Materias dentro de su búsqueda.
Mostrando 901 - 920 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.22s Limitar resultados
  1. 901
    “…Saddle flap technique, a modified coronally advanced flap approach for isolated gingival recession management was introduced and assessed in terms of clinical efficacy and patient satisfaction. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Modified coronally advanced flap design in management of isolated gingival recession: Saddle flap technique
  2. 902
    “…CONCLUSION: A combination of SNRB with PTED was effective for diagnosing and treating multi-segment lumbar lateral recess stenosis.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Accurate location and minimally invasive treatment of lumbar lateral recess stenosis with combined SNRB and PTED
  3. 903
    “…This hypothesis is that residential schools for the deaf, which concentrate signing deaf individuals together, have promoted assortative mating, which in turn has increased the prevalence of recessive deafness and also the commonest underlying deafness allele. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Deaf intermarriage has limited effect on the prevalence of recessive deafness and no effect on underlying allelic frequency
  4. 904
    por Urbanos-Garrido, Rosa M.
    Publicado 2020
    “…CONCLUSIONS: The Great Recession left its trace in form of a higher inequality in the access to dental care. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Income-related inequalities in unmet dental care needs in Spain: traces left by the Great Recession
  5. 905
    “…We noted that mutations in the NUBPL gene had been reported as causing autosomal recessive (AR) mitochondrial Complex I (CI) deficiency in children. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Loss-of-Function NUBPL Mutation May Link Parkinson's Disease to Recessive Complex I Deficiency
  6. 906
    “…The PCA design is fabricated with recessed metal electrodes in direct contact with the 2DEG region of the MDH. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    A modulation-doped heterostructure-based terahertz photoconductive antenna emitter with recessed metal contacts
  7. 907
    “…Mutations in the human desmin gene cause autosomal-dominant and recessive cardiomyopathies and myopathies with marked phenotypic variability. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies
  8. 908
    “…We postulate that this recessive missense mutation in CYP26C1 impacts the catalytic activity of the encoded enzyme, leading to excess RA resulting in the observed MD phenotype.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Mandibulofacial Dysostosis Attributed to a Recessive Mutation of CYP26C1 in Hereford Cattle
  9. 909
    por Wilkinson, Lindsay
    Publicado 2020
    “…Using longitudinal lagged dependent variable models that adjust for pre-recession self-rated health, the results reveal that both initial and increased financial strain due to the recession were associated with worsening self-rated health between 2006 and 2009. …”
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Financial Strain, Self-Rated Health, and the Mediating Role of Health Behaviors During the Great Recession
  10. 910
    “…We identified six families with biallelic mutations, five compound heterozygotes with no consanguinity, and one homozygous, with consanguineous parents, resulting in 30% of cases with possible autosomal recessive inheritance. We identified seven novel variants, four of them classified as pathogenic. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients
  11. 911
    “…Autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS) is a rare neurodegenerative disorder caused by biallelic mutations in the SACS gene. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
  12. 912
    “…INTRODUCTION: Bartsocas-Papas syndrome (BPS) is an autosomal recessive form of Popliteal Pterygium syndrome (PPS). …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Bartsocas-Papas syndrome: The first case report of severe autosomal recessive form from Indonesia
  13. 913
    “…NR2E3-associated recessive disease in humans is historically defined by congenital night blinding retinopathy, characterized by an initial increase in short-wavelength (S)-cone sensitivity and progressive loss of rod and cone function. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Interspecies Correlations between Human and Mouse NR2E3-Associated Recessive Disease
  14. 914
    “…Purpose: ARL3 (ADP-ribosylation factor-like 3) variants cause autosomal dominant retinitis pigmentosa (RP) or autosomal recessive Joubert syndrome. We found a family with rod-cone dystrophy (RCD) and verified it was associated with compound heterozygous variants in ARL3 gene. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene
  15. 915
    por Erickson, Robert P.
    Publicado 2021
    “…This led to an increased frequency of other autosomal recessive diseases. Recent advances in population genetics, pathophysiology of the diseases, and social/ethical issues concerning their study are reviewed.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Autosomal recessive diseases among the Athabaskans of the southwestern United States: anthropological, medical, and scientific aspects
  16. 916
    “…PURPOSE: To investigate the clinical course, genetic findings, and phenotypic spectrum of autosomal recessive bestrophinopathy (ARB) in a large cohort of children and adults. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical Trials
  17. 917
    por Zhang, Lujia, Li, Ya, Qin, Litao, Wu, Yu, Lei, Bo
    Publicado 2021
    “…Our data suggested that REEP6 c.268G>C may be a recurrent causative variant in Chinese autosomal recessive retinitis pigmentosa patients.…”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Population
  18. 918
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy
  19. 919
    “…Mutations in the transmembrane protein 38B (TMEM38B) gene have been reported in a rare autosomal recessive form of osteogenesis imperfecta.  TMEM38B encodes TRIC-B - a trimeric intracellular cation channel type B which is essential to modulate intracellular calcium signaling. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Detection of a Recurrent TMEM38B Gene Deletion Associated with Recessive Osteogenesis Imperfecta
  20. 920
    “…Based on the family’s pedigree, the variant acts in an autosomal recessive manner, which makes it the second autosomal recessive variant of PRKD1 to be identified with a link to CHDs, while all other previously described variants act dominantly. …”
    Enlace del recurso
    Enlace del recurso
    Enlace del recurso
    Online Artículo Texto
    Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart Disease
Herramientas de búsqueda: RSS