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1881.
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1882.
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1883.
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Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy. [electronic resource] by
- van Berge, Laura
- Hamilton, Eline M
- Linnankivi, Tarja
- Uziel, Graziella
- Steenweg, Marjan E
- Isohanni, Pirjo
- Wolf, Nicole I
- Krägeloh-Mann, Ingeborg
- Brautaset, Nils J
- Andrews, P Ian
- de Jong, Brigit A
- al Ghamdi, Malak
- van Wieringen, Wessel N
- Tannous, Bakhos A
- Hulleman, Esther
- Würdinger, Thomas
- van Berkel, Carola G M
- Polder, Emiel
- Abbink, Truus E M
- Struys, Eduard A
- Scheper, Gert C
- van der Knaap, Marjo S
Producer: 20140521
In:
Brain : a journal of neurology vol. 137
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1886.
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White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis. [electronic resource] by
- Perlstein, Matthew D
- Chohan, Moeed R
- Coman, Ioana L
- Antshel, Kevin M
- Fremont, Wanda P
- Gnirke, Matthew H
- Kikinis, Zora
- Middleton, Frank A
- Radoeva, Petya D
- Shenton, Martha E
- Kates, Wendy R
Producer: 20140829
In:
Schizophrenia research vol. 152
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1887.
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Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS. [electronic resource] by
- Konno, Takuya
- Tada, Masayoshi
- Tada, Mari
- Koyama, Akihide
- Nozaki, Hiroaki
- Harigaya, Yasuo
- Nishimiya, Jin
- Matsunaga, Akiko
- Yoshikura, Nobuaki
- Ishihara, Kenji
- Arakawa, Musashi
- Isami, Aiko
- Okazaki, Kenichi
- Yokoo, Hideaki
- Itoh, Kyoko
- Yoneda, Makoto
- Kawamura, Mitsuru
- Inuzuka, Takashi
- Takahashi, Hitoshi
- Nishizawa, Masatoyo
- Onodera, Osamu
- Kakita, Akiyoshi
- Ikeuchi, Takeshi
Producer: 20140307
In:
Neurology vol. 82
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1888.
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Progressive leukoencephalopathy impairs neurobehavioral development in sialin-deficient mice. [electronic resource] by
- Stroobants, Stijn
- Van Acker, Nathalie G G
- Verheijen, Frans W
- Goris, Ilse
- Daneels, Guy F T
- Schot, Rachel
- Verbeek, Elly
- Knaapen, Michiel W M
- De Bondt, An
- Göhlmann, Hinrich W
- Crauwels, Marion L A
- Mancini, Grazia M S
- Andries, Luc J
- Moechars, Dieder W E
- D'Hooge, Rudi
Producer: 20170516
In:
Experimental neurology vol. 291
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1889.
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Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. [electronic resource] by
- Netravathi, Manjunath
- Kumari, Renu
- Kapoor, Saketh
- Dakle, Pushkar
- Dwivedi, Manish Kumar
- Roy, Sumitabho Deb
- Pandey, Paritosh
- Saini, Jitender
- Ramakrishna, Anil
- Navalli, Devaraddi
- Satishchandra, Parthasarathy
- Pal, Pramod Kumar
- Kumar, Arun
- Faruq, Mohammed
Producer: 20150630
In:
BMC medical genetics vol. 16
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Juvenile striatal white matter is resistant to ischemia-induced damage. [electronic resource] by
- Ahrendsen, Jared T
- Grewal, Himmat S
- Hickey, Sean P
- Culp, Cecilia M
- Gould, Elizabeth A
- Shimizu, Takeru
- Strnad, Frank A
- Traystman, Richard J
- Herson, Paco S
- Macklin, Wendy B
Producer: 20180104
In:
Glia vol. 64
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1894.
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Gene therapy targeting oligodendrocytes provides therapeutic benefit in a leukodystrophy model. [electronic resource] by
- Georgiou, Elena
- Sidiropoulou, Kyriaki
- Richter, Jan
- Papaneophytou, Christos
- Sargiannidou, Irene
- Kagiava, Alexia
- von Jonquieres, Georg
- Christodoulou, Christina
- Klugmann, Matthias
- Kleopa, Kleopas A
Producer: 20170529
In:
Brain : a journal of neurology vol. 140
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