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Results: 1-25 | 26-50 | 51-75 | 76-91
Results: 1-25/91
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY IN A PATIENT WITH PHENOTYPIC FINDINGS OF ANGELMAN-SYNDROME
Authors: ARN PH WILLIAMS CA ZORI RT DRISCOLL DJ ROSENBLATT DS
Citation: Ph. Arn et al., METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY IN A PATIENT WITH PHENOTYPIC FINDINGS OF ANGELMAN-SYNDROME, American journal of medical genetics, 77(3), 1998, pp. 198-200
PREVALENCE OF 22Q11 REGION DELETIONS IN PATIENTS WITH VELOPHARYNGEAL INSUFFICIENCY
Authors: ZORI RT BOYAR FZ WILLIAMS WN GRAY BA BENTWILLIAMS A STALKER HJ RIMER LA NACKASHI JA DRISCOLL DJ RASMUSSEN SA DIXONWOOD V WILLIAMS CA
Citation: Rt. Zori et al., PREVALENCE OF 22Q11 REGION DELETIONS IN PATIENTS WITH VELOPHARYNGEAL INSUFFICIENCY, American journal of medical genetics, 77(1), 1998, pp. 8-11
USE OF HEPARIN IN THE TREATMENT OF PROTEIN-LOSING ENTEROPATHY AFTER FONTAN OPERATION FOR COMPLEX CONGENITAL HEART-DISEASE
Authors: KELLY AM FELDT RH DRISCOLL DJ DANIELSON GK
Citation: Am. Kelly et al., USE OF HEPARIN IN THE TREATMENT OF PROTEIN-LOSING ENTEROPATHY AFTER FONTAN OPERATION FOR COMPLEX CONGENITAL HEART-DISEASE, Mayo Clinic proceedings, 73(8), 1998, pp. 777-779
CARDIAC TRANSPLANTATION FOR END-STAGE CONGENITAL HEART-DEFECTS - THE MAYO-CLINIC EXPERIENCE
Authors: SPEZIALI G DRISCOLL DJ DANIELSON GK JULSRUD PR PORTER CBJ DEARANI JA DALY RC MCGREGOR CGA
Citation: G. Speziali et al., CARDIAC TRANSPLANTATION FOR END-STAGE CONGENITAL HEART-DEFECTS - THE MAYO-CLINIC EXPERIENCE, Mayo Clinic proceedings, 73(10), 1998, pp. 923-928
KLIPPEL-TRENAUNAY-SYNDROME - SPECTRUM AND MANAGEMENT
Authors: JACOB AG DRISCOLL DJ SHAUGHNESSY WJ STANSON AW CLAY RP GLOVICZKI P
Citation: Ag. Jacob et al., KLIPPEL-TRENAUNAY-SYNDROME - SPECTRUM AND MANAGEMENT, Mayo Clinic proceedings, 73(1), 1998, pp. 28-36
MEASUREMENT OF BLOOD-PLASMA CYCLOSPORINE LEVELS USING CAPILLARY (FINGERSTICK) SAMPLING - A VALIDATION-STUDY
Authors: PETTERSEN MD DRISCOLL DJ MOYER TP DEARANI JA MCGREGOR CGA
Citation: Md. Pettersen et al., MEASUREMENT OF BLOOD-PLASMA CYCLOSPORINE LEVELS USING CAPILLARY (FINGERSTICK) SAMPLING - A VALIDATION-STUDY, Circulation, 98(17), 1998, pp. 3629-3629
PREDICTORS OF EARLY-ONSET AND LATE-ONSET SUPRAVENTRICULAR TACHYARRHYTHMIAS AFTER FONTAN OPERATION
Authors: DURONGPISITKUL K PORTER CJ CETTA F OFFORD KP SLEZAK JM PUGA FJ SCHAFF HV DANIELSON GK DRISCOLL DJ
Citation: K. Durongpisitkul et al., PREDICTORS OF EARLY-ONSET AND LATE-ONSET SUPRAVENTRICULAR TACHYARRHYTHMIAS AFTER FONTAN OPERATION, Circulation, 98(11), 1998, pp. 1099-1107
CARDIOVASCULAR PREPARTICIPATION SCREENING OF COMPETITIVE ATHLETES - ADDENDUM - AN ADDENDUM TO A STATEMENT FOR HEALTH-PROFESSIONALS FROM THESUDDEN-DEATH COMMITTEE (COUNCIL ON CLINICAL CARDIOLOGY) AND THE CONGENITAL CARDIAC DEFECTS COMMITTEE (COUNCIL ON CARDIOVASCULAR-DISEASE IN THE YOUNG), AMERICAN-HEART-ASSOCIATION
Authors: MARON BJ THOMPSON PD PUFFER JC MCGREW CA STRONG WB DOUGLAS PS CLARK LT MITTEN MJ CRAWFORD MD ATKINS DL DRISCOLL DJ EPSTEIN AE
Citation: Bj. Maron et al., CARDIOVASCULAR PREPARTICIPATION SCREENING OF COMPETITIVE ATHLETES - ADDENDUM - AN ADDENDUM TO A STATEMENT FOR HEALTH-PROFESSIONALS FROM THESUDDEN-DEATH COMMITTEE (COUNCIL ON CLINICAL CARDIOLOGY) AND THE CONGENITAL CARDIAC DEFECTS COMMITTEE (COUNCIL ON CARDIOVASCULAR-DISEASE IN THE YOUNG), AMERICAN-HEART-ASSOCIATION, Circulation, 97(22), 1998, pp. 2294-2294
GENOMIC IMPRINTING - POTENTIAL FUNCTION AND MECHANISMS REVEALED BY THE PRADER-WILLI AND ANGELMAN SYNDROMES
Authors: GLENN CC DRISCOLL DJ YANG TP NICHOLLS RD
Citation: Cc. Glenn et al., GENOMIC IMPRINTING - POTENTIAL FUNCTION AND MECHANISMS REVEALED BY THE PRADER-WILLI AND ANGELMAN SYNDROMES, Molecular human reproduction, 3(4), 1997, pp. 321-332
NF1 MUTATION ANALYSIS USING A COMBINED HETERODUPLEX SSCP APPROACH/
Authors: ABERNATHY CR RASMUSSEN SA STALKER HJ ZORI R DRISCOLL DJ WILLIAMS CA KOUSSEFF BG WALLACE MR
Citation: Cr. Abernathy et al., NF1 MUTATION ANALYSIS USING A COMBINED HETERODUPLEX SSCP APPROACH/, Human mutation, 9(6), 1997, pp. 548-554
PREPARATION OF PARAMAGNETIC LIGANDS FOR COORDINATION-COMPLEXES AND NETWORKS WITH INTERESTING MAGNETIC-PROPERTIES
Authors: SHULTZ DA BOAL AK DRISCOLL DJ FARMER GT KITCHIN JR MILLER DB TEW GN
Citation: Da. Shultz et al., PREPARATION OF PARAMAGNETIC LIGANDS FOR COORDINATION-COMPLEXES AND NETWORKS WITH INTERESTING MAGNETIC-PROPERTIES, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 305, 1997, pp. 303-310
EXERCISE TOLERANCE IN PATIENTS WITH EBSTEINS-ANOMALY
Authors: MACLELLANTOBERT SG DRISCOLL DJ MOTTRAM CD MAHONEY DW WOLLAN PC DANIELSON GK
Citation: Sg. Maclellantobert et al., EXERCISE TOLERANCE IN PATIENTS WITH EBSTEINS-ANOMALY, Journal of the American College of Cardiology, 29(7), 1997, pp. 1615-1622
SYNCOPE IN CHILDREN AND ADOLESCENTS
Authors: DRISCOLL DJ JACOBSEN SJ PORTER CBJ WOLLAN PC
Citation: Dj. Driscoll et al., SYNCOPE IN CHILDREN AND ADOLESCENTS, Journal of the American College of Cardiology, 29(5), 1997, pp. 1039-1045
CARDIORESPIRATORY RESPONSE TO EXERCISE AFTER MODIFIED FONTAN OPERATION - DETERMINANTS OF PERFORMANCE
Authors: DURONGPISITKUL K DRISCOLL DJ MAHONEY DW WOLLAN PC MOTTRAM CD PUGA FJ DANIELSON GK
Citation: K. Durongpisitkul et al., CARDIORESPIRATORY RESPONSE TO EXERCISE AFTER MODIFIED FONTAN OPERATION - DETERMINANTS OF PERFORMANCE, Journal of the American College of Cardiology, 29(4), 1997, pp. 785-790
IMPRINTING MUTATIONS IN PRADER-WILLI (AND ANGELMAN) SYNDROME EXEMPLIFY A NEW GENETIC MECHANISM
Authors: OHTA T SAITOH S BUITING K GABRIEL JM SCHWARTZ S CASSIDY SB ROGAN PK GLENN CC DRISCOLL DJ HORSTHEMKE B NICHOLLS RD
Citation: T. Ohta et al., IMPRINTING MUTATIONS IN PRADER-WILLI (AND ANGELMAN) SYNDROME EXEMPLIFY A NEW GENETIC MECHANISM, American journal of medical genetics, 73(4), 1997, pp. 4-4
UNEXPECTED FAMILIAL RECURRENCE IN ANGELMAN SYNDROME
Authors: CONNERTONMOYER KJ NICHOLLS RD SCHWARTZ S DRISCOLL DJ HENDRICKSON JE WILLIAMS CA PAULI RM
Citation: Kj. Connertonmoyer et al., UNEXPECTED FAMILIAL RECURRENCE IN ANGELMAN SYNDROME, American journal of medical genetics, 70(3), 1997, pp. 253-260
CLINICAL SPECTRUM AND MOLECULAR DIAGNOSIS OF ANGELMAN AND PRADER-WILLI-SYNDROME PATIENTS WITH AN IMPRINTING MUTATION
Authors: SAITOH S BUITING K CASSIDY SB CONROY JM DRISCOLL DJ GABRIEL JM GILLESSENKAESBACH G GLENN CC GREENSWAG LR HORSTHEMKE B KONDO I KUWAJIMA K NIIKAWA N ROGAN PK SCHWARTZ S SEIP J WILLIAMS CA NICHOLLS RD
Citation: S. Saitoh et al., CLINICAL SPECTRUM AND MOLECULAR DIAGNOSIS OF ANGELMAN AND PRADER-WILLI-SYNDROME PATIENTS WITH AN IMPRINTING MUTATION, American journal of medical genetics, 68(2), 1997, pp. 195-206
HEALTH SUPERVISION FOR CHILDREN WITH TURNER SYNDROME
Authors: FREED MD MOODIE DS DRISCOLL DJ BRICKER JT
Citation: Md. Freed et al., HEALTH SUPERVISION FOR CHILDREN WITH TURNER SYNDROME, Pediatrics, 99(1), 1997, pp. 146-146
SURGICAL-MANAGEMENT OF EBSTEINS-ANOMALY - A 25-YEAR EXPERIENCE
Authors: THEODORO DA DANIELSON GK KIZILTAN HT DRISCOLL DJ MAIR DD WARNES CA ANDERSON BJ
Citation: Da. Theodoro et al., SURGICAL-MANAGEMENT OF EBSTEINS-ANOMALY - A 25-YEAR EXPERIENCE, Circulation, 96(8), 1997, pp. 2841-2841
RECOMBINATION BETWEEN LARGE, TRANSCRIPTIONALLY ACTIVE REPEATED ELEMENTS AT THE PROXIMAL AND DISTAL BREAKPOINTS IN PRADER-WILLI AND ANGELMAN-SYNDROMES
Authors: AMOSLANDGRAF JM JI Y WANDSTRAT AE DRISCOLL DJ SCHWARTZ S NICHOLLS RD
Citation: Jm. Amoslandgraf et al., RECOMBINATION BETWEEN LARGE, TRANSCRIPTIONALLY ACTIVE REPEATED ELEMENTS AT THE PROXIMAL AND DISTAL BREAKPOINTS IN PRADER-WILLI AND ANGELMAN-SYNDROMES, American journal of human genetics, 61(4), 1997, pp. 5-5
CYTOGENETIC AND MOLECULAR ABNORMALITIES IN 387 PATIENTS REFERRED FOR EVALUATION OF PRADER-WILLI AND ANGELMAN SYNDROMES
Authors: MCCANDLESS SE CASSIDY SB DRISCOLL DJ BECKER L HEEGER S NICHOLLS R SCHWARTZ S
Citation: Se. Mccandless et al., CYTOGENETIC AND MOLECULAR ABNORMALITIES IN 387 PATIENTS REFERRED FOR EVALUATION OF PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of human genetics, 61(4), 1997, pp. 155-155
GENETIC-ASPECTS OF EBSTEINS-ANOMALY, A CONGENITAL HEART-DISEASE
Authors: RAMIREZ M KAN E BOSQUES G CHEN Q WARNES CA DANIELSON GK DRISCOLL DJ DENNIS NR TOWBIN JA WANG Q
Citation: M. Ramirez et al., GENETIC-ASPECTS OF EBSTEINS-ANOMALY, A CONGENITAL HEART-DISEASE, American journal of human genetics, 61(4), 1997, pp. 620-620
LIGATION-MEDIATED METHYLATION-PCR FOR RAPID MOLECULAR DIAGNOSIS OF PRADER-WILLI AND ANGELMAN-SYNDROMES
Authors: SAITOH S WADA T DRISCOLL DJ SCHWARTZ S NICHOLLS RD
Citation: S. Saitoh et al., LIGATION-MEDIATED METHYLATION-PCR FOR RAPID MOLECULAR DIAGNOSIS OF PRADER-WILLI AND ANGELMAN-SYNDROMES, American journal of human genetics, 61(4), 1997, pp. 1315-1315
ANALYSIS OF UBE3A IN CLASSICAL AND ATYPICAL ANGELMAN PATIENTS
Authors: LOSSIE AC BOYAR FZ FILBRANDT MM ZORI RT WILLIAMS CA DRISCOLL DJ
Citation: Ac. Lossie et al., ANALYSIS OF UBE3A IN CLASSICAL AND ATYPICAL ANGELMAN PATIENTS, American journal of human genetics, 61(4), 1997, pp. 1835-1835
MOLECULAR ANALYSIS IN 2 LARGE AS IMPRINTING MUTATION (IM) FAMILIES AND IDENTIFICATION OF MICRODELETION JUNCTIONS IN AS AND PWS IM FAMILIES
Authors: OHTA T BUITING K KOKKONEN H SAITOH S MCCANDLESS S CASSIDY SB DRISCOLL DJ HORSTHEMKE B NICHOLLS RD
Citation: T. Ohta et al., MOLECULAR ANALYSIS IN 2 LARGE AS IMPRINTING MUTATION (IM) FAMILIES AND IDENTIFICATION OF MICRODELETION JUNCTIONS IN AS AND PWS IM FAMILIES, American journal of human genetics, 61(4), 1997, pp. 1850-1850
Risultati: 1-25 | 26-50 | 51-75 | 76-91