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Results: 1-25 | 26-45
Results: 1-25/45
SPATIAL AND TEMPORAL VARIABILITY OF NONMETHANE HYDROCARBON MIXING RATIOS AND THEIR RELATION TO PHOTOCHEMICAL LIFETIME
Authors: JOBSON BT PARRISH DD GOLDAN P KUSTER W FEHSENFELD FC BLAKE DR BLAKE NJ NIKI H
Citation: Bt. Jobson et al., SPATIAL AND TEMPORAL VARIABILITY OF NONMETHANE HYDROCARBON MIXING RATIOS AND THEIR RELATION TO PHOTOCHEMICAL LIFETIME, J GEO RES-A, 103(D11), 1998, pp. 13557-13567
GENOTYPE PHENOTYPE CORRELATION IN AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS/
Authors: HENNIES HC KUSTER W WIEBE V KREBSOVA A REIS A
Citation: Hc. Hennies et al., GENOTYPE PHENOTYPE CORRELATION IN AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS/, American journal of human genetics, 62(5), 1998, pp. 1052-1061
SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME
Authors: SILLEN A ANTONLAMPRECHT I BRAUNQUENTIN C KRAUS CS SAYLI BS AYUSO C JAGELL S KUSTER W WADELIUS C
Citation: A. Sillen et al., SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME, Human mutation, 12(6), 1998, pp. 377-384
NEVUS PSILOLIPARUS - A DISTINCT FATTY TISSUE NEVUS
Authors: HAPPLE R KUSTER W
Citation: R. Happle et W. Kuster, NEVUS PSILOLIPARUS - A DISTINCT FATTY TISSUE NEVUS, Dermatology, 197(1), 1998, pp. 6-10
EFFICACY OF UREA THERAPY IN CHILDREN WITH ICHTHYOSIS - A MULTICENTER RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, SEMILATERAL STUDY
Authors: KUSTER W BOHNSACK K RIPPKE F UPMEYER HJ GROLL S TRAUPE H
Citation: W. Kuster et al., EFFICACY OF UREA THERAPY IN CHILDREN WITH ICHTHYOSIS - A MULTICENTER RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, SEMILATERAL STUDY, Dermatology, 196(2), 1998, pp. 217-222
CONGENITAL ICHTHYOSIS, FOLLICULAR ATROPHODERMA, HYPOTRICHOSIS, AND HYPOHIDROSIS - A NEW GENODERMATOSIS
Authors: LESTRINGANT GG KUSTER W FROSSARD PM HAPPLE R
Citation: Gg. Lestringant et al., CONGENITAL ICHTHYOSIS, FOLLICULAR ATROPHODERMA, HYPOTRICHOSIS, AND HYPOHIDROSIS - A NEW GENODERMATOSIS, American journal of medical genetics, 75(2), 1998, pp. 186-189
NOVEL K5 AND K14 MUTATIONS IN GERMAN PATIENTS WITH THE WEBER-COCKAYNEVARIANT OF EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: MULLER FB KUSTER W BRUCKNERTUDERMAN L KORGE BP
Citation: Fb. Muller et al., NOVEL K5 AND K14 MUTATIONS IN GERMAN PATIENTS WITH THE WEBER-COCKAYNEVARIANT OF EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of investigative dermatology, 111(5), 1998, pp. 900-902
NEW KERATIN K5 AND K14 MUTATIONS IN 7 GERMAN FAMILIES WITH EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: MULLER FB KUSTER W BRUCKNERTUDERMAN L KORGE BP
Citation: Fb. Muller et al., NEW KERATIN K5 AND K14 MUTATIONS IN 7 GERMAN FAMILIES WITH EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of investigative dermatology, 110(4), 1998, pp. 511-511
LACK OF ASSOCIATION BETWEEN MUTANT ALLELE OF XENOBIOTIC-METABOLIZING ENZYMES CYTOCHROME-P450 2C19 AND 2E1 AND PSORIASIS
Authors: SACHS B RICHTERHINTZ D KRONENBERG S VONSCHMIEDEBERG S SCHUPPE HC RUZICKA T STANDER M KUSTER W GLEICHMANN E ESSER C
Citation: B. Sachs et al., LACK OF ASSOCIATION BETWEEN MUTANT ALLELE OF XENOBIOTIC-METABOLIZING ENZYMES CYTOCHROME-P450 2C19 AND 2E1 AND PSORIASIS, Journal of investigative dermatology, 110(4), 1998, pp. 621-621
GENERALIZED ERYTHROKERATODERMIA PROGRESSIVA SYMMETRICA DARIER-GOTTRON
Authors: EMMERT S KUSTER W SCHAUDER S NEUMANN C RUNGER TM
Citation: S. Emmert et al., GENERALIZED ERYTHROKERATODERMIA PROGRESSIVA SYMMETRICA DARIER-GOTTRON, Hautarzt, 49(8), 1998, pp. 666-671
ASN(141) IS ESSENTIAL FOR DNA RECOGNITION BY ECORI RESTRICTION-ENDONUCLEASE
Authors: FRITZ A KUSTER W ALVES J
Citation: A. Fritz et al., ASN(141) IS ESSENTIAL FOR DNA RECOGNITION BY ECORI RESTRICTION-ENDONUCLEASE, FEBS letters, 438(1-2), 1998, pp. 66-70
PHOTOCHEMISTRY OF FORMALDEHYDE DURING THE 1993 TROPOSPHERIC OH PHOTOCHEMISTRY EXPERIMENT
Authors: FRIED A MCKEEN S SEWELL S HARDER J HENRY B GOLDAN P KUSTER W WILLIAMS E BAUMANN K SHETTER R CANTRELL C
Citation: A. Fried et al., PHOTOCHEMISTRY OF FORMALDEHYDE DURING THE 1993 TROPOSPHERIC OH PHOTOCHEMISTRY EXPERIMENT, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 102(D5), 1997, pp. 6283-6296
HO2 OH AND RO(2)/HO2 RATIOS DURING THE TROPOSPHERIC OH PHOTOCHEMISTRYEXPERIMENT - MEASUREMENT AND THEORY/
Authors: STEVENS PS MATHER JH BRUNE WH EISELE F TANNER D JEFFERSON A CANTRELL C SHETTER R SEWALL S FRIED A HENRY B WILLIAMS E BAUMANN K GOLDAN P KUSTER W
Citation: Ps. Stevens et al., HO2 OH AND RO(2)/HO2 RATIOS DURING THE TROPOSPHERIC OH PHOTOCHEMISTRYEXPERIMENT - MEASUREMENT AND THEORY/, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 102(D5), 1997, pp. 6379-6391
PHOTOCHEMICAL MODELING OF HYDROXYL AND ITS RELATIONSHIP TO OTHER SPECIES DURING THE TROPOSPHERIC OH PHOTOCHEMISTRY EXPERIMENT
Authors: MCKEEN SA MOUNT G EISELE F WILLIAMS E HARDER J GOLDAN P KUSTER W LIU SC BAUMANN K TANNER D FRIED A SEWELL S CANTRELL C SHETTER R
Citation: Sa. Mckeen et al., PHOTOCHEMICAL MODELING OF HYDROXYL AND ITS RELATIONSHIP TO OTHER SPECIES DURING THE TROPOSPHERIC OH PHOTOCHEMISTRY EXPERIMENT, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 102(D5), 1997, pp. 6467-6493
AUTOSOMAL-DOMINANT INHERITANCE OF HID SYNDROME (HYSTRIX-LIKE ICHTHYOSIS WITH DEAFNESS)
Authors: KONIG A KUSTER W BERGER R HAPPLE R
Citation: A. Konig et al., AUTOSOMAL-DOMINANT INHERITANCE OF HID SYNDROME (HYSTRIX-LIKE ICHTHYOSIS WITH DEAFNESS), EJD. European journal of dermatology, 7(8), 1997, pp. 554-555
DISRUPTIVE ANOMALIES IN A NEWBORN WITH FOCAL DERMAL HYPOPLASIA (GOLTZ-SYNDROME)
Authors: RAMSING M NGO TKN HOLZGREVE W RACKOWITZ A KUSTER W REHDER H
Citation: M. Ramsing et al., DISRUPTIVE ANOMALIES IN A NEWBORN WITH FOCAL DERMAL HYPOPLASIA (GOLTZ-SYNDROME), EJD. European journal of dermatology, 7(1), 1997, pp. 15-18
OPERATING EXPERIENCES WITH AN ANAEROBIC F LUIDIZED-BED REACTOR FOR THE TREATMENT OF SUGAR FACTORY WASTE-WATER
Authors: JORDENING HJ KUSTER W
Citation: Hj. Jordening et W. Kuster, OPERATING EXPERIENCES WITH AN ANAEROBIC F LUIDIZED-BED REACTOR FOR THE TREATMENT OF SUGAR FACTORY WASTE-WATER, Zuckerindustrie, 122(12), 1997, pp. 934-936
CLAUEN-SUGAR-FACTORY OF ZUCKERVERBUND-NOR D-AG - COMPLETION OF 2ND RECONSTRUCTION PHASE OF BEET END
Authors: BUHRMANN S KUSTER W
Citation: S. Buhrmann et W. Kuster, CLAUEN-SUGAR-FACTORY OF ZUCKERVERBUND-NOR D-AG - COMPLETION OF 2ND RECONSTRUCTION PHASE OF BEET END, Zuckerindustrie, 122(11), 1997, pp. 849-853
ICHTHYOSIS VARIEGATA - A NEW NAME FOR A NEGLECTED DISEASE
Authors: HAPPLE R KUSTER W
Citation: R. Happle et W. Kuster, ICHTHYOSIS VARIEGATA - A NEW NAME FOR A NEGLECTED DISEASE, Journal of the American Academy of Dermatology, 36(3), 1997, pp. 500-500
THE LOCALISATA VARIANT OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA (JEB) IS ACOLLAGEN-XVII DISEASE
Authors: SCHUMANN H HAUASLI NH PULKKINEN L MAUVIEL A KUSTER W OWARIBE K UITTO J BRUCKNERTUDERMAN L
Citation: H. Schumann et al., THE LOCALISATA VARIANT OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA (JEB) IS ACOLLAGEN-XVII DISEASE, Journal of investigative dermatology, 109(3), 1997, pp. 410-410
CORRELATION OF THE GENOTYPE WITH BIOLOGICAL AND CLINICAL PHENOTYPES IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA (JEB)
Authors: SCHUMANN H HAUASLI NH PULKKINEN L MAUVIEL A KUSTER W LUTHI U OWARIBE K UITTO J BRUCKNERTUDERMAN L
Citation: H. Schumann et al., CORRELATION OF THE GENOTYPE WITH BIOLOGICAL AND CLINICAL PHENOTYPES IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA (JEB), Journal of investigative dermatology, 108(4), 1997, pp. 152-152
PATCHY DERMAL HYPOPLASIA AS A CHARACTERISTIC FEATURE OF PROTEUS SYNDROME
Authors: HAPPLE R STEIJLEN PM THEILE U KARITZKY D TINSCHERT S ALBRECHTNEBE H KUSTER W
Citation: R. Happle et al., PATCHY DERMAL HYPOPLASIA AS A CHARACTERISTIC FEATURE OF PROTEUS SYNDROME, Archives of dermatology, 133(1), 1997, pp. 77-80
SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME
Authors: SILLEN A KRAUS CS ANTONLAMBRECHT I JAGELL S KUSTER W SAYLI BS AYUSO C WADELIUS C
Citation: A. Sillen et al., SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 2029-2029
LOCALIZATION OF THE GENE CAUSING KERATOLYTIC WINTER ERYTHEMA TO CHROMOSOME 8P22-P23, AND EVIDENCE FOR A FOUNDER EFFECT IN SOUTH-AFRICAN AFRIKAANS-SPEAKERS
Authors: STARFIELD M HENNIES HC JUNG M JENKINS T WIENKER T HULL P SPURDLE A KUSTER W RAMSAY M REIS A
Citation: M. Starfield et al., LOCALIZATION OF THE GENE CAUSING KERATOLYTIC WINTER ERYTHEMA TO CHROMOSOME 8P22-P23, AND EVIDENCE FOR A FOUNDER EFFECT IN SOUTH-AFRICAN AFRIKAANS-SPEAKERS, American journal of human genetics, 61(2), 1997, pp. 370-378
3 NOVEL HOMOZYGOUS POINT MUTATIONS AND A NEW POLYMORPHISM IN THE COL17A1 GENE - RELATION TO BIOLOGICAL AND CLINICAL PHENOTYPES OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA
Authors: SCHUMANN H HAMMAMIHAUASLI N PULKKINEN L MAUVIEL A KUSTER W LUTHI U OWARIBE K UITTO J BRUCKNERTUDERMAN L
Citation: H. Schumann et al., 3 NOVEL HOMOZYGOUS POINT MUTATIONS AND A NEW POLYMORPHISM IN THE COL17A1 GENE - RELATION TO BIOLOGICAL AND CLINICAL PHENOTYPES OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA, American journal of human genetics, 60(6), 1997, pp. 1344-1353
Risultati: 1-25 | 26-45