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Neuropathological findings in phenyl-pyruvic oligophrenia (phenyl-ketonuria).

作者信息

ALVORD E C, STEVENSON L D, VOGEL F S, ENGLE R L

出版信息

J Neuropathol Exp Neurol. 1950 Jul;9(3):298-310. doi: 10.1097/00005072-195007000-00004.

DOI:10.1097/00005072-195007000-00004
PMID:15437204
Abstract
摘要

相似文献

1
Neuropathological findings in phenyl-pyruvic oligophrenia (phenyl-ketonuria).苯丙酮尿性智力发育不全(苯丙酮尿症)的神经病理学发现。
J Neuropathol Exp Neurol. 1950 Jul;9(3):298-310. doi: 10.1097/00005072-195007000-00004.
2
The neuropathology of oligophrenia.智力发育不全的神经病理学
Recent Progr Psychiatr. 1950;2:324-45.
3
Inhibition of brain glutamic acid decarboxylase by phenylalanine, valine, and leucine derivatives: a suggestion concerning the etiology of the neurological defect in phenylketonuria and branched-chain ketonuria.苯丙氨酸、缬氨酸和亮氨酸衍生物对脑谷氨酸脱羧酶的抑制作用:关于苯丙酮尿症和支链酮尿症神经缺陷病因的一种推测。
Metabolism. 1961 May;10:393-402.
4
[New biological explorations into phenyl-pyruvic oligophrenia].
C R Seances Soc Biol Fil. 1950 Feb;144(3-4):251-3.
5
[A case of infantile type of amaurotic idiocy (Tay-Sachs). Neuropathological and histochemical studies].[一例婴儿型黑蒙性白痴(泰-萨克斯病)。神经病理学和组织化学研究]
Patol Pol. 1962 Apr-Jun;13:159-71.
6
The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child.苯丙氨酸摄入对一名苯丙酮尿症患儿的生化指标及行为的影响。
Acta Paediatr (Stockh). 1954 Jan;43(1):64-77. doi: 10.1111/j.1651-2227.1954.tb04000.x.
7
A case of galactosaemia with the pathological and neuropathological findings.一例伴有病理和神经病理学发现的半乳糖血症病例。
Arch Dis Child. 1962 Aug;37(194):415-21. doi: 10.1136/adc.37.194.415.
8
Studies regarding glutamine and ammonia in the cerebrospinal fluid of patients with nervous and mental diseases (with some observations on insulin hypoglycemic shock and oligophrenia phenylpyruvica).关于神经和精神疾病患者脑脊液中谷氨酰胺和氨的研究(对胰岛素低血糖休克和苯丙酮尿症智力发育不全的一些观察)
J Nerv Ment Dis. 1945 Nov;102:466-76.
9
[Psychiatric sequelae in brain diseases; oligophrenia as symptom and oligophrenia as entity].
Rev Esp Pediatr. 1952 Sep-Oct;8(5):607-15.
10
[CLINICAL, BIOCHEMICAL, AND NEUROPATHOLOGIC ASPECTS OF MAPLE SYRUP URINE DISEASE. A KETOACIDURIA OF THE OPEN CHAIN AMINOACIDS LEUCINE, ISOLEUCINE AND VALINE].
An Fac Med Lima. 1963 Sep;46:339-65.

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Modeling the cognitive effects of diet discontinuation in adults with phenylketonuria (PKU) using pegvaliase therapy in PAH-deficient mice.使用缺乏苯丙氨酸羟化酶的小鼠中的培维索酶治疗模拟成人苯丙酮尿症(PKU)患者停止饮食对认知的影响。
Mol Genet Metab. 2022 May;136(1):46-64. doi: 10.1016/j.ymgme.2022.03.008. Epub 2022 Mar 21.
2
The effects of early-treated phenylketonuria on volumetric measures of the cerebellum.早期治疗苯丙酮尿症对小脑容积测量的影响。
Mol Genet Metab Rep. 2020 Sep 18;25:100647. doi: 10.1016/j.ymgmr.2020.100647. eCollection 2020 Dec.
3
Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.
血液苯丙氨酸降低可纠正中枢神经系统多巴胺和 5-羟色胺的缺乏,并部分改善成年苯丙酮尿症小鼠的行为表现。
Mol Genet Metab. 2018 Jan;123(1):6-20. doi: 10.1016/j.ymgme.2017.10.009. Epub 2017 Oct 19.
4
Motor development skills of 1- to 4-year-old Iranian children with early treated phenylketonuria.1至4岁早期接受治疗的苯丙酮尿症伊朗儿童的运动发育技能
JIMD Rep. 2014;12:85-9. doi: 10.1007/8904_2013_248. Epub 2013 Aug 6.
5
Diffusion MRI findings in phenylketonuria.苯丙酮尿症的扩散磁共振成像结果
Eur Radiol. 2003 Dec;13 Suppl 6:L226-9. doi: 10.1007/s00330-002-1778-3. Epub 2003 Feb 18.
6
PHENYLKETONURIA PRESENTING AN INTERMITTENT PROGRESSIVE COURSE.呈现间歇性进展病程的苯丙酮尿症。
J Neurol Neurosurg Psychiatry. 1965 Apr;28(2):165-70. doi: 10.1136/jnnp.28.2.165.
7
A chemical investigation of the defects of myelination in phenylketonuria.苯丙酮尿症髓鞘形成缺陷的化学研究。
J Neurol Neurosurg Psychiatry. 1962 May;25(2):143-8. doi: 10.1136/jnnp.25.2.143.
8
Phenylketonuria; a survey of cases at the Manitoba School.苯丙酮尿症;对曼尼托巴学校病例的调查
Can Med Assoc J. 1956 Jun 1;74(11):897-900.
9
The pathological report of a case of phenylpyruvic oligophrenia.
J Neurol Neurosurg Psychiatry. 1953 Aug;16(3):139-43. doi: 10.1136/jnnp.16.3.139.
10
[Metabolic disorders and central nervous system].[代谢紊乱与中枢神经系统]
Dtsch Z Nervenheilkd. 1953;169(6):446-78.