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Doris A Trauner

Showing results (31-40 of 35) with videos related to

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Journal of Child Neurology|December 21, 2004
Autism in several members of a family with generalized epilepsy with febrile seizures plusTracy J Dixon-Salazar, Lesley C Keeler, Doris A Trauner, et al.
Pediatric Nephrology (Berlin, Germany)|July 24, 2010
Neurological impairment in nephropathic cystinosis: motor coordination deficitsDoris A Trauner, Jennifer Williams, Angela O Ballantyne, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|May 12, 2009
Developmental changes in cerebral white matter microstructure in a disorder of lysosomal storageSunita Bava, Rebecca J Theilmann, Miriam Sach, et al.
Pediatric Nephrology (Berlin, Germany)|March 5, 2005
First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and futureRobert Kleta, Frederick Kaskel, Ranjan Dohil, et al.
American Journal of Human Genetics|May 14, 2019
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyAnne H O'Donnell-Luria, Lynn S Pais, Víctor Faundes, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Child Neurology|December 21, 2004
Autism in several members of a family with generalized epilepsy with febrile seizures plusTracy J Dixon-Salazar, Lesley C Keeler, Doris A Trauner, et al.
Pediatric Nephrology (Berlin, Germany)|July 24, 2010
Neurological impairment in nephropathic cystinosis: motor coordination deficitsDoris A Trauner, Jennifer Williams, Angela O Ballantyne, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|May 12, 2009
Developmental changes in cerebral white matter microstructure in a disorder of lysosomal storageSunita Bava, Rebecca J Theilmann, Miriam Sach, et al.
Pediatric Nephrology (Berlin, Germany)|March 5, 2005
First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and futureRobert Kleta, Frederick Kaskel, Ranjan Dohil, et al.
American Journal of Human Genetics|May 14, 2019
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyAnne H O'Donnell-Luria, Lynn S Pais, Víctor Faundes, et al.
Pageof 4