Results
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Disordered eating and food restrictions in children with PANDAS/PANS. [electronic resource] by
- Toufexis, Megan D
- Hommer, Rebecca
- Gerardi, Diana M
- Grant, Paul
- Rothschild, Leah
- D'Souza, Precilla
- Williams, Kyle
- Leckman, James
- Swedo, Susan E
- Murphy, Tanya K
Producer: 20151120
In:
Journal of child and adolescent psychopharmacology vol. 25
Availability: No items available.
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Prospective longitudinal overnight video-EEG evaluation in Phelan-McDermid Syndrome. [electronic resource] by
- Khan, Omar I
- Zhou, Xiangping
- Leon, Jill
- Kessler, Riley
- Gaughan, Thomas
- D'Souza, Precilla
- Gropman, Andrea
- Cohen, Ninette
- Rennert, Owen
- Buckley, Ashura
- Inati, Sara
- Thurm, Audrey
Producer: 20190207
In:
Epilepsy & behavior : E&B vol. 80
Availability: No items available.
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Randomized, Controlled Trial of Intravenous Immunoglobulin for Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections. [electronic resource] by
- Williams, Kyle A
- Swedo, Susan E
- Farmer, Cristan A
- Grantz, Heidi
- Grant, Paul J
- D'Souza, Precilla
- Hommer, Rebecca
- Katsovich, Liliya
- King, Robert A
- Leckman, James F
Producer: 20170713
In:
Journal of the American Academy of Child and Adolescent Psychiatry vol. 55
Availability: No items available.
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CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism. [electronic resource] by
- Shoffner, John
- Trommer, Barbara
- Thurm, Audrey
- Farmer, Cristan
- Langley, William A
- Soskey, Laura
- Rodriguez, Aldeboran N
- D'Souza, Precilla
- Spence, Sarah J
- Hyland, Keith
- Swedo, Susan E
Producer: 20170505
In:
Neurology vol. 86
Availability: No items available.
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Linked-read genome sequencing identifies biallelic pathogenic variants in [electronic resource] by
- Knapp, Karen M
- Sullivan, Rosie
- Murray, Jennie
- Gimenez, Gregory
- Arn, Pamela
- D'Souza, Precilla
- Gezdirici, Alper
- Wilson, William G
- Jackson, Andrew P
- Ferreira, Carlos
- Bicknell, Louise S
Producer: 20210226
In:
Journal of medical genetics vol. 57
Availability: No items available.
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Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. [electronic resource] by
- Macnamara, Ellen F
- Koehler, Alanna E
- D'Souza, Precilla
- Estwick, Tyra
- Lee, Paul
- Vezina, Gilbert
- Fauni, Harper
- Braddock, Stephen R
- Torti, Erin
- Holt, James Matthew
- Sharma, Prashant
- Malicdan, May Christine V
- Tifft, Cynthia J
Producer: 20200309
In:
Human mutation vol. 40
Availability: No items available.
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