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  1. 1261
    “…In this paper, we examined how educational inequalities in self-reported health have evolved in different European countries and welfare state regimes over the last decade, which was troubled by the Great Recession. METHODS: We used cross-sectional data from the EU-SILC survey for adults from 26 European countries, from 2005 to 2014 (n = 3,030,595). …”
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    Welfare states, the Great Recession and health: Trends in educational inequalities in self-reported health in 26 European countries
  2. 1262
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    Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  3. 1263
    “…CONCLUSIONS: Our study identified, for the first time, a private pathogenic splice site mutation in FKBP10 gene and further prove the involvement of this gene in the rare cases of autosomal recessive OI type XI with distinguished clinical manifestations. …”
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    Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report
  4. 1264
    “…Discovery of most autosomal recessive disease genes has involved analysis of large, often consanguineous, multiplex families or small cohorts of unrelated individuals with a well-defined clinical condition. …”
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    Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
  5. 1265
    “…Recessive genic male sterility (RGMS) has great potential for F(1) hybrid seeds production in sesame (Sesamum indicum L.). …”
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    Cytological characterization and molecular mapping of a novel recessive genic male sterility in sesame (Sesamum indicum L.)
  6. 1266
    “…Hence, PTES has been proposed to represent a satisfactory alternative for the treatment of lateral recess stenosis (LRS), being defined as percutaneous endoscopic ventral facetectomy (PEVF) in these cases. …”
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    Percutaneous endoscopic ventral facetectomy: An innovative substitute of open decompression surgery for lateral recess stenosis surgical treatment?
  7. 1267
    por Fong, Foo Mei, Che Ahmad, Aswani
    Publicado 2018
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    CRNC3: Gingival Veneer: A Prosthetic Solution to Enhance Smile by Masking Aesthetically Challenging Gum Recession
  8. 1268
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    Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects
  9. 1269
    “…BACKGROUND: Autosomal recessive nail dysplasia is characterized by thick and hard nails with a very slow growth on the hands and feet. …”
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    A possible founder mutation in FZD6 gene in a Turkish family with autosomal recessive nail dysplasia
  10. 1270
    “…It is caused by mutations of the VPS13A gene with an autosomal recessive transmission. We report a consanguineous Turkish family with a different and informative clinical and diagnostic course. …”
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    Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation
  11. 1271
    “…Six genes are associated with autosomal recessive OCA (TYR, OCA2, TYRP1, SLC45A2, SLC24A5 and LRMDA), and one gene, GPR143, is associated with X-linked ocular albinism (OA). …”
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    A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1
  12. 1272
    “…His genetic analysis showed a recessive splice-site mutation in the CLCN1 gene (IVS19+2T>A). …”
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    A case report of recessive myotonia congenita and early onset cognitive impairment: Is it a causal or casual link?
  13. 1273
    “…BACKGROUND: Autosomal recessive congenital ichthyosis (ARCI) is a genetically and phenotypically heterogeneous skin disease, associated with defects in the skin permeability barrier. …”
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    Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan
  14. 1274
    “…BACKGROUND: MYO15A variants are responsible for human non-syndromic autosomal recessive deafness (DFNB3). The majority of MYO15A variants are associated with a congenital severe-to-profound hearing loss phenotype, except for MYO15A variants in exon 2, which cause a milder auditory phenotype, suggesting a genotype-phenotype correlation of MYO15A. …”
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    Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss
  15. 1275
    “…Introduction  Posterior tympanotomy through facial recess (FR) is the conventional and most preferred approach to facilitate cochlear implantation, especially when the electrode is inserted through the round window. …”
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    Anatomical Study of the Facial Recess with Implications in Round Window Visibility for Cochlear Implantation: Personal Observations and Review of the Literature
  16. 1276
    “…Protein structure modeling points to loss of function of the novel recessive missense variants and to a dominant-negative effect of the reported dominant RAX2 alleles. …”
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    Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
  17. 1277
    por Hammarström, Ann, Virtanen, Pekka
    Publicado 2019
    “…Results: At age 21, those who studied during recession had more depressive and functional somatic symptoms than those who studied during boom. …”
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    The importance of financial recession for mental health among students: short- and long-term analyses from an ecosocial perspective
  18. 1278
    “…Pathogenic mutations in the gene encoding the giant skeletal muscle protein titin (TTN) are associated with several muscle disorders, including cardiomyopathy, recessive congenital myopathies and limb-girdle muscular dystrophy (LGMD) type10. …”
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    Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10
  19. 1279
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    Pathogenic Pathways in Early-Onset Autosomal Recessive Parkinson's Disease Discovered Using Isogenic Human Dopaminergic Neurons
  20. 1280
    “…BACKGROUND: Autosomal recessive bestrophinopathy (ARB) is a retinal degenerative disorder caused by BEST1 mutations with autosomal recessive inheritance. …”
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    Familial autosomal recessive bestrophinopathy: identification of a novel variant in BEST1 gene and the specific metabolomic profile
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