WordNet

a brief treatise on a subject of interest; published in the form of a booklet (同)pamphlet
an extended area of land (同)piece of land, piece of ground, parcel of land, parcel
a system of body parts that together serve some particular purpose
a drawing created by superimposing a semitransparent sheet of paper on the original image and copying on it the lines of the original image (同)trace
the act of drawing a plan or diagram or outline
the discovery and description of the course of development of something; "the tracing of genealogies"

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1. 気腫性尿路感染症 emphysematous urinary tract infections
2. 総胆管損傷の修復 repair of common bile duct injuries
3. 妊娠中の尿路感染症および無症候性細菌尿 urinary tract infections and asymptomatic bacteriuria in pregnancy
4. 腹腔鏡下胆嚢摘出術の合併症の内視鏡マネージメント endoscopic management of complications from laparoscopic cholecystectomy
5. 急性膀胱炎：2歳以上の小児や青年における臨床的特徴および診断 acute cystitis clinical features and diagnosis in children older than two years and adolescents

High-Resolution Diffusion Tensor Imaging and Tractography in Joubert Syndrome: Beyond Molar Tooth Sign.

Hsu CC1, Kwan GN1, Bhuta S2.
Pediatric neurology.Pediatr Neurol.2015 Jul;53(1):47-52. doi: 10.1016/j.pediatrneurol.2015.02.027. Epub 2015 Mar 5.
BACKGROUND: We undertook diffusion tensor imaging analysis of brainstem fiber tracts in two Joubert syndrome patients.METHODS: Two Joubert syndrome patients underwent magnetic resonance imaging brain examination with diffusion tensor imaging. Imaging findings were compared with five age- and sex-mat
PMID 25890865

Ruppert E, Kilic-Huck U, Wolff V, Tatu L, Ghobadi M, Bataillard M, Bourgin P.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.J Clin Sleep Med.2014 Sep 15;10(9):1037-8. doi: 10.5664/jcsm.4028.
The onset of restless legs syndrome (RLS) is usually progressive and the neural substrates underlying its pathophysiology remain to be identified. Here we report on a patient presenting with acute-onset RLS that was symptomatic of a right anteromedial pontine infarction. This case is exceptional bec
PMID 25142775

Zafeiriou DI1, Ververi A, Tsitlakidou A, Anastasiou A, Vargiami E.
Neuromuscular disorders : NMD.Neuromuscul Disord.2013 Feb;23(2):116-9. doi: 10.1016/j.nmd.2012.08.004. Epub 2012 Nov 22.
Pontocerebellar hypoplasia type 2 is an autosomal recessive disorder characterized by hypoplasia and atrophy of the cerebellum and pons, leading to microcephaly, dystonia/dyskinesia, seizures, and severe cognitive impairment. Until lately it was considered a CNS-refined disease, but recent reports h
PMID 23177318