1. A De Novo case of autosomal dominant mitochondrial membrane protein‐associated neurodegeneration. Issue 7 (27th May 2021) Authors: Fraser, Stuart; Koenig, Mary; Farach, Laura; Mancias, Pedro; Mowrey, Kate Journal: Molecular genetics & genomic medicine Issue: Volume 9:Issue 7(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. (June 2021) Authors: Calame, Daniel G.; Fatih, Jawid; Herman, Isabella; Akdemir, Zeynep Coban; Du, Haowei; Jhangiani, Shalini N.; Gibbs, Richard A.; Marafi, Dana; Pehlivan, Davut; Posey, Jennifer E.; Lotze, Timothy; Mancias, Pedro; Bhattacharjee, Meenakshi Bidwai; Lupski, James R. Journal: Neurology Issue: Volume 7:Number 3(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cerebral Sinovenous Thrombosis Associated With Iron Deficiency Anemia Secondary to Severe Menorrhagia: A Case Report. (September 2014) Authors: Corrales-Medina, Fernando F.; Grant, Leon; Egas-Bejar, Daniela; Valdivia-Ascuna, Zoila; Rodriguez, Nidra; Mancias, Pedro Other Names: Maria Bernard L. guest-editor. Journal: Journal of child neurology Issue: Volume 29:Number 9(2014:Sep.) Page Start: NP62 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dysferlinopathy Presenting as Rhabdomyolysis and Acute Renal Failure. (April 2013) Authors: Moody, Shadé; Mancias, Pedro Journal: Journal of child neurology Issue: Volume 28:Number 4(2013) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic Testing Practices of Genetic Counselors, Geneticists, and Pediatric Neurologists With Regard to Childhood-Onset Neurogenetic Conditions. (March 2019) Authors: Wofford, Sara; Noblin, Sarah; Davis, Jessica M; Farach, Laura S; Hashmi, S Shahrukh; Mancias, Pedro; Wagner, Victoria F Journal: Journal of child neurology Issue: Volume 34:Number 4(2019:Apr.) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of a novel microdeletion causative of Nance‐Horan syndrome. Issue 3 (5th February 2022) Authors: Lopez Martinolich, Mariana; Northrup, Hope; Mancias, Pedro; Hillman, Paul; Rao, Kavya; Mowrey, Kate Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 3(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mitochondria‐associated membrane collapse is a common pathomechanism in SIGMAR1‐ and SOD1‐linked ALS. Issue 12 (7th November 2016) Authors: Watanabe, Seiji; Ilieva, Hristelina; Tamada, Hiromi; Nomura, Hanae; Komine, Okiru; Endo, Fumito; Jin, Shijie; Mancias, Pedro; Kiyama, Hiroshi; Yamanaka, Koji Journal: EMBO molecular medicine Issue: Volume 8:Issue 12(2016) Page Start: 1421 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Strategies to Support Social Justice Activism in Medical School. (5th April 2022) Authors: McCleary-Gaddy, Asia T.; Mancias, Pedro Journal: Academic medicine Issue: Volume 97:Number 12(2022) Page Start: 1869 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Sural sparing pattern discriminates Guillain–Barré syndrome from its mimics. Issue 5 (24th September 2014) Authors: Derksen, Angelika; Ritter, Christian; Athar, Parveen; Kieseier, Bernd C.; Mancias, Pedro; Hartung, Hans‐Peter; Sheikh, Kazim A.; Lehmann, Helmar C. Journal: Muscle & nerve Issue: Volume 50:Issue 5(2014:Nov.) Page Start: 780 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗