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Cerebellar atrophy in patients with subcortical-type vascular cognitive impairment. [electronic resource] by
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- Park, Jun-Sung
- Kwak, Ki-Chang
- Yoon, Uicheul
- Suh, Mee Kyung
- Kim, Geon Ha
- Shin, Ji Soo
- Kim, Chi Hun
- Noh, Young
- Cho, Hanna
- Kim, Min-Jeong
- Kim, Jong Hun
- Roh, Jee Hoon
- Lee, Jong-Min
- Na, Duk L
Producer: 20130613
In:
Cerebellum (London, England) vol. 12
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1183.
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Spatial characteristics of white matter abnormalities in schizophrenia. [electronic resource] by
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- Caprihan, Arvind
- Schulz, S Charles
- Andreasen, Nancy C
- Gollub, Randy L
- Calhoun, Vince D
- Magnotta, Vincent A
Producer: 20140422
In:
Schizophrenia bulletin vol. 39
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1185.
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Protective effects of pentoxifylline on lipopolysaccharide-induced white matter injury in a rat model of periventricular leukomalasia. [electronic resource] by
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- Kumral, Abdullah
- Okyay, Emre
- Ozbal, Seda
- Tugyan, Kazim
- Tuzun, Funda
- Sever, Ali Haydar
- Yilmaz, Osman
- Duman, Nuray
- Ozkan, Hasan
Producer: 20140701
In:
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians vol. 26
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1187.
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1188.
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1189.
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Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene. [electronic resource] by
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- Di Donato, Ilaria
- Bianchi, Silvia
- Monti, Lucia
- Formichi, Patrizia
- Rufa, Alessandra
- Taglia, Ilaria
- Cerase, Alfonso
- Dotti, Maria Teresa
- Federico, Antonio
Producer: 20150202
In:
Journal of neurology vol. 261
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A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis. [electronic resource] by
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- Sasaki, Masayuki
- Hiraide, Takuya
- Sumitomo, Noriko
- Takeshita, Eri
- Shimizu-Motohashi, Yuko
- Ishiyama, Akihiko
- Saito, Takashi
- Komaki, Hirofumi
- Nakagawa, Eiji
- Sato, Noriko
- Nakashima, Mitsuko
- Saitsu, Hirotomo
Producer: 20210125
In:
Brain & development vol. 42
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1193.
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CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy. [electronic resource] by
- Mitsui, Jun
- Matsukawa, Takashi
- Ishiura, Hiroyuki
- Higasa, Koichiro
- Yoshimura, Jun
- Saito, Taro L
- Ahsan, Budrul
- Takahashi, Yuji
- Goto, Jun
- Iwata, Atsushi
- Niimi, Yuki
- Riku, Yuuichi
- Goto, Yoji
- Mano, Kazuo
- Yoshida, Mari
- Morishita, Shinichi
- Tsuji, Shoji
Producer: 20130507
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 159B
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KIF5A de novo mutation associated with myoclonic seizures and neonatal onset progressive leukoencephalopathy. [electronic resource] by
- Rydzanicz, M
- Jagła, M
- Kosinska, J
- Tomasik, T
- Sobczak, A
- Pollak, A
- Herman-Sucharska, I
- Walczak, A
- Kwinta, P
- Płoski, R
Producer: 20170602
In:
Clinical genetics vol. 91
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