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Mostrando 181 - 200 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.20s Limitar resultados
  1. 181
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    Mutation of TBCK causes a rare recessive developmental disorder
  2. 182
    “…Gingival recession has direct causes and predisposing factors. …”
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    Gingival recession: its causes and types, and the importance of orthodontic treatment
  3. 183
    “…OBJECTIVE: To evaluate the inter-rater and intra-rater reliability of ultrasonographic measurements of axillary recess (AR) thickness in healthy individuals, and to analyze the factors affecting the thickness of the AR capsule. …”
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    Ultrasonographic Measurement of the Thickness of Axillary Recess Capsule in Healthy Volunteers
  4. 184
    por Roy, Avik Kumar, Padhy, Debananda
    Publicado 2015
    “…An 18-year-old male with 360 degree angle recession after blunt trauma in his right eye developed uncontrolled intraocular pressure (IOP) despite four antiglaucoma medications (AGM) with advancing disc damage. …”
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    Serous retinal detachment after trabeculectomy in angle recession glaucoma
  5. 185
    “…Genetic associations involving both rare and common alleles have been reported for schizophrenia but there have been no systematic scans for rare recessive genotypes using fully phased trio data. Here, we use exome sequencing in 604 schizophrenia proband–parent trios to investigate the role of recessive (homozygous or compound heterozygous) nonsynonymous genotypes in the disorder. …”
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    Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia
  6. 186
    “…BACKGROUND: Cholesterol deficiency (CD), a newly identified autosomal recessive genetic defect in Holstein cattle, is associated with clinical signs of diarrhea, failure to thrive, and hypocholesterolemia. …”
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    Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle
  7. 187
    “…RESULTS: Cellular type of recess was found intraoperatively in 32% of ears and dome-shaped in 68% of the study group. …”
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    Intraoperative endoscopy of the anterior epitympanum recess through the posterior tympanotomy
  8. 188
    “…PURPOSE: To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family. …”
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    Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts
  9. 189
    “…Here we report the identification of biallelic mutations in Receptor Expression Enhancer Protein 6 (REEP6) in seven individuals with autosomal-recessive RP from five unrelated families. REEP6 is a member of the REEP/Yop1 family of proteins that influence the structure of the endoplasmic reticulum but is relatively unstudied. …”
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    Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
  10. 190
    “…INTRODUCTION: The detailed knowledge of the peritoneal recesses has great significance with respect to internal hernias. …”
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    Clinical importance of duodenal recesses with special reference to internal hernias
  11. 191
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    Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts
  12. 192
    “…BACKGROUND: The classification of autosomal recessive ataxias represents a significant challenge because of high genetic heterogeneity and complex phenotypes. …”
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    Systematic review of autosomal recessive ataxias and proposal for a classification
  13. 193
    “…Our aims were (1) to locate the gastrocnemius muscular-tendinous junction in relation to the mid-length of the fibula (from here on designated the mid-fibula), (2) to compare the dorsiflexion achieved with dorsal recession or ventral recession, and (3) to determine the risk of injury to the sural nerve during gastrocnemius recession. …”
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    Gastrocnemius recession: A cadaveric study of surgical safety and effectiveness
  14. 194
    “…To begin to answer these questions, we focused on one of the simplest cases: recessive mutations that alone cause lethal diseases or complete sterility. …”
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    The population genetics of human disease: The case of recessive, lethal mutations
  15. 195
    “…BACKGROUND: Gingival recession in dentitions with otherwise healthy periodontium is a common occurrence in adults. …”
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    Quantitative measures of gingival recession and the influence of gender, race, and attrition
  16. 196
    por Sironi, Maria
    Publicado 2017
    “…Using the Luxembourg Income Study, this work investigates the trends in income from work of young adults before and after the Great Recession of 2008 in five countries—US, UK, Norway, Germany, and Spain. …”
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    Economic Conditions of Young Adults Before and After the Great Recession
  17. 197
    “…After delivery, the neonate required several double volume exchange transfusions and ultimately was diagnosed with autosomal recessive hereditary spherocytosis weeks after birth. …”
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    Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
  18. 198
    “…We report on an ESCS phenotype in additional patients with autosomal recessive NRL (arNRL) mutations. Three Moroccan patients of two different families with arNRL mutations were enrolled in this study. …”
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    Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome
  19. 199
    “…Persisting embryonal infundibular recess (PEIR) is a rare anomaly of the development of the posterior pituitary wherein there is a defect in the third ventricular floor. …”
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    Persisting Embryonal Infundibular Recess Masquerading as a Nasal Mass
  20. 200
    “…Cytochrome b5 reductase 3 (CYB5R3) is a membrane-bound NADH-dependent redox enzyme anchored to the mitochondrial outer membrane, endoplasmic reticulum, and plasma membrane. Recessive hereditary methaemoglobinaemia (RHM) type II is caused by CYB5R3 deficiency and is an incurable disease characterized by severe encephalopathy with mental retardation, microcephaly, generalized dystonia, and movement disorders. …”
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    Cellular and Molecular Mechanisms of Recessive Hereditary Methaemoglobinaemia Type II
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