalsHumansPakistanInner earNonsyndromic deafnessChildClaudinGenetics (clinical)Exome sequencingnonsyndromic deafnessTight junctionGenetic heterogeneityclaudin 9; exome sequencing; Morocco; nonsyndromic deafness; Pakistan; tight junctionsHomozygotemedicine.diseaseMolecular biologyPedigreeMoroccomedicine.anatomical_structureClaudinsMutationexome sequencingHeLa CellsHuman Mutation
researchProduct

Time-like Proton Form Factors with Initial State Radiation Technique

2022

Electromagnetic form factors are fundamental quantities describing the internal structure of hadrons. They can be measured with scattering processes in the space-like region and annihilation processes in the time-like region. The two regions are connected by crossing symmetry. The measurements of the proton electromagnetic form factors in the time-like region using the initial state radiation technique are reviewed. Recent experimental studies have shown that initial state radiation processes at high luminosity electron-positron colliders can be effectively used to probe the electromagnetic structure of hadrons. The BABAR experiment at the B-factory PEP-II in Stanford and the BESIII experim…

time-likePhysics and Astronomy (miscellaneous)Chemistry (miscellaneous)General Mathematicselectromagnetic form factorsQA1-939Computer Science (miscellaneous)Computer Science::Programming Languagesinitial state radiationHigh Energy Physics::ExperimentComputer Science::Digital LibrariesMathematicsprotonSymmetry
researchProduct

Progress in HAXPES performance combining full-field k-imaging with time-of-flight recording

2019

Journal of synchrotron radiation 26(6), 1996-2012 (2019). doi:10.1107/S1600577519012773

time-of-flight microscopeDiffractionNuclear and High Energy PhysicsMaterials scienceMicroscopePhoton550530 Physics02 engineering and technologyKinetic energy01 natural scienceslaw.inventionOpticslaw0103 physical sciencesddc:550HAXPES010306 general physicsInstrumentationMonochromatorRadiationk-spacebusiness.industry021001 nanoscience & nanotechnology530 PhysikResearch PapersBrillouin zoneWavelengthTime of flightBrillouin zone0210 nano-technologybusinessX-ray photoelectron diffraction
researchProduct

Art. 1987 - Efficacia delle promesse

2009

tipicità/aticipitàpromesse unilateraliSettore IUS/01 - Diritto Privato
researchProduct

Extramedullary hematopoiesis within endothelial papillary hyperplasia (Masson?s pseudoangiosarcoma) of the tongue

2007

We report the unique association of Masson?s pseudoangiosarcoma (endothelial papillary hyperplasia) and extramedullary hematopoiesis. The lesion was present as a violaceous nodule on the side of the tongue of a 78-year-old man with history of multiple myeloma and long-standing mild anemia. This association between a peculiar form of thrombus organization and extramedullary hematopoiesis has been reported previously only once, in an infant with a cranial hematoma, and raises interesting pathogenetic questions.

tongueintravascular endothelial papillary hyperplasiaUNESCO::CIENCIAS MÉDICAScardiovascular systemthrombus organization:CIENCIAS MÉDICAS [UNESCO]Extramedullary hematopoiesis
researchProduct

Micromaterials lipid-based for topic release of fluticasone propionate for the COPD treatment

2016

topic release COPD micromaterials
researchProduct

Les discours de Libanios (discours 33-64) et la topographie d’Antioche

2012

The work is preparatory to elaborating a Libanius' lexicon attentive to the different nuances that seemingly common words can take on in a specific context such as that of his speech.

topographyspeechlexiconSettore L-ANT/03 - Storia RomanaAntiochLibaniu
researchProduct