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Mostrando 881 - 900 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.29s Limitar resultados
  1. 881
    por Tomiyama, Takami, Shimada, Hiroyuki
    Publicado 2020
    “…In this review, we describe the story behind the discovery of the Osaka mutation, summarize the mutant’s phenotypes, and propose a mechanism of its recessive inheritance.…”
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    APP Osaka Mutation in Familial Alzheimer’s Disease—Its Discovery, Phenotypes, and Mechanism of Recessive Inheritance
  2. 882
    por Chalaris, M., Gritzalis, S.
    Publicado 2020
    “…In this article we provide data from seven Greek Universities during the economic recession. Based on the data that has been collected we assess the strategic performance of the universities using the aggregation disaggregation theory of the Multiple Criteria Analysis. …”
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    Data on strategic performance of Greek universities during the economic recession: A multiple criteria approach
  3. 883
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    RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability
  4. 884
    “…The variants were filtered assuming autosomal recessive inheritance, rare variants in population databases, in silico analysis predicted as deleterious and pituitary and/or hypothalamus gene expression. …”
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    SAT-LB58 Molecular Investigation of Recessive Inheritance by Exome Sequencing of Patients With Congenital Hypopituitarism
  5. 885
    “…BACKGROUND: The causes for thousands of individually rare recessive diseases have been discovered since the adoption of next generation sequencing (NGS). …”
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    Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families
  6. 886
    “…We report the long-term surgical results of augmented lateral rectus muscle (LR) recession for dissociated horizontal deviation (DHD) without concomitant exotropia (XT) or esotropia (ET). …”
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    Long-term results of augmented unilateral lateral rectus muscle recession for dissociated horizontal deviation
  7. 887
    “…[Image: see text] Oxidative stress occurs when physiological antioxidant systems do not manage to counteract the excessive intracellular production of reactive oxygen species (ROS), which accumulate leading to irreversible oxidation of DNA and other biomacromolecules, and thus to the onset of pathological conditions. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disease characterized by autosomal recessive mutations in the sacsin gene (SACS). …”
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    Development of Nanostructured Lipid Carriers for the Delivery of Idebenone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
  8. 888
    por Sheetal, S, Kumar, S Amith, Byju, P
    Publicado 2020
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    SACS Mutation-Positive Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay (ARSACS) from Kerala
  9. 889
    “…Time series were divided into pre-recession (Jan 2000-Nov 2007) and recession/post-recession (Dec 2007-Sept 2015) periods. …”
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    The impact of the Great Recession on California domestic violence events, and related hospitalizations and emergency service visits
  10. 890
    “…BACKGROUND: Autosomal recessive bestrophinopathy (ARB) is caused by homozygous or compound heterozygous mutations in the BEST1 gene and always accompanied with refractory angle-closure glaucoma (ACG). …”
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    Pathogenic role of the vitreous in angle-closure glaucoma with autosomal recessive bestrophinopathy: a case report
  11. 891
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    Role of frataxin protein deficiency and metabolic dysfunction in Friedreich ataxia, an autosomal recessive mitochondrial disease
  12. 892
    por Akutsu, Noriko
    Publicado 2020
    “…The model used is a restricted solid-on-solid model with a discrete Hamiltonian without surface or volume diffusion (interface limited growth/recession). The temperature, driving force for growth, system size, and surface slope dependences of the surface width are calculated for vicinal surfaces tilted between the (001) and (111) surfaces. …”
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    Crossover from BKT-rough to KPZ-rough surfaces for interface-limited crystal growth/recession
  13. 893
    por Fan, Chao, Jiang, Xiangqi, Mostafavi, Ali
    Publicado 2020
    “…This study presents a mathematical contagion model to describe the spatial–temporal spread and recession process of floodwaters in urban road networks. …”
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    A network percolation-based contagion model of flood propagation and recession in urban road networks
  14. 894
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    Novel CHP1 mutation in autosomal-recessive cerebellar ataxia: autopsy features of two siblings
  15. 895
    “…Our data support further expansion of the clinical spectrum linked to MCM3AP variant and highlight that MCM3AP should be considered in patients with accompaniment of recessive motor axonal Charcot-Marie-Tooth neuropathy and multiple sclerosis.…”
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    Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
  16. 896
    “…BACKGROUND: Autosomal recessive dystrophic epidermolysis bullosa (RDEB) is an incurable and severe inherited skin disorder characterized by recurrent blistering at the sublamina densa beneath the cutaneous basement membrane. …”
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    Novel biallelic variants in COL7A1 cause recessive dystrophic epidermolysis bullosa
  17. 897
    “…Background: Classical Galactosemia (CG) is a rare autosomal recessive metabolic disease caused by mutations in the galactose-1-phosphate uridyl transferase (GALT) gene. …”
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    High-Throughput Sequencing Reveals the Loss-of-Function Mutations in GALT Cause Recessive Classical Galactosemia
  18. 898
    “…Gingival recessions are usually treated with surgical therapies which involve the use of connective tissue autograft in order to thicken the gingival tissue. …”
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    Bilaminar Technique with Coronally Advanced Flap and Cryopreserved Human Amniotic Membrane in the Treatment of Gingival Recessions
  19. 899
    por Erten, Bilge, Antonio Ocampo, José
    Publicado 2021
    “…The pandemic-driven global recession has already triggered a rapid decline in global commodity prices, particularly of energy products. …”
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    The future of commodity prices and the pandemic-driven global recession: Evidence from 150 years of data
  20. 900
    “…MYH2 mutations are responsible for an autosomal dominant (AD) progressive myopathy, characterized by the presence of rimmed vacuoles and by a reduction in the number and size of type 2A fibers, and a recessive early onset myopathy characterized by complete loss of type 2A fibers. …”
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    MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form
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