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Results:
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Results: 21
Authors:
CLARK KM
BINDOFF LA
LIGHTOWLERS RN
ANDREW RM
GRIFFITHS PG
JOHNSON MA
BRIERLEY EJ
TURNBULL DM
Citation: Km. Clark et al., REVERSAL OF A MITOCHONDRIAL-DNA DEFECT IN HUMAN SKELETAL-MUSCLE, Nature genetics, 16(3), 1997, pp. 222-224
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
Authors:
BLANK SC
SHAKIR RA
BINDOFF LA
BRADEY N
Citation: Sc. Blank et al., SPONTANEOUS INTRACRANIAL HYPOTENSION - CLINICAL AND MAGNETIC-RESONANCE-IMAGING CHARACTERISTICS, Clinical neurology and neurosurgery, 99(3), 1997, pp. 199-204
Authors:
HOWELL N
BINDOFF LA
Citation: N. Howell et La. Bindoff, THE NEUROPATHOLOGY OF LEBERS HEREDITARY OPTIC NEUROPATHY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1142-1142
Authors:
BIDOOKI SK
JOHNSON MA
CHRZANOWSKALIGHTOWLERS Z
BINDOFF LA
LIGHTOWLERS RN
Citation: Sk. Bidooki et al., INTRACELLULAR MITOCHONDRIAL TRIPLASMY IN A PATIENT WITH 2 HETEROPLASMIC BASE CHANGES, American journal of human genetics, 60(6), 1997, pp. 1430-1438
Authors:
WEBER K
WILSON JN
TAYLOR L
BRIERLEY E
JOHNSON MA
TURNBULL DM
BINDOFF LA
Citation: K. Weber et al., A NEW MTDNA MUTATION SHOWING ACCUMULATION WITH TIME AND RESTRICTION TO SKELETAL-MUSCLE, American journal of human genetics, 60(2), 1997, pp. 373-380
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
Authors:
MORRIS AAM
LEONARD IV
BROWN GK
BIDOUKI SK
BINDOFF LA
WOODWARD CE
HARDING AE
LAKE BD
HARDING BN
FARRELL MA
BELL JE
MIRAKHUR M
TURNBULL DM
Citation: Aam. Morris et al., DEFICIENCY OF RESPIRATORY-CHAIN COMPLEX-I IS A COMMON-CAUSE OF LEIGH-DISEASE, Annals of neurology, 40(1), 1996, pp. 25-30
Authors:
TAYLOR RW
BIRCHMACHIN MA
SCHAEFER J
TAYLOR L
SHAKIR R
ACKRELL BAC
COCHRAN B
BINDOFF LA
JACKSON MJ
GRIFFITHS P
TURNBULL DM
Citation: Rw. Taylor et al., DEFICIENCY OF COMPLEX-II OF THE MITOCHONDRIAL RESPIRATORY-CHAIN IN LATE-ONSET OPTIC ATROPHY AND ATAXIA, Annals of neurology, 39(2), 1996, pp. 224-232
Authors:
MORRIS AAM
TAYLOR RW
BIRCHMACHIN MA
JACKSON MJ
COULTHARD MG
BINDOFF LA
WELCH RJ
HOWELL N
TURNBULL DM
Citation: Aam. Morris et al., NEONATAL FANCONI-SYNDROME DUE TO DEFICIENCY OF COMPLEX III OF THE RESPIRATORY-CHAIN, Pediatric nephrology, 9(4), 1995, pp. 407-411
Authors:
WALKER M
TAYLOR RW
STEWART MW
BINDOFF LA
JACKSON MJ
ALBERTI GKMM
TURNBULL DM
Citation: M. Walker et al., INSULIN SENSITIVITY AND MITOCHONDRIAL GENE MUTATION, Diabetes care, 18(2), 1995, pp. 273-274
Authors:
WALKER M
TAYLOR RW
STEWART MW
BINDOFF LA
SHEARING PA
ANYAOKU V
JACKSON MJ
HUMPHRISS DB
JOHNSTON DG
ALBERTI KGMM
TURNBULL DM
Citation: M. Walker et al., INSULIN AND PROINSULIN SECRETION IN SUBJECTS WITH ABNORMAL GLUCOSE-TOLERANCE AND A MITOCHONDRIAL TRNA(LEU(UUR)) MUTATION, Diabetes care, 18(11), 1995, pp. 1507-1509
Authors:
MORRIS AAM
JACKSON MJ
BINDOFF LA
TURNBULL DM
Citation: Aam. Morris et al., THE INVESTIGATION OF MITOCHONDRIAL RESPIRATORY-CHAIN DISEASE, Journal of the Royal Society of Medicine, 88(4), 1995, pp. 217-222
Authors:
JACKSON MJ
SCHAEFER JA
JOHNSON MA
MORRIS AAM
TURNBULL DM
BINDOFF LA
Citation: Mj. Jackson et al., PRESENTATION AND CLINICAL INVESTIGATION OF MITOCHONDRIAL RESPIRATORY-CHAIN DISEASE - A STUDY OF 51 PATIENTS, Brain, 118, 1995, pp. 339-357
Authors:
BIRCHMACHIN MA
BRIGGS HL
SABORIDO AA
BINDOFF LA
TURNBULL DM
Citation: Ma. Birchmachin et al., AN EVALUATION OF THE MEASUREMENT OF THE ACTIVITIES OF COMPLEXES I-IV IN THE RESPIRATORY-CHAIN OF HUMAN SKELETAL-MUSCLE MITOCHONDRIA, Biochemical medicine and metabolic biology, 51(1), 1994, pp. 35-42
Authors:
JACKSON MJ
BINDOFF LA
WEVER K
WILSON JN
INCE P
ALBERTI KGMM
TURNBULL DM
Citation: Mj. Jackson et al., BIOCHEMICAL AND MOLECULAR STUDIES OF MITOCHONDRIAL-FUNCTION IN DIABETES-INSIPIDUS, DIABETES-MELLITUS, OPTIC ATROPHY, AND DEAFNESS, Diabetes care, 17(7), 1994, pp. 728-733
Authors:
GOODMAN SI
AXTELL KM
BINDOFF LA
BEARD SE
GILL RE
FRERMAN FE
Citation: Si. Goodman et al., MOLECULAR-CLONING AND EXPRESSION OF A CDNA-ENCODING HUMAN ELECTRON-TRANSFER FLAVOPROTEIN-UBIQUINONE OXIDOREDUCTASE, European journal of biochemistry, 219(1-2), 1994, pp. 277-286
Authors:
POULTON J
BINDOFF LA
Citation: J. Poulton et La. Bindoff, MTDNA - PATHOGENIC OR NONPATHOGENIC SEQUENCE CHANGES, American journal of human genetics, 54(2), 1994, pp. 385-385
Authors:
BINDOFF LA
HOWELL N
POULTON J
MCCULLOUGH DA
MORTEN KJ
LIGHTOWLERS RN
TURNBULL DM
WEBER K
Citation: La. Bindoff et al., ABNORMAL RNA PROCESSING ASSOCIATED WITH A NOVEL TRANSFER-RNA MUTATIONIN MITOCHONDRIAL-DNA - A POTENTIAL DISEASE MECHANISM, The Journal of biological chemistry, 268(26), 1993, pp. 19559-19564
Authors:
CHRZANOWSKALIGHTOWLERS ZMA
TURNBULL DM
BINDOFF LA
LIGHTOWLERS RN
Citation: Zma. Chrzanowskalightowlers et al., AN ANTISENSE OLIGODEOXYNUCLEOTIDE APPROACH TO INVESTIGATE THE FUNCTION OF THE NUCLEAR-ENCODED SUBUNITS OF HUMAN CYTOCHROME-C-OXIDASE, Biochemical and biophysical research communications, 196(1), 1993, pp. 328-335
Authors:
POULTON J
ROTIG A
MUNNICH A
MORTEN K
BINDOFF LA
BROWN GK
Citation: J. Poulton et al., FAMILIES OF MITOCHONDRIAL-DNA RE-ARRANGEMENTS IN PATIENTS WITH MESSENGER TRANSFER DNA DELETIONS AND PEARSON SYNDROME AND OR KEARNS-SAVRE SYNDROME - DUPLICATIONS ARE ASSOCIATED WITH PROGRESSION OF THE PHENOTYPETO KEARNS-SAVRE SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1214-1214
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