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Mostrando 621 - 640 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.41s Limitar resultados
  1. 621
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    Correction: Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
  2. 622
    “…PURPOSE: To identify the genetic origins of autosomal recessive congenital cataracts (arCC) in the Pakistani population. …”
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    Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening
  3. 623
    “…Sinonasal mucosal specimens were obtained from the frontal recess, ethmoid sinus, and nasal polyp separately. …”
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    IL-5 and IL-6 are increased in the frontal recess of eosinophilic chronic rhinosinusitis patients
  4. 624
    “…Isolated familial hypoparathyroidism is an extremely rare disorder, which to date has been linked to several loci including mutations in CASR, GCM2, and PTH, as well as a rare condition defined as X-linked recessive hypoparathyroidism, previously associated with a 1.5 Mb region on Xq26-q27. …”
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    A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
  5. 625
    “…These findings indicate recessive mutations in MSTO1 as a new cause for inherited neuromuscular disorders with multisystem features.…”
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    Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
  6. 626
    “…Among the recessive forms, OI types VII, VIII, and IX are due to mutations in CRTAP, P3H1, and PPIB genes, respectively. …”
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    Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective
  7. 627
    “…Autosomal recessive cutis laxa type-II (ARCLII) is a spectrum of clinical disorders with prenatal and postnatal growth retardation, cutis laxa, dysmorphism, and skeletal abnormalities. …”
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    Autosomal Recessive Cutis Laxa Type II: Report of Novel Mutation in a Child
  8. 628
    “…Recently, there had been several studies that reported better surgical results of augmented bilateral lateral rectus muscle recession procedure over the conventional procedure. …”
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    Long-term outcomes of augmented unilateral recess-resect procedure in children with intermittent exotropia
  9. 629
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    UFM1 founder mutation in the Roma population causes recessive variant of H-ABC
  10. 630
    “…CONCLUSION: It is generally safe to place the posterolateral incision more than 14cm above the calcaneal tuberosity to avoid the sural nerve if surgeons plan to use a posterolateral incision for endoscopic recession. The distance between the calcaneal tuberosity to the gastrocnemius tendon insertion into the Achilles tendon is too highly variable to be used as a landmark for locating the gastrocnemius insertion.…”
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    Cadaveric Anatomical Study of Sural Nerve: Where is The Safe Area for Endoscopic Gastrocnemius Recession?
  11. 631
    “…BACKGROUND: Lethal recessive variation can cause prenatal death of homozygous offspring. …”
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    A systematic survey to identify lethal recessive variation in highly managed pig populations
  12. 632
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    Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight
  13. 633
    “…BACKGROUND: Many of the genetic childhood disorders leading to death in the pre- or neonatal period or during early childhood follow autosomal recessive modes of inheritance and bear specific challenges for genetic counseling and prenatal diagnostics. …”
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    Targeted next-generation sequencing analysis in couples at increased risk for autosomal recessive disorders
  14. 634
    por Paryag, Amit, Lowe, Jenai, Rafeek, Reisha
    Publicado 2017
    “…In this case of extensive gingival recession (Miller’s Class II) and mild physiologic pigmentation, an alternative method for the placement of Amaris Gingiva-Colored Composite was used to produce a non-invasive, aesthetic result acceptable to the patient. …”
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    Colored Gingiva Composite Used for the Rehabilitation of Gingiva Recessions and Non-Carious Cervical Lesions
  15. 635
    “…PURPOSE: To present the results of bilateral superior rectus transposition with medial rectus recession in a case of chronic bilateral sixth nerve palsy. …”
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    Bilateral superior rectus transposition and medial rectus recession for bilateral sixth nerve palsy
  16. 636
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    Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
  17. 637
    “…INTRODUCTION: During the recent “Great Recession,” many families in the United Kingdom experienced increased financial strain (FS). …”
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    Financial Strain, Parental Smoking, and the Great Recession: An Analysis of the UK Millennium Cohort Study
  18. 638
    “…Objectives  To measure the distances of the simulated trajectory to the facial recess, cochlea, ossicular chain and tympanic membrane, while performing the minimally invasive cochlear implant technique, using the Improvise imaging software (Vanderbilt University, Nashville, TN, US). …”
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    Evaluation of the Facial Recess and Cochlea on the Temporal Bone of Stillbirths regarding the Percutaneous Cochlear Implant
  19. 639
    “…OBJECTIVE: To address the relationship between mutations in the DNA strand break repair protein tyrosyl DNA phosphodiesterase 2 (TDP2) and spinocerebellar ataxia autosomal recessive 23 (SCAR23) and to characterize the cellular phenotype of primary fibroblasts from this disease. …”
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    Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)
  20. 640
    “…We report the first case of nonimmune hydrops fetalis (NIHF) associated with a recessive, in-frame deletion of V205 in the G protein–coupled receptor, Calcitonin Receptor-Like Receptor (hCALCRL). …”
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    hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia
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