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  1. 1441
    “…A Japanese family with autosomal recessive cerebellar ataxia type 8 (SCAR8, MIM 610743) is described. …”
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    A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8
  2. 1442
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    Economic insecurity during the Great Recession and metabolic, inflammatory and liver function biomarkers: analysis of the UK Household Longitudinal Study
  3. 1443
    “…We remind readers of the grey-line approach to levator recession (LR) and lamellar repositioning surgery. …”
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    Upper eyelid levator-recession and anterior lamella repositioning through the grey-line: Avoiding a skin-crease incision
  4. 1444
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    Erratum. Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 2017;66:2316–2322
  5. 1445
    “…BACKGROUND: Unmet medical need (UMN) had been declining steadily across Europe until the 2008 Recession, a period characterized by rising unemployment. …”
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    The Great Recession and inequalities in access to health care: a study of unemployment and unmet medical need in Europe in the economic crisis
  6. 1446
    “…Mutations in the ALS5/SPG11/ KIAA1840 gene are a frequent cause of autosomal recessive hereditary spastic paraplegia with thin corpus callosum and peripheral axonal neuropathy, and account for ∼40% of autosomal recessive juvenile amyotrophic lateral sclerosis. …”
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    ALS5/SPG11/ KIAA1840 mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease
  7. 1447
    “…BACKGROUND: Several researchers have tried to improve the results of gingival recession treatment techniques. One of the methods is to use growth factors The present study was undertaken to evaluate the effect of CAF (coronally advanced flap) + CTG (connective tissue graft) + PRGF (plasma rich in growth factors) in the treatment of Miller Class I buccal gingival recession. …”
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    Coronally advanced flap and connective tissue graft with or without plasma rich in growth factors (PRGF) in treatment of gingival recession
  8. 1448
    “…Clinical parameters were recorded at baseline, 3 months and 6 months which include plaque index, gingival index, recession depth, recession width, clinical attachment loss and width of keratinized tissue. …”
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    Comparison of two surgical techniques in the treatment of multiple gingival recessions sandwiched with a combination of A-PRF and L-PRF
  9. 1449
    “…BACKGROUND: Autosomal recessive primary microcephaly (MCPH) is a rare genetically heterogeneous disorder of neurogenic brain development characterized by a reduced head circumference at birth with no remarkable anomalies of brain architecture and variable degrees of intellectual impairment. …”
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    A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report
  10. 1450
    “…Recessive dystrophic epidermolysis bullosa (RDEB) is a devastating inherited skin blistering disease caused by mutations in the COL7A1 gene that encodes type VII collagen (C7), a major structural component of anchoring fibrils at the dermal‐epidermal junction (DEJ). …”
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    Efficacy of Human Placental‐Derived Stem Cells in Collagen VII Knockout (Recessive Dystrophic Epidermolysis Bullosa) Animal Model
  11. 1451
    “…BACKGROUND: Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) is a recessive neurological disorder with cerebellar, pyramidal and neuropathic features. …”
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    From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay
  12. 1452
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    Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphoma
  13. 1453
    por Sams, Aaron J., Boyko, Adam R.
    Publicado 2018
    “…In domestic dogs, nearly 200 mutations are known to cause recessive diseases, most of which can be efficiently assayed using SNP arrays. …”
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    Fine-Scale Resolution of Runs of Homozygosity Reveal Patterns of Inbreeding and Substantial Overlap with Recessive Disease Genotypes in Domestic Dogs
  14. 1454
    “…Balancing selection provides a plausible explanation for the maintenance of deleterious alleles at moderate frequency in livestock, including lethal recessives exhibiting heterozygous advantage in carriers. …”
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    Balancing selection at a premature stop mutation in the myostatin gene underlies a recessive leg weakness syndrome in pigs
  15. 1455
    “…BACKGROUND: Gingival recession is a frequent issue encountered by both the clinician and the patient. …”
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    Free Gingival Graft as a Single Step Procedure for Treatment of Mandibular Miller Class I and II Recession Defects
  16. 1456
    por Atherwood, Serge, Sparks, Corey S.
    Publicado 2019
    “…OBJECTIVE: The goal of this study was to analyze differences in the employment and wage trajectories of college-educated young workers in the United States, as distinguished by the timing of their entry into the labor market relative to the onset of the 2008–09 recession. METHODS AND FINDINGS: Using annual American Community Survey microdata, we analyzed the first six years of employment and wage outcomes for cohorts of young workers on traditional-student pathways entering the market (1) in 2006, shortly before recession onset; (2) in 2009, during the recession; and (3) in 2012, three years after the recession officially ended. …”
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    Early-career trajectories of young workers in the U.S. in the context of the 2008–09 recession: The effect of labor market entry timing
  17. 1457
    “…CONCLUSION: These observations point to a recessive mode of inheritance reported for the first time for this combination of gene/disease.…”
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    A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)
  18. 1458
    “…In total, 38% of diagnosed cases were caused by recessive genes, of which two cases escaped automatic calling due to one allele occurring de novo. …”
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    The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study
  19. 1459
    “…Autosomal recessive cornea plana is a very rare hereditary ocular disease, characterized by a flattened corneal curvature, marked hyperopia due to low refractive power and frequently consequent accommodative esotropia. …”
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    Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case report
  20. 1460
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    A homozygous frameshift variant in the KRT5 gene is compatible with life and results in severe recessive epidermolysis bullosa simplex
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