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Titolo:
PHOSPHOMANNOMUTASE DEFICIENCY IS THE MAIN CAUSE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME WITH TYPE-I ISOELECTROFOCUSING PATTERN OF SERUM SIALOTRANSFERRINS
Autore:
JAEKEN J; ARTIGAS J; BARONE R; FIUMARA A; DEKONING TJ; POLLTHE BT; DERIJKVANANDEL JF; HOFFMANN GF; ASSMANN B; MAYATEPEK E; PINEDA M; VILASECA MA; SAUDUBRAY JM; SCHLUTER B; WEVERS R; VANSCHAFTINGEN E;
Indirizzi:
UNIV HOSP GASTHUISBERG,DEPT PEDIAT,CTR METAB DIS,HERESTR 49 B-3000 LOUVAIN BELGIUM CATHOLIC UNIV LEUVEN,DEPT PEDIAT B-3000 LOUVAIN BELGIUM PARC TAULI HOSP,DEPT PEDIAT SABADELL SPAIN UNIV CATANIA,DEPT PEDIAT I-95124 CATANIA ITALY WILHELMINA CHILDRENS HOSP UTRECHT NETHERLANDS IGNATIUS HOSP BREDA,DEPT NEUROL BREDA NETHERLANDS UNIV MARBURG,CHILDRENS HOSP D-35032 MARBURG GERMANY UNIV HEIDELBERG,DEPT PEDIAT D-6900 HEIDELBERG GERMANY UNIV BARCELONA,HOSP SANT JOAN DEU E-08007 BARCELONA SPAIN HOP NECKER ENFANTS MALAD,DEPT PEDIAT PARIS FRANCE VEST KINDERKLIN DATTELN GERMANY UNIV NIJMEGEN HOSP,INST NEUROL NL-6500 HB NIJMEGEN NETHERLANDS UNIV NIJMEGEN HOSP,INST PEDIAT NL-6500 HB NIJMEGEN NETHERLANDS UNIV NIJMEGEN HOSP,INST RADIOL NL-6500 HB NIJMEGEN NETHERLANDS UNIV LOUVAIN LOUVAIN BELGIUM ICP,PHYSIOL CHEM LAB LOUVAIN BELGIUM
Titolo Testata:
Journal of inherited metabolic disease
fascicolo: 3, volume: 20, anno: 1997,
pagine: 447 - 449
SICI:
0141-8955(1997)20:3<447:PDITMC>2.0.ZU;2-I
Fonte:
ISI
Lingua:
ENG
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
14
Recensione:
Indirizzi per estratti:
Citazione:
J. Jaeken et al., "PHOSPHOMANNOMUTASE DEFICIENCY IS THE MAIN CAUSE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME WITH TYPE-I ISOELECTROFOCUSING PATTERN OF SERUM SIALOTRANSFERRINS", Journal of inherited metabolic disease, 20(3), 1997, pp. 447-449


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/11/20 alle ore 08:10:14