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  1. 561
    “…BACKGROUND: School recess provides a daily opportunity for children to engage in physically active behaviours. …”
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    Variables associated with children's physical activity levels during recess: the A-CLASS project
  2. 562
    “…An 11 year-old girl, whose condition was diagnosed as juvenile-type autosomal recessive polycystic kidney disease (ARPKD) at five years of age, presented with chest pain and dyspnea that had developed suddenly two months previously. …”
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    Pulmonary hypertension in a child with juvenile-type autosomal recessive polycystic kidney disease.
  3. 563
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    Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes
  4. 564
    “…Autosomal Recessive Primary Microcephaly (MCPH) is a rare disorder of neurogenic mitosis characterized by reduced head circumference at birth with variable degree of mental retardation. …”
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    Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum
  5. 565
    “…Here we demonstrate the use of whole-exome sequencing to overcome these obstacles by identifying recessive mutations in WDR62 as the cause of a wide spectrum of severe cerebral cortical malformations including microcephaly, pachygria with cortical thickening as well as hypoplasia of the corpus callosum. …”
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    Whole exome sequencing identifies recessive WDR62 mutations in severe brain malformations
  6. 566
    “…To the best of our knowledge, the effect of pregnancy as well as treatment in genetically confirmed autosomal recessive juvenile parkinsonism (ARJP) has never been reported. …”
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    Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism
  7. 567
    “…PURPOSE: To compare the outcomes of unilateral lateral rectus recession between the first operation and second operation for exotropia. …”
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    Comparison of Outcomes of Unilateral Lateral Rectus Recession for Exotropia between First and Second Operations
  8. 568
    “…In this case series study, we assessed the effects of recession-resection surgery augmented with botulinum toxin A chemodenervation for patients with chronic paralytic horizontal strabismus. …”
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    Recession-Resection Surgery Augmented with Botulinum Toxin A Chemodenervation for Paralytic Horizontal Strabismus
  9. 569
    “…Autosomal recessive osteopetrosis (ARO) is a genetically heterogeneous disorder attributed to reduced bone resorption by osteoclasts. …”
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    RANK-Dependent Autosomal Recessive Osteopetrosis: Characterization of Five New Cases With Novel Mutations
  10. 570
    “…The RDX gene anchors cytoskeletal actin of stereocilia to hair cell transmembrane and is responsible for autosomal recessive nonsyndromic hearing impairment (ARNSHI) due to DFNB24. …”
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    Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene
  11. 571
    “…Each patient had undergone unilateral or bilateral rectus recession associated with uni- or bilateral inferior oblique (IO) 14 mm recession, using a modified surgical normogram for lateral rectus (LR) recession, which resulted in 1 to 2 mm of reduction of LR recession. …”
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    Contemplation of the Surgical Normogram of Lateral Rectus Recession for Exotropia Associated with Superior Oblique Palsy
  12. 572
    “…PURPOSE: Nonsyndromic autosomal recessive optic atrophy (arOA) is extremely rare and its existence was disputed until a locus, optic atrophy 6 (OPA6), was mapped to 8q. …”
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    TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy
  13. 573
    “…BACKGROUND: Gingival recession is a common occurrence and patients often report to dental clinic with associated problems such as root surface hypersensitivity, esthetic concerns, cervical root abrasions, and root caries that make it a concern for patients. …”
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    Interest and satisfaction of dentists in practicing periodontics: A survey based on treatment of gingival recession
  14. 574
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    Mutation of SPATA7 in a family with autosomal recessive early-onset retinitis pigmentosa
  15. 575
    “…Here we describe the initial characterization and mapping of a recessive mutation that leads to degeneration of the incisors, failure of molars to erupt, a grey coat colour, and mild osteopetrosis. …”
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    Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1
  16. 576
    “…We aimed at identifying a novel gene for an autosomal recessive form of early onset severe retinal dystrophy in a patient carrying no previously described mutations in known genes. …”
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    The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy
  17. 577
    “…PURPOSE: To compare bilateral medial rectus advancement (BMRA) and bilateral lateral rectus recession (BLRR) for the treatment of consecutive exotropia. …”
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    Bilateral Medical Rectus Advancement versus Bilateral Lateral Rectus Recession for Consecutive Exotropia
  18. 578
    “…Since nearly 50% of HCM cases occur in the absence of a family history, a recessive inheritance pattern may be involved. METHODS: A pedigree was identified with suspected autosomal recessive transmission of HCM. …”
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    Autosomal Recessive Transmission of MYBPC3 Mutation Results in Malignant Phenotype of Hypertrophic Cardiomyopathy
  19. 579
    “…Our analyses revealed compound heterozygous DES variants, both of which are predicted to lead to a loss-of-function. Consistent with recessive inheritance, each variant was identified in an unaffected parent. …”
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    Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathy
  20. 580
    “…Although the autosomal recessive (AR) form of CMD had been mapped to 6q21-22 the mutation has been elusive. …”
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    A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia
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