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  1. 1241
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    Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency
  2. 1242
    por Lu, Cong, Zheng, Yi-Cen, Dong, Yi, Li, Hong-Fu
    Publicado 2016
    “…BACKGROUND: Autosomal recessive cerebellar ataxias (ARCA) are a group of neurodegenerative disorders characterized by early onset of gait impairment, disturbed limb coordination, dysarthria, and eye movement abnormalities, most likely due to the degeneration of cerebellum, brainstem, and spinal cord. …”
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    Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing
  3. 1243
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    SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss
  4. 1244
    “…Renal failure and infectious disease are strongly associated with morbidity and mortality in patients with severe generalized recessive dystrophic epidermolysis bullosa (RDEB-sev gen). …”
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    Maintenance Hemodialysis Using Native Arteriovenous Fistula in a Patient with Severe Generalized Recessive Dystrophic Epidermolysis Bullosa
  5. 1245
    “…In the present study, this approach was applied to four families with autosomal recessive (AR) congenital sensorineural hearing loss. …”
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    Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR
  6. 1246
    “…BACKGROUND: To discuss the strategy of suprapedicular foraminal endoscopic approach to lumbar lateral recess decompression and evaluate the safety and effectiveness of this strategy. …”
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    Suprapedicular Foraminal Endoscopic Approach to Lumbar Lateral Recess Decompression Surgery to Treat Degenerative Lumbar Spinal Stenosis
  7. 1247
    “…Mutations in PINK1 are the second most common agents causing autosomal recessive, early onset PD. We aimed to identify the pathogenic SNPs in PARK2 and PINK1 using in silico prediction software and their effect on the structure, function, and regulation of the proteins. …”
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    In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease
  8. 1248
    “…CONCLUSION: Synovial osteochondromatosis of shoulder joint, subscapular recess and along the long head of biceps is a rare case (less than 5% cases reported till date). …”
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    A Rare Case of Multiple Rice Bodies in Glenohumeral Joint, Subscapular Recess and Along Long Head of Biceps
  9. 1249
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    Depression in Sardinian immigrants in Argentina and residents in Sardinia at the time of the Argentinian default (2001) and the Great Recession in Italy (2015)
  10. 1250
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    A nationwide survey of training satisfaction and employment prospects among Greek gastroenterology fellows during the economic recession
  11. 1251
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    Coping with the Double Crisis: Lake Chilwa Recession and the Great Depression on Chisi Island in Colonial Malawi, 1930–1935
  12. 1252
    “…Possible explanations include the weak impact of the recession on wages, as well as the generous unemployment insurance and social benefit system in Finland. …”
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    Are some populations resilient to recessions? Economic fluctuations and mortality during a period of economic decline and recovery in Finland
  13. 1253
    “…BACKGROUND: There is a growing body of evidence associating financial strain (FS) with poor health but most of this research has been cross-sectional and adult-focused. During the ‘Great Recession’ many UK households experienced increased FS. …”
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    Increased household financial strain, the Great Recession and child health—findings from the UK Millennium Cohort Study
  14. 1254
    “…METHODS: Thirty families investigated in Shahrekord University of Medical Sciences in 2014, genetic linkage analysis via four short tandem repeat markers linked to MYO7A was performed for two consanguineous families originating from Hamedan (family-13) and Chaharmahal-Bakhtiari (family-32) provinces of Iran, co-segregating autosomal recessive HL and showed no mutation in GJB2 gene in our preliminary investigation. …”
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    Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran
  15. 1255
    “…We report a rare case of an 18-month-old female with autosomal recessive polycystic kidney disease, Caroli syndrome, and pure fetal type hepatoblastoma. …”
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    A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome—Review of the Literature
  16. 1256
    por Liao, Chen-Mao, Lin, Chih-Ming
    Publicado 2017
    “…The reduction of the alcohol tax resulted in increased rates of AADs among both the low and high income groups. The economic recession and the reduction of the alcohol tax resulted in an increased rate of AAD among low income men.…”
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    The Effects of the Global Economic Recession and a Reduced Alcohol Tax on Hospitalizations Due to Alcohol-Attributed Diseases in Taiwan
  17. 1257
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    Correction: Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)
  18. 1258
    “…This study describes the use of exome sequencing to identify a homozygous recessive variant in MAP3K14, NIK(Val345Met), in a patient with combined immunodeficiency, disseminated BCG-osis, and paradoxically elevated lymphocytes. …”
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    Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency
  19. 1259
    “…The treatment of buccal gingival recession is a common requirement due to aesthetic concern or root sensitivity. …”
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    Comparative Evaluation of Platelet-Rich Fibrin with Connective Tissue Grafts in the Treatment of Miller's Class I Gingival Recessions
  20. 1260
    “…Previously, we introduced a noninvasive prenatal testing (NIPT) protocol for diagnosing compound heterozygous autosomal recessive point mutations via maternal plasma DNA and simulated control genomic DNA sampling based on fetal DNA fraction. …”
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    One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR
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