نتایج جستجو برای: papillon lefevre syndrome
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Clusterwise regression is applied to functional data, using PCR and PLS as regularization methods for the functional linear regression model. We compare these two approaches on simulated data as well as on stock-exchange data.
Many of the conclusions in this chapter can be summarised in an acronym that can be remembered by the phrase " Please Think " — PLS –T. 1. PROCESS — Managers will be most effective in targeting riparian revegetation if they first understand the erosion mechanisms (the processes) that are acting in a particular stream or river reach. 2. LEVERAGE — Once we understand the erosion mechanism, then w...
A variety of neutral serine proteases are important for the effector functions of immune cells. The neutrophil-derived serine proteases cathepsin G and neutrophil elastase are implicated in the host defense against invading bacterial and fungal pathogens. Likewise, the cytotoxic lymphocyte and NK cell granule-associated granzymes A and B are important for the elimination of virus-infected cells...
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disease that presents clinically with palmoplantar keratoderma and periodontitis results in early-onset dental loss. PLS management difficult. We report 30-year-old female who had unfavourable response to topical keratolytic creams, oral isotretinoin narrow-band ultraviolet-B (NB-UVB) phototherapy but showed significant clinical impr...
Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive disorder, characterized by diffuse palmoplantar keratoderma and precocious aggressive periodontitis, leading to premature loss of deciduous and permanent dentition at a very young age. Various etiopathogenic factors are associated with the syndrome, like immunologic alterations, genetic mutations, and the role of bacteria. Dentists p...
INTRODUCTION Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar keratoderma and severe, early onset periodontitis, which results from deficiency of cathepsin C activity secondary to mutations in the cathepsin C gene. To date, 13 different cathepsin C mutations have been reported in PLS patients, all of which are homozygous for a given mutation, refl...
مقدمه: سندرم papillon-lefevre یک بیماری نادر اتوزومال مغلوب است. این بیماری با هایپرکراتوز کف دست و پا و پریودنتیت سریع پیشرونده مشخص می شود و منجر به از دست رفتن پیش از موعد دندان های شیری و دائمی می گردد. تشخیص و درمان به موقع می تواند مانع از درگیری دندان های دایمی و بهبود پریودنتال و ماندگاری بیشتر دندان های شیری گردد و در پیشگیری از تحلیل ریج استخوانی زودهنگام و ایجاد مشکلات پروتزی برای بی...
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