نتایج جستجو برای: larsson syndrome

تعداد نتایج: 622429  

2006
Hiie Allik

Asperger syndrome (AS) and high-functioning autism (HFA) are pervasive developmental disorders (PDD) in children of normal range intelligence. Individuals with AS/HFA have impairments in social interaction, communication, and restricted behavioural repertoire, deficits that significantly interfere with their well-being and ability to adapt to ordinary everyday life. Moreover, AS and HFA are pre...

Journal: :IEEE Trans. Information Theory 1998
Adrian Mardjuadi Jos H. Weber

A new construction method for codes correcting multiple localized burst errors is proposed. The codes obtained by this method improve upon codes presented by Larsson in size, while keeping the encoding and decoding complexity low. Like the Larsson codes, the proposed codes are asymptotically optimal when the number of bursts to be corrected is fixed and the correctable burst length grows linear...

2013
Hannes Olauson

Chronic kidney disease (CKD) is a global health burden of growing incidence and prevalence. As renal function declines disturbances in mineral metabolism, such as hyperphosphatemia and secondary hyperparathyroidism, inevitably develop. These metabolic changes are closely associated with poor prognosis and survival. The bonederived hormone fibroblast growth factor-23 (FGF23) and its co-receptor ...

2017
Isabell Brikell Ralf Kuja-Halkola Jan-Olov Larsson Benjamin B. Lahey Samuele Cortese

Citation for published version (APA): Brikell, I., Kuja-Halkola, R., Larsson, J-O., Lahey, B. B., Kuntsi, J., Lichtenstein, P., ... Larsson, H. (2016). Relative Immaturity in Childhood and Attention-Deficit/Hyperactivity Disorder Symptoms From Childhood to Early Adulthood: Exploring Genetic and Environmental Overlap Across Development. Journal of the American Academy of Child and Adolescent Psy...

Journal: :Arquivos de neuro-psiquiatria 2006
Mauro Nakayama Daniel G F Távora Thereza C L Alvim Alexandre C B Araújo Rômulo L Gama

Sjögren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder caused by deficiency of the microsomal enzyme fatty aldehyde dehydrogenase. Patients present the classical triad of congenital ichthyosis, mental retardation and spastic di- or tetraplegia. Magnetic resonance imaging (MRI) of the brain usually shows hypomyelination involving the periventricular white matter. Ce...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید