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Results: 1-25 | 26-27
Results: 1-25/27
RETRIEVAL OF AEROSOL SINGLE-SCATTERING ALBEDO FROM GROUND-BASED MEASUREMENTS - APPLICATION TO OBSERVATIONAL DATA
Authors: DEVAUX C VERMEULEN A DEUZE JL DUBUISSON P HERMAN M SANTER R VERBRUGGHE M
Citation: C. Devaux et al., RETRIEVAL OF AEROSOL SINGLE-SCATTERING ALBEDO FROM GROUND-BASED MEASUREMENTS - APPLICATION TO OBSERVATIONAL DATA, J GEO RES-A, 103(D8), 1998, pp. 8753-8761
MUTATIONS IN GLUT2, THE GENE FOR THE LIVER-TYPE GLUCOSE-TRANSPORTER, IN PATIENTS WITH FANCONI-BICKEL-SYNDROME (VOL 17, PG 324, 1997)
Authors: SANTER R SCHNEPPENHEIM R DOMBROWSKI A GOTZE H STEINMANN B SCHAUB J
Citation: R. Santer et al., MUTATIONS IN GLUT2, THE GENE FOR THE LIVER-TYPE GLUCOSE-TRANSPORTER, IN PATIENTS WITH FANCONI-BICKEL-SYNDROME (VOL 17, PG 324, 1997), Nature genetics, 18(3), 1998, pp. 298-298
FANCONI-BICKEL-SYNDROME - THE ORIGINAL PATIENT AND HIS NATURAL-HISTORY, HISTORICAL STEPS LEADING TO THE PRIMARY DEFECT, AND A REVIEW OF THELITERATURE
Authors: SANTER R SCHNEPPENHEIM R SUTER D SCHAUB J STEINMANN B
Citation: R. Santer et al., FANCONI-BICKEL-SYNDROME - THE ORIGINAL PATIENT AND HIS NATURAL-HISTORY, HISTORICAL STEPS LEADING TO THE PRIMARY DEFECT, AND A REVIEW OF THELITERATURE, European journal of pediatrics, 157(10), 1998, pp. 783-797
FANCONI-BICKEL-SYNDROME - A CONGENITAL DEFECT OF THE LIVER-TYPE FACILITATIVE GLUCOSE-TRANSPORTER
Authors: SANTER R SCHNEPPENHEIM R DOMBROWSKI A GOTZE H STEINMANN B SCHAUB J
Citation: R. Santer et al., FANCONI-BICKEL-SYNDROME - A CONGENITAL DEFECT OF THE LIVER-TYPE FACILITATIVE GLUCOSE-TRANSPORTER, Journal of inherited metabolic disease, 21(3), 1998, pp. 191-194
AEROSOL REMOTE-SENSING USING GROUND-BASED MEASUREMENTS AND POLDER AIRBORNE SENSOR ABOVE COASTAL WATERS
Authors: CHAMI M SANTER R
Citation: M. Chami et R. Santer, AEROSOL REMOTE-SENSING USING GROUND-BASED MEASUREMENTS AND POLDER AIRBORNE SENSOR ABOVE COASTAL WATERS, Remote sensing of environment, 66(2), 1998, pp. 203-221
FURTHER EVIDENCE FOR A DOMINANT FORM OF FAMILIAL PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY - A FAMILY WITH DOCUMENTED HYPERINSULINEMIA IN 2 GENERATIONS
Authors: HUFNAGEL M EICHMANN D STIEH J SANTER R
Citation: M. Hufnagel et al., FURTHER EVIDENCE FOR A DOMINANT FORM OF FAMILIAL PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY - A FAMILY WITH DOCUMENTED HYPERINSULINEMIA IN 2 GENERATIONS, The Journal of clinical endocrinology and metabolism, 83(6), 1998, pp. 2215-2216
MUTATIONS IN GLUT2, THE GENE FOR THE LIVER-TYPE GLUCOSE-TRANSPORTER, IN PATIENTS WITH FANCONI-BICKEL-SYNDROME
Authors: SANTER R SCHNEPPENHEIM R DOMBROWSKI A GOTZE H STEINMANN B SCHAUB J
Citation: R. Santer et al., MUTATIONS IN GLUT2, THE GENE FOR THE LIVER-TYPE GLUCOSE-TRANSPORTER, IN PATIENTS WITH FANCONI-BICKEL-SYNDROME, Nature genetics, 17(3), 1997, pp. 324-326
A FIELD EXPERIMENT IN SAHARAN ALGERIA FOR THE CALIBRATION OF OPTICAL SATELLITE SENSORS
Authors: COSNEFROY H BRIOTTET X LEROY M LECOMTE P SANTER R
Citation: H. Cosnefroy et al., A FIELD EXPERIMENT IN SAHARAN ALGERIA FOR THE CALIBRATION OF OPTICAL SATELLITE SENSORS, International journal of remote sensing, 18(16), 1997, pp. 3337-3359
FANCONI-BICKEL-SYNDROME PRESENTING IN NEONATAL SCREENING FOR GALACTOSEMIA
Authors: MULLER D SANTER R KRAWINKEL M CHRISTIANSEN B SCHAUB J
Citation: D. Muller et al., FANCONI-BICKEL-SYNDROME PRESENTING IN NEONATAL SCREENING FOR GALACTOSEMIA, Journal of inherited metabolic disease, 20(4), 1997, pp. 607-608
A SURVEY OF THE NEWBORN POPULATIONS IN BELGIUM, GERMANY, POLAND, CZECH-REPUBLIC, HUNGARY, BULGARIA, SPAIN, TURKEY, AND JAPAN FOR THE G985 VARIANT ALLELE WITH HAPLOTYPE ANALYSIS AT THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE LOCUS - CLINICAL AND EVOLUTIONARY CONSIDERATION
Authors: TANAKA K GREGERSEN N RIBES A KIM J KOLVRAA S WINTER V EIBERG H MARTINEZ G DEUFEL T LEIFERT B SANTER R FRANCOIS B PRONICKA E LASZLO A KMOCH S KREMENSKY I KALAYDJICVA L OZALP I ITO M
Citation: K. Tanaka et al., A SURVEY OF THE NEWBORN POPULATIONS IN BELGIUM, GERMANY, POLAND, CZECH-REPUBLIC, HUNGARY, BULGARIA, SPAIN, TURKEY, AND JAPAN FOR THE G985 VARIANT ALLELE WITH HAPLOTYPE ANALYSIS AT THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE LOCUS - CLINICAL AND EVOLUTIONARY CONSIDERATION, Pediatric research, 41(2), 1997, pp. 201-209
A NOVEL MISSENSE (E163G) MUTATION IN THE CATALYTIC SUBUNIT OF LIPOPROTEIN-LIPASE CAUSES FAMILIAL CHYLOMICRONEMIA
Authors: WIEBUSCH H FUNKE H SANTER R RICHTER W ASSMANN G
Citation: H. Wiebusch et al., A NOVEL MISSENSE (E163G) MUTATION IN THE CATALYTIC SUBUNIT OF LIPOPROTEIN-LIPASE CAUSES FAMILIAL CHYLOMICRONEMIA, Human mutation, 8(4), 1996, pp. 392-392
CEREBROSPINAL-FLUID CONCENTRATIONS OF LEUKOTRIENE B-4 IN BACTERIAL-MENINGITIS
Authors: SANTER R SIEVERS E SCHAUB J
Citation: R. Santer et al., CEREBROSPINAL-FLUID CONCENTRATIONS OF LEUKOTRIENE B-4 IN BACTERIAL-MENINGITIS, Acta paediatrica, 85(8), 1996, pp. 902-905
WILLIAMS-BEUREN SYNDROME AND CELIAC-DISEASE
Authors: SANTER R PANKAU R SCHAUB J BURGINWOLFF A
Citation: R. Santer et al., WILLIAMS-BEUREN SYNDROME AND CELIAC-DISEASE, Journal of pediatric gastroenterology and nutrition, 23(3), 1996, pp. 339-340
THE PREVALENCE OF THE G985 ALLELE OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY AMONG SUDDEN INFANT DEATH VICTIMS AND HEALTHY NEWBORNS IN NORTHERN GERMANY
Authors: SANTER R GREGERSEN N TANAKA K HINCKKNEIP C KRAWINKEL M SCHAUB J
Citation: R. Santer et al., THE PREVALENCE OF THE G985 ALLELE OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY AMONG SUDDEN INFANT DEATH VICTIMS AND HEALTHY NEWBORNS IN NORTHERN GERMANY, European journal of pediatrics, 154(6), 1995, pp. 497-497
DECREASED ACTIVITY OF RESPIRATORY-CHAIN ENZYMES IN GLUTARIC ACIDURIA TYPE-II
Authors: SANTER R CLAASS A KRAWINKEL M SCHAUB J RUITENBEEK W
Citation: R. Santer et al., DECREASED ACTIVITY OF RESPIRATORY-CHAIN ENZYMES IN GLUTARIC ACIDURIA TYPE-II, Journal of inherited metabolic disease, 18(1), 1995, pp. 75-76
NAG IN TYPE-I DIABETES-MELLITUS - DO WE NEED RANDOM OR 24-HOUR URINE SPECIMENS FOR THE REPRESENTATIVE ASSESSMENT OF NAG EXCRETION
Authors: SIEVERS E EGGERT P MULLER D SANTER R
Citation: E. Sievers et al., NAG IN TYPE-I DIABETES-MELLITUS - DO WE NEED RANDOM OR 24-HOUR URINE SPECIMENS FOR THE REPRESENTATIVE ASSESSMENT OF NAG EXCRETION, Pediatric research, 37(4), 1995, pp. 370-370
SUDDEN UNEXPECTED INFANT DEATH AND MEDIUM -CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY
Authors: SANTER R SCHMIDTSOMMERFELD E GREGERSEN N HINCKKNEIP C KRAWINKEL M SCHAUB J
Citation: R. Santer et al., SUDDEN UNEXPECTED INFANT DEATH AND MEDIUM -CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY, Monatsschrift fur Kinderheilkunde, 143(8), 1995, pp. 749-753
GASTROINTESTINAL PASSAGE TIME IN PRETERM INFANTS
Authors: SIEVERS E SANTER R OLDIGS HD HAASE S SCHLEYERBACH U SCHAUB J
Citation: E. Sievers et al., GASTROINTESTINAL PASSAGE TIME IN PRETERM INFANTS, Monatsschrift fur Kinderheilkunde, 143(7), 1995, pp. 76-80
DISCORDANCE FOR HYPERINSULINEMIC HYPOGLYCEMIA IN MONOZYGOTIC TWINS
Authors: SANTER R HOFFMANN H SUTTORP M SIMEONI E SCHAUB J
Citation: R. Santer et al., DISCORDANCE FOR HYPERINSULINEMIC HYPOGLYCEMIA IN MONOZYGOTIC TWINS, The Journal of pediatrics, 126(6), 1995, pp. 1017-1017
URSODESOXYCHOLIC ACID - EFFECT ON XANTHOMAS IN ALAGILLE-WATSON SYNDROME
Authors: KRAWINKEL MB SANTER R OLDIGS HD
Citation: Mb. Krawinkel et al., URSODESOXYCHOLIC ACID - EFFECT ON XANTHOMAS IN ALAGILLE-WATSON SYNDROME, Journal of pediatric gastroenterology and nutrition, 19(4), 1994, pp. 476-477
ASSOCIATION OF MALONYL-COA DECARBOXYLASE DEFICIENCY AND HETEROZYGOTE STATE FOR HEMOGLOBIN-C DISEASE
Authors: KRAWINKEL MB OLDIGS HD SANTER R LEHNERT W WENDEL U SCHAUB J
Citation: Mb. Krawinkel et al., ASSOCIATION OF MALONYL-COA DECARBOXYLASE DEFICIENCY AND HETEROZYGOTE STATE FOR HEMOGLOBIN-C DISEASE, Journal of inherited metabolic disease, 17(5), 1994, pp. 636-637
POLARIZATION OF THE SOLAR LIGHT SCATTERED BY THE EARTH ATMOSPHERE SYSTEM AS OBSERVED FROM THE UNITED-STATES-SHUTTLE
Authors: ROGER JC SANTER R HERMAN M DEUZE JL
Citation: Jc. Roger et al., POLARIZATION OF THE SOLAR LIGHT SCATTERED BY THE EARTH ATMOSPHERE SYSTEM AS OBSERVED FROM THE UNITED-STATES-SHUTTLE, Remote sensing of environment, 48(3), 1994, pp. 275-290
ASCITES - AN UNUSUAL PRESENTATION OF CHRO NIC GRANULOMATOUS-DISEASE
Authors: SANTER R SCHNEPPENHEIM R OPPERMANN H HARMS D GAHR M
Citation: R. Santer et al., ASCITES - AN UNUSUAL PRESENTATION OF CHRO NIC GRANULOMATOUS-DISEASE, Monatsschrift fur Kinderheilkunde, 142(3), 1994, pp. 185-188
POPULATION SCREENING FOR MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - ANALYSIS OF MEDIUM-CHAIN FATTY-ACIDS AND ACYLGLYCINES IN BLOOD SPOTS
Authors: BENNETT MJ RAGNI MC OSTFELD RJ SANTER R SCHMIDTSOMMERFELD E
Citation: Mj. Bennett et al., POPULATION SCREENING FOR MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - ANALYSIS OF MEDIUM-CHAIN FATTY-ACIDS AND ACYLGLYCINES IN BLOOD SPOTS, Annals of clinical biochemistry, 31, 1994, pp. 72-77
SANTER,J.F. - OBITUARY
Authors: SANTER R
Citation: R. Santer, SANTER,J.F. - OBITUARY, BMJ. British medical journal, 307(6916), 1993, pp. 1419-1419
Risultati: 1-25 | 26-27