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Results: 1-25 | 26-50 | 51-58
Results: 1-25/58
DISPARITY IN EXPRESSION OF PROTEIN-KINASE-C-ALPHA IN HUMAN GLIOMA VERSUS GLIOMA-DERIVED PRIMARY-CELL LINES - THERAPEUTIC IMPLICATIONS
Authors: ZELLNER A FETELL MR BRUCE JN DEVIVO DC ODRISCOLL KR
Citation: A. Zellner et al., DISPARITY IN EXPRESSION OF PROTEIN-KINASE-C-ALPHA IN HUMAN GLIOMA VERSUS GLIOMA-DERIVED PRIMARY-CELL LINES - THERAPEUTIC IMPLICATIONS, Clinical cancer research, 4(7), 1998, pp. 1797-1802
GLUT-1 DEFICIENCY SYNDROME CAUSED BY HAPLOINSUFFICIENCY OF THE BLOOD-BRAIN-BARRIER HEXOSE CARRIER
Authors: SEIDNER G ALVAREZ MG YEH JI ODRISCOLL KR KLEPPER J STUMP TS WANG D SPINNER NB BIRNBAUM MJ DEVIVO DC
Citation: G. Seidner et al., GLUT-1 DEFICIENCY SYNDROME CAUSED BY HAPLOINSUFFICIENCY OF THE BLOOD-BRAIN-BARRIER HEXOSE CARRIER, Nature genetics, 18(2), 1998, pp. 188-191
NEONATAL BLOOD CARNITINE CONCENTRATIONS - ESTABLISHING NORMATIVE VALUES
Authors: DEVIVO DC KWAN A MCMAHON D CHIRIBOGA CA NAYLOR EW CHACE DH
Citation: Dc. Devivo et al., NEONATAL BLOOD CARNITINE CONCENTRATIONS - ESTABLISHING NORMATIVE VALUES, Annals of neurology, 44(3), 1998, pp. 26-26
BALLISTIC MOVEMENT DISORDER ASSOCIATED WITH LOW CEREBROSPINAL-FLUID HOMOVANILLIC-ACID - A DEFECT IN THE DOPAMINE TRANSPORTER
Authors: HYLAND K CHANG YT ARNOLD LA FORD B DEVIVO DC
Citation: K. Hyland et al., BALLISTIC MOVEMENT DISORDER ASSOCIATED WITH LOW CEREBROSPINAL-FLUID HOMOVANILLIC-ACID - A DEFECT IN THE DOPAMINE TRANSPORTER, Annals of neurology, 44(3), 1998, pp. 32-32
COMPARATIVE CLINICAL ANALYSIS OF MITOCHONDRIAL ENCEPHALOMYOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES AND MYOCLONIC EPILEPSY AND RAGGED-RED FIBERS
Authors: SANO M POLANCO Y DEVIVO DC
Citation: M. Sano et al., COMPARATIVE CLINICAL ANALYSIS OF MITOCHONDRIAL ENCEPHALOMYOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES AND MYOCLONIC EPILEPSY AND RAGGED-RED FIBERS, Annals of neurology, 44(3), 1998, pp. 48-48
INFANTILE ENCEPHALOPATHY ASSOCIATED WITH THE MELAS A3243G MUTATION
Authors: SUE CM BRUNO C ANDREU AL CARGAN A MENDELL JR TSAO CY SHANSKE S DIMAURO S DEVIVO DC
Citation: Cm. Sue et al., INFANTILE ENCEPHALOPATHY ASSOCIATED WITH THE MELAS A3243G MUTATION, Annals of neurology, 44(3), 1998, pp. 61-61
CYTOCHROME-C-OXIDASE DEFICIENCY IN THE MICROVASCULATURE OF CORTICAL REGIONS OF MELAS-3243 BRAINS
Authors: TANJI K SCHON EA DEVIVO DC DIMAURO S BONILLA E
Citation: K. Tanji et al., CYTOCHROME-C-OXIDASE DEFICIENCY IN THE MICROVASCULATURE OF CORTICAL REGIONS OF MELAS-3243 BRAINS, Annals of neurology, 44(3), 1998, pp. 70-70
DEFICIENT TRANSPORT OF DEHYDROASCORBIC ACID IN THE GLUCOSE-TRANSPORTER PROTEIN SYNDROME
Authors: KLEPPER J VERA JC DEVIVO DC
Citation: J. Klepper et al., DEFICIENT TRANSPORT OF DEHYDROASCORBIC ACID IN THE GLUCOSE-TRANSPORTER PROTEIN SYNDROME, Annals of neurology, 44(2), 1998, pp. 286-287
COMPLEXITIES OF THE PYRUVATE-DEHYDROGENASE COMPLEX
Authors: DEVIVO DC
Citation: Dc. Devivo, COMPLEXITIES OF THE PYRUVATE-DEHYDROGENASE COMPLEX, Neurology, 51(5), 1998, pp. 1247-1249
CLINICAL MANIFESTATIONS OF MITOCHONDRIAL-DNA DEPLETION
Authors: VU TH SCIACCO M TANJI K NICHTER C BONILLA E CHATKUPT S MAERTENS P SHANSKE S MENDELL J KOENIGSBERGER MR SHARER L SCHON EA DIMAURO S DEVIVO DC
Citation: Th. Vu et al., CLINICAL MANIFESTATIONS OF MITOCHONDRIAL-DNA DEPLETION, Neurology, 50(6), 1998, pp. 1783-1790
GTPS - DEFINING A NEW SYNDROME
Authors: KLEPPER J WANG D ALVAREZ MG HINTON VJ NORDLI DR ODRISCOLL KR DEVIVO DC
Citation: J. Klepper et al., GTPS - DEFINING A NEW SYNDROME, Neurology, 50(4), 1998, pp. 3001-3001
L-CARNITINE SUPPLEMENTATION IN CHILDHOOD EPILEPSY - CURRENT PERSPECTIVES
Authors: DEVIVO DC BOHAN TP COULTER DL DREIFUSS FE GREENWOOD RS NORDLI DR SHIELDS D STAFSTROM CE TEIN I
Citation: Dc. Devivo et al., L-CARNITINE SUPPLEMENTATION IN CHILDHOOD EPILEPSY - CURRENT PERSPECTIVES, Epilepsia, 39(11), 1998, pp. 1216-1225
MITOCHONDRIAL MORPHOLOGY AND INTRACELLULAR CALCIUM HOMEOSTASIS IN CYTOCHROME OXIDASE-DEFICIENT HUMAN FIBROBLASTS
Authors: HANDRAN SD WERTH JL DEVIVO DC ROTHMAN SM
Citation: Sd. Handran et al., MITOCHONDRIAL MORPHOLOGY AND INTRACELLULAR CALCIUM HOMEOSTASIS IN CYTOCHROME OXIDASE-DEFICIENT HUMAN FIBROBLASTS, Neurobiology of disease, 3(4), 1997, pp. 287-298
MATERNALLY INHERITED ENCEPHALOPATHY ASSOCIATED WITH A SINGLE-BASE INSERTION IN THE MITOCHONDRIAL TRNA(TRP) GENE
Authors: SANTORELLI FM TANJI K SANO M SHANSKE S ELSHAHAWI M KRANZEBLE P DIMAURO S DEVIVO DC
Citation: Fm. Santorelli et al., MATERNALLY INHERITED ENCEPHALOPATHY ASSOCIATED WITH A SINGLE-BASE INSERTION IN THE MITOCHONDRIAL TRNA(TRP) GENE, Annals of neurology, 42(2), 1997, pp. 256-260
DEFICIENT MUSCLE CARNITINE TRANSPORT IN PRIMARY CARNITINE DEFICIENCY
Authors: PONS R CARROZZO R TEIN I WALKER WF ADDONIZIO LJ RHEAD W MIRANDA AF DIMAURO S DEVIVO DC
Citation: R. Pons et al., DEFICIENT MUSCLE CARNITINE TRANSPORT IN PRIMARY CARNITINE DEFICIENCY, Pediatric research, 42(5), 1997, pp. 583-587
INCREASED SENSITIVITY TO OLIGOMYCIN OF FIBROBLASTS HARBORING THE MTDNA T8993G (NARP MILS) MUTATION/
Authors: MANFREDI G VAZQUEZMEMIJE ME SADLOCK J SANTORELLI FM DEVIVO DC SCHON EA
Citation: G. Manfredi et al., INCREASED SENSITIVITY TO OLIGOMYCIN OF FIBROBLASTS HARBORING THE MTDNA T8993G (NARP MILS) MUTATION/, Neurology, 48(3), 1997, pp. 4084-4084
BOYS WITH DUCHENNE MUSCULAR-DYSTROPHY HAVE IMPAIRED AUDITORY COMPREHENSION OF COMPLEX VERBAL MATERIAL
Authors: HINTON VJ NEREO NE STERN Y DEVIVO DC
Citation: Vj. Hinton et al., BOYS WITH DUCHENNE MUSCULAR-DYSTROPHY HAVE IMPAIRED AUDITORY COMPREHENSION OF COMPLEX VERBAL MATERIAL, Neurology, 48(3), 1997, pp. 5002-5002
CHARACTERIZATION OF THE HUMAN PYRUVATE-CARBOXYLASE GENE
Authors: ODRISCOLL KR ALVAREZ MBG WANG D PONS R KRANZEBLE PJ DEVIVO DC
Citation: Kr. Odriscoll et al., CHARACTERIZATION OF THE HUMAN PYRUVATE-CARBOXYLASE GENE, Neurology, 48(3), 1997, pp. 6002-6002
THE KETOGENIC DIET REVISITED - BACK TO THE FUTURE
Authors: NORDLI DR DEVIVO DC
Citation: Dr. Nordli et Dc. Devivo, THE KETOGENIC DIET REVISITED - BACK TO THE FUTURE, Epilepsia, 38(7), 1997, pp. 743-749
MITOCHONDRIAL MYOPATHY SIMULATING SPINAL MUSCULAR-ATROPHY
Authors: PONS R ANDREETTA F WANG CH VU TH BONILLA E DIMAURO S DEVIVO DC
Citation: R. Pons et al., MITOCHONDRIAL MYOPATHY SIMULATING SPINAL MUSCULAR-ATROPHY, Pediatric neurology, 15(2), 1996, pp. 153-158
PYRUVATE-DEHYDROGENASE DEFICIENCY - THE RELATION OF THE E1-ALPHA MUTATION TO THE E1-BETA SUBUNIT DEFICIENCY
Authors: FUJII T ALVAREZ MBG SHEU KFR KRANZEBLE PJ DEVIVO DC
Citation: T. Fujii et al., PYRUVATE-DEHYDROGENASE DEFICIENCY - THE RELATION OF THE E1-ALPHA MUTATION TO THE E1-BETA SUBUNIT DEFICIENCY, Pediatric neurology, 14(4), 1996, pp. 328-334
CLINICAL AND MOLECULAR ANALYSIS OF PYRUVATE-DEHYDROGENASE DEFICIENCY
Authors: ALVAREZ MG FUJII T DEVIVO DC
Citation: Mg. Alvarez et al., CLINICAL AND MOLECULAR ANALYSIS OF PYRUVATE-DEHYDROGENASE DEFICIENCY, Annals of neurology, 40(2), 1996, pp. 15-15
DOES DICHLOROACETATE MINIMIZE THE NEUROTOXICITY OF CHRONIC CEREBRAL ACIDOSIS
Authors: DEVIVO DC SHUNGU D MILLAR W DIMAURO S
Citation: Dc. Devivo et al., DOES DICHLOROACETATE MINIMIZE THE NEUROTOXICITY OF CHRONIC CEREBRAL ACIDOSIS, Annals of neurology, 40(2), 1996, pp. 126-126
ADIE-HOLMES PUPILS, MOTOR AND SENSORY NEUROPATHY, PYRAMIDAL TRACT INVOLVEMENT AND AUTOSOMIC DYSFUNCTION IN A FAMILY
Authors: HAENGGELI CA DEVIVO DC
Citation: Ca. Haenggeli et Dc. Devivo, ADIE-HOLMES PUPILS, MOTOR AND SENSORY NEUROPATHY, PYRAMIDAL TRACT INVOLVEMENT AND AUTOSOMIC DYSFUNCTION IN A FAMILY, Annals of neurology, 40(2), 1996, pp. 164-164
GENETIC-HETEROGENEITY IN LEIGH-SYNDROME
Authors: DIMAURO S DEVIVO DC
Citation: S. Dimauro et Dc. Devivo, GENETIC-HETEROGENEITY IN LEIGH-SYNDROME, Annals of neurology, 40(1), 1996, pp. 5-7
Risultati: 1-25 | 26-50 | 51-58