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Results: 1-25 |
Results: 25
MITOCHONDRIAL DEFECTS AND ENDOCRINE DYSFUNCTION
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, MITOCHONDRIAL DEFECTS AND ENDOCRINE DYSFUNCTION, QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS, 91(5), 1998, pp. 376-376
MITOCHONDRIAL-DNA AND DISEASE
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, MITOCHONDRIAL-DNA AND DISEASE, Netherlands journal of medicine, 53(1), 1998, pp. 4-6
MITOCHONDRIAL GENOTYPE AND CLINICAL PHENOTYPE
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, MITOCHONDRIAL GENOTYPE AND CLINICAL PHENOTYPE, Journal of inherited metabolic disease, 21(4), 1998, pp. 321-325
VOMITING, ANOREXIA, AND MITOCHONDRIAL-DNA DISEASE
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, VOMITING, ANOREXIA, AND MITOCHONDRIAL-DNA DISEASE, Lancet, 351(9100), 1998, pp. 448-448
MITOCHONDRIAL-DNA MUTATIONS AND PATHOGENICITY
Authors: CHINNERY PF TURNBULL DM HOWELL N ANDREWS RM
Citation: Pf. Chinnery et al., MITOCHONDRIAL-DNA MUTATIONS AND PATHOGENICITY, Journal of Medical Genetics, 35(8), 1998, pp. 701-702
MITOCHONDRIAL DIABETES - INVESTIGATION AND IDENTIFICATION OF A NOVEL MUTATION
Authors: LYNN S WARDELL T JOHNSON MA CHINNERY PF DALY ME WALKER M TURNBULL DM
Citation: S. Lynn et al., MITOCHONDRIAL DIABETES - INVESTIGATION AND IDENTIFICATION OF A NOVEL MUTATION, Diabetes, 47(11), 1998, pp. 1800-1802
A NOVEL MITOCHONDRIAL-DNA POINT MUTATION IN THE TRNA(ILE) GENE - STUDIES IN A PATIENT PRESENTING WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND MULTIPLE-SCLEROSIS
Authors: TAYLOR RW CHINNERY PF BATES MJD JACKSON MJ JOHNSON MA ANDREWS RM TURNBULL DM
Citation: Rw. Taylor et al., A NOVEL MITOCHONDRIAL-DNA POINT MUTATION IN THE TRNA(ILE) GENE - STUDIES IN A PATIENT PRESENTING WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND MULTIPLE-SCLEROSIS, Biochemical and biophysical research communications, 243(1), 1998, pp. 47-51
MITOCHONDRIAL MEDICINE
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, MITOCHONDRIAL MEDICINE, Quarterly Journal of Medicine, 90(11), 1997, pp. 657-667
SELECTIVE-INHIBITION OF MUTANT HUMAN MITOCHONDRIAL-DNA REPLICATION IN-VITRO BY PEPTIDE NUCLEIC-ACIDS
Authors: TAYLOR RW CHINNERY PF TURNBULL DM LIGHTOWLERS RN
Citation: Rw. Taylor et al., SELECTIVE-INHIBITION OF MUTANT HUMAN MITOCHONDRIAL-DNA REPLICATION IN-VITRO BY PEPTIDE NUCLEIC-ACIDS, Nature genetics, 15(2), 1997, pp. 212-215
MATERNALLY INHERITED DIABETES AND DEAFNESS - PREVALENCE IN A HOSPITALDIABETIC POPULATION
Authors: NEWKIRK JE TAYLOR RW HOWELL N BINDOFF LA CHINNERY PF ALBERTI KGMM TURNBULL DM WALKER M
Citation: Je. Newkirk et al., MATERNALLY INHERITED DIABETES AND DEAFNESS - PREVALENCE IN A HOSPITALDIABETIC POPULATION, Diabetic medicine, 14(6), 1997, pp. 457-460
A NOVEL MITOCHONDRIAL TRANSFER-RNA PHENYLALANINE MUTATION PRESENTING WITH ACUTE RHABDOMYOLYSIS
Authors: CHINNERY PF JOHNSON MA TAYLOR RW LIGHTOWLERS RN TURNBULL DM
Citation: Pf. Chinnery et al., A NOVEL MITOCHONDRIAL TRANSFER-RNA PHENYLALANINE MUTATION PRESENTING WITH ACUTE RHABDOMYOLYSIS, Annals of neurology, 41(3), 1997, pp. 408-410
MAMMALIAN MITOCHONDRIAL GENETICS - HEREDITY, HETEROPLASMY AND DISEASE
Authors: LIGHTOWLERS RN CHINNERY PF TURNBULL DM HOWELL N
Citation: Rn. Lightowlers et al., MAMMALIAN MITOCHONDRIAL GENETICS - HEREDITY, HETEROPLASMY AND DISEASE, Trends in genetics, 13(11), 1997, pp. 450-455
TREATMENT OF MITOCHONDRIAL DISEASE
Authors: TAYLOR RW CHINNERY PF CLARK KM LIGHTOWLERS RN TURNBULL DM
Citation: Rw. Taylor et al., TREATMENT OF MITOCHONDRIAL DISEASE, Journal of bioenergetics and biomembranes, 29(2), 1997, pp. 195-205
DRIVING AND STROKE - REPLY
Authors: CHINNERY PF TURNBULL DM WALLS TJ READING PJ
Citation: Pf. Chinnery et al., DRIVING AND STROKE - REPLY, Lancet, 350(9088), 1997, pp. 1402-1403
RECURRENT STROKES IN A 34-YEAR-OLD MAN
Authors: CHINNERY PF TURNBULL DM WALLS TJ READING PJ
Citation: Pf. Chinnery et al., RECURRENT STROKES IN A 34-YEAR-OLD MAN, Lancet, 350(9077), 1997, pp. 560-560
CSF ANTIGLIADIN ANTIBODIES AND THE RAMSAY-HUNT-SYNDROME
Authors: CHINNERY PF READING PJ MILNE D GARDNERMEDWIN D TURNBULL DM
Citation: Pf. Chinnery et al., CSF ANTIGLIADIN ANTIBODIES AND THE RAMSAY-HUNT-SYNDROME, Neurology, 49(4), 1997, pp. 1131-1133
A NOVEL MITOCHONDRIAL TRANSFER-RNA ISOLEUCINE GENE MUTATION CAUSING CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
Authors: CHINNERY PF JOHNSON MA TAYLOR RW DURWARD WF TURNBULL DM
Citation: Pf. Chinnery et al., A NOVEL MITOCHONDRIAL TRANSFER-RNA ISOLEUCINE GENE MUTATION CAUSING CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Neurology, 49(4), 1997, pp. 1166-1168
GENE-THERAPY FOR MITOCHONDRIAL-DNA DISEASES
Authors: TAYLOR RF CHINNERY PF LIGHTOWLERS RN TURNBULL DM
Citation: Rf. Taylor et al., GENE-THERAPY FOR MITOCHONDRIAL-DNA DISEASES, Neurology, 48(3), 1997, pp. 4085-4085
GENETIC-COUNSELING FOR PATIENTS WITH MITOCHONDRIAL-DNA DEFECTS - PREDICTING THE OUTCOME OF PREGNANCY BASED ON MATERNAL MUTANT LOAD
Authors: CHINNERY PF HOWELL N LIGHTOWLERS RN TURNBULL DM
Citation: Pf. Chinnery et al., GENETIC-COUNSELING FOR PATIENTS WITH MITOCHONDRIAL-DNA DEFECTS - PREDICTING THE OUTCOME OF PREGNANCY BASED ON MATERNAL MUTANT LOAD, Neurology, 48(3), 1997, pp. 49002-49002
CLINICAL-FEATURES, INVESTIGATION, AND MANAGEMENT OF PATIENTS WITH DEFECTS OF MITOCHONDRIAL-DNA
Authors: CHINNERY PF TURNBULL DM
Citation: Pf. Chinnery et Dm. Turnbull, CLINICAL-FEATURES, INVESTIGATION, AND MANAGEMENT OF PATIENTS WITH DEFECTS OF MITOCHONDRIAL-DNA, Journal of Neurology, Neurosurgery and Psychiatry, 63(5), 1997, pp. 559-563
MANAGEMENT OF PARKINSONISM AND PSYCHOTIC DEPRESSION IN A CASE OF ACUTE INTERMITTENT PORPHYRIA
Authors: CHINNERY PF CARTLIDGE N BURN DJ CLELAND PG MCKEITH I
Citation: Pf. Chinnery et al., MANAGEMENT OF PARKINSONISM AND PSYCHOTIC DEPRESSION IN A CASE OF ACUTE INTERMITTENT PORPHYRIA, Journal of Neurology, Neurosurgery and Psychiatry, 62(5), 1997, pp. 542-542
FULMINANT ENCEPHALOPATHY DUE TO THE CATASTROPHIC PRIMARY ANTIPHOSPHOLIPID SYNDROME
Authors: CHINNERY PF SHAW PJ INCE PG JACKSON GH BISHOP RI
Citation: Pf. Chinnery et al., FULMINANT ENCEPHALOPATHY DUE TO THE CATASTROPHIC PRIMARY ANTIPHOSPHOLIPID SYNDROME, Journal of Neurology, Neurosurgery and Psychiatry, 62(3), 1997, pp. 300-301
MOLECULAR PATHOLOGY OF MELAS AND MERRF - THE RELATIONSHIP BETWEEN MUTATION LOAD AND CLINICAL PHENOTYPES
Authors: CHINNERY PF HOWELL N LIGHTOWLERS RN TURNBULL DM
Citation: Pf. Chinnery et al., MOLECULAR PATHOLOGY OF MELAS AND MERRF - THE RELATIONSHIP BETWEEN MUTATION LOAD AND CLINICAL PHENOTYPES, Brain, 120, 1997, pp. 1713-1721
MELAS ASSOCIATED WITH A MUTATION IN THE VALINE TRANSFER-RNA GENE OF MITOCHONDRIAL-DNA
Authors: TAYLOR RW CHINNERY PF HALDANE F MORRIS AAM BINDOFF LA WILSON J TURNBULL DM
Citation: Rw. Taylor et al., MELAS ASSOCIATED WITH A MUTATION IN THE VALINE TRANSFER-RNA GENE OF MITOCHONDRIAL-DNA, Annals of neurology, 40(3), 1996, pp. 459-462
THE BLOODY HEART OF THE MATTER
Authors: CHINNERY PF
Citation: Pf. Chinnery, THE BLOODY HEART OF THE MATTER, British Journal of Hospital Medicine, 53(3), 1995, pp. 114-114
Risultati: 1-25 |