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Results: 1-11 |
Results: 11
DEJERINE-SOTTAS NEUROPATHY ASSOCIATED WITH DE-NOVO S79P MUTATION OF THE PERIPHERAL MYELIN PROTEIN-22 (PMP22) GENE
Authors: BORT S SEVILLA T GARCIAPLANELLS J BLESA D PARICIO N VILCHEZ JJ PRIETO F PALAU F
Citation: S. Bort et al., DEJERINE-SOTTAS NEUROPATHY ASSOCIATED WITH DE-NOVO S79P MUTATION OF THE PERIPHERAL MYELIN PROTEIN-22 (PMP22) GENE, Human mutation, 1998, pp. 95-98
CLINICAL, GENETIC AND ELECTROPHYSIOLOGIC CORRELATION IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES WITH INVOLVEMENT OF PMP22 GENE AT CHROMOSOME 17P11.2
Authors: CRUZMARTINEZ A BORT S ARPA J DUARTE J PALAU F
Citation: A. Cruzmartinez et al., CLINICAL, GENETIC AND ELECTROPHYSIOLOGIC CORRELATION IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES WITH INVOLVEMENT OF PMP22 GENE AT CHROMOSOME 17P11.2, European journal of neurology, 4(3), 1997, pp. 274-286
MUTATIONAL ANALYSIS OF THE MPZ, PMP22 AND CX32 GENES IN PATIENTS OF SPANISH ANCESTRY WITH CHARCOT-MARIE-TOOTH-DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: BORT S NELIS E TIMMERMAN V SEVILLA T CRUZMARTINEZ A MARTINEZ F MILLAN JM ARPA J VILCHEZ JJ PRIETO F VANBROECKHOVEN C PALAU F
Citation: S. Bort et al., MUTATIONAL ANALYSIS OF THE MPZ, PMP22 AND CX32 GENES IN PATIENTS OF SPANISH ANCESTRY WITH CHARCOT-MARIE-TOOTH-DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Human genetics, 99(6), 1997, pp. 746-754
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) REVEALED AFTER WEIGHT-LOSS
Authors: CRUZMARTINEZ A BORT S ARPA J PALAU F
Citation: A. Cruzmartinez et al., HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) REVEALED AFTER WEIGHT-LOSS, European neurology, 37(4), 1997, pp. 257-260
THE ROLE OF NFAT ENHANCED IL-4 GENE-EXPRESSION
Authors: CRON RO BORT S WANG YX BRUNVAND M LEWIS D
Citation: Ro. Cron et al., THE ROLE OF NFAT ENHANCED IL-4 GENE-EXPRESSION, Arthritis and rheumatism, 40(9), 1997, pp. 46-46
PREVALENCE AND PARENTAL ORIGIN OF DE-NOVO 1.5-MB DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A
Authors: BORT S MARTINEZ F PALAU F
Citation: S. Bort et al., PREVALENCE AND PARENTAL ORIGIN OF DE-NOVO 1.5-MB DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A, American journal of human genetics, 60(1), 1997, pp. 230-233
COEXPRESSION OF THE INTERLEUKIN-13 AND INTERLEUKIN-4 GENES CORRELATESWITH THEIR PHYSICAL LINKAGE IN THE CYTOKINE GENE-CLUSTER ON HUMAN-CHROMOSOME 5Q23-31
Authors: DOLGANOV G BORT S LOVETT M BURR J SCHUBERT L SHORT D MCGURN M GIBSON C LEWIS DB
Citation: G. Dolganov et al., COEXPRESSION OF THE INTERLEUKIN-13 AND INTERLEUKIN-4 GENES CORRELATESWITH THEIR PHYSICAL LINKAGE IN THE CYTOKINE GENE-CLUSTER ON HUMAN-CHROMOSOME 5Q23-31, Blood, 87(8), 1996, pp. 3316-3326
DIAGNOSIS AND PREVALENCE OF THE MT1-A LOC US IN TYPE-1 CHARCOT-MARIE-TOOTH DISEASE (VOL 104, PG 648, 1995)
Authors: BORT S
Citation: S. Bort, DIAGNOSIS AND PREVALENCE OF THE MT1-A LOC US IN TYPE-1 CHARCOT-MARIE-TOOTH DISEASE (VOL 104, PG 648, 1995), Medicina Clinica, 105(5), 1995, pp. 179-179
THE DIAGNOSIS AND PREVALENCE OF DUPLICATI ON OF THE CMT1A LOCUS IN CHARCOT-MARIE-TOOTH TYPE-I DISEASE
Authors: BORT S SEVILLA T VILCHEZ JJ PRIETO F PALAU F
Citation: S. Bort et al., THE DIAGNOSIS AND PREVALENCE OF DUPLICATI ON OF THE CMT1A LOCUS IN CHARCOT-MARIE-TOOTH TYPE-I DISEASE, Medicina Clinica, 104(17), 1995, pp. 648-652
NUCLEAR PROTEINS BINDING TO THE P-ELEMENT OF THE HUMAN INTERLEUKIN-4 GENE PROMOTER IN PRIMED MEMORY AND UNPRIMED ANTIGENICALLY NAIVE T-CELLS
Authors: LEWIS DB BORT S
Citation: Db. Lewis et S. Bort, NUCLEAR PROTEINS BINDING TO THE P-ELEMENT OF THE HUMAN INTERLEUKIN-4 GENE PROMOTER IN PRIMED MEMORY AND UNPRIMED ANTIGENICALLY NAIVE T-CELLS, Journal of cellular biochemistry, 1994, pp. 417-417
ORIGIN OF THE DE-NOVO DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE1A - UNEQUAL NONSISTER CHROMATID EXCHANGE DURING SPERMATOGENESIS
Authors: PALAU F LOFGREN A DEJONGHE P BORT S NELIS E SEVILLA T MARTIN JJ VILCHEZ J PRIETO F VANBROECKHOVEN C
Citation: F. Palau et al., ORIGIN OF THE DE-NOVO DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE1A - UNEQUAL NONSISTER CHROMATID EXCHANGE DURING SPERMATOGENESIS, Human molecular genetics, 2(12), 1993, pp. 2031-2035
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