1. Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome. Issue 10 (5th August 2013) Authors: Lee, Ryan W.Y.; Conley, Sandra K.; Gropman, Andrea; Porter, Forbes D.; Baker, Eva H. Journal: American journal of medical genetics Issue: Volume 161:Issue 10(2013:Oct.) Page Start: 2407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Evaluation of disease progression in INCL by MR spectroscopy. Issue 8 (1st July 2015) Authors: Baker, Eva H.; Levin, Sondra W.; Zhang, Zhongjian; Mukherjee, Anil B. Journal: Annals of clinical and translational neurology Issue: Volume 2:Issue 8(2015:Aug.) Page Start: 797 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Long-Term Follow-Up of CD19-CAR T-Cell Therapy in Children and Young Adults With B-ALL. Issue 15 (20th May 2021) Authors: Shah, Nirali N.; Lee, Daniel W.; Yates, Bonnie; Yuan, Constance M.; Shalabi, Haneen; Martin, Staci; Wolters, Pamela L.; Steinberg, Seth M.; Baker, Eva H.; Delbrook, Cindy P.; Stetler-Stevenson, Maryalice; Fry, Terry J.; Stroncek, David F.; Mackall, Crystal L. Journal: Journal of clinical oncology Issue: Volume 39:Issue 15(2021) Page Start: 1650 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. MRI/MRS as a surrogate marker for clinical progression in GM1 gangliosidosis. Issue 3 (8th December 2015) Authors: Regier, Debra S.; Kwon, Hyuk Joon; Johnston, Jean; Golas, Gretchen; Yang, Sandra; Wiggs, Edythe; Latour, Yvonne; Thomas, Sarah; Portner, Cindy; Adams, David; Vezina, Gilbert; Baker, Eva H.; Tifft, Cynthia J. Journal: American journal of medical genetics Issue: Volume 170:Issue 3(2016) Page Start: 634 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Neurologic involvement in patients with atypical Chediak-Higashi disease. (14th February 2017) Authors: Introne, Wendy J.; Westbroek, Wendy; Groden, Catherine A.; Bhambhani, Vikas; Golas, Gretchen A.; Baker, Eva H.; Lehky, Tanya J.; Snow, Joseph; Ziegler, Shira G.; Malicdan, May Christine V.; Adams, David R.; Dorward, Heidi M.; Hess, Richard A.; Huizing, Marjan; Gahl, William A.; Toro, Camilo Journal: Neurology Issue: Volume 88:Number 7(2017) Page Start: e57 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Neurologic involvement in patients with atypical Chediak-Higashi disease. (5th April 2016) Authors: Introne, Wendy J.; Westbroek, Wendy; Cullinane, Andrew R.; Groden, Catherine A.; Bhambhani, Vikas; Golas, Gretchen A.; Baker, Eva H.; Lehky, Tanya J.; Snow, Joseph; Ziegler, Shira G.; Adams, David R.; Dorward, Heidi M.; Hess, Richard A.; Huizing, Marjan; Gahl, William A.; Toro, Camilo Journal: Neurology Issue: Volume 86:Number 14(2016)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Propofol administration in patients with methylmalonic acidemia and intracellular cobalamin metabolism disorders: a review of theoretical concerns and clinical experiences in 28 patients. Issue 5 (19th May 2015) Authors: Ktena, Yiouli P.; Ramstad, Trygg; Baker, Eva H.; Sloan, Jennifer L.; Mannes, Andrew J.; Manoli, Irini; Venditti, Charles P. Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 5(2015) Page Start: 847 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Seizure phenotype in CLN3 disease and its relation to other neurologic outcome measures. Issue 4 (15th February 2021) Authors: Abdennadher, Myriam; Inati, Sara; Soldatos, Ariane; Norato, Gina; Baker, Eva H.; Thurm, Audrey; Bartolini, Luca; Masvekar, Ruturaj; Theodore, William; Bielekova, Bibiana; Porter, Forbes D.; Dang Do, An N. Journal: Journal of inherited metabolic disease Issue: Volume 44:Issue 4(2021) Page Start: 1013 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis. Issue 10 (23rd August 2016) Authors: Keppler‐Noreuil, Kim M.; Baker, Eva H.; Sapp, Julie C.; Lindhurst, Marjorie J.; Biesecker, Leslie G. Other Names: Hennekam Raoul C.M. guestEditor.; Biesecker Leslie G. guestEditor. Journal: American journal of medical genetics Issue: Volume 170:Issue 10(2016) Page Start: 2605 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Spontaneously regressing brain lesions in Smith–Lemli–Opitz syndrome. Issue 2 (11th December 2017) Authors: Dang Do, An N.; Baker, Eva H.; Warren, Katherine E.; Bianconi, Simona E.; Porter, Forbes D. Journal: American journal of medical genetics Issue: Volume 176:Issue 2(2018) Page Start: 386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗