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Results: 1-21 |
Results: 21
EVALUATION OF GD-DOTA-LABELED DEXTRAN POLYMER AS AN INTRAVASCULAR MR CONTRAST AGENT FOR MYOCARDIAL PERFUSION
Authors: CASALI C JANIER M CANET E OBADIA JF BENDERBOUS S COROT C REVEL D
Citation: C. Casali et al., EVALUATION OF GD-DOTA-LABELED DEXTRAN POLYMER AS AN INTRAVASCULAR MR CONTRAST AGENT FOR MYOCARDIAL PERFUSION, Academic radiology, 5, 1998, pp. 214-218
CLINICAL AND MOLECULAR CORRELATIONS IN PROGRESSIVE EXTERNAL OPHTHALMOPARESIS WITH MULTIPLE MTDNA DELETIONS
Authors: CARROZZO R SANTORO L CASALI C SANTORELLI FM
Citation: R. Carrozzo et al., CLINICAL AND MOLECULAR CORRELATIONS IN PROGRESSIVE EXTERNAL OPHTHALMOPARESIS WITH MULTIPLE MTDNA DELETIONS, European journal of human genetics, 6, 1998, pp. 1002-1002
ATYPICAL CLINICAL AND MOLECULAR PRESENTATION OF THE MTDNA A3243G MUTATION
Authors: DEJOANNA G CASALI C SANTORO L PERRETTI A SANTORELLI FM
Citation: G. Dejoanna et al., ATYPICAL CLINICAL AND MOLECULAR PRESENTATION OF THE MTDNA A3243G MUTATION, European journal of human genetics, 6, 1998, pp. 1003-1003
THE RISING ROLE OF MTDNA MUTATIONS IN LETHAL INFANTILE CARDIOMYOPATHIES
Authors: SANTORELLI FM BRUNO C CASALI C SHANSKE S HIRANO M DIMAURO S
Citation: Fm. Santorelli et al., THE RISING ROLE OF MTDNA MUTATIONS IN LETHAL INFANTILE CARDIOMYOPATHIES, European journal of human genetics, 6, 1998, pp. 4080-4080
GENETIC-HETEROGENEITY OF MYOCLONUS EPILEPSY WITH RAGGED-RED FIBERS SYNDROME
Authors: SANTORELLI FM CASALI C
Citation: Fm. Santorelli et C. Casali, GENETIC-HETEROGENEITY OF MYOCLONUS EPILEPSY WITH RAGGED-RED FIBERS SYNDROME, Muscle & nerve, 21(5), 1998, pp. 681-682
MULTIPLE MTDNA DELETIONS FEATURES IN AUTOSOMAL-DOMINANT AND RECESSIVEDISEASES SUGGEST DISTINCT PATHOGENESES
Authors: CARROZZO R HIRANO M FROMENTY B CASALI C SANTORELLI FM BONILLA E DIMAURO S SCHON EA MIRANDA AF
Citation: R. Carrozzo et al., MULTIPLE MTDNA DELETIONS FEATURES IN AUTOSOMAL-DOMINANT AND RECESSIVEDISEASES SUGGEST DISTINCT PATHOGENESES, Neurology, 50(1), 1998, pp. 99-106
MITOCHONDRIAL TRNA(CYS) GENE MUTATION (A5814G) - A 2ND FAMILY WITH MITOCHONDRIAL ENCEPHALOPATHY
Authors: SANTORELLI FM SICILIANO G CASALI C BASIRICO MG CARROZZO R CALVOSA F SARTUCCI F BONFIGLIO L MURRI L DIMAURO S
Citation: Fm. Santorelli et al., MITOCHONDRIAL TRNA(CYS) GENE MUTATION (A5814G) - A 2ND FAMILY WITH MITOCHONDRIAL ENCEPHALOPATHY, Neuromuscular disorders, 7(3), 1997, pp. 156-159
DESIGN OF AN ISOLATED PIG-HEART PREPARATION FOR POSITRON-EMISSION-TOMOGRAPHY AND MAGNETIC-RESONANCE-IMAGING
Authors: CASALI C OBADIA JF CANET E BENDJELID K ANDREFOUET X REVEL D JANIER MF
Citation: C. Casali et al., DESIGN OF AN ISOLATED PIG-HEART PREPARATION FOR POSITRON-EMISSION-TOMOGRAPHY AND MAGNETIC-RESONANCE-IMAGING, Investigative radiology, 32(11), 1997, pp. 713-720
MITRAL SUBVALVULAR APPARATUS - DIFFERENT FUNCTIONS OF PRIMARY AND SECONDARY CHORDAE
Authors: OBADIA JF CASALI C CHASSIGNOLLE JF JANIER M
Citation: Jf. Obadia et al., MITRAL SUBVALVULAR APPARATUS - DIFFERENT FUNCTIONS OF PRIMARY AND SECONDARY CHORDAE, Circulation, 96(9), 1997, pp. 3124-3128
DEFECT-11 SYNDROME - REPORT OF A NEW FAMILY WITH UNUSUAL NEUROLOGICALMANIFESTATIONS
Authors: CASALI C WUYTS W DIGENNARO G VANHUL W FORTINI D SPADARO M PIERELLI F WILLEMS P MOROCUTTI C
Citation: C. Casali et al., DEFECT-11 SYNDROME - REPORT OF A NEW FAMILY WITH UNUSUAL NEUROLOGICALMANIFESTATIONS, American journal of human genetics, 61(4), 1997, pp. 518-518
MULTIPLE SYMMETRICAL LIPOMATOSIS IN MITOCHONDRIAL DISORDERS
Authors: DIGENNARO G SANTORELLI FM TOLLI VS SCOPPETTA C PIERELLI C SPADARO M CASALI C
Citation: G. Digennaro et al., MULTIPLE SYMMETRICAL LIPOMATOSIS IN MITOCHONDRIAL DISORDERS, American journal of human genetics, 61(4), 1997, pp. 1793-1793
MATERNALLY INHERITED CARDIOMYOPATHY - AN ATYPICAL CLINICAL PRESENTATION OF THE MITOCHONDRIAL-DNA A1555G MUTATION
Authors: SANTORELLI FM DIMAURO S TANJI K CASALI C ADDONIZIO L MANCINI D HIRANO M
Citation: Fm. Santorelli et al., MATERNALLY INHERITED CARDIOMYOPATHY - AN ATYPICAL CLINICAL PRESENTATION OF THE MITOCHONDRIAL-DNA A1555G MUTATION, Neurology, 46(2), 1996, pp. 3010-3010
MULTIPLE MITOCHONDRIAL-DNA REARRANGEMENTS IN MITOCHONDRIAL DISEASES
Authors: CARROZZO R FROMENTY B CASALI C SANTORELLI FM HIRANO M DIMAURO S SCHON EA MIRANDA AF
Citation: R. Carrozzo et al., MULTIPLE MITOCHONDRIAL-DNA REARRANGEMENTS IN MITOCHONDRIAL DISEASES, Neurology, 46(2), 1996, pp. 60001-60001
NOVEL MTDNA POINT MUTATION IN MATERNALLY INHERITED CARDIOMYOPATHY
Authors: DAMATI G CASALI C SANTORELLI FM GALLO P DIMAURO S DEBIASE L LAURENTI A BERNUCCI P
Citation: G. Damati et al., NOVEL MTDNA POINT MUTATION IN MATERNALLY INHERITED CARDIOMYOPATHY, Laboratory investigation, 74(1), 1996, pp. 147-147
MATERNALLY INHERITED CARDIOMYOPATHY AND HEARING-LOSS ASSOCIATED WITH A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(LYS) GENE (G8363A)
Authors: SANTORELLI FM MAK SC ELSCHAHAWI M CASALI C SHANSKE S BARAM TZ MADRID RE DIMAURO S
Citation: Fm. Santorelli et al., MATERNALLY INHERITED CARDIOMYOPATHY AND HEARING-LOSS ASSOCIATED WITH A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(LYS) GENE (G8363A), American journal of human genetics, 58(5), 1996, pp. 933-939
A NOVEL MTDNA MUTATION ASSOCIATED WITH HUMAN CARDIOMYOPATHY
Authors: SANTORELLI FM ELSHAHAWI M SHANSKE S CASALI C BARAM TZ MADRID RE DIMAURO S
Citation: Fm. Santorelli et al., A NOVEL MTDNA MUTATION ASSOCIATED WITH HUMAN CARDIOMYOPATHY, Circulation, 92(8), 1995, pp. 1107-1107
A NOVEL MTDNA POINT MUTATION IN MATERNALLY INHERITED CARDIOMYOPATHY
Authors: CASALI C SANTORELLI FM DAMATI G BERNUCCI P DEBIASE L DIMAURO S
Citation: C. Casali et al., A NOVEL MTDNA POINT MUTATION IN MATERNALLY INHERITED CARDIOMYOPATHY, Biochemical and biophysical research communications, 213(2), 1995, pp. 588-593
INFANTILE AUTOSOMAL-DOMINANT DISTAL MYOPATHY
Authors: SCOPPETTA C CASALI C LACESA I SERMONI A MERCURI B PIERELLI F VACCARIO ML
Citation: C. Scoppetta et al., INFANTILE AUTOSOMAL-DOMINANT DISTAL MYOPATHY, Acta neurologica Scandinavica, 92(2), 1995, pp. 122-126
MITOCHONDRIAL-DNA DEPLETION - AN AUTOSOMAL RECESSIVE, TISSUE-SPECIFICDISORDER
Authors: SHANSKE S DANON MJ BONILLA E CASALI C MORAES CT GRIFFIN A DIMAURO S
Citation: S. Shanske et al., MITOCHONDRIAL-DNA DEPLETION - AN AUTOSOMAL RECESSIVE, TISSUE-SPECIFICDISORDER, Neurology, 44(4), 1994, pp. 10000403-10000403
PATHOPHYSIOLOGY OF HEMIMASTICATORY SPASM
Authors: CRUCCU G INGHILLERI M BERARDELLI A PAULETTI G CASALI C CORATTI P FRISARDI G THOMPSON PD MANFREDI M
Citation: G. Cruccu et al., PATHOPHYSIOLOGY OF HEMIMASTICATORY SPASM, Journal of Neurology, Neurosurgery and Psychiatry, 57(1), 1994, pp. 43-50
FAMILIAL OCCURRENCE OF A SYNDROME RESEMBLING SUBACUTE COMBINED DEGENERATION - A NEW INHERITED DISORDER OF COBALAMIN METABOLISM
Authors: SCOPPETTA C PEPPE A SERMONI A SCIORTINO GR CASALI C
Citation: C. Scoppetta et al., FAMILIAL OCCURRENCE OF A SYNDROME RESEMBLING SUBACUTE COMBINED DEGENERATION - A NEW INHERITED DISORDER OF COBALAMIN METABOLISM, Neurology, 43(4), 1993, pp. 217-217
Risultati: 1-21 |