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  1. 841
    “…PURPOSE: The aim of the present case report was to describe the retreatment of the single gingival recession in aesthetic area, in the presence of scar formation and consequent impairment of aesthetic appearance. …”
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    Fifteen-Year Follow-Up of a Case of Surgical Retreatment of a Single Gingival Recession
  2. 842
    por Wang, Ho-Wei, Chen, Duan-Rung
    Publicado 2018
    “…RESULTS: During an economic recession, the RSV of obesity awareness and health behaviors declined (r=.441, P<.001; r=.593, P<.001, respectively); however, the RSV for fast food restaurants increased (r=−.437, P<.001). …”
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    Economic Recession and Obesity-Related Internet Search Behavior in Taiwan: Analysis of Google Trends Data
  3. 843
    “…Autosomal recessive hereditary spastic paraparesis is rare.We present 4 patients with slowly progressive predominantly lower limb spasticity and ataxia. …”
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    Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene
  4. 844
    “…PURPOSE: To compare the surgical outcomes of unilateral lateral rectus recession–medial rectus resection (RR) according to forced duction test (FDT) results with those of conventional RR in intermittent exotropia. …”
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    Surgical outcomes of unilateral recession and resection in intermittent exotropia according to forced duction test results
  5. 845
    “…BACKGROUND: Autosomal recessive primary microcephaly (MCPH) is a clinically and genetically heterogeneous disorder. …”
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    A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly
  6. 846
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    Use of dermatoscopy in the detection of squamous cell carcinoma in a patient with recessive dystrophic epidermolysis bullosa
  7. 847
    por Badawi, Nermeen, Ismail, Ahmed Taha
    Publicado 2018
    “…PURPOSE: This study compares the results of Y-split recession versus de Decker's (modified Cüppers) Faden techniques of medial rectus (MR) muscles for the management of essential infantile esotropia (IET). …”
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    Comparative Study of Y-Split Recession versus Faden Technique for Management of Infantile Esotropia in Egyptians
  8. 848
    “…PURPOSE: Mutations in ARL2BP, encoding ADP-ribosylation factor-like 2 binding protein, have recently been implicated as a cause of autosomal recessive retinitis pigmentosa (arRP), with three homozygous variants identified to date. …”
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    Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
  9. 849
    “…SYNE1-related disease is most commonly reported in autosomal recessive spinocerebellar ataxia 8, which demonstrates variable age of onset with a median of 30 years of age. …”
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    SYNE1-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairment
  10. 850
    “…OBJECTIVE: The aim of this study was to investigate the risk factors contributing to gingival recession among patients undergoing orthodontic treatment. …”
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    Risk factors contributing to gingival recession among patients undergoing different orthodontic treatment modalities
  11. 851
    “…Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder but even rarer in Africans and it is one of the causes of nephropathies in childhood. …”
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    Autosomal recessive polycystic kidney disease (ARPKD) in a Nigerian newborn: a case report
  12. 852
    “…Caroli syndrome, which is characterized by saccular and fusiform dilatation of the biliary ducts, is usually observed in association with autosomal recessive polycystic kidney disease (ARPKD). Although the diagnosis of ARPKD is generally easy to make in postnatal ultrasound, the diagnosis of Caroli syndrome may be challenging in prenatal ultrasound. …”
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    Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease
  13. 853
    “…BACKGROUND: Guided tissue regeneration-based root coverage has emerged as a promising treatment modality in the treatment of gingival recession. A variety of nonresorbable and bioresorbable membranes have been successfully used. …”
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    Comparative efficacy of placental membrane and Healiguide™ in treatment of gingival recession using guided tissue regeneration
  14. 854
    “…Several morphological phenotypes have been associated to RYR1-recessive myopathies. We recharacterized the RYR1-recessive morphological spectrum by a large monocentric study performed on 54 muscle biopsies from a large cohort of 48 genetically confirmed patients, using histoenzymology, immunohistochemistry, and ultrastructural studies. …”
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    ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies
  15. 855
    “…Our findings suggest that the homozygous recessive H2665L missense sequence variant impairs the normal morphology of the teeth roots via loss of cementum synthesis, and is also associated with early onset, recessive, Wagner syndrome, thus expanding both the phenotype mutation scenario and the inheritance mode of VCAN mutations.…”
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    Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family
  16. 856
    “…OBJECTIVES: Our objective in this study is to evaluate the impact the Great Recession (2008–2014) had on self-perceived health in Spain. …”
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    Impact of the great recession on self-perceived health in Spain: a longitudinal study with individual data
  17. 857
    “…AIM: The aim of this study is to report root coverage outcomes in single deep gingival recessions (GR) following a proposed decision-making algorithm. …”
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    Root Coverage for Single Deep Gingival Recessions: Outcomes Based on a Decision-Making Algorithm
  18. 858
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    Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy
  19. 859
    “…In contrast to other tissues, cardiac and skeletal muscle express two FXR1P isoforms that incorporate an additional exon-15. We report that recessive mutations in this particular exon of FXR1 cause congenital multi-minicore myopathy in humans and mice. …”
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    Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
  20. 860
    “…Moreover, several families with autosomal recessive Marfan syndrome caused by pathogenic variants in FBN1 have been described. …”
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    Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant
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