نتایج جستجو برای: falx

تعداد نتایج: 378  

Journal: :Journal 1985
A E Swanson

Nevoid basal cell carcinoma, known as Gorlin Goltz Syndrome, is a rare hereditary condition, characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. In this report, we discuss a case of a patient with Gorlin Goltz Syndrome, who was 16 years old when first admitted for an initial appointment. The patient was diagnosed, treated and followed up for 7 years t...

Journal: :Vision Research 1995
I. Cravo F. Campos M. Novais L. Gouveia-Andrade A. Castanheira-Dinis A. Monteiro-Trindade J. Ribeiro-da-Silva

w The major difficulty in albino diagnosis is that although foveal hypoplasii seems a consistent feature, it is not uncommon for an albino to have normal fundus pigmentation, normal iris pigmentation and/or no nystagmus. Only a retina-ge.nicula-coni misprojection seems pathognomonic to albinism since all species of albino mammals share this feature. With appropriate stimulus and recording condi...

Journal: :Zoological Journal of the Linnean Society 2022

Abstract The pan-sirenian Bauplan is conservative, probably owing to the constraints of adaptation an aquatic lifestyle. Gathering morphological data from extinct forms complex, resulting in poorly resolved phylogenies for stem pan-sirenians. Extant sirenians ossify falx cerebri and tentorium cerebelli, membranes dura mater brain attached parietal bone. Nevertheless, these ossifications are not...

Journal: :International Journal of Science and Research Archive 2023

Complex partial seizure are often associated with impaired or loss of consciousness clinically proved to have an impact on masial temporal sclerosis (Hippocampus) region brain. Seizures admits several etiopathophysiological events leading neuro functional changes in the reticulothalamocortical circuitry zones CNS .This paves episodes complex seizures events. A clinical case report a 47 years ag...

انصار, اکرم, فرشچیان, محمود, فریدون نژاد, مرتضی,

Introduction: Nevoid BCC syndrome (Gorline syndrome) is a familial disorder with autosomal dominant inheritense. This syndrome is combination of multiple BCC that occurs at an early age, characteristic faces with: frontal bossing, broad nasal bridge and hypertelorism, jaw cysts, palmoplanter pitting, macrocephaly, skeletal and spinal anomalies include bifid ribes, cervical rib and kyphoscoliosi...

2007
Wei-Da Chang Ming-Chi Shih Cheng-Pei Chang Lee-Shing Chu Su-Quin Liao Shyh-Jen Wang Ren-Shyan Liu

Received 4/5/2006; revised 6/20/2006; accepted 6/23/2006. For correspondence or reprints contact: Ren-Shyan Liu, M.D., Department of Nuclear Medicine, Taipei Veterans General Hospital, 201 Section 2, Shih-Pai Road, Taipei 112, Taiwan. Tel: (886)2-28757301 ext. 299, Fax: (886)2-28749431, E-mail: [email protected] Tuberculosis of the central nervous system accounts for about 5% of extrapulmonar...

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