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Soft tissue small avascular tumor imaging with x-ray phase-contrast micro-CT in-line holography. [electronic resource] by
- Nesterets, Yakov
- Gureyev, Tim
- Stevenson, Andrew
- Pogany, Andrew
- Wilkins, Steve
- Kincaid, Russell
- Ye, Hongwei
- Vogelsang, Levon
- Lipson, Edward
- Coman, Ioana
- Fourmaux, Sylvain
- Kieffer, Jean-Claude
- Krol, Andrzej
Publication details: Proceedings of SPIE--the International Society for Optical Engineering 2008
In:
Proceedings of SPIE--the International Society for Optical Engineering vol. 6913
Availability: No items available.
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16.
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Intrinsic Connectivity Network-Based Classification and Detection of Psychotic Symptoms in Youth With 22q11.2 Deletions. [electronic resource] by
- Schreiner, Matthew
- Forsyth, Jennifer K
- Karlsgodt, Katherine H
- Anderson, Ariana E
- Hirsh, Nurit
- Kushan, Leila
- Uddin, Lucina Q
- Mattiacio, Leah
- Coman, Ioana L
- Kates, Wendy R
- Bearden, Carrie E
Producer: 20180319
In:
Cerebral cortex (New York, N.Y. : 1991) vol. 27
Availability: No items available.
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17.
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Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome. [electronic resource] by
- Kikinis, Zora
- Makris, Nikos
- Sydnor, Valerie J
- Bouix, Sylvain
- Pasternak, Ofer
- Coman, Ioana L
- Antshel, Kevin M
- Fremont, Wanda
- Kubicki, Marek R
- Shenton, Martha E
- Kates, Wendy R
- Rathi, Yogesh
Producer: 20191211
In:
NeuroImage. Clinical vol. 21
Availability: No items available.
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18.
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White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosis. [electronic resource] by
- Kates, Wendy R
- Olszewski, Amy K
- Gnirke, Matthew H
- Kikinis, Zora
- Nelson, Joshua
- Antshel, Kevin M
- Fremont, Wanda
- Radoeva, Petya D
- Middleton, Frank A
- Shenton, Martha E
- Coman, Ioana L
Producer: 20150824
In:
Schizophrenia research vol. 161
Availability: No items available.
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19.
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Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. [electronic resource] by
- Thompson, Carlie A
- Karelis, Jason
- Middleton, Frank A
- Gentile, Karen
- Coman, Ioana L
- Radoeva, Petya D
- Mehta, Rashi
- Fremont, Wanda P
- Antshel, Kevin M
- Faraone, Stephen V
- Kates, Wendy R
Producer: 20170921
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 174
Availability: No items available.
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20.
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Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes. [electronic resource] by
- Radoeva, Petya D
- Coman, Ioana L
- Salazar, Cynthia A
- Gentile, Karen L
- Higgins, Anne Marie
- Middleton, Frank A
- Antshel, Kevin M
- Fremont, Wanda
- Shprintzen, Robert J
- Morrow, Bernice E
- Kates, Wendy R
Producer: 20150625
In:
Psychiatric genetics vol. 24
Availability: No items available.
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