Results 1 to 10 of about 273,560 (330)

Fundamental review of the trading book: State of art on implementation of Standardised Approach Fundamental review of the trading book: Stato dell’arte sulle implementazioni dello Standardised Approach [PDF]

open access: yesRisk Management Magazine, 2021
Following the publication of the regulatory framework for the Fundamental Review of the Trading Book (FRTB) by both the Basel Committee (BCBS) and the EU Regulator, the Financial Institutions have started the mandatory actions to comply with the new ...
Nicoletta Figurelli   +9 more
doaj   +1 more source

Determination of Spatial Scale in Martian Landscape Images Acquired by the Curiosity Rover, and Viewing Image Scale and Target Chemistry Using the ASIC Website

open access: yesEarth and Space Science, 2023
In this paper we describe a method to compute spatial scales for images acquired by NASA's Mars Curiosity rover (Mars Science Laboratory, MSL). The method is based on the assumption that the rover stands on an infinite plane that may have any orientation
Walter Goetz   +4 more
doaj   +1 more source

The importance of early diagnosis and views on newborn screening in metachromatic leukodystrophy: results of a Caregiver Survey in the UK and Republic of Ireland

open access: yesOrphanet Journal of Rare Diseases, 2022
Metachromatic Leukodystrophy (MLD) is a rare, autosomal recessive lysosomal storage disorder caused by a deficiency of the enzyme arylsulfatase A (ARSA).
Georgina Morton   +5 more
doaj   +1 more source

GREATER LONDON POLICE: ORIGINS AND CURRENT STATUS

open access: yesВестник Брянского государственного университета, 2021
The article is devoted to the interaction of the police and the elected bodies of Greater London-its Administration and municipal districts (boroughs) - in ensuring law and order. Both the history of the issue and its current state are touched upon.
Pronkin S.V.
doaj   +1 more source

Impact of the COVID-19 pandemic on access to the cerliponase alfa managed access agreement in England for CLN2 treatment

open access: yesOrphanet Journal of Rare Diseases, 2022
Background Cerliponase alfa, an enzyme replacement therapy for neuronal ceroid lipofuscinosis type 2 (CLN2), is currently available in England through a managed access agreement (MAA).
Amanda Mortensen   +2 more
doaj   +1 more source

Covid-19 crisis and its impacts on the economic and financial sector [PDF]

open access: yesRisk Management Magazine, 2021
The World Bank data confirm that the recovery scenario will be different depending on the type of nation, the fundamentals of its economy, etc.. The Bank of Italy expects a growth of more than 4% for Italy at the end of 2021.
Camillo Giliberto
doaj   +1 more source

Nuove policy nazionali ed internazionale: possibili implicazioni sulle Banche Italiane [PDF]

open access: yesRisk Management Magazine, 2020
The article proposes some reflections on the funding and bank credit policies of italian banks in the light of the considering originated by some factors although different in times, in the modalities and certainty of manifestation are expected to ...
Camillo Giliberto
doaj   +1 more source

Mucopolysaccharidosis: A broad review

open access: yesIndian Journal of Ophthalmology, 2022
Mucopolysaccharidosis (MPS) is a group of genetic disorders with seven types and 13 subgroups which are characterized by an inherent deficiency of the enzymes responsible for the degradation of glycosaminoglycans (GAGs).
Ritu Nagpal   +6 more
doaj   +1 more source

Differences in MPS I and MPS II Disease Manifestations [PDF]

open access: yesInternational Journal of Molecular Sciences, 2021
Mucopolysaccharidosis (MPS) type I and II are two closely related lysosomal storage diseases associated with disrupted glycosaminoglycan catabolism. In MPS II, the first step of degradation of heparan sulfate (HS) and dermatan sulfate (DS) is blocked by a deficiency in the lysosomal enzyme iduronate 2-sulfatase (IDS), while, in MPS I, blockage of the ...
Christiane S. Hampe   +5 more
openaire   +2 more sources

Clinical, molecular, and genetic characteristics of the hereditary spastic paraplegia type 3

open access: yesАнналы клинической и экспериментальной неврологии, 2020
Introduction. The autosomal dominant hereditary spastic paraplegia type 3 (SPG3), associated with the ATL1 gene, is a common form of the hereditary spastic paraplegia (HSP).
Galina E. Rudenskaya   +10 more
doaj   +1 more source

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