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Freezing lesions to the developing cortical plate of rodents results in a focal malformation resembling human 4-layered microgyria, and this malformation has been shown to result in local and widespread disruptions of neuronal architecture, connectivity, and physiology.
The incidence of vascular malformation has been reported in approximately 7%% of all benign tumors, the majority of which develop in the head and neck region.
Sclerotherapy of venous malformation has been reported by numerous researchers to be effective for the treatment of venous malformations in the head and neck region.
No human congenital malformation has been associated with SALL2 so far.
Early gestation embryo loss or malformation has been linked to yolk sac vasculopathy and congenital heart defects (CHDs).
The role of FGF signaling in the SHFM malformation has been partly clarified.
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Many surgical techniques to correct the malformation have been described.
Neuroradiological findings of Chiari malformation have been rarely reported in LDS.
A 39-year-old woman with renal failure secondary to a congenital kidney malformation had been on renal haemodialysis treatment 3 days every week for the previous 17 years.
The association between syringomyelia and malformative conditions, and in particular the Chiari malformations has been examined in some depth, with a wealth of clinical, radiological, pathological, surgical and experimental studies see, for review [ 1- 6].
Certain craniospinal malformations could be diagnosed as early as the dawn of ultrasonography and this group of malformations has been the focus of attention ever since.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com