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Results: 1-12 |
Results: 12
A MOLECULAR-GENETIC STUDY OF HYPERKINETIC DISORDER ATTENTION DEFICIT HYPERACTIVITY DISORDER/
Authors: POULTON K HOLMES J HEVER T TRUMPER A FITZPATRICK H MCGUFFIN P OWEN M WORTHINGTON J OLLIER W HARRINGTON R THAPAR A
Citation: K. Poulton et al., A MOLECULAR-GENETIC STUDY OF HYPERKINETIC DISORDER ATTENTION DEFICIT HYPERACTIVITY DISORDER/, American journal of medical genetics, 81(6), 1998, pp. 458-458
A CASE OF OHTAHARA-SYNDROME WITH CYTOCHROME-OXIDASE DEFICIENCY
Authors: WILLIAMS AN GRAY RG POULTON K RAMANI P WHITEHOUSE WPA
Citation: An. Williams et al., A CASE OF OHTAHARA-SYNDROME WITH CYTOCHROME-OXIDASE DEFICIENCY, Developmental Medicine and Child Neurology, 40(8), 1998, pp. 568-570
GIANT-CELL ARTERITIS AND POLYMYALGIA-RHEUMATICA CAN BE DIFFERENTIATEDBY DISTINCT PATTERNS OF HLA CLASS-II ASSOCIATION
Authors: DEBABNEH A GONZALEZGAY M GARCIAPORRURA C HAJEER A POULTON K THOMSON W OLLIER W
Citation: A. Debabneh et al., GIANT-CELL ARTERITIS AND POLYMYALGIA-RHEUMATICA CAN BE DIFFERENTIATEDBY DISTINCT PATTERNS OF HLA CLASS-II ASSOCIATION, Arthritis and rheumatism, 41(9), 1998, pp. 511-511
ETHYLMALONIC ADIPIC ACIDURIA - A TREATABLE HEPATOMUSCULAR DISORDER IN2 ADULT BROTHERS
Authors: ELIAS E GRAY RGF POULTON K GREEN A
Citation: E. Elias et al., ETHYLMALONIC ADIPIC ACIDURIA - A TREATABLE HEPATOMUSCULAR DISORDER IN2 ADULT BROTHERS, Journal of hepatology, 26(2), 1997, pp. 433-436
MUSCLE BIOCHEMISTRY IN THIAMIN-RESPONSIVE ANEMIA
Authors: BARRETT TG POULTON K BAINES M MCCOWEN C
Citation: Tg. Barrett et al., MUSCLE BIOCHEMISTRY IN THIAMIN-RESPONSIVE ANEMIA, Journal of inherited metabolic disease, 20(3), 1997, pp. 404-406
BLOOD-TRANSFUSION - A POSSIBLE RISK FACTOR FOR THE DEVELOPMENT OF RHEUMATOID-ARTHRITIS
Authors: HARRISON B BANKHEAD C SILMAN A POULTON K BARRETT E SCOTT D SYMMONS D
Citation: B. Harrison et al., BLOOD-TRANSFUSION - A POSSIBLE RISK FACTOR FOR THE DEVELOPMENT OF RHEUMATOID-ARTHRITIS, Arthritis and rheumatism, 40(9), 1997, pp. 1697-1697
TNF MICROSATELLITE A2, B3 AND D2 ALLELES ARE ASSOCIATED WITH SYSTEMICLUPUS-ERYTHEMATOSUS
Authors: HAJEER AH WORTHINGTON J DAVIES EJ HILLARBY MC POULTON K OLLIER WER
Citation: Ah. Hajeer et al., TNF MICROSATELLITE A2, B3 AND D2 ALLELES ARE ASSOCIATED WITH SYSTEMICLUPUS-ERYTHEMATOSUS, Tissue antigens, 49(3), 1997, pp. 222-227
DIDMOAD SYNDROME - FURTHER-STUDIES AND MUSCLE BIOCHEMISTRY
Authors: BARRETT TG POULTON K BUNDEY S
Citation: Tg. Barrett et al., DIDMOAD SYNDROME - FURTHER-STUDIES AND MUSCLE BIOCHEMISTRY, Journal of inherited metabolic disease, 18(2), 1995, pp. 218-220
A 6-B, 4 GSA S GAAS HBT ADC
Authors: POULTON K KNUDSEN KL CORCORAN JJ WANG KC NUBLING RB PIERSON RL CHANG MCF ASBECK PM HUANG RT
Citation: K. Poulton et al., A 6-B, 4 GSA S GAAS HBT ADC, IEEE journal of solid-state circuits, 30(10), 1995, pp. 1109-1118
HLA ALLELE DETECTION USING MOLECULAR TECHNIQUES
Authors: DYER PA JAWAHEER D OLLIER B POULTON K SINNOTT P THOMSON W
Citation: Pa. Dyer et al., HLA ALLELE DETECTION USING MOLECULAR TECHNIQUES, Disease markers, 11(4), 1993, pp. 145-160
HLA GENOTYPING OF A CHILD WITH SEVERE COMBINED IMMUNODEFICIENCY DISORDER (SCID) - A STRATEGY USING A RAPID AND COMPREHENSIVE MOLECULAR ANALYSIS
Authors: SINNOTT PJ POULTON K SUMMERS CW YAP PL MILLER WN DYER PA
Citation: Pj. Sinnott et al., HLA GENOTYPING OF A CHILD WITH SEVERE COMBINED IMMUNODEFICIENCY DISORDER (SCID) - A STRATEGY USING A RAPID AND COMPREHENSIVE MOLECULAR ANALYSIS, Human immunology, 37, 1993, pp. 87-87
WOLFRAM-SYNDROME - MITOCHONDRIAL DISORDER
Authors: BUNDEY S FIELDER A POULTON K
Citation: S. Bundey et al., WOLFRAM-SYNDROME - MITOCHONDRIAL DISORDER, Lancet, 342(8878), 1993, pp. 1059-1060
Risultati: 1-12 |