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Results: 1-25/28
Authors:
EHIRIM PU
KERR DS
COHEN AR
Citation: Pu. Ehirim et al., PRIMARY HYPOTHYROIDISM MIMICKING A PITUITARY MACROADENOMA, Pediatric neurosurgery, 28(4), 1998, pp. 195-197
Authors:
WEXLER ID
KERR DS
DU YF
KAUNG MM
STEPHENSON W
LUSK MM
WAPPNER RS
HIGGINS JJ
Citation: Id. Wexler et al., MOLECULAR CHARACTERIZATION OF PYRUVATE-CARBOXYLASE DEFICIENCY IN 2 CONSANGUINEOUS FAMILIES, Pediatric research, 43(5), 1998, pp. 579-584
Authors:
CAFFREY M
KERR DS
FENG L
KOYNOVA R
DING L
Citation: M. Caffrey et al., LIPIDAT - A WEB-BASED RELATIONAL DATABASE OF LIPID PHASE-TRANSITION TYPES, TEMPERATURES, ENTHALPY CHANGES AND MOLECULAR-STRUCTURES, Biophysical journal, 74(2), 1998, pp. 315-315
Authors:
KERR DS
Citation: Ds. Kerr, PROTEAN MANIFESTATIONS OF MITOCHONDRIAL DISEASES - A MINIREVIEW, Journal of pediatric hematology/oncology, 19(4), 1997, pp. 279-286
Authors:
HONG YS
KERR DS
LIU TC
LUSK M
POWELL BR
PATEL MS
Citation: Ys. Hong et al., DEFICIENCY OF DIHYDROLIPOAMIDE DEHYDROGENASE DUE TO 2 MUTANT ALLELES (E340K AND G101DEL) - ANALYSIS OF A FAMILY AND PRENATAL TESTING, Biochimica et biophysica acta. Molecular basis of disease, 1362(2-3), 1997, pp. 160-168
Authors:
HONG YS
LIU TC
KERR DS
LUSK M
POWELL B
PATEL MS
Citation: Ys. Hong et al., DEFICIENCY OF DIHYDROLIPOAMIDE DEHYDROGENASE DUE TO 2 MUTANT ALLELES (E240K AND G101DEL), The FASEB journal, 11(9), 1997, pp. 515-515
Authors:
WEXLER ID
HEMALATHA SG
MCCONNELL J
BUIST NRM
DAHL HHM
BERRY SA
CEDERBAUM SD
PATEL MS
KERR DS
Citation: Id. Wexler et al., OUTCOME OF PYRUVATE-DEHYDROGENASE DEFICIENCY TREATED WITH KETOGENIC DIETS - STUDIES IN PATIENTS WITH IDENTICAL MUTATIONS, Neurology, 49(6), 1997, pp. 1655-1661
Authors:
COUSSENS CM
KERR DS
ABRAHAM WC
Citation: Cm. Coussens et al., GLUCOCORTICOID RECEPTOR ACTIVATION LOWERS THE THRESHOLD FOR NMDA-RECEPTOR-DEPENDENT HOMOSYNAPTIC LONG-TERM DEPRESSION IN THE HIPPOCAMPUS THROUGH ACTIVATION OF VOLTAGE-DEPENDENT CALCIUM CHANNELS, Journal of neurophysiology, 78(1), 1997, pp. 1-9
Authors:
STACPOOLE PW
BARNES CL
HURBANIS MD
CANNON SL
KERR DS
Citation: Pw. Stacpoole et al., TREATMENT OF CONGENITAL LACTIC-ACIDOSIS WITH DICHLOROACETATE, Archives of Disease in Childhood, 77(6), 1997, pp. 535-541
Authors:
TRIPARARA A
KERR DS
LUSK MM
KOLLI M
TAN J
PATEL MS
Citation: A. Triparara et al., 3 NEW MUTATIONS OF THE PYRUVATE-DEHYDROGENASE ALPHA-SUBUNIT - A POINTMUTATION (M181V), 3-BP DELETION (-R282), AND 16-BP INSERTION FRAMESHIFT (K358SVS-]TVDQS)/, Human mutation, 8(2), 1996, pp. 180-182
Authors:
KERR DS
ABRAHAM WC
Citation: Ds. Kerr et Wc. Abraham, LTD - MANY MEANS TO HOW MANY ENDS, Hippocampus, 6(1), 1996, pp. 30-34
Authors:
HONG YS
KERR DS
CRAIGEN WJ
TAN J
PAN YZ
LUSK M
PATEL MS
Citation: Ys. Hong et al., IDENTIFICATION OF 2 MUTATIONS IN A COMPOUND HETEROZYGOUS CHILD WITH DIHYDROLIPOAMIDE DEHYDROGENASE-DEFICIENCY, Human molecular genetics, 5(12), 1996, pp. 1925-1930
Authors:
GRIFFIN TA
HOSTOFFER RW
TSERNG KY
LEBOVITZ DJ
HOPPEL CL
MOSSER JL
KAPLAN D
KERR DS
Citation: Ta. Griffin et al., PARATHYROID-HORMONE RESISTANCE AND B-CELL LYMPHOPENIA IN PROPIONIC ACIDEMIA, Acta paediatrica, 85(7), 1996, pp. 875-878
Authors:
KARAN V
KERR DS
MURTHY US
VINZE AS
Citation: V. Karan et al., INFORMATION TECHNOLOGY SUPPORT FOR COLLABORATIVE DECISION-MAKING IN AUDITING - AN EXPERIMENTAL INVESTIGATION, Decision support systems, 16(3), 1996, pp. 181-194
Authors:
WEXLER ID
DU YF
KERR DS
STEPHENSON W
KAUNG M
SCHWARTZ S
Citation: Id. Wexler et al., THE GENOMIC STRUCTURE OF HUMAN PYRUVATE-CARBOXYLASE (PC), Pediatric research, 39(4), 1996, pp. 883-883
Authors:
TSERNG KY
GRIFFIN RL
KERR DS
Citation: Ky. Tserng et al., DISTINCTION OF DICARBOXYLIC ACIDURIA DUE TO MEDIUM-CHAIN TRIGLYCERIDEFEEDING FROM THAT DUE TO ABNORMAL FATTY-ACID OXIDATION AND FASTING INCHILDREN, Metabolism, clinical and experimental, 45(2), 1996, pp. 162-167
Authors:
HEMALATHA SG
KERR DS
WEXLER ID
LUSK MM
KAUNG M
DU YF
KOLLI M
SCHELPER RL
PATEL MS
Citation: Sg. Hemalatha et al., PYRUVATE-DEHYDROGENASE COMPLEX DEFICIENCY DUE TO A POINT MUTATION (P188L) WITHIN THE THIAMINE PYROPHOSPHATE BINDING LOOP OF THE E(1)ALPHA SUBUNIT, Human molecular genetics, 4(2), 1995, pp. 315-318
Authors:
KERR DS
SMITH LM
Citation: Ds. Kerr et Lm. Smith, IMPORTANCE OF AND APPROACHES TO INCORPORATING ETHICS INTO THE ACCOUNTING CLASSROOM, Journal of business ethics, 14(12), 1995, pp. 987-995
Authors:
KERR DS
ABRAHAM WC
Citation: Ds. Kerr et Wc. Abraham, COOPERATIVE INTERACTIONS AMONG AFFERENTS GOVERN THE INDUCTION OF HOMOSYNAPTIC LONG-TERM DEPRESSION IN THE HIPPOCAMPUS, Proceedings of the National Academy of Sciences of the United Statesof America, 92(25), 1995, pp. 11637-11641
Authors:
PATEL MS
NAIK S
WEXLER ID
KERR DS
Citation: Ms. Patel et al., GENE-REGULATION AND GENETIC-DEFECTS IN THE PYRUVATE-DEHYDROGENASE COMPLEX, The Journal of nutrition, 125(6), 1995, pp. 1753-1757
Authors:
CHRISTIE BR
KERR DS
ABRAHAM WC
Citation: Br. Christie et al., FLIP SIDE OF SYNAPTIC PLASTICITY - LONG-TERM DEPRESSION MECHANISMS INTHE HIPPOCAMPUS, Hippocampus, 4(2), 1994, pp. 127-135
Authors:
WEXLER ID
DU YF
LISGARIS MV
MANDAL SK
FREYTAG SO
YANG BS
LIU TC
KWON M
PATEL MS
KERR DS
Citation: Id. Wexler et al., PRIMARY AMINO-ACID-SEQUENCE AND STRUCTURE OF HUMAN PYRUVATE-CARBOXYLASE, Biochimica et biophysica acta. Molecular basis of disease, 1227(1-2), 1994, pp. 46-52
Authors:
KERR DS
HUGGETT AM
ABRAHAM WC
Citation: Ds. Kerr et al., MODULATION OF HIPPOCAMPAL LONG-TERM POTENTIATION AND LONG-TERM DEPRESSION BY CORTICOSTEROID RECEPTOR ACTIVATION, Psychobiology, 22(2), 1994, pp. 123-133
Authors:
HIGGINS JJ
GLASGOW AM
LUSK M
KERR DS
Citation: Jj. Higgins et al., MRI, CLINICAL, AND BIOCHEMICAL FEATURES OF PARTIAL PYRUVATE-CARBOXYLASE DEFICIENCY, Journal of child neurology, 9(4), 1994, pp. 436-439
Authors:
HIGGINS JJ
GLASGOW AM
LUSK M
KERR DS
Citation: Jj. Higgins et al., MRI, CLINICAL, AND BIOCHEMICAL FEATURES OF PARTIAL PYRUVATE-CARBOXYLASE DEFICIENCY, Journal of child neurology, 9(4), 1994, pp. 436-439