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Mostrando 161 - 180 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.21s Limitar resultados
  1. 161
    “…By exome sequencing we identify recessive mutations in DGKE (diacylglycerol kinase epsilon) that co-segregate with aHUS in 9 unrelated kindreds, defining a distinctive Mendelian disease. …”
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    Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
  2. 162
    “…To date, no clear patterns have been identified in these recessive mutations, though no systematic examination has yet been performed. …”
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    Genotype-phenotype correlations in recessive RYR1-related myopathies
  3. 163
    por Modrek, Sepideh, Cullen, Mark R
    Publicado 2013
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    Job insecurity during recessions: effects on survivors’ work stress
  4. 164
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    Prenatal diagnosis of autosomal recessive osteopetrosis: a case report
  5. 165
    “…Their previous child also had a similar condition. Autosomal recessive AED (AR-AED) can have its full expression both in males and females and it is clinically indistinguishable from the x-linked recessive AED (XL-AED), which is the most common type of ectodermal dysplasia. …”
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    Autosomal Recessive Anhidrotic Ectodermal Dysplasia: A Rare Entity
  6. 166
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    Uniform versus Asymmetric Shading Mediates Crown Recession in Conifers
  7. 167
    “…BACKGROUND: Autosomal recessive limb-girdle muscular dystrophies (LGMD2) include a number of disorders with heterogeneous etiology that cause predominantly weakness and wasting of the shoulder and pelvic girdle muscles. …”
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    Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
  8. 168
    por Shah, Rucha, Sowmya, N. K., Mehta, D. S.
    Publicado 2014
    “…DISCUSSION: Because of its inherent wound-modulating properties, amnion allograft may be used to enhance periodontal wound healing and enable tissue regeneration such as that in the coverage of gingival recession. CONCLUSION: Amnion allograft may provide an alternative to other conventional methods of treating gingival recession.…”
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    Amnion membrane for coverage of gingival recession: A novel application
  9. 169
    “…We investigated a strategy for diagnosing autosomal recessive lethal disorders in non-consanguineous pedigrees with multiple affected fetuses. …”
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    An exome sequencing strategy to diagnose lethal autosomal recessive disorders
  10. 170
    “…Due to minimal trauma at the recipient site, this procedure may be advantageous in treatment of recession as compared to other treatment modalities.…”
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    The pouch and tunnel technique for management of multiple gingival recession defects
  11. 171
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    Peripheral neuro-immune pathology in recessive dystrophic epidermolysis bullosa
  12. 172
    “…BACKGROUND/AIMS: Donohue and Rabson-Mendenhall syndrome are rare autosomal recessive disorders caused by mutations in the insulin receptor gene, INSR. …”
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    Insulin Receptor and the Kidney: Nephrocalcinosis in Patients with Recessive INSR Mutations
  13. 173
    “…Reports of primary isolated dystonia inherited in an autosomal-recessive (AR) manner, often lumped together as “DYT2 dystonia,” have appeared in the scientific literature for several decades, but no genetic cause has been identified to date. …”
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    Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia
  14. 174
    “…The effects of inbreeding on human health depend critically on the number and severity of recessive, deleterious mutations carried by individuals. …”
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    An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans
  15. 175
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    Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta
  16. 176
    “…AIM: To compare the surgical outcome of adjustable with the conventional recession in patients with horizontal comitant strabismus. …”
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    Adjustable recessions in horizontal comitant strabismus: A pilot study
  17. 177
    “…We aimed to identify the causative genetic lesions in two families in which eight affected individuals displayed variable learning disability, spasticity and abnormal gait. METHODS: Autosomal recessive inheritance was suggested by consanguinity in one family and by sibling recurrences with normal parents in the second. …”
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    HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome
  18. 178
    “…In contrast just 32% of nonparticipating boys and 31% of girls reached this level. With longer recess time the recommendation was met by 43% of boys (42% of girls) compared with 26% of boys (23% of girls) with shorter recess time. …”
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    The Role of Physical Education Lessons and Recesses in School Lifestyle of Adolescents
  19. 179
    “…BACKGROUND: Patients with recessive dystrophic epidermolysis bullosa (RDEB) exhibit blisters and erosions since birth, causing pain, pruritus and various complications. …”
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    Quality of Life and Economic Burden in Recessive Dystrophic Epidermolysis Bullosa
  20. 180
    por Corti, Olga
    Publicado 2015
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    Mechanisms of mitochondrial quality control in autosomal recessive Parkinson’s disease
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