Detalles de la búsqueda
1.
Expression of N-methyl-D-aspartate receptor subunits in the bovine ovum: ova as a potential source of autoantigens causing anti-NMDAR encephalitis.
Tohoku J Exp Med
; 235(3): 223-31, 2015 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-25786541
2.
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Estimation of pathological lesion stage from brain images.
J Neurol Sci
; 461: 123027, 2024 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38805875
3.
Identification of the N-Methyl-D-aspartate receptor (NMDAR)-related epitope, NR2B, in the normal human ovary: implication for the pathogenesis of anti-NMDAR encephalitis.
Tohoku J Exp Med
; 230(1): 13-6, 2013 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-23648631
4.
[An autopsy case report of a patient with frontotemporal dementia with motor neuron disease in totally locked-in state showing hyperosmolar hyperosmotic state].
Rinsho Shinkeigaku
; 62(8): 595-601, 2022 Aug 27.
Artículo
en Japonés
| MEDLINE | ID: mdl-35871561
5.
Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP).
eNeurologicalSci
; 22: 100310, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33553700
6.
An Elderly Case of Paraneoplastic Anti-NMDA Receptor Encephalitis Associated with Small-cell Lung Cancer Expressing NR1 Subunits.
Intern Med
; 59(18): 2307-2309, 2020 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-32493856
7.
Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: lesion staging and dynamic changes of axons and microglial subsets.
Brain Pathol
; 27(6): 748-769, 2017 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-27608278
8.
Corpus callosum atrophy in patients with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: an MRI-based study.
Intern Med
; 53(1): 21-7, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24390523
9.
Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R.
Intern Med
; 52(4): 503-6, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23411710
10.
Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: case report.
J Neurol Sci
; 318(1-2): 115-8, 2012 Jul 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22503135
11.
Calciphylaxis as a Catastrophic Complication in a Patient with POEMS Syndrome.
Case Rep Neurol
; 1(1): 47-53, 2009 Dec 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-20847836
12.
A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine.
Clin Neurol Neurosurg
; 115(8): 1542-5, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23369404
Resultados
1 -
12
de 12
1
Próxima >
>>