And thou shalt set upon the table loaves of proposition in my sight always.

The woman knelt before the altar to pray to God for her son's safe return.

妇人跪在供桌前祈祷：保佑她儿子平安归来。

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In front of the tomb, there is an altar for offering.

墓前有石五供，设供桌以摆放祭品。

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Craniocerebral Imaging Analysis of Neurofibromatosis ( Analysis of 9 Cases)

神经纤维瘤病的颅脑影像分析（附9例报告）

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Clinicopathological study of neurofibromatosis type 1: An experience in Nigeria

尼日利亚Ⅰ型神经纤维瘤病的临床病理学研究

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Neurofibromatosis& A Radiologic Analysis of Bone Changes in 30 Cases

多发性神经纤维瘤病&骨骼改变30例X线分析

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Objective: To recognise the predisposing factors, clinical manifestations, diagnosis and treatment of neurofibromatosis type 2 ( NF2).

目的：提高对神经纤维瘤病Ⅱ型（NF2）的病因、临床表现、诊断及治疗的认识。

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Objective To explore the effects of 17 β-estradiol ( E_2) and E_2 receptor antagonist on the formation and development of neurofibromas in patients with neurofibromatosis type 1 ( NF1).

目的探讨17β-雌二醇（E2）和E2受体拮抗剂对Ⅰ型神经纤维瘤病（NF1）神经纤维瘤的形成和发展的影响。

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Neurofibromatosis type 1 ( NF1) is a common, autosomal-dominant disorder caused by mutations in the NF1 tumor suppressor gene.

神经纤维瘤病（NF1）是常见的常染色体显性遗传性疾病，国外报道，其发病率高达1：3000。这种疾病是由于NF1基因的突变而发生的。

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Objective: To investigate the characteristics of the intellectual disability of neurofibromatosis type 1 ( NF1) and it's relative factors.

目的：研究1型神经纤维瘤病（neurofibromatosis type1，NF1）智力损害的特征及其影响因素。

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All of patients had no neurofibromatosis type 1 ( NF-1) and had impaired vision.

24例患者均不伴有神经纤维瘤病1型（NF-1），临床表现均有视力下降。

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Distinctive clinical presentation of a NF-1 patient with loss of heterozygosity of PTCH in his epithelial tumors

伴上皮肿瘤内PTCH杂合子缺失的1型神经纤维瘤病患者的特征性临床表现

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Objective To detect the mutation on exons 32,33 of Chinese the neurofibromatosis type 1 ( NF1) gene.

目的检测中国人神经纤维瘤病1型（NF1）基因32、33外显子突变。

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POEMS syndrome and hereditary neurofibromatosis type I ( NF I) are two different diseases with different causes and pathogenesis but both can cause multiple system lesions. The coexisting case was rare.

POEMS综合征和遗传性神经纤维瘤病I型（NFⅠ）是不同病因不同发病机制致病的两种疾病，但均可引起多系统损害，症状体征有交叉，二者合并病例很罕见。

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Objective To investigate the growth characteristic, clinical manifestation, diagnosis and treatment of neurofibromatosis ( NF) in otorhinolaryngology.

目的探讨耳鼻咽部多发性神经纤维瘤病（neurofibromatosis，NF）的病理、临床表现及诊断和治疗。

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Effect of p-AKT and PTEN on Neurofibromatosis ⅰ Pathogenesis

p-AKT和PTEN在Ⅰ型神经纤维瘤病中的表达及意义

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Materials and Methods: We collected 3 cases of neurofibromatosis type ⅱ proven by surgery and MR imaging system. The cranial MR appearences were reported.

材料与方法：搜集我院行MR检查并经手术证实符合神经纤维瘤病诊断标准者3例，分析其头部MRI表现。

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Objective To understand MRI findings of neurofibromatosis in cranium and spinal column is helpful in providing reliable informations for further clinical management.

目的认识神经纤维瘤病的颅脑及脊柱MRI表现，为临床进一步诊治提供客观依据。

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Diagnostic Analysis of MRI in 16 Patients with Neurilemoma of Cauda Equina The incidence of neurofibromatosis in neurilemoma was 1.66%.

马尾神经鞘瘤16例MRI诊断分析40～49岁组发病率最高为28.78%，神经纤维瘤病患者并发神经鞘瘤占神经鞘瘤的1.66%。

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Purpose: To understand cranial involvement of neurofibromatosis type I and to evaluate the value of CT and MRI in diagnostic aspect.

目的：认识神经纤维瘤病Ⅰ型的颅脑影像学表现，评价MRI和CT在诊断方面的价值。

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Objective: To emphasize the diagnostic value of cranial MRI examination and enhanced scanning in neurofibromatosis type ⅱ.

目的：强调Ⅱ型神经纤维瘤病头部MRI的诊断和增强扫描价值。

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