Mental Retardation & Developmental Disabilities (MRDD) Branch Supported Projects for 2009
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|
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| F32 - Postdoctoral Individual National Research Service Award |
| Project Number |
Description |
| 5F32HD055745-03 |
MALONEY, MICHAEL T
STANFORD UNIVERSITY
RETROGRADE TRANSPORT AT THE CROSSROADS OF COGNITIVE DELCINE AND NEURODEGENERATION
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| |
| K08 - Clinical Investigator Award |
| Project Number |
Description |
| 1K08HD058022-01A1 |
SONDHEIMER, NEAL
CHILDREN'S HOSPITAL OF PHILADELPHIA
MITOCHONDRIAL TRANSCRIPTION AND PEDIATRIC DISEASE
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| |
| K23 - Mentored Patient-Oriented Research Devel Awd |
| Project Number |
Description |
| 1K23HD058043-01A1 |
VISOOTSAK, JEANNIE J
EMORY UNIVERSITY
NEURODEVELOPMENTAL IMPACT OF CONGENITAL HEART DEFECTS IN DOWN SYNDROME
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| 5K23HD048502-05 |
RAUEN, KATHERINE ANNA
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
ELUCIDATION OF THE GENETIC ETIOLOGY OF COSTELLO SYNDROME
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| |
| K24 - Midcareer Investigator Awd in Patient-Oriented Res |
| Project Number |
Description |
| 5K24HD046712-05 |
GLASS, IAN A
UNIVERSITY OF WASHINGTON
GENETIC ANALYSES OF CEREBELLAR MALFORMATIONS
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| |
| P01 - Research Program Projects |
| Project Number |
Description |
| 5P01HD018955-23 |
SAUNDERS, RICHARD R
UNIVERSITY OF KANSAS LAWRENCE
COMMUNICATION OF PEOPLE WITH MENTAL RETARDATION
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| 5P01HD032062-15 |
DIMAURO, SALVATORE
COLUMBIA UNIVERSITY HEALTH SCIENCES
MITOCHONDRIAL ENCEPHALOMYOPATHIES AND MENTAL RETARDATION
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| 5P01HD035946-10 |
FLETCHER, JACK M
UNIVERSITY OF HOUSTON
SPINA BIFIDA: COGNITIVE AND NEUROBIOLOGICAL VARIABILITY
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| 5P01HD057247-02 |
WILSON, JAMES M
UNIVERSITY OF PENNSYLVANIA
GENE THERAPY FOR UREA CYCLE DISORDERS
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| |
| P30 - Center Core Grants |
| Project Number |
Description |
| 3P30HD024061-21S1 |
CATALDO, MICHAEL F
HUGO W. MOSER RES INST KENNEDY KRIEGER
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH CENTERS 2008
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| |
| P50 - Specialized Center |
| Project Number |
Description |
| 5P50MH081756-02 |
KLIN, AMI
YALE UNIVERSITY
MECHANISMS OF SOCIAL ENGAGEMENT IN AUTISM SPECTRUM DISORDERS
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| |
| R01 - Research Project |
| Project Number |
Description |
| 1R01HD055345-01A2 |
CONNERS, FRANCES A
UNIVERSITY OF ALABAMA IN TUSCALOOSA
COGNITIVE PREDICTORS OF LANGUAGE IMPAIRMENT IN DOWN SYNDROME
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| 1R01HD056370-01A2 |
GIBSON, JAY ROBERT
UNIVERSITY OF TEXAS SW MED CTR/DALLAS
CORTICAL CIRCUIT CHANGES AND MECHANISMS IN A MOUSE MODEL OF FRAGILE X SYNDROME
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| 1R01HD057033-01A1 |
HARDING, CARY O.
OREGON HEALTH AND SCIENCE UNIVERSITY
AUGMENTED PHENYLALANINE CLEARANCE BY MUSCLES AS NOVEL THERAPY FOR PHENYLKETONURIA
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| 1R01HD057136-01A1 |
RAYMOND, GERALD V
HUGO W. MOSER RES INST KENNEDY KRIEGER
NEWBORN SCREENING FOR ADRENOLEUKODYSTROPHY
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| 1R01HD058553-01 |
GIBSON, K MICHAEL
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
NOVEL TREATMENT AND SCREENING STRATEGIES IN HERITABLE GAMMA-HYDROXYBUTYRIC ACIDUR
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| 1R01HD058880-01 |
SLONIM, DONNA
TUFTS UNIVERSITY MEDFORD
TRANSLATIONAL BIOINFORMATICS FOR HUMAN DEVELOPMENTAL GENOMICS
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| 1R01HD059762-01 |
HONG, YOUNG-KWON
UNIVERSITY OF SOUTHERN CALIFORNIA
MOLECULAR BASIS OF NUCHAL EDEMA
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| 2R01HD034879-11A2 |
BAKER, BRUCE L
UNIVERSITY OF CALIFORNIA LOS ANGELES
CHILDREN WITH MR: FAMILY PROCESSES AND DUAL DIAGNOSIS
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| 2R01HD039961-06A2 |
FEIN, DEBORAH A.
UNIVERSITY OF CONNECTICUT STORRS
EARLY DETECTION OF PERVASIVE DEVELOPMENTAL DISORDERS
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| 2R01HD042053-06 |
BIANCHI, DIANA W
TUFTS MEDICAL CENTER
FETO-MATERNAL DNA/RNA TRAFFICKING: BIOLOGY AND APPLICATION
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| 2R01HD042182-06A2 |
LAMANTIA, ANTHONY S
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
REGULATION OF 22Q11 GENES IN EMBROYONIC AND ADULT FOREBRAIN
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| 3R01HD052731-01A2S1 |
HUBER, KIMBERLY M
UNIVERSITY OF TEXAS SW MED CTR/DALLAS
STUDY OF FRAGILE X MENTAL RETARDATION PROTEIN IN SYNAPTIC FUNCTION AND PLASTICITY
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| 5R01ES016443-02 |
NEWSCHAFFER, CRAIG J
DREXEL UNIVERSITY
EARLY AUTISM RISK LONGITUDINAL INVESTIGATION (EARLI) NETWORK
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| 5R01HD020521-23 |
WARREN, STEPHEN T.
EMORY UNIVERSITY
MOLECULAR CLONING OF THE FRAGILE X SITE
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| 5R01HD023333-17 |
WIGHTMAN, FREDERIC L
UNIVERSITY OF LOUISVILLE
LISTENING SKILLS IN CHILDREN WITH AND WITHOUT COCHLEAR IMPLANTS
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| 5R01HD027592-17 |
DI PIETRO, JANET A.
JOHNS HOPKINS UNIVERSITY
FETAL NEUROBEHAVIORAL DEVELOPMENT & POSTNATAL CONTINUITY
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| 5R01HD028607-18 |
SCHUCHMAN, EDWARD H
MOUNT SINAI SCHOOL OF MEDICINE OF NYU
ACID SPHINGOMYELINASE & NIEMANN-PICK DISEASE
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| 5R01HD033470-16 |
TAGER-FLUSBERG, HELEN B.
BOSTON UNIVERSITY MEDICAL CAMPUS
SOCIAL COGNITION IN WILLIAMS SYNDROME
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| 5R01HD034852-11 |
XIA, YING
YALE UNIVERSITY
HYPOXIA AND NEURONAL EXCITABILITY: CELLULAR MECHANISMS
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| 5R01HD036071-11 |
HAGERMAN, RANDI J
UNIVERSITY OF CALIFORNIA DAVIS
GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE X FAMILIES
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| 5R01HD037872-08 |
RESNICK, JAMES L
UNIVERSITY OF FLORIDA
GENETIC COMPLEMENTATION OF A MOUSE MODEL FOR PWS
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| 5R01HD038384-09 |
REEVES, ROGER H
JOHNS HOPKINS UNIVERSITY
GENOMIC APPROACHES TO ANEUPLOIDY
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| 5R01HD038466-09 |
BUSCIGLIO, JORGE A
UNIVERSITY OF CALIFORNIA IRVINE
MITOCHONDRIAL DYSFUNCTION IN DOWN'S SYNDROME
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| 5R01HD038819-08 |
LOSH, MOLLY
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
PRAGMATIC SKILLS OF YOUNG MALES AND FEMALES WITH FRAGILE X SYNDROME
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| 5R01HD039708-08 |
PROHASKA, JOSEPH ROBERT
UNIVERSITY OF MINNESOTA DULUTH
NUTRITIONAL COPPER STATUS AND THE NERVOUS SYSTEM
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| 5R01HD040182-09 |
VALLEE, RICHARD B
COLUMBIA UNIVERSITY HEALTH SCIENCES
MECHANISM OF ACTION OF THE LISSENCEPHALY GENE LIS-1
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| 5R01HD040647-08 |
DARNELL, JENNIFER C
ROCKEFELLER UNIVERSITY
IDENTIFICATION AND VALIDATION OF FMRP TARGET RNAS
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| 5R01HD040661-07 |
HAGERMAN, PAUL J
UNIVERSITY OF CALIFORNIA DAVIS
EXPRESSION OF THE FRAGILE X GENE
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| 5R01HD041590-08 |
SVAREN, JOHN P
UNIVERSITY OF WISCONSIN MADISON
GENETIC CONTROL OF MYELINATION BY EGR2 AND NAB PROTEINS
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| 5R01HD042908-06 |
FRANCESCHINI, MARIA ANGELA
MASSACHUSETTS GENERAL HOSPITAL
OPTICAL MONITORING OF CEREBRAL OXYGENATION IN INFANTS
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| 5R01HD046609-05 |
LANDRY, SUSAN
UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
LONGITUDINAL EFFECTS OF SPINA BIFIDA ON LEARNING
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| 5R01HD046667-05 |
VASSILEV, PETER M
BRIGHAM AND WOMEN'S HOSPITAL
ELUCIDATION AND RESCUE OF PHENOTYPIC ALTERATIONS IN MLIV
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| 5R01HD047567-04 |
ULRICH, BEVERLY D
UNIVERSITY OF MICHIGAN AT ANN ARBOR
SENSORIMOTOR DEVELOPMENT: INFANTS BORN WITH SPINA BIFIDA
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| 5R01HD047656-05 |
WENGER, GALEN R
UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK
AGE AND COGNITION IN A MOUSE MODEL OF DOWN SYNDROME
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| 5R01HD048489-05 |
AKBARIAN, SCHAHRAM
UNIV OF MASSACHUSETTS MED SCH WORCESTER
CHROMATIN ALTERATIONS IN RETT SYNDROME
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| 5R01HD048947-04 |
SANDMAN, CURT A.
UNIVERSITY OF CALIFORNIA IRVINE
EMERGENCE OF SIB IN DEVELOPMENTALLY DELAYED INDIVIDUALS
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| 5R01HD049686-04 |
KUPPERMANN, MIRIAM
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
EXPANDED PRENATAL TESTING OPTIONS AND INFORMED CHOICE
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| 5R01HD050557-03 |
LOBATO, DEBRA J
RHODE ISLAND HOSPITAL (PROVIDENCE, RI)
LATINO SIBLINGS AND MR/DD
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| 5R01HD052083-04 |
FALLON, JUSTIN R
BROWN UNIVERSITY
EXPERIENCE-DEPENDENT REGULATION OF THE FRAGILE X GENE
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| 5R01HD052664-03 |
OLNEY, JOHN W
WASHINGTON UNIVERSITY
ANESTHESIA-INDUCED DEVELOPMENTAL NEUROAPOPTOSIS IN NON-HUMAN PRIMATES
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| 5R01HD052682-03 |
FULLER, DAVID D
UNIVERSITY OF FLORIDA
CONTROL OF BREATHING & GLYCOGEN STORAGE DISEASE
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| 5R01HD052731-02 |
HUBER, KIMBERLY M
UNIVERSITY OF TEXAS SW MED CTR/DALLAS
STUDY OF FRAGILE X MENTAL RETARDATION PROTEIN IN SYNAPTIC FUNCTION AND PLASTICITY
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| 5R01HD052804-02 |
DOBKINS, KAREN R
UNIVERSITY OF CALIFORNIA SAN DIEGO
DEVELOPMENT OF NEURAL PATHWAYS IN INFANTS AT RISK FOR AUTISM SPECTRUM DISORDERS
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| 5R01HD053036-04 |
SHACKLETON, CEDRIC HOWARD
CHILDREN'S HOSPITAL & RES CTR AT OAKLAND
PATHOGENESIS/TREATMENT-INHERITED CHOLESTEROL DEFICIENCY
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| 5R01HD053814-02 |
KLINE, JENNIE KATHERINE
COLUMBIA UNIVERSITY HEALTH SCIENCES
TRISOMY AND OVARIAN AGE: AN EPIDEMIOLOGIC STUDY
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| 5R01HD054453-03 |
PORTERA-CAILLIAU, CARLOS
UNIVERSITY OF CALIFORNIA LOS ANGELES
IMAGING THE ORIGIN OF DENDRITIC SPINE ABNORMALITIES IN FRAGILE X MICE
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| 5R01HD054744-03 |
LAI, KENT
UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
INNOVATIVE THERAPIES AND CLINICAL STUDIES FOR CLASSIC GALACTOSEMIA
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| 5R01HD054764-02 |
ABBEDUTO, LEONARD J
UNIVERSITY OF WISCONSIN MADISON
SOCIAL-AFFECTIVE BASES OF WORD LEARNING IN FRAGILE X SYNDROME AND AUTISM
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| 5R01HD054905-03 |
BROWN, STEPHEN A
UNIVERSITY OF VERMONT & ST AGRIC COLLEGE
PRENATAL DIAGNOSIS THROUGH SELECTIVE DNA AMPLIFICATION
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| 5R01HD054979-03 |
IVERSON, JANA M
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
EARLY IDENTIFICATION OF AUTISM: A PROSPECTIVE STUDY
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| 5R01HD055391-02 |
CRABTREE, GERALD R.
STANFORD UNIVERSITY
NFAT SIGNALING AND DOWN SYNDROME
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| 5R01HD055461-03 |
SANDS, MARK S
WASHINGTON UNIVERSITY
NOVEL THERAPIES FOR GLOBOID-CELL LEUKODYSTROPHY
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| 5R01HD056235-02 |
GARDINER, KATHELEEN
UNIVERSITY OF COLORADO DENVER
SYSTEMS BIOLOGY FOR STUDIES OF COGNITION IN DOWN SYNDROME
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| 5R01HD056503-02 |
MANDEL, GAIL
OREGON HEALTH AND SCIENCE UNIVERSITY
NEURONAL: GLIAL INTERACTIONS UNDERLYING RETT SYNDROME
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| 5R01HD057564-02 |
STRUPP, BARBARA J
CORNELL UNIVERSITY ITHACA
PERINATAL CHOLINE THERAPY IN A MOUSE MODEL OF DOWN SYNDROME & ALZHEIMER'S DISEASE
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| 5R01MH081754-02 |
GESCHWIND, DANIEL H
UNIVERSITY OF CALIFORNIA LOS ANGELES
A COMPREHENSIVE APPROACH TO IDENTIFICATION OF AUTISM SUSCEPTIBILITY GENES
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| |
| R03 - Small Research Grants |
| Project Number |
Description |
| 1R03HD057292-01A1 |
MERRILL, EDWARD C
UNIVERSITY OF ALABAMA IN TUSCALOOSA
WAYFINDING SKILLS OF PERSONS WITH DOWN SYNDROME
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| 3R03HD058220-02S1 |
WEISS, ROBERT S
CORNELL UNIVERSITY ITHACA
COOPERATIVE ROLES FOR ATM AND HUS1 IN GENOME MAINTENANCE
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| 5R03HD054507-02 |
RAKISON, DAVID H
CARNEGIE-MELLON UNIVERSITY
PRECURSORS OF THEORY OF MIND IN YOUNG CHILDREN WITH AUTISM
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| 5R03HD057244-02 |
HECK, DETLEF H.
UNIVERSITY OF TENNESSEE HEALTH SCI CTR
ROLE OF INHIBITION IN SHAPING NEOCORTICAL ACTIVITY: NORMAL VS FMR1 KNOCKOUT MOUSE
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| 5R03HD057321-02 |
WEBB, SARA JANE
UNIVERSITY OF WASHINGTON
NEURAL CORRELATES OF EYE GAZE PROCESSING IN FRAGILE X SYNDROME AND AUTISM SPECTRU
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| 5R03HD057560-02 |
DE VELLIS, JEAN
UNIVERSITY OF CALIFORNIA LOS ANGELES
EARLY INTERVENTION TO RESTORE OL AND MYELIN DEVELOPMENT IN LEUKODYSTROPHY MODEL
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| 5R03HD058220-02 |
WEISS, ROBERT S
CORNELL UNIVERSITY ITHACA
COOPERATIVE ROLES FOR ATM AND HUS1 IN GENOME MAINTENANCE
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| R13 - Conferences |
| Project Number |
Description |
| 1R13HD061140-01 |
RAUEN, KATHERINE ANNA
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
GENETIC SYNDROMES OF THE RAS/MAPK PATHWAY: FROM BEDSIDE TO BENCH AND BACK
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| 1R13MH085352-01 |
ROBERTSON, ANDREW D
KEYSTONE SYMPOSIA
EPIGENETIC BASIS OF NEURODEVELOPMENTAL DISORDERS
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| 1R13NS065534-01 |
POLLEUX, FRANCK
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
WIRING THE BRAIN: FROM GENETIC TO NEURONAL NETWORKS
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| 1R13NS065535-01 |
OSORIO, IVAN
UNIVERSITY OF KANSAS MEDICAL CENTER
FOURTH INTERNATIONAL SEIZURE PREDICTION WORKSHOP
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| 2R13HD048170-06 |
GOLDEN, JEFFREY A
CHILDREN'S HOSPITAL OF PHILADELPHIA
DAVID W. SMITH WORKSHOP ON MALFORMATIONS AND MORPHOGENESIS
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| 5R13HD038335-11 |
SELTZER, MARSHA MAILICK
UNIVERSITY OF WISCONSIN MADISON
THE GATLINBURG CONFERENCE ON RESEARCH IN ID/DD
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| 5R13MH063153-09 |
GREENOUGH, WILLIAM T
UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN
FRAGILE X SYNDROME: BANBURY CONFERENCES
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| 5R13MH070772-06 |
ROGERS, SALLY J
UNIVERSITY OF CALIFORNIA DAVIS
INTERNATIONAL MEETING FOR AUTISM RESEARCH (IMFAR)
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| 5R13MH072277-03 |
CHASE, MICHAEL H
WEBSCIENCES INTERNATIONAL
TRAINING WORKSHOPS IN BASIC SLEEP RESEARCH
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| 5R13MH079632-03 |
SPRUSTON, NELSON P.
GORDON RESEARCH CONFERENCES
2006 DENDRITES: MOLECULES, STRUCTURE AND FUNCTION (GORDON RESEARCH CONFERENCE)
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| R21 - Exploratory/Developmental Grants |
| Project Number |
Description |
| 1R21HD055178-01A2 |
MOSES, PAMELA A
UNIVERSITY OF CALIFORNIA SAN DIEGO
ASSESSMENT OF COGNITIVE NEURODEVELOPMENT IN CHILDREN WITH CEREBRAL PALSY IN CHINA
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| 1R21HD056293-01A2 |
KIPNIS, JONATHAN
UNIVERSITY OF VIRGINIA CHARLOTTESVILLE
IMMUNE SYSTEM IN RETT SYNDROME
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| 1R21HD059823-01 |
GRABOWSKI, GREGORY A.
CHILDREN'S HOSPITAL MED CTR (CINCINNATI)
THERAPY OF NEURONOPATHIC GAUCHER DISEASE
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| 1R21HD060120-01 |
SOBIN, CHRISTINA
UNIVERSITY OF TEXAS EL PASO
LEAD, GENES, AND COGNITION IN UNDERSERVED CHILDREN
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| 1R21HD060909-01 |
GANGWANI, LAXMAN DASS
MEDICAL COLLEGE OF GEORGIA (MCG)
ANIMAL MODELS TO EXAMINE ROLE OF ZPR1 PROTEIN COMPLEXES
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| 1R21HD060959-01 |
JIANG, CHUN
GEORGIA STATE UNIVERSITY
POSTNATAL CCR DISRUPTION IN MECP2-DEFECTIVE MICE
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| 5R21HD053114-02 |
HIROI, NOBORU
YESHIVA UNIVERSITY
22Q11 GENES AND COMPLEX BEHAVIOR IN MICE
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| 5R21HD054347-02 |
SHEEN, VOLNEY L
BETH ISRAEL DEACONESS MEDICAL CENTER
HUMAN NEURAL PRECURSORS FROM CNS DEVELOPMENTAL DISORDERS: DOWN SYNDROME
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| 5R21HD055550-02 |
MAYER-PROSCHEL, MARGOT
UNIVERSITY OF ROCHESTER
GLIAL DYSFUNCTION IN ATAXIA TELANGIECTASIA
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| 5R21HD057488-02 |
RONCA, APRIL ELIZABETH
WAKE FOREST UNIVERSITY HEALTH SCIENCES
APPLICATION OF MR SPECTROSCOPY TECHNIQUES TO ANIMAL MODELS OF OBSTETRIC COMPLICAT
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| 5R21HD058196-02 |
CHEN, CHINFEI
CHILDREN'S HOSPITAL BOSTON
SYNAPSE REMODELING IN MECP2 MOUSE MODELS
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| 5R21HD058207-02 |
MCCARTHY, KEN D
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
ANALYSIS OF GENOMIC AND PROTEOMIC CHANGES IN GLIA THAT LEAD TO HYDROCEPHALUS
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| |
| R34 - Clinical Trial Planning Grant |
| Project Number |
Description |
| 1R34HD057967-01A1 |
MAHONEY, GERALD J
CASE WESTERN RESERVE UNIVERSITY
A RANDOMIZED CONTROL STUDY OF RELATIONSHIP FOCUSED INTERVENTION WITH YOUNG CHILDR
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| |
| R37 - Method to Extend Research in Time (MERIT) Award |
| Project Number |
Description |
| 4R37HD029957-17 |
MERVIS, CAROLYN B.
UNIVERSITY OF LOUISVILLE
EARLY DEVELOPMENT WITH WILLIAMS OR DOWN SYNDROME
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| |
| R41 - Small Business Technology Transfer (STTR) Grants - Phase I |
| Project Number |
Description |
| 1R41HD061163-01 |
CHEN, LIANGJING
AMBION DIAGNOSTICS, INC.
SINGLE MOLECULE FLUORESCENCE DETECTION OF FRAGILE X MUTATIONS
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| |
| T32 - Institutional National Research Service Award |
| Project Number |
Description |
| 1T32HD057844-01A1 |
SAUNDERS, KATHRYN J
UNIVERSITY OF KANSAS LAWRENCE
POSTDOCTORAL TRAINING IN TRANSLATIONAL IDD RESEARCH
|
| 5T32HD007149-32 |
LIFTON, RICHARD P
YALE UNIVERSITY
GENETICS AND GENOMICS OF HUMAN DISEASE
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| 5T32HD007473-15 |
QUITTNER, ALEXANDRA L
UNIVERSITY OF MIAMI CORAL GABLES
TRAINING-MENTAL RETARDATION/DEVELOPMENTAL DISABILITIES
|
| 5T32HD007489-15 |
ABBEDUTO, LEONARD J
UNIVERSITY OF WISCONSIN MADISON
POSTDOCTORAL TRAINING IN MENTAL RETARDATION RESEARCH
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| 5T32HD046388-04 |
GALLO, VITTORIO
CHILDREN'S RESEARCH INSTITUTE
POSTDOCTORAL TRAINING IN DEVELOPMENTAL DISABILITIES RESEARCH
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