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Its pathophysiology is characterised by a negative protein and energy balance driven by a variable combination of reduced food intake and abnormal metabolism.
Multiple system atrophy (MSA) is a sporadic adult-onset neurodegenerative disorder clinically characterized by a variable combination of dysautonomia, levodopa-unresponsive parkinsonian and cerebellar symptoms.
That aspirations are time-dependent (hence call for diachronic and life-course related research), and that they are affected by a variable combination of micro-, meso- and macro- factors, is important.
Genetic predisposition to lung cancer is likely to be both polygenic and heterogeneous, conferred by a variable combination of relatively common polymorphisms with low penetrance and modest effect sizes [9], [10].
Second, the genetic factors underlying lung cancer risk are likely to be both polygenic and heterogeneous, conferred by a variable combination of genetic variants (i.e. SNPs with low penetrance and small effect sizes).
It is characterised by a variable combination of gluten-induced symptoms and signs, specific antibodies, a specific human leukocyte antigen (HLA) type (DQ2 or DQ8) and enteropathy [ 38].
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According to the ESPGHAN definition, "Coeliac disease is an immune-mediated systemic disorder elicited by gluten and related prolamines in genetically susceptible individuals, characterised by the presence of a variable combination of gluten dependent clinical manifestations, coeliac disease specific antibodies, HLA-DQ2 and DQ8 haplotypes and enteropathy" [ 1].
Sirenomelia, also known as sirenomelia sequence, is a severe malformation of the lower body characterized by fusion of the legs and a variable combination of visceral abnormalities.
The resultant decrease in model fit for those species best fitted by a different variable combination was marginal in all cases.
Multiple system atrophy (MSA) denotes an adult-onset neurodegenerative disorder of relentless progression and unknown aetiology that is clinically characterized by the variable combination of autonomic failure, levodopa-unresponsive parkinsonism, cerebellar ataxia, and pyramidal signs.
We ascribe this higher accordance of selected features by SANN/LDA and GA/MLHD to a more extensive variable combination caused by a similar evolutionary algorithm of both methods compared to greedy/LDA.
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by a certain combination
by a variable pulse
by a variable speed
by a variable wavelength
by a variable course
by a variable capacitor
by a variable risk
by a variable value
by a variable hallucal
by a variable frequency
by a variable thickness
by a variable number
by a variable delay
by a variable gain
by a variable range
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