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DISCUSSION OF "GEOELECTRIC SOUNDINGS FOR PREDICTING AQUIFER PROPERTIES," BY WALTER K. KOSINSKI AND WILLIAM E. KELLY, MARCH-APRIL 1981 ISSUE, VOL. 19, NO. 2, P. 163-171 = DISCUSSION DE "SONDAGES GEOELECTRIQUES POUR LA PREVISION DES PROPRIETES DES AQUIFERES" PAR WALTER K. KOSINSKY ET WILLIAM E. KELLY, MARS-AVRIL 1981, VOL. 19, NO 2, P. 163-171LEONARD MAYER PATRICIA J; TAYLOR ROBERT W.1982; GROUND WATER; ISSN 0017-467X; USA; DA. 1982-02; VOL. 20; NO 1; PP. 111-112; BIBL. 8 REF.Article

INORGANIC PHOSPHORUS IN CALCAREOUS ROCKLAND SOILS OF THE BAHAMAS = LE PHOSPHORE MINERAL DES SOLS DES TERRAINS ROCHEUX CALCAIRES DES BAHAMASTAYLOR ROBERT W; WOODS JONATHAN; STEWART BA et al.1981; SOIL SCI. SOC. AM. J.; ISSN 0361-5995; USA; DA. 1981; VOL. 45; NO 1-6; PP. 730-734; BIBL. 28 REF.; 7 TAB. ; ILL.Conference Paper

1st International conference on office automation, New Orleans LA, December 17-19, 1984Taylor, Robert W.International conference on office automation. 1984, 173 p., isbn 0-8186-0596-0Conference Proceedings

Mitochondrial DNA mutations in human diseaseTAYLOR, Robert W; TURNBULL, Doug M.Nature reviews. Genetics (Print). 2005, Vol 6, Num 5, pp 389-402, issn 1471-0056, 14 p.Article

Central venous catheterizationTAYLOR, Robert W; PALAGIRI, Ashok V.Critical care medicine. 2007, Vol 35, Num 5, pp 1390-1396, issn 0090-3493, 7 p.Article

Disease progression in patients with single, large-scale mitochondrial DNA deletionsGRADY, John P; CAMPBELL, Georgia; TURNBULL, Doug M et al.Brain. 2014, Vol 137, pp 323-334, issn 0006-8950, 12 p., 2Article

Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3HORVATH, Rita; CZERMIN, Birgit; BRODHUN, Michael et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 2, pp 174-178, issn 0022-3050, 5 p.Article

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIIe mutation causing hypertrophic cardiomyopathyPERLI, Elena; GIORDANO, Carla; AUTORE, Camillo et al.Human molecular genetics (Print). 2012, Vol 21, Num 1, pp 85-100, issn 0964-6906, 16 p.Article

Isolated Distal Myopathy of the Upper Limbs Associated With Mitochondrial DNA Depletion and Polymerase γ MutationsGIORDANO, Carla; PICHIORRI, Floriana; BLAKELY, Emma L et al.Archives of neurology (Chicago). 2010, Vol 67, Num 9, pp 1144-1146, issn 0003-9942, 3 p.Article

A New Mitochondrial Transfer RNAPro Gene Mutation Associated With Myoclonic Epilepsy With Ragged-Red Fibers and Other Neurological FeaturesBLAKELY, Emma L; ANAND TRIP, S; SWALWELL, Helen et al.Archives of neurology (Chicago). 2009, Vol 66, Num 3, pp 399-402, issn 0003-9942, 4 p.Article

Phosphatase activity of ultisols and relationship to soil fertility indicesSENWO, Zachary N; RANATUNGA, Thilini D; TAZISONG, Irenus A et al.International journal of food, agriculture and environment (Print). 2007, Vol 5, Num 1, pp 262-266, issn 1459-0255, 5 p.Article

Ophthalmoplegia due to mitochondrial dna disease : The need for genetic diagnosisSCHAEFER, Andrew M; BLAKELY, Emma L; GRIFFITHS, Philip G et al.Muscle & nerve. 2005, Vol 32, Num 1, pp 104-107, issn 0148-639X, 4 p.Article

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutationMCFARLAND, Robert; CLARK, Kim M; MORRIS, Andrew A. M et al.Nature genetics. 2002, Vol 30, Num 2, pp 145-146, issn 1061-4036Article

In-vitro genetic modification of mitochondrial functionTAYLOR, Robert W; CHINNERY, Patrick F; TURNBULL, Douglass M et al.Human reproduction (Oxford. Print). 2000, Vol 15, pp 79-85, issn 0268-1161, SUP2Conference Paper

LATE-ONSET RESPIRATORY FAILURE DUE TO TK2 MUTATIONS CAUSING MULTIPLE mtDNA DELETIONSALSTON, Charlotte L; SCHAEFER, Andrew M; NIXON, John et al.Neurology. 2013, Vol 81, Num 23, pp 2051-2053, issn 0028-3878, 3 p.Article

Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiencyALSTON, Charlotte L; DAVISON, James E; WASSMER, Evangeline et al.Journal of medical genetics. 2012, Vol 49, Num 9, pp 569-577, issn 0022-2593, 9 p.Article

Maternally inherited mitochondrial DNA disease in consanguineous familiesALSTON, Charlotte L; LANGPING HE; MORRIS, Andrew A et al.European journal of human genetics. 2011, Vol 19, Num 12, pp 1226-1229, issn 1018-4813, 4 p.Article

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple familiesTUPPEN, Helen A. L; HOGAN, Vanessa E; JONES, Simon et al.Brain. 2010, Vol 133, pp 2952-2963, issn 0006-8950, 12 p., 10Article

Inorganic Phosphorus Forms in Soufriere Hills Volcanic Ash and Volcanic Ash-Derived SoilRANATUNGA, Thilini D; TAYLOR, Robert W; BHAT, Kamala N et al.Soil science. 2009, Vol 174, Num 8, pp 430-438, issn 0038-075X, 9 p.Article

A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation : are two mutations better than one?SWALWELL, Helen; BLAKELY, Emma L; DAVIDSON, Mercy M et al.European journal of human genetics. 2008, Vol 16, Num 10, pp 1265-1274, issn 1018-4813, 10 p.Article

Mutation of OPAI causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions : a novel disorder of mtDNA maintenance. CommentaryZEVIANI, Massimo; HUDSON, Gavin; REYNIER, Pascal et al.Brain. 2008, Vol 131, issn 0006-8950, 314-317, 329-337 [13 p.], 2Article

POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth DiseaseHARROWER, Timothy; STEWART, Joanna D; HUDSON, Gavin et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 133-136, issn 0003-9942, 4 p.Article

Induction of mitochondrial biogenesis is a maladaptive mechanism in mitochondrial cardiomyopathiesSEBASTIANI, Mariangela; GIORDANO, Carla; GALLO, Pietro et al.Journal of the American College of Cardiology. 2007, Vol 50, Num 14, pp 1362-1369, issn 0735-1097, 8 p.Article

Sporadic intragenic inversion of the mitochondrial DNA MTND1 gene causing fatal infantile lactic acidosisBLAKELY, Emma L; RENNIE, Katherine J; TAYLOR, Robert W et al.Pediatric research. 2006, Vol 59, Num 3, pp 440-444, issn 0031-3998, 5 p.Article

Changes in the human mitochondrial genome after treatment of malignant diseaseWARDELL, Theresa M; FERGUSON, Elaine; CHINNERY, Patrick F et al.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2003, Vol 525, Num 1-2, pp 19-27, issn 1386-1964, 9 p.Article

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