AAAAAA

   
Results: 1-25 | 26-31
Results: 1-25/31
GENETIC-MAPPING OF THE GENE FOR VAN-BUCHEM-DISEASE TO CHROMOSOME 17Q12-Q21
Authors: BALEMANS W VANHUL E DIKKERS F STOKROOS R VANCAMP G WILLEMS P VANHUL W
Citation: W. Balemans et al., GENETIC-MAPPING OF THE GENE FOR VAN-BUCHEM-DISEASE TO CHROMOSOME 17Q12-Q21, European journal of human genetics, 6, 1998, pp. 507-507
PAGETS-DISEASE OF BONE - EVIDENCE FOR A SUSCEPTIBILITY LOCUS ON CHROMOSOME 18Q AND FOR GENETIC-HETEROGENEITY
Authors: HASLAM SI VANHUL W MORALESPIGA A BALEMANS W SANMILLAN JL NAKATSUKA K WILLEMS P HAITES NE RALSTON SH
Citation: Si. Haslam et al., PAGETS-DISEASE OF BONE - EVIDENCE FOR A SUSCEPTIBILITY LOCUS ON CHROMOSOME 18Q AND FOR GENETIC-HETEROGENEITY, Journal of bone and mineral research, 13(6), 1998, pp. 911-917
CLINICAL, BIOCHEMICAL AND MOLECULAR FINDINGS IN A PATIENT WITH X-LINKED LIVER GLYCOGENOSIS FOLLOWED FOR 40 YEARS
Authors: HENDRICKX J BOSSHARD NU WILLEMS P GITZELMANN R
Citation: J. Hendrickx et al., CLINICAL, BIOCHEMICAL AND MOLECULAR FINDINGS IN A PATIENT WITH X-LINKED LIVER GLYCOGENOSIS FOLLOWED FOR 40 YEARS, European journal of pediatrics, 157(11), 1998, pp. 919-923
NONSYNDROMIC AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS - AUDIOLOGICAL ANALYSIS OF A PEDIGREE LINKED TO DFNA2
Authors: KUNST H MARRES H HUYGEN P ENSINK R VANCAMP G VANHAUWE P COUCKE P WILLEMS P CREMERS C
Citation: H. Kunst et al., NONSYNDROMIC AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS - AUDIOLOGICAL ANALYSIS OF A PEDIGREE LINKED TO DFNA2, The Laryngoscope, 108(1), 1998, pp. 74-80
SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS
Authors: BUITING K DITTRICH B GROSS S LICH C FARBER C BUCHHOLZ T SMITH E REIS A BURGER J NOTHEN MM BARTHWITTE U JANSSEN B ABELIOVICH D LERER I VANDENOUWELAND AMW HALLEY DJJ SCHRANDERSTUMPEL C SMEETS H MEINECKE P MALCOLM S GARDNER A LALANDE M NICHOLLS RD FRIEND K SCHULZE A MATTHIJS G KOKKONEN H HILBERT P VANMALDERGEM L GLOVER G CARBONELL P WILLEMS P GILLESSENKAESBACH G HORSTHEMKE B
Citation: K. Buiting et al., SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS, American journal of human genetics, 63(1), 1998, pp. 170-180
DISCUSSION ON ALTERNATIVE SYSTEMS FOR FILM RADIOGRAPHY
Authors: VAESSEN B PERDIEUS P WILLEMS P
Citation: B. Vaessen et al., DISCUSSION ON ALTERNATIVE SYSTEMS FOR FILM RADIOGRAPHY, Insight, 39(10), 1997, pp. 719-723
REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA, European journal of human genetics, 5(6), 1997, pp. 397-405
SAFETY AND IMMUNOGENICITY OF A COMBINED PENTAVALENT DIPHTHERIA, TETANUS, ACELLULAR PERTUSSIS, INACTIVATED POLIOVIRUS AND HAEMOPHILUS-INFLUENZAE TYPE-B TETANUS CONJUGATE VACCINE IN INFANTS, COMPARED WITH A WHOLE-CELL PERTUSSIS PENTAVALENT VACCINE
Authors: DAGAN R IGBARIA K PIGLANSKY L MELAMED R WILLEMS P GROSSI A KAUFHOLD A
Citation: R. Dagan et al., SAFETY AND IMMUNOGENICITY OF A COMBINED PENTAVALENT DIPHTHERIA, TETANUS, ACELLULAR PERTUSSIS, INACTIVATED POLIOVIRUS AND HAEMOPHILUS-INFLUENZAE TYPE-B TETANUS CONJUGATE VACCINE IN INFANTS, COMPARED WITH A WHOLE-CELL PERTUSSIS PENTAVALENT VACCINE, The Pediatric infectious disease journal, 16(12), 1997, pp. 1113-1121
INHERITED NONSYNDROMIC HEARING-LOSS - AN AUDIOVESTIBULAR STUDY IN A LARGE FAMILY WITH AUTOSOMAL-DOMINANT PROGRESSIVE HEALING LOSS RELATED TO DFNA2
Authors: MARRES H VANEWIJK M HUYGEN P KUNST H VANCAMP G COUCKE P WILLEMS P CREMERS C
Citation: H. Marres et al., INHERITED NONSYNDROMIC HEARING-LOSS - AN AUDIOVESTIBULAR STUDY IN A LARGE FAMILY WITH AUTOSOMAL-DOMINANT PROGRESSIVE HEALING LOSS RELATED TO DFNA2, Archives of otolaryngology, head & neck surgery, 123(6), 1997, pp. 573-577
FEASIBILITY STUDY OF A COMBINED DIPHTHERIA TETANUS ACELLULAR PERTUSSIS HEPATITIS-B (DTPA-HBV) VACCINE, AND COMPARISON OF CLINICAL REACTIONSAND IMMUNE-RESPONSES WITH DIPHTHERIA TETANUS ACELLULAR PERTUSSIS (DTPA) AND HEPATITIS-B VACCINES APPLIED AS MIXED OR INJECTED INTO SEPARATELIMBS
Authors: USONIS V BAKASENAS V WILLEMS P CLEMENS R
Citation: V. Usonis et al., FEASIBILITY STUDY OF A COMBINED DIPHTHERIA TETANUS ACELLULAR PERTUSSIS HEPATITIS-B (DTPA-HBV) VACCINE, AND COMPARISON OF CLINICAL REACTIONSAND IMMUNE-RESPONSES WITH DIPHTHERIA TETANUS ACELLULAR PERTUSSIS (DTPA) AND HEPATITIS-B VACCINES APPLIED AS MIXED OR INJECTED INTO SEPARATELIMBS, Vaccine, 15(15), 1997, pp. 1680-1686
DOES WALKING SPEED INFLUENCE THE TIME-PATTERN OF MUSCLE ACTIVATION INNORMAL-CHILDREN
Authors: DETREMBLEUR C WILLEMS P PLAGHKI L
Citation: C. Detrembleur et al., DOES WALKING SPEED INFLUENCE THE TIME-PATTERN OF MUSCLE ACTIVATION INNORMAL-CHILDREN, Developmental Medicine and Child Neurology, 39(12), 1997, pp. 803-807
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
REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE, American journal of human genetics, 61(4), 1997, pp. 1743-1743
7TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X-LINKED AND X-LINKED MENTAL-RETARDATION
Authors: TRANEBJAERG L LUBS HA BORGHGRAEF M BROWN WT FISCH G FRYNS JP HAGERMAN R JACOBS PA MANDEL JL MULLEY J OOSTRA B SCHWARTZ C SHERMAN S WILLARD H WILLEMS P
Citation: L. Tranebjaerg et al., 7TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X-LINKED AND X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 64(1), 1996, pp. 1-14
LUMPING X-LINKED HYDROCEPHALUS (MIM-ASTERISK-307000) AND MASA-SYNDROME (MIM-ASTERISK-303350)
Authors: SCHRANDERSTUMPEL C HOWELER C MEYER H WILLEMS P FRYNS JP
Citation: C. Schranderstumpel et al., LUMPING X-LINKED HYDROCEPHALUS (MIM-ASTERISK-307000) AND MASA-SYNDROME (MIM-ASTERISK-303350), American journal of medical genetics, 64(1), 1996, pp. 17-17
SIMULTANEOUS DETERMINATION OF INHIBITION-KINETICS OF CARBON OXIDATIONAND NITRIFICATION WITH A RESPIROMETER
Authors: KONG Z VANROLLEGHEM P WILLEMS P VERSTRAETE W
Citation: Z. Kong et al., SIMULTANEOUS DETERMINATION OF INHIBITION-KINETICS OF CARBON OXIDATIONAND NITRIFICATION WITH A RESPIROMETER, Water research, 30(4), 1996, pp. 825-836
PHOTOSTIMULATION REDSHIFT FOR NONSTOICHIOMETRIC BA1-XSRXFBR-EU2+
Authors: DIETZE C HANGLEITER T WILLEMS P LEBLANS PJR STRUYE L SPAETH JM
Citation: C. Dietze et al., PHOTOSTIMULATION REDSHIFT FOR NONSTOICHIOMETRIC BA1-XSRXFBR-EU2+, Journal of applied physics, 80(2), 1996, pp. 1074-1078
ELECTRON TRAPS IN CA2-DOPED OR SR2+-DOPED BAFBR-EU2+ X-RAY STORAGE PHOSPHORS()
Authors: SCHWEIZER S WILLEMS P LEBLANS PJR STRUYE L SPAETH JM
Citation: S. Schweizer et al., ELECTRON TRAPS IN CA2-DOPED OR SR2+-DOPED BAFBR-EU2+ X-RAY STORAGE PHOSPHORS(), Journal of applied physics, 79(8), 1996, pp. 4157-4165
CD34 SELECTIONS FROM MYELOMA PERIPHERAL-BLOOD CELL AUTOGRAFTS CONTAINRESIDUAL TUMOR-CELLS DUE TO IMPURITY, NOT TO CD34(+) MYELOMA CELLS
Authors: WILLEMS P CROOCKEWIT A RAYMAKERS R HOLDRINET R VANDERBOSCH G HUYS E MENSINK E
Citation: P. Willems et al., CD34 SELECTIONS FROM MYELOMA PERIPHERAL-BLOOD CELL AUTOGRAFTS CONTAINRESIDUAL TUMOR-CELLS DUE TO IMPURITY, NOT TO CD34(+) MYELOMA CELLS, British Journal of Haematology, 93(3), 1996, pp. 613-622
RETARDED AND ABERRANT SPLICINGS CAUSED BY SINGLE EXON MUTATION IN A PHOSPHOGLYCERATE KINASE VARIANT
Authors: OOKAWARA T DAVE V WILLEMS P MARTIN JJ DEBARSY T MATTHYS E YOSHIDA A
Citation: T. Ookawara et al., RETARDED AND ABERRANT SPLICINGS CAUSED BY SINGLE EXON MUTATION IN A PHOSPHOGLYCERATE KINASE VARIANT, Archives of biochemistry and biophysics, 327(1), 1996, pp. 35-40
LINKAGE OF A GENE FOR DOMINANT NON-SYNDROMIC DEAFNESS TO CHROMOSOME-19
Authors: CHEN AH NI L FUKUSHIMA K MARIETTA J ONEILL M COUCKE P WILLEMS P SMITH RJH
Citation: Ah. Chen et al., LINKAGE OF A GENE FOR DOMINANT NON-SYNDROMIC DEAFNESS TO CHROMOSOME-19, Human molecular genetics, 4(6), 1995, pp. 1073-1076
MUTATIONS IN THE CELL-ADHESION MOLECULE LI CAUSE MENTAL-RETARDATION
Authors: WONG EV KENWRICK S WILLEMS P LEMMON V
Citation: Ev. Wong et al., MUTATIONS IN THE CELL-ADHESION MOLECULE LI CAUSE MENTAL-RETARDATION, Trends in neurosciences, 18(4), 1995, pp. 168-172
CONFINED COMPRESSION OF CANINE ANNULUS FIBROSUS UNDER CHEMICAL AND MECHANICAL LOADING
Authors: DROST MR WILLEMS P SNIJDERS H HUYGHE JM JANSSEN JD HUSON A
Citation: Mr. Drost et al., CONFINED COMPRESSION OF CANINE ANNULUS FIBROSUS UNDER CHEMICAL AND MECHANICAL LOADING, Journal of biomechanical engineering, 117(4), 1995, pp. 390-396
MYOCARDIAL PERFUSION IMAGING WITH TC-99M TETROFOSMIN - COMPARISON TO (TL)-T-201 IMAGING AND CORONARY ANGIOGRAPHY IN A PHASE-III MULTICENTER
Authors: ZARET BL RIGO P WACKERS FJT HENDEL RC BRAAT SH ISKANDRIAN AS SRIDHARA BS JAIN D ITTI R SERAFINI AN GORIS ML LAHIRI A HALDERS S KOPPEJANS L CAJOB I WILLEMS P BONTEMPS L EGROIZARD P SAYEGH Y FRAYSSE M BENOIT TR LELLERLO B FOULON J KLINE R MORRISSETTE G PRICE L JACKSON R SPIES S BELLOW S LEONARD S BULL C SRIDHARA B RAVAL U CRAWLEY J SMITH T ISKANDRIAN A HEO J UNTEEKER W FEINSMITH N CAVE V WASSERLEBEN V MCDOUGALL R BLAKE L GUREVICH N FUJII C EZUDDIN S SEQUEIRA R LOWERY M WACKERS FJ MATTERA J MCMAHON M SAARI M
Citation: Bl. Zaret et al., MYOCARDIAL PERFUSION IMAGING WITH TC-99M TETROFOSMIN - COMPARISON TO (TL)-T-201 IMAGING AND CORONARY ANGIOGRAPHY IN A PHASE-III MULTICENTER, Circulation, 91(2), 1995, pp. 313-319
MOLECULAR DELINEATION OF A NEW CONTIGUOUS GENE SYNDROME WITH MULTIPLEEXOSTOSES ASSOCIATED WITH DELETIONS ON THE SHORT ARM OF CHROMOSOME-11
Authors: VANHUL W WUYTS W HECHT JT BARTSCH O MEINECKE P ZABEL B WERNER W HINKEL GK WILLEMS P
Citation: W. Vanhul et al., MOLECULAR DELINEATION OF A NEW CONTIGUOUS GENE SYNDROME WITH MULTIPLEEXOSTOSES ASSOCIATED WITH DELETIONS ON THE SHORT ARM OF CHROMOSOME-11, American journal of human genetics, 57(4), 1995, pp. 31-31
Risultati: 1-25 | 26-31