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Management of an older Marshall-Smith syndrome patient: a review of literature of MSS and craniosynostosis
Marshall-Smith Syndrome (MSS) is a rare progressive developmental disorder that severely impairs a patient’s intellectual development and physical...
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Smith-Kingsmore syndrome with nystagmus as the initial symptom
BackgroundSmith-Kingsmore syndrome (SKS) is a rare autosomal dominant disorder caused by de novo mutations of gene MTOR in most cases and germline...
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A comparative study of stretch-and-flow voice therapy versus Smith accent method in rehabilitation of hyperfunctional dysphonia: a randomized controlled trial
BackgroundThis work aims to compare between stretch-and-flow voice therapy and Smith accent method of voice therapy in treatment of hyperfunctional...
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Influence of sex and strength differences on the load–velocity relationship of the Smith-machine back squat
PurposeWe aimed at determining whether the load–velocity relationship of the Smith machine concentric-back squat differs between sexes and persons...
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De-epithelialized overlap flap to secure urethroplasty in second stage hypospadias repair: revisiting the Smith technique
BackgroundThe application of a second layer between the neourethra and skin was a major contribution, which has improved the outcome of hypospadias...
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Modified Smith–Petersen approach with rectus-sparing reduces severe avascular necrosis for developmental dysplasia of the hip at walking age: minimum 5-year follow-up
BackgroundDevelopmental dysplasia of the hip (DDH) is one of the most common orthopedic malformations in children. Open reduction for DDH at walking...
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Hybrid of Smith-Peterson and Watson-Jones minimally invasive direct anterior approach to the hip joint
BackgroundMuscle-sparing techniques, more consistent acetabular component positioning with fluoroscopy guidance, development in implants and...
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Co-positivity of anti-dsDNA, anti-nucleosome, and anti-smith autoantibodies as serological biomarkers for disease activity in systemic lupus erythematosus
BackgroundEvaluation of disease activity in systemic lupus erythematosus (SLE) patients is important for modulating the therapeutic plan and...
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Retinoic Acid-Induced 1 gene variants associated with Smith–Magenis syndrome circadian phenotypes enriched in autism spectrum disorder: whole-genome sequencing study
BackgroundThis study aimed to characterize the frequency of RAI1 genetic aberrations associated with Smith–Magenis syndrome (SMS), in a large cohort...
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Lupus nephritis correlates with B cell interferon-β, anti-Smith, and anti-DNA: a retrospective study
BackgroundIn systemic lupus erythematosus (SLE), detection of interferon-β (IFNβ) in B cells was found to be most prominent in patients with high...
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Caregivers’ experience of sleep management in Smith–Magenis syndrome: a mixed-methods study
BackgroundSmith–Magenis syndrome (SMS) is a rare genetic syndrome associated with a unique profile of early morning waking and daytime sleepiness....
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Smith and Nesi’s Ophthalmic Plastic and Reconstructive Surgery
This landmark book is the most extensive and complete oculofacial plastic surgery guide available in the market. Updated and broadened from the three...
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Management of Sleep Disturbances Associated with Smith-Magenis Syndrome
Smith-Magenis syndrome is a genetic disorder caused by a microdeletion involving the retinoic acid-induced 1 ( RAI1 ) gene that maps on the short arm...
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Methylphenidate for attention-deficit/hyperactivity disorder in patients with Smith–Magenis syndrome: protocol for a series of N-of-1 trials
BackgroundSmith–Magenis syndrome (SMS) is a rare genetic neurodevelopmental disorder characterized by intellectual disability and severe behavioural...
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Comparison of blood tonic efficacy and chemical constituents of Kadsura interior A.C. Smith and its closely related species
BackgroundThe stems of Kadsura interior A. C. Smith are used as traditional Chinese medicine (TCM) Kadsurae Caulis, with the traditional efficacy of...
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Carrier frequency and incidence estimation of Smith–Lemli–Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis
BackgroundSmith–Lemli–Opitz syndrome (SLOS) is an autosomal, recessively inherited congenital malformation syndrome characterized by multiple...
