WordNet

use or deal in (as of stock or commercial transaction) in a pyramid deal
(stock market) a series of transactions in which the speculator increases his holdings by using the rising market value of those holdings as margin for further purchases
a polyhedron having a polygonal base and triangular sides with a common vertex
increase rapidly and progressively step by step on a broad base
arrange or build up as if on the base of a pyramid
enlarge ones holdings on an exchange on a continued rise by using paper profits as margin to buy additional amounts
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"
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
resembling a pyramid (同)pyramidic, pyramidical

PrepTutorEJDIC

(エジプト・メキシコなどの)『ピラミッド』 / ピラミッド形の物 / (幾何の)角錐(かくすい) / ピラミッド形になる / 〈物価などが〉上昇する,増加する / …‘を'ピラミッド形にする(積み上げる)
広大な土地(地域),(土地・海・空などの)広がり《+of+名》 / (器官の)管,(神経の)索
(おもに宗教・政治などの宣伝用の)小冊子,パンフレット
跡を追うこと,追跡;透写,複写 / 〈C〉 / 透写(複写)によってできたもの(地図・図案など),透写図
(疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
ピラミッド[状]の

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Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation.

Shimazaki H1, Honda J1, Naoi T1, Namekawa M1, Nakano I2, Yazaki M3, Nakamura K3, Yoshida K3, Ikeda S3, Ishiura H4, Fukuda Y4, Takahashi Y4, Goto J4, Tsuji S4, Takiyama Y5.
Journal of neurology, neurosurgery, and psychiatry.J Neurol Neurosurg Psychiatry.2014 Sep;85(9):1024-8. doi: 10.1136/jnnp-2013-306981. Epub 2014 Feb 12.
BACKGROUND: Autosomal-recessive hereditary spastic paraplegias (AR-HSP) consist of a genetically diverse group of neurodegenerative diseases characterised by pyramidal tracts dysfunction. The causative genes for many types of AR-HSP remain elusive. We tried to identify the gene mutation for AR-HSP w
PMID 24521565

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.

Miyata H1, Miyata M, Ohama E.
Neuropathology : official journal of the Japanese Society of Neuropathology.Neuropathology.2014 Jun;34(3):219-26. doi: 10.1111/neup.12081. Epub 2013 Dec 9.
Trisomy 18 or Edwards syndrome is known to exhibit various developmental abnormalities in the central nervous system. We report dominant uncrossed pyramidal tract in trisomy 18 syndrome, based on the postmortem neuropathologic study of eight consecutive autopsied fetuses and infants with trisomy 18
PMID 24313853

[Cerebrotendinous xanthomatosis: a multicentric retrospective study of 15 adults, clinical and paraclinical typical and atypical aspects].

Lionnet C1, Carra C1, Ayrignac X1, Levade T2, Gayraud D3, Castelnovo G4, Besson G5, Androdias G6, Vukusic S6, Confavreux C6, Zaenker C7, De Seze J8, Collongues N8, Blanc F8, Tranchant C8, Wallon D9, Hannequin D9, Gerdelat-Mas A10, Brassat D10, Clanet M10, Zephir H11, Outteryck O11, Vermersch P11, Labauge P12.
Revue neurologique.Rev Neurol (Paris).2014 Jun-Jul;170(6-7):445-53. doi: 10.1016/j.neurol.2014.01.675. Epub 2014 Apr 16.
INTRODUCTION: Cerebrotendinous xanthomatosis, a metabolic leukodystrophy with an autosomal recessive inheritance, is secondary to deficiency of sterol 27-hydroxylase, an enzyme involved in cholesterol catabolism. Classical symptoms include clinical or infraclinical xanthomas affecting the skin and t
PMID 24746394