Results
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1461.
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1462.
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Life-span changes of the human brain white matter: diffusion tensor imaging (DTI) and volumetry. [electronic resource] by
- Westlye, Lars T
- Walhovd, Kristine B
- Dale, Anders M
- Bjørnerud, Atle
- Due-Tønnessen, Paulina
- Engvig, Andreas
- Grydeland, Håkon
- Tamnes, Christian K
- Ostby, Ylva
- Fjell, Anders M
Producer: 20110421
In:
Cerebral cortex (New York, N.Y. : 1991) vol. 20
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1463.
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Clinical and neuroimaging findings of Cree leukodystrophy: a retrospective case series. [electronic resource] by
- Harder, S
- Gourgaris, A
- Frangou, E
- Hopp, K
- Huntsman, R
- Lowry, N
- Seshia, S
- Lemire, E
- Robinson, C
- Tynan, J
Producer: 20110104
In:
AJNR. American journal of neuroradiology vol. 31
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1464.
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1465.
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1466.
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1467.
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1468.
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Do cardiovascular risk factors explain the link between white matter hyperintensities and brain volumes in old age? A population-based study. [electronic resource] by
- Wang, R
- Fratiglioni, L
- Laveskog, A
- Kalpouzos, G
- Ehrenkrona, C-H
- Zhang, Y
- Bronge, L
- Wahlund, L-O
- Bäckman, L
- Qiu, C
Producer: 20151026
In:
European journal of neurology vol. 21
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1469.
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1470.
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1471.
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1472.
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1473.
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1474.
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1475.
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1476.
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None [electronic resource] by
- Ma, Shenghong
- Sun, Renqiang
- Jiang, Bowen
- Gao, Jun
- Deng, Wanglong
- Liu, Peng
- He, Ruoyu
- Cui, Jing
- Ji, Minbiao
- Yi, Wei
- Yang, Pengyuan
- Wu, Xiaohui
- Xiong, Yue
- Qiu, Zilong
- Ye, Dan
- Guan, Kun-Liang
Producer: 20170630
In:
Molecular and cellular biology vol. 37
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1477.
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Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum. [electronic resource] by
- Emrick, Lisa T
- Rosenfeld, Jill A
- Lalani, Seema R
- Jain, Mahim
- Desai, Nilesh K
- Larson, Austin
- Kripps, Kimberly
- Vanderver, Adeline
- Taft, Ryan J
- Bluske, Krista
- Perry, Denise
- Nagakura, Honey
- Immken, LaDonna L
- Burrage, Lindsay C
- Bacino, Carlos A
- Belmont, John W
- Network, Undiagnosed Diseases
- Lee, Brendan
Producer: 20200128
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 21
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1478.
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1479.
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A novel complex neurological phenotype due to a homozygous mutation in FDX2. [electronic resource] by
- Gurgel-Giannetti, Juliana
- Lynch, David S
- Paiva, Anderson Rodrigues Brandão de
- Lucato, Leandro Tavares
- Yamamoto, Guilherme
- Thomsen, Christer
- Basu, Somsuvro
- Freua, Fernando
- Giannetti, Alexandre Varella
- de Assis, Bruno Della Ripa
- Ribeiro, Mara Dell Ospedale
- Barcelos, Isabella
- Sayão Souza, Katiane
- Monti, Fernanda
- Melo, Uirá Souto
- Amorim, Simone
- Silva, Leonardo G L
- Macedo-Souza, Lúcia Inês
- Vianna-Morgante, Angela M
- Hirano, Michio
- Van der Knaap, Marjo S
- Lill, Roland
- Vainzof, Mariz
- Oldfors, Anders
- Houlden, Henry
- Kok, Fernando
Producer: 20190715
In:
Brain : a journal of neurology vol. 141
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1480.
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Brief Report: Impact of ART Classes on the Increasing Risk of Cerebral Small-Vessel Disease in Middle-Aged, Well-Controlled, cART-Treated, HIV-Infected Individuals. [electronic resource] by
- Januel, Edouard
- Godin, Ophelia
- Moulignier, Antoine
- Lescure, François-Xavier
- Savatovsky, Julien
- Lamirel, Cédric
- Valin, Nadia
- Tubiana, Roland
- Canestri, Ana
- Roux, Pascal
- Sadik, Jean-Claude
- Salomon, Laurence
- Katlama, Christine
- Yazdanpanah, Yazdan
- Pialoux, Gilles
- Girard, Pierre-Marie
- Costagliola, Dominique
- Assoumou, Lambert
Producer: 20200414
In:
Journal of acquired immune deficiency syndromes (1999) vol. 81
Availability: No items available.
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