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Results: 1-20 |
Results: 20
NEONATAL BLOOD CARNITINE CONCENTRATIONS - ESTABLISHING NORMATIVE VALUES
Authors: DEVIVO DC KWAN A MCMAHON D CHIRIBOGA CA NAYLOR EW CHACE DH
Citation: Dc. Devivo et al., NEONATAL BLOOD CARNITINE CONCENTRATIONS - ESTABLISHING NORMATIVE VALUES, Annals of neurology, 44(3), 1998, pp. 26-26
3-METHYLCROTONYL-COENZYME-A CARBOXYLASE DEFICIENCY IN AMISH MENNONITEADULTS IDENTIFIED BY DETECTION OF INCREASED ACYLCARNITINES IN BLOOD SPOTS OF THEIR CHILDREN/
Authors: GIBSON KM BENNETT MJ NAYLOR EW MORTON DH
Citation: Km. Gibson et al., 3-METHYLCROTONYL-COENZYME-A CARBOXYLASE DEFICIENCY IN AMISH MENNONITEADULTS IDENTIFIED BY DETECTION OF INCREASED ACYLCARNITINES IN BLOOD SPOTS OF THEIR CHILDREN/, The Journal of pediatrics, 132(3), 1998, pp. 519-523
PETARCH AND GOMEZ,ALVAR - THE TRANSLATION OF THE 'TRIUNFO DE AMOR' - SPANISH - RECIO,R
Authors: NAYLOR EW
Citation: Ew. Naylor, PETARCH AND GOMEZ,ALVAR - THE TRANSLATION OF THE 'TRIUNFO DE AMOR' - SPANISH - RECIO,R, Revista de filologia espanola, 77(3-4), 1997, pp. 365-366
DIRECT ANALYSIS OF FILTER-PAPER BLOOD SPECIMENS FOR IDENTIFICATION OFSMITH-LEMLI-OPITZ SYNDROME USING TIME-OF-FLIGHT SECONDARY-ION MASS-SPECTROMETRY
Authors: ZIMMERMAN PA HERCULES DM NAYLOR EW
Citation: Pa. Zimmerman et al., DIRECT ANALYSIS OF FILTER-PAPER BLOOD SPECIMENS FOR IDENTIFICATION OFSMITH-LEMLI-OPITZ SYNDROME USING TIME-OF-FLIGHT SECONDARY-ION MASS-SPECTROMETRY, American journal of medical genetics, 68(3), 1997, pp. 300-304
TESTING INFANTS WHO DIE OF UNKNOWN CAUSES FOR METABOLIC AND OTHER DISEASES USING A DRIED BLOOD SPOT
Authors: HOFMAN LF POLANA PA MITCHELL BL NAYLOR EW SWANSON JR
Citation: Lf. Hofman et al., TESTING INFANTS WHO DIE OF UNKNOWN CAUSES FOR METABOLIC AND OTHER DISEASES USING A DRIED BLOOD SPOT, Clinical chemistry, 43, 1997, pp. 444-444
RAPID DIAGNOSIS OF MCAD DEFICIENCY - QUANTITATIVE-ANALYSIS OF OCTANOYLCARNITINE AND OTHER ACYLCARNITINES IN NEWBORN BLOOD SPOTS BY TANDEM MASS-SPECTROMETRY
Authors: CHACE DH HILLMAN SL VANHOVE JLK NAYLOR EW
Citation: Dh. Chace et al., RAPID DIAGNOSIS OF MCAD DEFICIENCY - QUANTITATIVE-ANALYSIS OF OCTANOYLCARNITINE AND OTHER ACYLCARNITINES IN NEWBORN BLOOD SPOTS BY TANDEM MASS-SPECTROMETRY, Clinical chemistry, 43(11), 1997, pp. 2106-2113
IMMEDIATELY ELEVATED POSTOPERATIVE SERUM BRANCHED-CHAIN AMINO-ACIDS FOLLOWING EFFECTIVE GI DECOMPRESSION AND ENTERAL FEEDING
Authors: NASSIF AC NAYLOR EW
Citation: Ac. Nassif et Ew. Naylor, IMMEDIATELY ELEVATED POSTOPERATIVE SERUM BRANCHED-CHAIN AMINO-ACIDS FOLLOWING EFFECTIVE GI DECOMPRESSION AND ENTERAL FEEDING, Nutrition, 12(3), 1996, pp. 159-162
SPANISH POETRY OF THE 20TH-CENTURY - MODERNITY AND BEYOND - DEBICKI,AP
Authors: NAYLOR EW
Citation: Ew. Naylor, SPANISH POETRY OF THE 20TH-CENTURY - MODERNITY AND BEYOND - DEBICKI,AP, The Sewanee review, 104(2), 1996, pp. 39-40
MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN PENNSYLVANIA - NEONATAL SCREENING SHOWS HIGH-INCIDENCE AND UNEXPECTED MUTATION FREQUENCIES
Authors: ZIADEH R HOFFMAN EP FINEGOLD DN HOOP RC BRACKETT JC STRAUSS AW NAYLOR EW
Citation: R. Ziadeh et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN PENNSYLVANIA - NEONATAL SCREENING SHOWS HIGH-INCIDENCE AND UNEXPECTED MUTATION FREQUENCIES, Pediatric research, 37(5), 1995, pp. 675-678
FREQUENCY OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY AMONG CALIFORNIA CHILDREN DYING OF SUDDEN-INFANT-DEATH-SYNDROME (SIDS) OR LIVER-DISEASE - 2-TIERED ANALYSIS OF NEWBORN SCREENING SPECIMENS
Authors: ZHANG YH YBARRA A MCCABE LL LOREY F RIGGLE S MORALES D NAYLOR EW CUNNINGHAM GC MCCABE ERB
Citation: Yh. Zhang et al., FREQUENCY OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY AMONG CALIFORNIA CHILDREN DYING OF SUDDEN-INFANT-DEATH-SYNDROME (SIDS) OR LIVER-DISEASE - 2-TIERED ANALYSIS OF NEWBORN SCREENING SPECIMENS, Pediatric research, 37(4), 1995, pp. 156-156
RAPID DIAGNOSIS OF MAPLE-SYRUP-URINE-DISEASE IN BLOOD SPOTS FROM NEWBORNS BY TANDEM MASS-SPECTROMETRY
Authors: CHACE DH HILLMAN SL MILLINGTON DS KAHLER SG ROE CR NAYLOR EW
Citation: Dh. Chace et al., RAPID DIAGNOSIS OF MAPLE-SYRUP-URINE-DISEASE IN BLOOD SPOTS FROM NEWBORNS BY TANDEM MASS-SPECTROMETRY, Clinical chemistry, 41(1), 1995, pp. 62-68
DIAGNOSIS OF CYSTIC-FIBROSIS IN A PREMATURE-INFANT VIA NEONATAL SCREENING
Authors: ALLEN JL STAVIS R KAPLAN GS NAYLOR EW
Citation: Jl. Allen et al., DIAGNOSIS OF CYSTIC-FIBROSIS IN A PREMATURE-INFANT VIA NEONATAL SCREENING, Archives of pediatrics & adolescent medicine, 148(9), 1994, pp. 995-996
DELETION OF THE FERROCHELATASE GENE IN A PATIENT WITH PROTOPORPHYRIA
Authors: MAGNESS ST TUGORES A CHRISTENSEN SR WAGNERMCPHERSON C EVANS GA NAYLOR EW BRENNER DA
Citation: St. Magness et al., DELETION OF THE FERROCHELATASE GENE IN A PATIENT WITH PROTOPORPHYRIA, Human molecular genetics, 3(9), 1994, pp. 1695-1697
'DON QUIXOTE' - CERVANTES, MOTTEUX,PA
Authors: NAYLOR EW
Citation: Ew. Naylor, 'DON QUIXOTE' - CERVANTES, MOTTEUX,PA, The Sewanee review, 102(2), 1994, pp. 180000042-180000044
THE SANCTIFICATION OF DON-QUIXOTE - FROM HIDALGO TO PRIEST - ZIOLKOWSKI,E
Authors: NAYLOR EW
Citation: Ew. Naylor, THE SANCTIFICATION OF DON-QUIXOTE - FROM HIDALGO TO PRIEST - ZIOLKOWSKI,E, The Sewanee review, 102(2), 1994, pp. 180000042-180000044
AESOP FABLES, WITH A LIFE OF AESOP - KELLER,JE, KEATING,LC, TRANSLATORS
Authors: NAYLOR EW
Citation: Ew. Naylor, AESOP FABLES, WITH A LIFE OF AESOP - KELLER,JE, KEATING,LC, TRANSLATORS, Hispania, 77(4), 1994, pp. 815-815
THE 'BOOK OF TALES BY A.B.C.' - SANCHEZDEVERCIAL,C
Authors: NAYLOR EW
Citation: Ew. Naylor, THE 'BOOK OF TALES BY A.B.C.' - SANCHEZDEVERCIAL,C, Hispania, 77(4), 1994, pp. 815-815
NEONATAL SCREENING FOR CYSTIC-FIBROSIS - ADDITION OF MOLECULAR DIAGNOSTICS TO INCREASE SPECIFICITY
Authors: SPENCE WC PAULUSTHOMAS J ORENSTEIN DM NAYLOR EW
Citation: Wc. Spence et al., NEONATAL SCREENING FOR CYSTIC-FIBROSIS - ADDITION OF MOLECULAR DIAGNOSTICS TO INCREASE SPECIFICITY, Biochemical medicine and metabolic biology, 49(2), 1993, pp. 200-211
NEONATAL SCREENING FOR INBORN-ERRORS OF FATTY-ACID OXIDATION AND AMINO-ACID-METABOLISM USING FAST-ATOM-BOMBARDMENT TANDEM MASS-SPECTROMETRY
Authors: NAYLOR EW ZIADEH R FINEGOLD DN
Citation: Ew. Naylor et al., NEONATAL SCREENING FOR INBORN-ERRORS OF FATTY-ACID OXIDATION AND AMINO-ACID-METABOLISM USING FAST-ATOM-BOMBARDMENT TANDEM MASS-SPECTROMETRY, American journal of human genetics, 53(3), 1993, pp. 934-934
MUTATION IN THE 4A-CARBINOLAMINE DEHYDRATASE GENE LEADS TO MILD HYPERPHENYLALANINEMIA WITH DEFECTIVE COFACTOR METABOLISM
Authors: CITRON BA KAUFMAN S MILSTIEN S NAYLOR EW GREENE CL DAVIS MD
Citation: Ba. Citron et al., MUTATION IN THE 4A-CARBINOLAMINE DEHYDRATASE GENE LEADS TO MILD HYPERPHENYLALANINEMIA WITH DEFECTIVE COFACTOR METABOLISM, American journal of human genetics, 53(3), 1993, pp. 768-774
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