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Results: 1-24 |
Results: 24
IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N BOSSUYT P WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY, Genomics, 47(2), 1998, pp. 230-237
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
MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W DEBOULLE K HENDRICKX J BAKKER E VANHOENACKER F MOLLICA F LUDECKE HJ SAYLI BS PAZZAGLIA UE MORTIER G HAMEL B CONRAD EU MATSUSHITA M RASKIND WH WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2
Authors: WUYTS W VANHUL W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N VANAGTMAEL T BOSSUYT P WILLEMS PJ
Citation: W. Wuyts et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2, European journal of human genetics, 5(6), 1997, pp. 382-389
IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J WAUTERS J DEBOULLE K WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY, Journal of bone and mineral research, 12, 1997, pp. 661-661
IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES
Authors: WUYTS W VANHUL W HENDRICKX J DEBOULLE K WILLEMS PW
Citation: W. Wuyts et al., IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES, American journal of human genetics, 61(4), 1997, pp. 2059-2059
PROGNOSIS OF GASTRIC-CARCINOMA WITH EMPHASIS ON LYMPH-NODE STATUS
Authors: TOPAL B TRIMPENEERS F HENDRICKX J
Citation: B. Topal et al., PROGNOSIS OF GASTRIC-CARCINOMA WITH EMPHASIS ON LYMPH-NODE STATUS, Acta Chirurgica Belgica, 97(3), 1997, pp. 118-122
LOCATION OF THE HYDROXYL FUNCTIONS IN HYDROXYLATED METABOLITES OF NEBIVOLOL IN DIFFERENT ANIMAL SPECIES AND HUMAN-SUBJECTS AS DETERMINED BYONLINE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY DIODE-ARRAY DETECTION
Authors: HENDRICKX J BOCKX M ZWIJSEN C BORGMANS C MANNENS G MEULDERMANS W HEYKANTS J
Citation: J. Hendrickx et al., LOCATION OF THE HYDROXYL FUNCTIONS IN HYDROXYLATED METABOLITES OF NEBIVOLOL IN DIFFERENT ANIMAL SPECIES AND HUMAN-SUBJECTS AS DETERMINED BYONLINE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY DIODE-ARRAY DETECTION, Journal of chromatography, 729(1-2), 1996, pp. 341-354
X-LINKED LIVER GLYCOGENOSIS TYPE-II (XLG-II) IS CAUSED BY MUTATIONS IN PHKA2, THE GENE ENCODING THE LIVER A SUBUNIT OF PHOSPHORYLASE-KINASE
Authors: HENDRICKX J DAMS E COUCKE P LEE P FERNANDES J WILLEMS PJ
Citation: J. Hendrickx et al., X-LINKED LIVER GLYCOGENOSIS TYPE-II (XLG-II) IS CAUSED BY MUTATIONS IN PHKA2, THE GENE ENCODING THE LIVER A SUBUNIT OF PHOSPHORYLASE-KINASE, Human molecular genetics, 5(5), 1996, pp. 649-652
POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W WAUTERS J NEMTSOVA M REYNIERS E VANHUL E DEBOULLE K DEVRIES BBA HENDRICKX J HERRYGERS I BOSSUYT P BALEMANS W FRANSEN E VITS L COUCKE P NOWAK NJ SHOWS TB MALLET L VANDENOUWELAND AMW MCGAUGHRAN J HALLEY DJJ WILLEMS PJ
Citation: W. Wuyts et al., POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES, Human molecular genetics, 5(10), 1996, pp. 1547-1557
GENETIC DEFICIENCIES OF THE GLYCOGEN-PHOSPHORYLASE SYSTEM
Authors: HENDRICKX J WILLEMS PJ
Citation: J. Hendrickx et Pj. Willems, GENETIC DEFICIENCIES OF THE GLYCOGEN-PHOSPHORYLASE SYSTEM, Human genetics, 97(5), 1996, pp. 551-556
TECHNIQUES OF EVENT HISTORY MODELING - NEW APPROACHES TO CAUSAL-ANALYSIS - BLOSSFELD,HP, ROHWER,G
Authors: HENDRICKX J
Citation: J. Hendrickx, TECHNIQUES OF EVENT HISTORY MODELING - NEW APPROACHES TO CAUSAL-ANALYSIS - BLOSSFELD,HP, ROHWER,G, European sociological review, 12(3), 1996, pp. 329-331
MUTATIONS IN THE PHOSPHORYLASE-KINASE GENE PHKA2 ARE RESPONSIBLE FOR X-LINKED LIVER-GLYCOGEN STORAGE DISEASE
Authors: HENDRICKX J COUCKE P DAMS E LEE P ODIEVRE M CORBEEL L FERNANDES JF WILLEMS PJ
Citation: J. Hendrickx et al., MUTATIONS IN THE PHOSPHORYLASE-KINASE GENE PHKA2 ARE RESPONSIBLE FOR X-LINKED LIVER-GLYCOGEN STORAGE DISEASE, Human molecular genetics, 4(1), 1995, pp. 77-83
ENDOSCOPIC EXTRAPERITONEAL LUMBAR SYMPATHECTOMY
Authors: HOURLAY P VANGERTRUYDEN G VERDUYCKT F TRIMPENEERS F HENDRICKX J
Citation: P. Hourlay et al., ENDOSCOPIC EXTRAPERITONEAL LUMBAR SYMPATHECTOMY, Surgical endoscopy, 9(5), 1995, pp. 530-533
REDUCTION OF THE PRODRUG LOPERAMIDE OXIDE TO ITS ACTIVE-DRUG LOPERAMIDE IN THE GUT OF RATS, DOGS, AND HUMANS
Authors: LAVRIJSEN K VANDYCK D VANHOUDT J HENDRICKX J MONBALIU J WOESTENBORGHS R MEULDERMANS W HEYKANTS J
Citation: K. Lavrijsen et al., REDUCTION OF THE PRODRUG LOPERAMIDE OXIDE TO ITS ACTIVE-DRUG LOPERAMIDE IN THE GUT OF RATS, DOGS, AND HUMANS, Drug metabolism and disposition, 23(3), 1995, pp. 354-362
LOCALIZATION OF A NEW-TYPE OF X-LINKED LIVER GLYCOGENOSIS TO THE CHROMOSOMAL REGION XP22 CONTAINING THE LIVER ALPHA-SUBUNIT OF PHOSPHORYLASE-KINASE (PHKA2)
Authors: HENDRICKX J COUCKE P HORSCAYLA MC SMIT GPA SHIN YS DEUTSCH J SMEITINK J BERGER R LEE P FERNANDES J WILLEMS PJ
Citation: J. Hendrickx et al., LOCALIZATION OF A NEW-TYPE OF X-LINKED LIVER GLYCOGENOSIS TO THE CHROMOSOMAL REGION XP22 CONTAINING THE LIVER ALPHA-SUBUNIT OF PHOSPHORYLASE-KINASE (PHKA2), Genomics, 21(3), 1994, pp. 620-625
THE METABOLISM AND EXCRETION OF RISPERIDONE AFTER ORAL-ADMINISTRATIONIN RATS AND DOGS
Authors: MEULDERMANS W HENDRICKX J MANNENS G LAVRIJSEN K JANSSEN C BRACKE J LEJEUNE L LAUWERS W HEYKANTS J
Citation: W. Meuldermans et al., THE METABOLISM AND EXCRETION OF RISPERIDONE AFTER ORAL-ADMINISTRATIONIN RATS AND DOGS, Drug metabolism and disposition, 22(1), 1994, pp. 129-138
RELIGIOUS ASSORTIVE MARRIAGES IN GERMANY (1901-1986) AND THE NETHERLANDS (1914-1986)
Authors: HENDRICKX J SCHREUDER O ULTEE W
Citation: J. Hendrickx et al., RELIGIOUS ASSORTIVE MARRIAGES IN GERMANY (1901-1986) AND THE NETHERLANDS (1914-1986), Kolner Zeitschrift fur Soziologie und Sozialpsychologie, 46(4), 1994, pp. 619-645
COSTS OF ADMINISTERING DESFLURANE OR ISOFLURANE VIA A CLOSED-CIRCUIT
Authors: HENDRICKX J DEWOLF AM
Citation: J. Hendrickx et Am. Dewolf, COSTS OF ADMINISTERING DESFLURANE OR ISOFLURANE VIA A CLOSED-CIRCUIT, Anesthesiology, 80(1), 1994, pp. 240-242
X-LINKED LIVER GLYCOGENOSIS - FROM PATIENT TO GENE
Authors: WILLEMS PJ HENDRICKX J
Citation: Pj. Willems et J. Hendrickx, X-LINKED LIVER GLYCOGENOSIS - FROM PATIENT TO GENE, American journal of human genetics, 55(3), 1994, pp. 10000004-10000004
X-LINKED LIVER GLYCOGENOSIS - LOCALIZATION AND ISOLATION OF A CANDIDATE GENE
Authors: HENDRICKX J COUCKE P BOSSUYT P WAUTERS J RAEYMAEKERS P MARCHAU F PETER G SMIT A STOLTE I SARDHARWALLA IB BERTHELOT J VANDENBERGH I BERGER R VANBROECKHOVEN C BAUSSAN C WAPENAAR M FERNANDES J WILLEMS PJ
Citation: J. Hendrickx et al., X-LINKED LIVER GLYCOGENOSIS - LOCALIZATION AND ISOLATION OF A CANDIDATE GENE, Human molecular genetics, 2(5), 1993, pp. 583-589
ABSORPTION, METABOLISM, AND EXCRETION OF RISPERIDONE IN HUMANS
Authors: MANNENS G HUANG ML MEULDERMANS W HENDRICKX J WOESTENBORGHS R HEYKANTS J
Citation: G. Mannens et al., ABSORPTION, METABOLISM, AND EXCRETION OF RISPERIDONE IN HUMANS, Drug metabolism and disposition, 21(6), 1993, pp. 1134-1141
MODELS FOR STATUS-INCONSISTENCY AND MOBILITY - A COMPARISON OF THE APPROACHES BY HOPE AND SOBEL WITH THE MAINSTREAM SQUARE ADDITIVE-MODEL
Authors: HENDRICKX J DEGRAAF ND LAMMERS J ULTEE W
Citation: J. Hendrickx et al., MODELS FOR STATUS-INCONSISTENCY AND MOBILITY - A COMPARISON OF THE APPROACHES BY HOPE AND SOBEL WITH THE MAINSTREAM SQUARE ADDITIVE-MODEL, Quality & quantity, 27(4), 1993, pp. 335-352
MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY - THE PREVALENTMUTATION G985 (K304E) IS SUBJECT TO A STRONG FOUNDER EFFECT FROM NORTHWESTERN EUROPE
Authors: GREGERSEN N WINTER V CURTIS D DEUFEL T MACK M HENDRICKX J WILLEMS PJ PONZONE A PARELLA T PONZONE R DING JH ZHANG W CHEN YT KAHLER S ROE CR KOLVRAA S SCHNEIDERMAN K ANDRESEN BS BROSS P BOLUND L
Citation: N. Gregersen et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY - THE PREVALENTMUTATION G985 (K304E) IS SUBJECT TO A STRONG FOUNDER EFFECT FROM NORTHWESTERN EUROPE, Human heredity, 43(6), 1993, pp. 342-350
Risultati: 1-24 |