Gotowe bibliografie tematyczne / Hydranencephaly

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji

Gotowa bibliografia na temat „Hydranencephaly”

Autor: Grafiati
Data publikacji: 2 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Hydranencephaly"

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Malheiros, José Augusto, Felipe Padovani Trivelato, Marcelo Magaldi Oliveira, Sebastião Gusmão, David Douglas Cochrane, and Paul Steinbok. "Endoscopic Choroid Plexus Cauterization Versus Ventriculoperitoneal Shunt for Hydranencephaly and Near Hydranencephaly." Neurosurgery 66, no. 3 (2010): 459–64. http://dx.doi.org/10.1227/01.neu.0000365264.99133.ca.

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Abstract OBJECTIVE To prospectively evaluate the results of endoscopic choroid plexus cauterization (ECPC) and ventriculoperitoneal shunts (VPSs) in infants with hydranencephaly or near hydranencephaly. METHODS We prospectively collected clinical data from all untreated hydranencephalic and near hydranencephalic children from October 2006 to March 2008. All patients treated were randomly divided into 2 groups, ECPC or VPS, and submitted to either endoscopic choroid plexus cauterization or ventriculoperitoneal shunt placement. RESULTS Seventeen patients were entered into the study. ECPC was com
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Gentry, Millicent, and Mary Connell. "Hydranencephaly." Ultrasound Quarterly 29, no. 3 (2013): 267–68. http://dx.doi.org/10.1097/ruq.0b013e3182a33715.

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Pinar, Halit. "Hydranencephaly." Pathology Case Reviews 16, no. 5 (2011): 186–88. http://dx.doi.org/10.1097/pcr.0b013e318229862e.

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Sharma, Akshay, Deeksha Sharma, and Pranav Pandoh. "HYDRANCEPHALY : RARE ENTITY WITH INCIDENCE LESS THAN 1 IN 10000 LIVE BIRTHS." International Journal of Advanced Research 9, no. 02 (2021): 678–80. http://dx.doi.org/10.21474/ijar01/12497.

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Hydranencephaly is a rare entity with incidence of 1 in 10000 live births and is characterized by near total absence of cerebral cortex and basal ganglia which are replaced by cerebrospinal fluid. Various aetiologies of hydranencephaly have been suggested which include: Infarction, leukomalacia, diffuse hypoxic-ischemic brain necrosis, intrauterine infections leading to necrotizing vasculitis. Ultrasonography, Computed Tomography and Magnetic Resonance Imaging can easily detect and diagnose hydranencephaly. We present a case of 2-month-old term infant diagnosed with hydranencephaly on computed
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Baidi, H., M. Sellouti, A. Ayad, and R. Abilkassem. "Monochorionic Twin Pregnancy with Hydranencephaly and Co-Twin Death: A Case Report." Asian Journal of Pediatric Research 14, no. 8 (2024): 18–24. http://dx.doi.org/10.9734/ajpr/2024/v14i8377.

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Background: Hydranencephaly is a rare congenital brain malformation with an incidence estimated to be between 1 in 10 000 and 1 in 5 000 pregnancies. It is characterized by the absence of development of the cerebral hemispheres, which are replaced by cerebrospinal fluid. The diagnosis of hydranencephaly can be made from 15 weeks of amenorrhea via obstetric ultrasound, with antenatal nuclear MRI being the definitive test to establish the diagnosis. The condition results from an anomaly in embryogenesis after the formation of the neural plate, though the exact pathophysiology of hydranencephaly
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Andreeva, E. Yu, D. S. Bokieva, and M. M. Bulanova. "Prenatal diagnosis of hydranencephaly: a clinical case." Ultrasound & Functional Diagnostics, no. 2 (June 21, 2024): 63–71. http://dx.doi.org/10.24835/1607-0771-269.

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Hydranencephaly is a rare abnormality of the central nervous system (CNS) of the fetus, in which the cerebral hemispheres are absent and replaced with cerebrospinal fluid, while the structures of the posterior fossa, thalami and falx cerebri remains normal. The ischemic, hemorrhagic complications, infection of the fetus, the toxic effects of carbon monoxide, butane and genetic abnormalities are potential causes of a hydranencephaly development. The article presents the modern data on the possible causes of the hydranencephaly development, and clinical case of prenatal ultrasound diagnosis of h
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Dehneh, Younes, Mohammed Khoulali, Noureddine Oulali, and Faycel Moufid. "Hydranencephaly Associated with Bilateral Megalocornea and Bilateral Cleft Lip in an Infant of Mother with Gestational Diabetes Mellitus." Indian Pediatrics Case Reports 4, no. 1 (2024): 48–50. http://dx.doi.org/10.4103/ipcares.ipcares_186_23.

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Abstract Background: Hydranencephaly is a rare congenital disorder of the central nervous system, in which the cerebrum is replaced by a membranous sac of cerebrospinal fluid. Clinical Description: A 2-month-old baby girl presented with abnormal body movements. She was born to a mother with gestational diabetes and had been diagnosed with hydrocephalus antenatally. The baby had features of facial dysmorphism such as bilateral megalocornea, bilateral cleft lip, and cleft palate. A magnetic resonance imaging (MRI) brain revealed the absence of cerebral hemispheres with remnants of parenchyma in
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M. Al-Abdallat, Imad, Ibrahim H. Alhabash, Asma M. Alshaeb, and Hasan A. Abder-Rahman. "Was the Hydranencephaly Defense Valid for the Death of a Child?: A Case Report." Arab Journal of Forensic Sciences and Forensic Medicine 3, no. 2 (2021): 331–35. http://dx.doi.org/10.26735/rbjb7151.

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Hydranencephaly is a central nervous system disorder at birth in which brain's cerebral hemispheres are absent and replaced by sacks filled with CSF. The prevalence of hydranencephaly is less than 1 in 10,000 births, with 0.2 percent of children autopsies showing the condition.
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Oriaifo, Bosede Belinda, Stephen Ohikhuemei Izevbekhai, Chukwudi Nnaedozie Ahunanya, Pamela Faith Isioma Irabor, and Evelyn Oshodin. "Ultrasound Diagnosed Fetal Hydranencephaly in the Prenatal Period." Journal of Radiation Medicine in the Tropics 5, no. 1 (2024): 31–33. http://dx.doi.org/10.4103/jrmt.jrmt_5_24.

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Abstract Hydranencephaly is a rare congenital encephalopathy characterized by a near complete absence of the cerebral cortical mantle and basal ganglia, with consequent replacement by cerebrospinal fluid (CSF). Although hydranencephaly is an extremely rare congenital entity with an incidence <1/10,000 live births, there are no known gender or racial predilections. However, polyhydramnios is a recognized association. Brain infarction from bilateral internal carotid artery occlusion, fetal hypoxia, leukomalacia, and congenital infections have all been implicated as possible etiologies for thi
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Ramesh, Vengalathur Ganesan. "Hydranencephaly Vs Hydrocephalus." Neurosurgery 67, no. 5 (2010): E1472. http://dx.doi.org/10.1227/neu.0b013e3181f36010.

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Rozprawy doktorskie na temat "Hydranencephaly"

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Ku, Kuo-Chi, and 顧國極. "Morphogenesis and pathogenesis of hydranencephaly." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/44839245931937463318.

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碩士<br>中國醫藥學院<br>醫學類<br>84<br>Hydranencephaly是一種罕見的中樞神經系統畸型,在臨床上常與嚴重的水 腦症無法區分,並且嚴重危害到新生兒的生存.其病理結構為兩側大腦半球 的缺失,但卻又保存有腦幹,小腦,延腦等天幕下結構,其形成機轉仍未完全 明瞭.本報告是以每公斤240mg的ethylenethiourea(ETU)給予懷孕第十五 天的大白鼠經胃管灌食,分別在懷孕的第十六,十七,十八,十九天剖腹取出 胎兒,並利用正中矢狀切片來追蹤整個大腦的變化,以及形成 hydranencephaly的過程.由實驗結果顯示,給藥後的大白鼠胚胎在給藥的 二十四個小時之後大腦即產生極為嚴重的大腦破壞(destructive encephalopathy),而逐漸被吞噬細胞所清除,形成一個由硬腦膜所包圍的 空腔,而且由形成的過程我們可以看到大腦是一邊發育一邊被破壞,這與先 前的假說指出大腦是在發育之後才遭到破壞有所出入.另外在頸部的橫切 片中並
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Książki na temat "Hydranencephaly"

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Publications, ICON Health. The Official Parent's Sourcebook on Hydranencephaly: A Revised and Updated Directory for the Internet Age. ICON Health Publications, 2002.

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Części książek na temat "Hydranencephaly"

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Chen, Harold. "Hydranencephaly." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-6430-3_262-1.

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Chen, Harold. "Hydranencephaly." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-2401-1_262.

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Friede, Reinhard L. "Porencephaly, Hydranencephaly, Multicystic Encephalopathy." In Developmental Neuropathology. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-73697-1_3.

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Dezena, Roberto Alexandre. "Beyond the Third Ventricle: Hydranencephaly." In Atlas of Endoscopic Neurosurgery of the Third Ventricle. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-50068-3_7.

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Paladini, Dario, and Paolo Volpe. "Intracranial Hemorrhage and Stroke, Hydranencephaly." In Ultrasound of Congenital Fetal Anomalies, 3rd ed. CRC Press, 2024. http://dx.doi.org/10.1201/9781003048268-16.

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Takada, Kuniyasu, Madoka Shiota, Masashi Ando, Masahiko Kimura, and Kazuhiko Inoue. "Porencephaly and Hydranencephaly: A neuropathological study of four autopsy cases." In Annual Review of Hydrocephalus. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-11158-1_3.

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"Hydranencephaly." In Diagnostic Imaging: Obstetrics. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39256-3.50046-7.

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"Hydranencephaly." In Diagnostic Imaging: Brain. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37754-6.50100-7.

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Chung, Ellen. "Hydranencephaly." In Pediatric Imaging Cases. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199758968.003.0094.

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Stevenson, Roger E., Charles E. Schwartz, and R. Curtis Rogers. "Hydranencephaly with Abnormal Genitalia (See Also ARX-Associated XLID)." In Atlas of X-Linked Intellectual Disability Syndromes. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199811793.003.0056.

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Streszczenia konferencji na temat "Hydranencephaly"

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Köhler, C., and T. Lücke. "7-Month-Old Girl with Hydranencephaly: Example of Interdisciplinary Cooperation Ethical Issues." In Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1739657.

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Wünsch, A., R. Fröber, and E. Schleußner. "Palliative Betreuung eines Kindes mit Hydranencephalie." In Kongressabstracts zur 16. Jahrestagung der Mitteldeutschen Gesellschaft für Frauenheilkunde und Geburtshilfe e.V. (MGFG). Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1769860.

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