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| Discipline Coordinators: |
Medicine Neurology |
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| Discipline(s): |
Medicine-Pediatrics |
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| AUCD Council Membership: |
No Council Membership |
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| Research: | Child neurology, Rett Syndrome | ||||||||||||||||||
| Education: | Child neurology, neurodevelopmental disorders, neurodegenerative disorders, Rett Syndrome, lysosomal dtorage disorders leukodystrophies | ||||||||||||||||||
Vita/Bio
BIOGRAPHICAL SKETCH
Give the following information for all professional personnel contributing to the training program. Use continuation page to expand any item.
(DO NOT EXCEED 2 PAGES ON ANY INDIVIDUAL)
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Name (Last, first, middle initial)
PERCY, ALAN K.
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Title Professor and Director Clinical Neuroscience, CIRC
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Birth Date (Mo, Day, Year) 05-12-38 |
EDUCATION (Begin with baccalaureate or other initial professional education and include postdoctoral training)
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INSTITUTION AND LOCATION |
DEGREE |
YEAR CONFERRED |
FIELD OF STUDY |
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Harvard College, Cambridge, MA Stanford University, Stanford, CA Stanford University, Stanford, CA Stanford University, Stanford, CA Johns Hopkins Hospital, Baltimore, MD |
A.B. M.D. Intern Resident Resident |
1960 1965 1965-66 1968-69 1969-71 |
Liberal Arts Medicine Medicine & Pediatrics Pediatrics Pediatric Neurology |
PROFESSIONAL CREDENTIALS, LICENSURE, CERTIFICATION
Licensure: Alabama - 1992
Certification: Am Brd of Pediatr-1974; Am Brd of Psychiatr & Neurol with Competence in Chd Neurol-1978 and Neurodevelopmental Disabilities-2001
OFFICES/MEMBERSHIP IN PROFESSIONAL ORGANIZATIONS, ADVISORY COUNCILS, BOARDS, ETC.
American Neurological Association; Child Neurology Society (President 1997-1999); International Child Neurology Association; American Academy of Neurology; President, Child Neurology Foundation 2003-2006
Member, National Advisory Council, NINDS, 1993-96
Editorial Boards: Neurology 2003-present
Director, American Board of Psychiatry & Neurology, 1997-2005 (President-2005)
Ad Hoc Member, Special Study Sections, DRG, NIH, 1981-pres; Ad Hoc Reviewer, various NIH review groups
MAJOR RESEARCH/PROFESSIONAL INTEREST: Rett Syndrome, Inherited Neurometabolic Diseases
RESEARCH OR TRAINING SUPPORT (List all grants on which you currently contribute effort and/or from which you receive support and specify the percent effort on each.)
MCH LEND MCJ019143 (Percy) 07/01/90 - 06/30/06 20%
ADD 04DD000162 (Percy) 07/01/02 - 06/30/07 15%
NIH P01HD4030101 (Percy) 07/23/01- 05/31/06 8%
NIH/NHGRI/NINDS R01HG02449-01 (Shoulson) 07/01/02-06/30/07 <1%
NICHD P30 HD38985 (PI-Percy) 08/04/00-06/30/05 20%
NCRR U54 RR019478 (PI-Beaudet) 09/30/03-07/31/08 20%
ATSDR U50/ATU473215 (PI-Lavender, Cash, Frumkin) 10/1/03-9/30/06 10%
HONORS/AWARDS
Doctor Honoris Causa-Göteborg University, Göteborg, Sweden-2002; Hower Award, Child Neurology Society-2005
PROFESSIONAL EXPERIENCE AND APPOINTMENTS: Starting with present position, list professional employment and academic appointments.
1992-present: Director, Clinical Neuroscience, Assoc Director (2003), Civitan International Research Center-UAB
1992-2003: Professor and Director, Child Neurology, University of Alabama at Birmingham School of Medicine
1994-2002: Vice Chairman, Dept. of Pediatrics, UAB
PUBLICATIONS:
Tofil N, Buckmaster M,...Percy A. Deep sedation with Propofol in patients with Rett syndrome. J Child Neurol 2005, in press.
Hogarth P, Kayson E,..., and the Huntington Study Group. Interrater Agreement in the Assessment of Motor Manifestations of Huntington's Disease. Movement Dis 20:293-297,2005.
Neul JL, Maricich SM,..., Percy A, Glaze D. Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett Syndrome. Neurology 64:2151-2152, 2005.
Amir RE, Fang P, Yu Z, Glaze D, Percy AK, Zoghbi HY, Roa BB, Van den Veyver, IB. Mutations in exon 1 of MECP2 are a rare cause of Rett Syndrome. J Medical Genet, on-line publication, 2004.
Schanen C,...Lane J, Everett R, Feng A, Cantor RM, Percy A. Phenotypic Manifestations of MECP2 Mutations in Classical and Atypical Rett Syndrome. Am J Med Genet 126A:129-140, 2004.
Breedveld G, van Dongen JWF, Danesino C, Guala A, Percy AK.... Mutations in TITF-1 are associated with Benign Hereditary Chorea. Hum Molecul Genet 11:971-979, 2002.
Breedveld G, Percy AK, Srinidhi L, de Vries BBA, Yapijakis C, Dure LS, Ippel E, Sandkuijl LA.... Clinical and Genetic Heterogeneity in Benign Hereditary Chorea. Neurology 59(4): 579-584, 2002.
Palmer CA, Percy AK. Neuropathology of the Occipital Horn Syndrome. J Child Neurol 16:764-766, 2001
Amir R, Van den Veyver I, Schultz R, Malicki D, Tran C, Philippi A, Percy AK, Motil K, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY. Influence of mutation type and X chromosome inactivation on the phenotype of Rett syndrome. Ann Neurol 47: 670-679, 2000.