Directory

Perry Boryee Shieh, M.D., Ph.D. [ Edit Your Profile ]

Email Address: pshieh@mednet.ucla.edu

Work Phone Number: 310-794-1195
310-794-7491

Mailing Address:
BOX 956975, B200, 300 Medical Plaza
Los Angeles, CA 90095

Work
Position/Title
Associate Professor & Director of the Neurouscular Program, Neurology

Education:
Degrees:
M.D., Ph.D., Johns Hopkins University School of Medicine, 2000
Ph.D., John Hopkins School of Medicine, 1998 - 2000
Fellowship:
EMG, Brigham & Women's Hospital, 2004-2005
Internship:
Yale-New Haven Hospital, 2000-2001
Residency:
Stanford University Medical Center, 2001-2004

Certifications:
Certifications:
American Board of Psychiatry and Neurology, 2007
American Board of Psychiatry and Neurology, 2008
American Board of Psychiatry and Neurology, 2006

Publications
Middlekauff Holly R, Verity M Anthony, Horwich Tamara B, Fonarow Gregg C, Hamilton Michele A, Shieh Perry, Intact skeletal muscle mitochondrial enzyme activity but diminished exercise capacity in advanced heart failure patients on optimal medical and device therapy. Clinical research in cardiology : official journal of the German Cardiac Society. 2013; 80(17): .
Bharucha-Goebel Diana Xerxes, Santi Mariarita, Medne Livija, Zukosky Kristin, Dastgir Jahannaz, Shieh Perry B, Winder Thomas, Tennekoon Gihan, Finkel Richard S, Dowling James J, Monnier Nicole, Bönnemann Carsten G, Severe congenital RYR1-associated myopathy: the expanding clinicopathologic and genetic spectrum. Neurology. 2013; 80(17): 1584-9.
Middlekauff Holly R, Vigna Chris, Verity M Anthony, Fonarow Gregg C, Horwich Tamara B, Hamilton Michele A, Shieh Perry, Tupling A Russell, Abnormalities of calcium handling proteins in skeletal muscle mirror those of the heart in humans with heart failure: a shared mechanism?. Journal of cardiac failure. 2012; 18(9): 724-33.
Wan Jijun, Yourshaw Michael, Mamsa Hafsa, Rudnik-Schöneborn Sabine, Menezes Manoj P, Hong Ji Eun, Leong Derek W, Senderek Jan, Salman Michael S, Chitayat David, Seeman Pavel, von Moers Arpad, Graul-Neumann Luitgard, Kornberg Andrew J, Castro-Gago Manuel, Sobrido María-Jesús, Sanefuji Masafumi, Shieh Perry B, Salamon Noriko, Kim Ronald C, Vinters Harry V, Chen Zugen, Zerres Klaus, Ryan Monique M, Nelson Stanley F, Jen Joanna C, Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration. Nature genetics. 2012; 44(6): 704-8.
Chan Nora, Le Cindy, Shieh Perry, Mozaffar Tahseen, Khare Manaswitha, Bronstein Jeff, Kimonis Virginia, Valosin-containing protein mutation and Parkinson's disease. Parkinsonism & related disorders. 2012; 18(1): 107-9.
Shieh Perry B, Kudryashova Elena, Spencer Melissa J, Limb-girdle muscular dystrophy 2H and the role of TRIM32. Handbook of clinical neurology. 2011; 101(1): 125-33.
Hao Minqi, Akrami Kevan, Wei Ke, De Diego Carlos, Che Nam, Ku Jeong-Hee, Tidball James, Graves Michael C, Shieh Perry B, Chen Fabian, Muscleblind-like 2 (Mbnl2) -deficient mice as a model for myotonic dystrophy. Developmental dynamics : an official publication of the American Association of Anatomists. 2008; 237(2): 403-10.
Desmond John E, Chen S H Annabel, Shieh Perry B, Cerebellar transcranial magnetic stimulation impairs verbal working memory. Annals of Neurology. 2005; 58(4): 553-60.
Gang Qiang, Bettencourt Conceicao, Machado Pedro M, Fox Zoe, Brady Stefen, Healy Estelle, Parton Matt, Holton Janice L, Hilton-Jones David, Shieh Perry B, Zanoteli Edmar, De Paepe Boel, De Bleecker Jan, Shaibani Aziz, Ripolone Michela, Violano Raffaella, Moggio Maurizio, Barohn Richard J, Dimachkie Mazen M, Mora Marina, Mantegazza Renato, Zanotti Simona, Hanna Michael G, Houlden Henry, Houlden Henry, The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis. Neurobiology of aging. 2015; 36(4): 1766.e1-3.
Lee Hane, Deignan Joshua L, Dorrani Naghmeh, Strom Samuel P, Kantarci Sibel, Quintero-Rivera Fabiola, Das Kingshuk, Toy Traci, Harry Bret, Yourshaw Michael, Fox Michelle, Fogel Brent L, Martinez-Agosto Julian A, Wong Derek A, Chang Vivian Y, Shieh Perry B, Palmer Christina G S, Dipple Katrina M, Grody Wayne W, Vilain Eric, Nelson Stanley F, Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA. 2014; 312(18): 1880-7.