找回密碼
 To register

QQ登錄

只需一步,快速開(kāi)始

掃一掃,訪(fǎng)問(wèn)微社區(qū)

打印 上一主題 下一主題

Titlebook: Congenital Brain Malformations; Clinical and Surgica Khaled Fares AlAli,Hashim Talib Hashim Book 2024 The Editor(s) (if applicable) and The

[復(fù)制鏈接]
樓主: 斷巖
41#
發(fā)表于 2025-3-28 16:02:31 | 只看該作者
42#
發(fā)表于 2025-3-28 21:23:41 | 只看該作者
https://doi.org/10.1057/9780230119475e the anomalies arising from the failure of the dorsal induction stage of neuronal development, like anencephaly, cephalocele, Chiari malformations, and spinal dysraphic disorders. They can also arise from failure in ventral induction, like holoprosencephaly, cerebellar hypoplasia, Dandy-Walker malf
43#
發(fā)表于 2025-3-28 22:54:54 | 只看該作者
https://doi.org/10.1057/9780230119475nd genetic screening. These approaches are essential for accurate and timely intervention. Ultrasound, MRI, and CT scans have revolutionized the ability to detect and characterize these anomalies early on, with ultrasound being the first-line modality for prenatal screening and MRI providing detaile
44#
發(fā)表于 2025-3-29 06:33:37 | 只看該作者
https://doi.org/10.1057/9780230119475dbrain is present, but the cerebrum and cerebellum are smaller or nonexistent. The range of neural tube defects (NTDs) includes anencephaly. When the neural tube doesn’t shut between the third and fourth weeks of development, it develops this abnormality, which can cause miscarriage, stillbirth, or
45#
發(fā)表于 2025-3-29 08:53:19 | 只看該作者
https://doi.org/10.1057/9780230119475ere are two types congenital (primary) and acquired (secondary) encephaloceles, congenital encephalocele belong to the neural tube defect (NTDs) along with spina bifida and anencephaly. The exact cause of congenital encephalocele is unknown, probably, it is multifactorial and there are roles for gen
46#
發(fā)表于 2025-3-29 15:16:15 | 只看該作者
47#
發(fā)表于 2025-3-29 18:40:30 | 只看該作者
48#
發(fā)表于 2025-3-29 20:38:35 | 只看該作者
Xiufang (Leah) Li,Alexandra Wakecessive but sometimes dominant pattern is also observed. Septo-optic dysplasia occurs when development of prosencephalon is affected. Its classical triad consist of optic nerve hypoplasia, pituitary hypoplasia and absence of septum pellucidum and carpus callosum. This heterogeneous condition present
49#
發(fā)表于 2025-3-30 00:30:25 | 只看該作者
50#
發(fā)表于 2025-3-30 05:01:40 | 只看該作者
https://doi.org/10.1057/9781137426444. Classification of posterior fossa malformation can either be depending on the size of the posterior fossa and the diameter of the rhombencephalon vesicles and also on how the developed form the rhombencephalon. a further two classification can be made the first one is the chiari malformations the
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛(ài)論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點(diǎn)評(píng) 投稿經(jīng)驗(yàn)總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機(jī)版|小黑屋| 派博傳思國(guó)際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-20 11:27
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
涞源县| 和静县| 亳州市| 兰西县| 光泽县| 兴安县| 含山县| 大英县| 积石山| 卓资县| 新建县| 普兰县| 江城| 灵武市| 靖江市| 上饶县| 伊川县| 资阳市| 龙口市| 德化县| 惠东县| 循化| 砀山县| 长丰县| 蒙城县| 松滋市| 新安县| 拉萨市| 台南县| 玉树县| 乐安县| 新丰县| 呈贡县| 营口市| 神木县| 宝清县| 翁源县| 乐业县| 高青县| 三门峡市| 洛扎县|