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Mostrando 921 - 940 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.19s Limitar resultados
  1. 921
    “…For the purposes of the present analysis, the 2005–2006 cycle were considered “Pre-recession”, data from the 2007–2010 cycles were considered “Recession period”, and data from the 2011–2014 cycle were considered “Recession recovery period”. …”
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    Nutritional Impact of Economic Downturn: How the Great Recession Shaped Dietary Behaviors in US Adults
  2. 922
    “…He was diagnosed with severe recessive dystrophic epidermolysis bullosa (RDEB) due to the lack of type VII collagen by performing an immunofluorescence mapping method from a skin biopsy specimen of the patient's bulla. …”
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    Dominance of Methicillin-Resistant Staphylococcus aureus in a Japanese Infant with Recessive Dystrophic Epidermolysis Bullosa
  3. 923
    por Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O’Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry
    Publicado 2021
    “…By interrogating the genome sequences of 74 180 individuals from the 100K Genomes Project in combination with international gene-matching efforts and targeted sequencing, we identified 17 individuals from 15 families with an autosomal-recessive, non-length dependent, hereditary motor neuropathy and rare biallelic variants in VWA1. …”
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    An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
  4. 924
    “…Our simulation experiments demonstrate that a recessive model is better than the additive model. …”
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    Recessive/dominant model: Alternative choice in case-control-based genome-wide association studies
  5. 925
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    Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
  6. 926
    “…The forkhead transcription factor FOXE3 is critical for vertebrate eye development. Recessive and dominant variants cause human ocular disease but the full range of phenotypes and mechanisms of action for the two classes of variants are unknown. …”
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    Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders
  7. 927
    “…BACKGROUND: Autosomal recessive Alport syndrome (ARAS) is caused by pathogenic variants in both alleles of either COL4A3 or COL4A4 genes. …”
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    Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome
  8. 928
    “…PURPOSE: The aim of this study was to evaluate the changes in astigmatism after unilateral recession of horizontal rectus muscles in pediatric patients. …”
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    Changes in astigmatism after horizontal muscle recession strabismus surgery: A retrospective cohort study
  9. 929
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    Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features
  10. 930
    por Paulsen, Richard J.
    Publicado 2021
    “…This study uses American Community Survey data to examine the impact of the Great Recession on college graduates majoring in the arts. …”
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    Arts majors and the Great Recession: a cross-sectional analysis of educational choices and employment outcomes
  11. 931
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    A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
  12. 932
    “…METHODS: Fifty-four Chinese index patients with unexplained autosomal recessive or sporadic ataxia were investigated by whole-exome sequencing (WES) and copy number variation (CNV) calling with ExomeDepth. …”
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    Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias
  13. 933
    “…CONCLUSIONS: Gingival recession was a prevalent condition among young individuals. …”
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    Prevalance and clinical characteristics of gingival recession in Greek young adults: A cross‐sectional study
  14. 934
    “…OBJECTIVES: Maxillary gingival recessions can be managed by both semilunar coronally repositioned flap (SLCRF) and coronally advanced flap (CAF). …”
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    Comparison of coronally advanced versus semilunar coronally repositioned flap in the management of maxillary gingival recessions
  15. 935
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    Inequality in the Face of Death: The Income Gradient in Mortality of the Spanish Pre-Recession Working-Age Population
  16. 936
    “…The current literature supports the gastrocnemius recession for non-insertional cases, but is inconsistent in its efficacy for insertional cases. …”
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    Treatment of Insertional Achilles Tendinopathy with MRI Confirmed Small or No Tear Using a Gastrocnemius Recession
  17. 937
    “…METHODS: Whole‐exome sequencing was applied for investigation of various variants of ID, then Sanger sequencing and in silico analysis in ten patients from five Iranian consanguineous families diagnosed with autosomal recessive neurodevelopmental disorders, intellectual disability, performed for confirming the causative mutation within the probands. …”
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    Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families
  18. 938
    “…Here we describe efficient methods for precise genome editing in this insect. A spontaneous recessive white-eyed phenotype maps to a frameshift deletion (c.737delC) in the white gene. …”
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    Mapping and CRISPR homology-directed repair of a recessive white eye mutation in Plodia moths
  19. 939
    “…METHODS: Multi-institutional, retrospective cohort study comparing NAT rates in children <18 y old during the COVID-19 pandemic (March-August 2020) with a recent historical data (January 2015-February 2020) and during a previous economic recession (January 2007-December 2011) at level 1 Pediatric Trauma Centers. …”
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    Association of Economic Recession and Social Distancing With Pediatric Non-accidental Trauma During COVID-19
  20. 940
    “…Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a hereditary cerebral small vascular disease caused by a homozygous mutation in the high-temperature requirement A serine peptidase 1 (HTRA1) gene. …”
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    Case Report: Diffuse Cerebral Microbleeds in Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts and Leukoencephalopathy
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