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Results: 1-25 | 26-32
Results: 1-25/32
PULMONARY MANIFESTATIONS OF GAUCHER-DISEASE - AN INCREASED RISK FOR L444P HOMOZYGOTES
Authors: SANTAMARIA F PARENTI G GUIDI G FILOCAMO M STRISCIUGLIO P GRILLO G FARINA V SARNELLI P RIZZOLO MG ROTONDO A ANDRIA G
Citation: F. Santamaria et al., PULMONARY MANIFESTATIONS OF GAUCHER-DISEASE - AN INCREASED RISK FOR L444P HOMOZYGOTES, American journal of respiratory and critical care medicine, 157(3), 1998, pp. 985-989
DETECTION OF SUBCLINICAL CENTRAL-NERVOUS-SYSTEM ABNORMALITIES IN 2 PATIENTS WITH MUCOLIPIDOSIS-III BY THE USE OF MOTOR AND SOMATOSENSORY-EVOKED POTENTIALS
Authors: TOSCANO E PERRETTI A BALBI P SILVESTRO E ANDRIA G PARENTI G
Citation: E. Toscano et al., DETECTION OF SUBCLINICAL CENTRAL-NERVOUS-SYSTEM ABNORMALITIES IN 2 PATIENTS WITH MUCOLIPIDOSIS-III BY THE USE OF MOTOR AND SOMATOSENSORY-EVOKED POTENTIALS, Neuropediatrics, 29(1), 1998, pp. 40-42
ULTRAFAST 3-DIMENSIONAL ULTRASOUND - APPLICATION TO CAROTID-ARTERY IMAGING
Authors: PALOMBO C KOZAKOVA M MORIZZO C ANDREUCCETTI F TONDINI A PALCHETTI P MIRRA G PARENTI G PANDIAN NG
Citation: C. Palombo et al., ULTRAFAST 3-DIMENSIONAL ULTRASOUND - APPLICATION TO CAROTID-ARTERY IMAGING, Stroke, 29(8), 1998, pp. 1631-1637
MILD PHENOTYPE ASSOCIATED WITH AN INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-1
Authors: MELIS D PERONE L SPERANDEO MP SABBATINO MS TUZZI MR ROMANO A PARENTI G ANDRIA G
Citation: D. Melis et al., MILD PHENOTYPE ASSOCIATED WITH AN INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-1, Journal of Medical Genetics, 35(12), 1998, pp. 1047-1049
STRUCTURE AND MUTATION ANALYSIS OF THE GLYCOGEN-STORAGE-DISEASE TYPE IB GENE
Authors: MARCOLONGO P BARONE V PRIORI G PIROLA B GIGLIO S BIASUCCI G ZAMMARCHI E PARENTI G BURCHELL A BENEDETTI A SORRENTINO V
Citation: P. Marcolongo et al., STRUCTURE AND MUTATION ANALYSIS OF THE GLYCOGEN-STORAGE-DISEASE TYPE IB GENE, FEBS letters, 436(2), 1998, pp. 247-250
A NOVEL MUTATION OF THE BETA-GLUCOCEREBROSIDASE GENE ASSOCIATED WITH NEUROLOGIC MANIFESTATIONS IN 3 SIBS
Authors: PARENTI G FILOCAMO M TITOMANLIO L RIZZOLO G SILVESTRO E PERRETTI A GATTI R ANDRIA G
Citation: G. Parenti et al., A NOVEL MUTATION OF THE BETA-GLUCOCEREBROSIDASE GENE ASSOCIATED WITH NEUROLOGIC MANIFESTATIONS IN 3 SIBS, Clinical genetics, 53(4), 1998, pp. 281-285
REAL-TIME 3-DIMENSIONAL ULTRASOUND FOR ASSESSMENT OF CAROTID-ARTERY STENOSIS - VALIDATION AGAINST ANGIOGRAPHY
Authors: PALOMBO C KOZAKOVA M MORIZZO C PALCHETTI P VASSALLE C ANDREUCCETTI F PARENTI G
Citation: C. Palombo et al., REAL-TIME 3-DIMENSIONAL ULTRASOUND FOR ASSESSMENT OF CAROTID-ARTERY STENOSIS - VALIDATION AGAINST ANGIOGRAPHY, Circulation, 98(17), 1998, pp. 512-512
BIOCHEMICAL-CHARACTERIZATION OF ARYLSULFATASE-E AND FUNCTIONAL-ANALYSIS OF MUTATIONS FOUND IN PATIENTS WITH X-LINKED CHONDRODYSPLASIA PUNCTATA
Authors: DANIELE A PARENTI G DADDIO M ANDRIA G BALLABIO A MERONI G
Citation: A. Daniele et al., BIOCHEMICAL-CHARACTERIZATION OF ARYLSULFATASE-E AND FUNCTIONAL-ANALYSIS OF MUTATIONS FOUND IN PATIENTS WITH X-LINKED CHONDRODYSPLASIA PUNCTATA, American journal of human genetics, 62(3), 1998, pp. 562-572
THE SULFATASE GENE FAMILY
Authors: PARENTI G MERONI G BALLABIO A
Citation: G. Parenti et al., THE SULFATASE GENE FAMILY, Current opinion in genetics & development, 7(3), 1997, pp. 386-391
COMBINED TRANSCRANIAL DOPPLER AND ELECTROPHYSIOLOGIC MONITORING FOR CAROTID ENDARTERECTOMY
Authors: FIORI L PARENTI G MARCONI F
Citation: L. Fiori et al., COMBINED TRANSCRANIAL DOPPLER AND ELECTROPHYSIOLOGIC MONITORING FOR CAROTID ENDARTERECTOMY, Journal of neurosurgical anesthesiology, 9(1), 1997, pp. 11-16
X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA DUE TO A NEW POINT MUTATION OF THE ARSE GENE
Authors: PARENTI G BUTTITTA P MERONI G FRANCO B BERNARD L RIZZOLO MG BRUNETTIPIERRI N BALLABIO A ANDRIA G
Citation: G. Parenti et al., X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA DUE TO A NEW POINT MUTATION OF THE ARSE GENE, American journal of medical genetics, 73(2), 1997, pp. 139-143
PHENYLKETONURIA IN ITALY - DISTINCT DISTRIBUTION PATTERN OF 3 MUTATIONS OF THE PHENYLALANINE-HYDROXYLASE GENE
Authors: GUZZETTA V BONAPACE G DIANZANI I PARENTI G LECORA M GIANNATTASIO S CONCOLINO D STRISCIUGLIO P SEBASTIO G ANDRIA G
Citation: V. Guzzetta et al., PHENYLKETONURIA IN ITALY - DISTINCT DISTRIBUTION PATTERN OF 3 MUTATIONS OF THE PHENYLALANINE-HYDROXYLASE GENE, Journal of inherited metabolic disease, 20(5), 1997, pp. 619-624
CEREBRAL OXIMETRY DURING CAROTID ENDARTERECTOMY
Authors: PARENTI G PAOLI C ORLANDI G MURRI L
Citation: G. Parenti et al., CEREBRAL OXIMETRY DURING CAROTID ENDARTERECTOMY, Stroke, 28(4), 1997, pp. 878-878
SILENT CEREBRAL MICROEMBOLISM IN ASYMPTOMATIC AND SYMPTOMATIC CAROTID-ARTERY STENOSES OF LOW AND HIGH-DEGREE
Authors: ORLANDI G PARENTI G BERTOLUCCI A MURRI L
Citation: G. Orlandi et al., SILENT CEREBRAL MICROEMBOLISM IN ASYMPTOMATIC AND SYMPTOMATIC CAROTID-ARTERY STENOSES OF LOW AND HIGH-DEGREE, European neurology, 38(1), 1997, pp. 39-43
CAROTID PLAQUE FEATURES ON ANGIOGRAPHY AND ASYMPTOMATIC CEREBRAL MICROEMBOLISM
Authors: ORLANDI G PARENTI G BERTOLUCCI A PUGLIOLI M COLLAVOLI P MURRI L
Citation: G. Orlandi et al., CAROTID PLAQUE FEATURES ON ANGIOGRAPHY AND ASYMPTOMATIC CEREBRAL MICROEMBOLISM, Acta neurologica Scandinavica, 96(3), 1997, pp. 183-186
EARLY DETECTION OF LUNG INVOLVEMENT IN LYSINURIC PROTEIN INTOLERANCE - ROLE OF HIGH-RESOLUTION COMPUTED-TOMOGRAPHY AND RADIOISOTOPIC METHODS
Authors: SANTAMARIA F PARENTI G GUIDI G ROTONDO A GRILLO G LAROCCA MR CELENTANO L STRISCIUGLIO P SEBASTIO G ANDRIA G
Citation: F. Santamaria et al., EARLY DETECTION OF LUNG INVOLVEMENT IN LYSINURIC PROTEIN INTOLERANCE - ROLE OF HIGH-RESOLUTION COMPUTED-TOMOGRAPHY AND RADIOISOTOPIC METHODS, American journal of respiratory and critical care medicine, 153(2), 1996, pp. 731-735
CLINICAL AND BIOCHEMICAL SCREENING FOR SMITH-LEMLI-OPITZ SYNDROME
Authors: GUZZETTA V DEFABIANI E GALLI G COLOMBO C CORSO G LECORA M PARENTI G STRISCIUGLIO P ANDRIA G DIROCCO M GIANNOTTI S LUPI L SELICORNI A CLEMENTI G GABRIELLI O PINTO L RIZZO A ZELANTE L
Citation: V. Guzzetta et al., CLINICAL AND BIOCHEMICAL SCREENING FOR SMITH-LEMLI-OPITZ SYNDROME, Acta paediatrica, 85(8), 1996, pp. 937-942
RESPIRATORY-CHAIN AND PYRUVATE METABOLISM DEFECTS - ITALIAN COLLABORATIVE SURVEY ON 72 PATIENTS
Authors: CARUSO U ADAMI A BERTINI E BURLINA AB CARNEVALE F CERONE R DIONISIVICI C GIORDANO G LEUZZI E PARENTI G SAVASTA S UZIEL G ZEVIANI M
Citation: U. Caruso et al., RESPIRATORY-CHAIN AND PYRUVATE METABOLISM DEFECTS - ITALIAN COLLABORATIVE SURVEY ON 72 PATIENTS, Journal of inherited metabolic disease, 19(2), 1996, pp. 143-148
CAN THE PRESENCE OF TCD-DETECTED MICROEMBOLI SELECT A HIGH-RISK GROUPOF LESS-THAN-70-PERCENT CAROTID STENOSIS FOR APPROPRIATE PROPHYLACTICSURGICAL-TREATMENT
Authors: ORLANDI G MURRI L PARENTI G
Citation: G. Orlandi et al., CAN THE PRESENCE OF TCD-DETECTED MICROEMBOLI SELECT A HIGH-RISK GROUPOF LESS-THAN-70-PERCENT CAROTID STENOSIS FOR APPROPRIATE PROPHYLACTICSURGICAL-TREATMENT, Stroke, 27(4), 1996, pp. 767-767
REACTIONS AND RESPONSES IN THE CITY OF FL ORENCE - 30-YEARS AFTER THEARNO RIVER FLOOD OF 1966
Authors: PARENTI G
Citation: G. Parenti, REACTIONS AND RESPONSES IN THE CITY OF FL ORENCE - 30-YEARS AFTER THEARNO RIVER FLOOD OF 1966, Il Ponte : rivista mensile di politica e letteratura, 1996, pp. 172-175
RESECTION OF SINGLE BRAIN METASTASIS IN NON-SMALL-CELL LUNG-CANCER - PROGNOSTIC FACTORS
Authors: MUSSI A PISTOLESI M LUCCHI M JANNI A CHELLA A PARENTI G ROSSI G ANGELETTI CA
Citation: A. Mussi et al., RESECTION OF SINGLE BRAIN METASTASIS IN NON-SMALL-CELL LUNG-CANCER - PROGNOSTIC FACTORS, Journal of thoracic and cardiovascular surgery, 112(1), 1996, pp. 146-153
CFC SYNDROME - REPORT OF FAMILIAL CASES
Authors: LECORA M PARENTI G ANDRIA G
Citation: M. Lecora et al., CFC SYNDROME - REPORT OF FAMILIAL CASES, Clinical genetics, 50(6), 1996, pp. 558-559
ELECTROPHYSIOLOGICAL MONITORING FOR SELECTIVE SHUNTING DURING CAROTIDENDARTERECTOMY
Authors: FIORI L PARENTI G
Citation: L. Fiori et G. Parenti, ELECTROPHYSIOLOGICAL MONITORING FOR SELECTIVE SHUNTING DURING CAROTIDENDARTERECTOMY, Journal of neurosurgical anesthesiology, 7(3), 1995, pp. 168-173
ANTERIOR FOSSA DURAL ARTERIOVENOUS MALFORMATION DISCOVERED BY MEANS OF PW-DOPPLER EXAMINATION
Authors: FIORI L PARENTI G PUGLIOLI M PADOLECCHIA R
Citation: L. Fiori et al., ANTERIOR FOSSA DURAL ARTERIOVENOUS MALFORMATION DISCOVERED BY MEANS OF PW-DOPPLER EXAMINATION, Neurological research, 17(3), 1995, pp. 226-228
VARIABLE PENETRANCE OF HYPOGONADISM IN A SIBSHIP WITH KALLMANN SYNDROME DUE TO A DELETION OF THE KAL GENE
Authors: PARENTI G RIZZOLO MG GHEZZI M DIMAIO S SPERANDEO MP INCERTI B FRANCO B BALLABIO A ANDRIA G
Citation: G. Parenti et al., VARIABLE PENETRANCE OF HYPOGONADISM IN A SIBSHIP WITH KALLMANN SYNDROME DUE TO A DELETION OF THE KAL GENE, American journal of medical genetics, 57(3), 1995, pp. 476-478
Risultati: 1-25 | 26-32