نتایج جستجو برای: bulbous plants

تعداد نتایج: 198583  

Journal: : 2022

The results of experimental studies the ice propulsion CNF22 project passenger-and-freight ferry model are given in article. vessel has a bulbous bow, transom stern and is designed for class Russian Maritime Register Shipping with reinforcements Ice2. choice broken justified resistance curves clear deep water 0.5 m thick concentration 4, 6, 8 points when moving bow forward were obtained. An alg...

Journal: :Agriculture 2022

In arid areas, it is necessary to apply phytomelioration widely create an organized, stable and ecologically well-maintained forest–agrarian landscape in which agricultural lands can provide diverse products, optimum ecologyfor the existence of a natural anthropogenic system. The aim this work select shrub herbaceous plant species for restoration degraded zone European part Russia with prospect...

Journal: :JAMA facial plastic surgery 2014
Anthony Bared Ali Rashan Benjamin P Caughlin Dean M Toriumi

IMPORTANCE In recent years, with the advent of 3-dimensional (3D) imaging techniques, it has become possible to objectively measure rhinoplasty results. However, few studies have used 3D imaging software to assess postoperative rhinoplasty results of the nasal tip. OBJECTIVE To analyze nasal tip volumes of patients with bulbous tips and measure postoperative nasal tip volume changes in patien...

2008
Marian H. Pettibone

•Among the Lepidonotinae, two species of Lepidonotus are referred to new genera: L. dictyolepis Haswell, from Australia, to Augenerilepidonotus, and L. kumari Rullier, from Malaya, to Olgalepidonotus. As part of an on-going study on the polynoid polychaetes, two species that were described under Lepidonotus Leach, 1816, L. dictyolepis Haswell, 1883, from Australia, and L. kumari Rullier, 1970, ...

Journal: :Acta dermato-venereologica 2015
Akitaka Shibata Kana Tanahashi Kazumitsu Sugiura Masashi Akiyama

Trichorhinophalangeal syndrome types I and III (TRPS1, OMIM 190350; TRPS3, OMIM 190351) are rare hereditary diseases with autosomal dominant inheritance (1, 2). The first case was reported in 1966 (3). In 2000 the TRPS1 gene was identified as one of its causative genes and mapped to chromosomal region 8q24.1 (1). These syndromes have characteristic sparse and slow-growing hair, craniofacial abn...

Journal: :Journal of medical genetics 1992
B Dallapiccola L Zelante L Accadia R Mingarelli

A family is reported in which the 'acromegaloid facial appearance' (AFA) phenotype was segregating through two generations. The five affected persons showed a striking resemblance to the patients previously reported, including progressively coarse acromegaloid-like facial appearance, narrow palpebral fissures, bulbous nose, and thickening of the lips and intraoral mucosa, resulting in exaggerat...

Journal: :Journal of anatomy 1984
J Calvo J Boya E Garcia-Mauriño

The adult dog pineal gland was studied with the electron microscope. Pineal connective tissue spaces were poorly developed and showed capillaries with nonfenestrated endothelial cells. Two cell types, pinealocytes and astrocytes, could be identified in pineal parenchyma. Dog pinealocytes showed microtubules, centrioles, occasional cilia, and well-developed Golgi complexes. These cells showed th...

2011
Mahul B. Amin

DIAGNOSIS: A. All that is papillary in the bladder is not papillary urothelial neoplasia: i. Diagnostic pitfalls: papillary hyperplasia, nephrogenic adenoma, fibroepithelial polyp and papillary/polypoid cystitis ii. Artifacts: pseudopapillary folds and avulsed urothelium B. All urothelial proliferations that expand the lamina propria are not invasive carcinoma: i. Diagnostic pitfalls: florid vo...

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