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santé - iate.europa.eu
santé - iate.europa.eu
santé - iate.europa.eu
santé - iate.europa.eu
Meeting abstract open access asthma and hypoxia... The main disorders associated with atopic disease are: Atopic myelitis Hopkins syndrome Hirayama disease Spinal progressive muscular atrophy (SPMA) The occurrence of myelitis in patients with atopic dia-thesis (atopic myelitis) affecting young adults has been widely reported especially...
général - core.ac.uk - PDF: ftp:
santé - iate.europa.eu
Journal of neurology, neurosurgery, and psychiatry 1988;51:440-442 short report haptoglobin groups in motor neuron disease... A significant excess of heterozygotes was observed, accentuated among males and in the progressive spinal muscular atrophy subgroup....
général - core.ac.uk - PDF: jnnp.bmj.com
Mimic syndromes in sporadic cases of progressive spinal muscular atrophyDescribed are patients initially diagnosed with progressive spinal muscular atrophy (PSMA), in whom further evaluation established another diagnosis....
santé - iate.europa.eu
santé - iate.europa.eu
Disease course and prognostic factors of progressive muscular atrophyOBJECTIVE: To investigate the natural history and prognostic factors in patients with nonhereditary, adult-onset progressive muscular atrophy....
général - core.ac.uk - PDF: www.loc.gov
Post syringomyelia progressive muscular atrophy: a late sequel to syringomyelia?... Spinal cord regions (cervical, thoracic, lumbosacral) involved on initial presentation predicted the regions of late progression of motor neuron loss, suggesting that pathogenesis may involve an initial loss of motor neurons due to the syrinx, and then age related loss as seen in post-poliomyelitis progressive muscular atrophy....
 PDF: dx.doi.org
santé - iate.europa.eu
santé - iate.europa.eu
Evaluation of the role of an antioxidant gene in nsc-34 motor neuron-like cells as a model of a motor neuron diseaseBackground: Spinal muscular atrophy is a rare genetic disease, which primarily affects motor neurons and predominantly occurs in children....
santé - core.ac.uk - PDF: journals.viamedica.pl
Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in the netherlandsSpinal muscular atrophy with respiratory distress type 1 is an autosomal recessive disorder with early respiratory difficulties, distal muscle weakness, and contractures leading...

Publications scientifiques

Bmk1 (erk5) regulates squamous differentiation marker sprr1b transcription in clara-like h441 cells... We have recently shown that phorbol 13-myristate 12acetate (PMA)–stimulated SPRR1B transcription in Clara-like H441 cells is mainly mediated by activator protein–1 (AP-1) and c-Jun N-terminal kinase-1 (JNK1)....
santé - core.ac.uk - PDF: citeseerx.ist.psu.edu
Modulation of 1,25-dihydroxyvitamin d3-dependent ca2+ uptake in skeletal muscle by protein kinase c.... The PKC activator phorbol 12-myristate 13-acetate (PMA, 100 nM) was found to rapidly stimulate muscle 45Ca uptake, mimicking 1,25(OH)2D3....
santé / détérioration de l'environnement / produit animal - core.ac.uk - PDF: www.pubmedcentral.nih.gov
Nested pcr amplification secures dna template quality and quantity in real-time mcop-pcr screening for smaBACKGROUND: Spinal Muscular Atrophy (SMA) is a common autosomal recessive disorder caused by SMN1 gene deletion....
santé - core.ac.uk - PDF: www.lib.kobe-u.ac.jp
Investigations and cause analysis of early diseases in sma pavement... Since the asphalt overlay of freeway in Hubei Province was opened, it appeared undue early diseases....
santé / activité agricole / bâtiment et travaux publics - core.ac.uk - PDF: www.scientific.net
Association of s-phenylmercapturic acid (spma) with dna methylation in alu, line-1, mage and p15 methylation.Fitted beta regression models of repeated-element and gene-specific methylation % versus log(SPMA), adjusted for potential confounders as described in the text....
général - core.ac.uk - PDF: figshare.com

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