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La ricerca find articoli where soggetti phrase all words 'DNA mutation' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 218 riferimenti
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    1. Przygodzki, RM; Koss, MN; O'Leary, TJ
      Pleomorphic (giant and/or spindle cell) carcinoma of lung shows a high percentage of variant CYP1A1*2

      MOLECULAR DIAGNOSIS
    2. Ravn, K; Wibrand, F; Hansen, FJ; Horn, N; Rosenberg, T; Schwartz, M
      An mtDNA mutation, 14453G -> A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Hutchin, TP; Lench, NJ; Arbuzova, S; Markham, AF; Mueller, RF
      Maternally inherited hearing impairment in a family with the mitochondrialDNA A7445G mutation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Klemm, T; Neumann, S; Trulzsch, B; Pistrosch, F; Hanefeld, M; Paschke, R
      Search for mitochondrial DNA, mutation ate position 3243 in German patients with a positive family history of maternal diabetes mellitus

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    5. Maassen, JA; van Essen, E; van den Ouweland, JMW; Lemkes, HHJP
      Molecular and clinical aspects of mitochondrial diabetes mellitus

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    6. Pantaleoni, C; D'Arrigo, S; Bagnasco, I; Piozzi, E; Carrara, F; Scaioli, V; Riva, D
      Papillitis as an onset sign of Leber's hereditary optic neuropathy: a casereport

      BRAIN & DEVELOPMENT
    7. Brown, MD; Zhadanov, S; Allen, JC; Hosseini, S; Newman, NJ; Atamonov, VV; Mikhailovskaya, IE; Sukernik, RI; Wallace, DC
      Novel mtDNA mutations and oxidative phosphorylation dysfunction in RussianLHON families

      HUMAN GENETICS
    8. Biousse, V; Newman, NJ
      Neuro-ophthalmology of mitochondrial diseases

      SEMINARS IN NEUROLOGY
    9. Zhu, L; Lee, HK; Lin, BC; Yeung, ES
      Spatial temperature gradient capillary electrophoresis for DNA mutation detection

      ELECTROPHORESIS
    10. Triepels, RH; Van den Heuvel, LP; Trijbels, JM; Smeitink, JA
      Respiratory chain complex I deficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Brown, MD; Allen, JC; Van Stavern, GP; Newman, NJ; Wallace, DC
      Clinical, genetic, and biochemical characterization of a leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    12. Hotta, O; Inoue, CN; Miyabayashi, S; Furuta, T; Takeuchi, A; Taguma, Y
      Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNA(Leu(UUR)) gene mutation

      KIDNEY INTERNATIONAL
    13. Berdanier, CD
      Mitochondrial gene expression in diabetes mellitus: Effect of nutrition

      NUTRITION REVIEWS
    14. Inglese, M; Rovaris, M; Bianchi, S; Comi, G; Filippi, M
      Magnetization transfer and diffusion tensor MR imaging of the optic radiations and calcarine cortex from patients with Leber's hereditary optic neuropathy

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    15. Vogel, H
      Mitochondrial myopathies and the role of the pathologist in the molecular era

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    16. Liu, C
      Magnetic resonance, magnetisation transfer, and diffusion weighted imagingcorrelates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    17. Inglese, M; Rovaris, M; Bianchi, S; La Mantia, L; Mancardi, GL; Ghezzi, A; Montagna, P; Salvi, F; Filippi, M
      Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damagein Leber's hereditary optic neuropathy

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    18. Murphy, EC; Zhurkin, VB; Louis, JM; Cornilescu, G; Clore, GM
      Structural basis for SRY-dependent 46-X,Y sex reversal: Modulation of DNA bending by a naturally occurring point mutation

      JOURNAL OF MOLECULAR BIOLOGY
    19. Kelley, SO; Steinberg, SV; Schimmel, P
      Fragile T-stem in disease-associated human mitochondrial tRNA sensitizes structure to local and distant mutations

      JOURNAL OF BIOLOGICAL CHEMISTRY
    20. Finsterer, J; Gharehbaghi-Schnell, E; Stollberger, C; Fheodoroff, K; Seiser, A
      Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy

      CLINICAL GENETICS
    21. Marin-Garcia, J; Goldenthal, MJ; Moe, GW
      Mitochondrial pathology in cardiac failure

      CARDIOVASCULAR RESEARCH
    22. Chinnery, PF; Brown, DT; Andrews, RM; Singh-Kler, R; Riordan-Eva, P; Lindley, J; Applegarth, DA; Turnbull, DM; Howell, N
      The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

      BRAIN
    23. Spellberg, B; Carroll, RM; Robinson, E; Brass, E
      mtDNA disease in the primary care setting

      ARCHIVES OF INTERNAL MEDICINE
    24. Tran, M; Bhargava, R; MacDonald, IM
      Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    25. Niemela, JE; Puck, JM; Fischer, RE; Fleisher, TA; Hsu, AP
      Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency

      CLINICAL IMMUNOLOGY
    26. Hutchin, TP; Cortopassi, GA
      Mitochondrial defects and hearing loss

      CELLULAR AND MOLECULAR LIFE SCIENCES
    27. Kopsidas, G; Kovalenko, SA; Islam, MM; Gingold, EB; Linnane, AW
      Preferential amplification is minimised in long-PCR systems

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    28. Kelley, SO; Steinberg, SV; Schimmel, P
      Functional defects of pathogenic human mitochondrial tRNAs related to structural fragility

      NATURE STRUCTURAL BIOLOGY
    29. Alexander, C; Votruba, M; Pesch, UEA; Thiselton, DL; Mayer, S; Moore, A; Rodriguez, M; Kellner, U; Leo-Kottler, B; Auburger, G; Bhattacharya, SS; Wissinger, B
      OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

      NATURE GENETICS
    30. Loeffen, JLCM; Smeitink, JAM; Trijbels, JMF; Janssen, AJM; Triepels, RH; Sengers, RCA; van den Heuvel, LP
      Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects

      HUMAN MUTATION
    31. Wei, YH; Kao, SH
      Mitochondrial DNA mutation and depletion are associated with decline of fertility and motility of human sperm

      ZOOLOGICAL STUDIES
    32. DiMauro, S; Andreu, AL
      Mutations in mtDNA: Are we scraping the bottom of the barrel?

      BRAIN PATHOLOGY
    33. Manfredi, G; Beal, MF
      The role of mitochondria in the pathogenesis of neurodegenerative diseases

      BRAIN PATHOLOGY
    34. Dey, R; Tengan, CH; Morita, MPA; Kiyomoto, BH; Moraes, CT
      A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loop

      NEUROMUSCULAR DISORDERS
    35. Leo-Kottler, B; Jacobi, F; Christ-Adler, M
      Leber's hereditary optic neuropathy with spontaneous recovery

      OPHTHALMOLOGE
    36. Besch, D; Wissinger, B; Zrenner, E; Leo-Kottler, B
      A case of liver optic neuropathy with a new point mutation in the cytochrome b gene

      OPHTHALMOLOGE
    37. Nissenkorn, A; Zeharia, A; Lev, D; Watemberg, N; Fattal-Valevski, A; Barash, V; Gutman, A; Harel, S; Lerman-Sagie, T
      Neurologic presentations of mitochondrial disorders

      JOURNAL OF CHILD NEUROLOGY
    38. Sparaco, M; Cavallaro, T; Rossi, G; Rizzuto, N
      Immunohistochemical demonstration of spinal ventral horn cells involvementin a case of "myoclonus epilepsy with ragged red fibers" (MERRF)

      CLINICAL NEUROPATHOLOGY
    39. Triepels, R; Smeitink, J; Loeffen, J; Smeets, R; Trijbels, F; van den Heuvel, L
      Characterization of the human complex INDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients

      HUMAN GENETICS
    40. Horvath, R; Abicht, A; Shoubridge, EA; Karcagi, V; Rozsa, C; Komoly, S; Lochmuller, H
      Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS

      JOURNAL OF NEUROLOGY
    41. Purvin, VA
      Optic neuropathies for the neurologist

      SEMINARS IN NEUROLOGY
    42. Perez-Gomez, C; Olalla, L; Blanca, M; Mates, JM
      DNA point mutations in the promoter of the human histidine decarboxylase (HDC) gene in patients suffering from allergic ashtma

      BIOGENIC AMINES
    43. Hwang, JM; Lee, JJ; Chang, BL; Park, SS
      Visual prognosis of Leber's hereditary optic neuropathy with 14484/ND6 mutation in Koreans

      NEURO-OPHTHALMOLOGY
    44. Sato, Y; Nakagawa, M; Higuchi, I; Osame, M; Naito, E; Oizumi, K
      Mitochondrial myopathy and familial thiamine deficiency

      MUSCLE & NERVE
    45. Van Camp, G; Smith, RJH
      Maternally inherited hearing impairment

      CLINICAL GENETICS
    46. Moslemi, AR; Selimovic, N; Bergh, CH; Oldfors, A
      Fatal dilated cardiomyopathy associated with a mitochondrial DNA deletion

      CARDIOLOGY
    47. Martin, L; Toutain, A; Guillen, C; Haftek, M; Machet, MC; Toledano, C; Arbeille, B; Lorette, G; Rotig, A; Vaillant, L
      Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome

      BRITISH JOURNAL OF DERMATOLOGY
    48. Mann, ES; Handler, SP; Chung, SM
      Leber's hereditary optic neuropathy masquerading as retinal vasculitis

      ARCHIVES OF OPHTHALMOLOGY
    49. Kerrison, JB; Miller, NR; Hsu, FC; Beaty, TH; Maumenee, IH; Smith, KH; Savino, PJ; Stone, EM; Newman, NJ
      A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    50. Hanna, MG; Nelson, IP
      Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases

      CELLULAR AND MOLECULAR LIFE SCIENCES
    51. Beckman, KB; Ames, BN
      Endogenous oxidative damage of mtDNA

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    52. Lu, CY; Lee, HC; Fahn, HJ; Wei, YH
      Oxidative damage elicited by imbalance of free radical scavenging enzymes is associated with large-scale mtDNA deletions in aging human skin

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    53. Bhatti, MT; Newman, NJ
      A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation

      JOURNAL OF NEURO-OPHTHALMOLOGY
    54. Leo-Kottler, B; Christ-Adler, M
      Leber's hereditary optic neuropathy (LHON) in women and children

      OPHTHALMOLOGE
    55. Chariot, P; Brugieres, P; Eliezer-Vanerot, MC; Geny, C; Binaghi, M; Cesaro, P
      Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy

      MOVEMENT DISORDERS
    56. Thieme, H; Wissinger, B; Jandeck, C; Christ-Adler, M; Kraus, H; Kellner, U; Foerster, MH
      A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    57. Besch, D; Leo-Kottler, B; Zrenner, E; Wissinger, B
      Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    58. Carelli, V; Ghelli, A; Bucchi, L; Montagna, P; De Negri, A; Leuzzi, V; Carducci, C; Lenaz, G; Lugaresi, E; Degli Esposti, M
      Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy

      ANNALS OF NEUROLOGY
    59. Howell, N
      Leber hereditary optic neuropathy: Potential opportunities potential pitfalls for drug therapy of optic nerve degenerative disorders

      DRUG DEVELOPMENT RESEARCH
    60. Nakamura, S; Yoshinari, M; Doi, Y; Yoshizumi, H; Katafuchi, R; Yokomizo, Y; Nishiyama, K; Wakisaka, M; Fujishima, M
      Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine tRNA

      DIABETES RESEARCH AND CLINICAL PRACTICE
    61. Brenner, L; Bynke, G; Bynke, H
      Leber's hereditary optic neuropathy - A report of two unusual cases

      NEURO-OPHTHALMOLOGY
    62. Tulinius, MH
      Mitochondrial myopathies. Clinical and diagnostic aspects

      SCANDINAVIAN JOURNAL OF REHABILITATION MEDICINE
    63. Barrera-Ramirez, CF; Barragan-Campos, HM; Sanchez-Guerrero, J; Garcia-Ramos, G; Vega-Boada, F; Estanol, B
      The other genome: Clinical spectrum of mitochondrial cytopathies or oxidative phosphorylation diseases

      REVISTA DE INVESTIGACION CLINICA
    64. Wallace, DC; Murdock, DG
      Mitochondria and dystonia: The movement disorder connection?

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    65. Brown, MD
      The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neuropathy

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    66. Chinnery, PF; Howell, N; Andrews, RM; Turnbull, DM
      Clinical mitochondrial genetics

      JOURNAL OF MEDICAL GENETICS
    67. Schapira, AHV; Cock, HR
      Mitochondrial myopathies and encephalomyopathies

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    68. Isotani, H; Kameoka, K; Nagano, Y; Kitaoka, H; Ohsawa, N
      Characteristic neuroimaging findings in patients with diabetes and the 8296 mitochondrial tRNA(Lys)

      DIABETOLOGIA
    69. Chowers, I; Lerman-Sagie, T; Elpeleg, ON; Shaag, A; Merin, S
      Cone and rod dysfunction in the NARP syndrome

      BRITISH JOURNAL OF OPHTHALMOLOGY
    70. Veldhoen, N; Watterson, J; Brash, M; Milner, J
      Identification of tumour-associated and germ line p53 mutations in canine mammary cancer

      BRITISH JOURNAL OF CANCER
    71. Morgan-Hughes, JA; Hanna, MG
      Mitochondrial encephalomyopathies: the enigma of genotype versus phenotype

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
    72. Chalmers, RM; Schapira, AHV
      Clinical, biochemical and molecular genetic features of Leber's hereditaryoptic neuropathy

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
    73. Hutchin, T
      Sensorineural hearing loss and the 1555G mitochondrial DNA mutation

      ACTA OTO-LARYNGOLOGICA
    74. KOPSIDAS G; KOVALENKO SA; KELSO JM; LINNANE AW
      AN AGE-ASSOCIATED CORRELATION BETWEEN CELLULAR BIOENERGY DECLINE AND MTDNA REARRANGEMENTS IN HUMAN SKELETAL-MUSCLE

      Mutation research. Fundamental and molecular mechanisms of mutagenesis
    75. AJAX ET; KARDON R
      LATE-ONSET LEBERS HEREDITARY OPTIC NEUROPATHY

      Journal of neuro-ophthalmology
    76. SUDOYO H; SITEPU M; MALIK S; POESPONEGORO HD; MARZUKI S
      LEBERS HEREDITARY OPTIC NEUROPATHY IN INDONESIA - 2 FAMILIES WITH THEMTDNA 11778G-GREATER-THAN-A AND 14484T-GREATER-THAN-C MUTATIONS

      Human mutation
    77. THORNS C; WIDJAJA A; BOECK N; SKAMIRA C; ZUHLKE H
      MATERNALLY-INHERITED DIABETES AND DEAFNESS - REPORT OF 2 AFFECTED GERMAN FAMILIES WITH THE A3243G MITOCHONDRIAL-DNA MUTATION

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    78. LEOKOTTLER B; CHRISTADLER M; WISSINGER B; ZRENNER E
      MISDIAGNOSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) - ROLE OF CLINICAL AND MOLECULAR-GENETIC EXAMINATIONS

      Der Ophthalmologe
    79. PEZZI PP; DENEGRI AM; SADUN F; CARELLI V; LEUZZI V
      CHILDHOOD LEBER HEREDITARY OPTIC NEUROPATHY (ND1 3460) WITH VISUAL RECOVERY/

      Pediatric neurology
    80. HUSAIN S; GOILA R; SHAHI S; BANERJEA AC
      FIRST REPORT OF A HEALTHY INDIAN HETEROZYGOUS FOR DELTA-32 MUTANT OF HIV-1 CO-RECEPTOR-CCR5 GENE

      Gene
    81. COCK HR; TABRIZI SJ; COOPER JM; SCHAPIRA AHV
      THE INFLUENCE OF NUCLEAR BACKGROUND ON THE BIOCHEMICAL EXPRESSION OF 3460-LEBERS HEREDITARY OPTIC NEUROPATHY

      Annals of neurology
    82. DOTTI MT; PLEWNIA K; CARDAIOLI E; MANNESCHI L; RUFA A; ALEMA G; FEDERICO A
      A CASE OF ETHAMBUTOL-INDUCED OPTIC NEUROPATHY HARBORING THE PRIMARY MITOCHONDRIAL LHON MUTATION AT NT-11778

      Journal of neurology
    83. BAI YD; ATTARDI G
      THE MTDNA-ENCODED ND6 SUBUNIT OF MITOCHONDRIAL NADH DEHYDROGENASE IS ESSENTIAL FOR THE ASSEMBLY OF THE MEMBRANE ARM AND THE RESPIRATORY-FUNCTION OF THE ENZYME

      EMBO journal (Print)
    84. ATHA DH; WENZ HM; MOREHEAD H; TIAN J; OCONNELL CD
      DETECTION OF P53 POINT MUTATIONS BY SINGLE-STRAND CONFORMATION POLYMORPHISM - ANALYSIS BY CAPILLARY ELECTROPHORESIS

      Electrophoresis
    85. HOWELL N
      LEBER HEREDITARY OPTIC NEUROPATHY - RESPIRATORY-CHAIN DYSFUNCTION ANDDEGENERATION OF THE OPTIC-NERVE

      Vision research
    86. PARAD RB
      BUCCAL CELL-DNA MUTATION ANALYSIS FOR DIAGNOSIS OF CYSTIC-FIBROSIS INNEWBORNS AND INFANTS INACCESSIBLE TO SWEAT CHLORIDE MEASUREMENT

      Pediatrics
    87. MACMILLAN C; KIRKHAM T; FU K; ALLISON V; ANDERMANN E; CHITAYAT D; FORTIER D; GANS M; HARE H; QUERCIA N; ZACKON D; SHOUBRIDGE EA
      PEDIGREE ANALYSIS OF FRENCH-CANADIAN FAMILIES WITH T14484C LEBERS HEREDITARY OPTIC NEUROPATHY

      Neurology
    88. CARELLI V; BARBONI P; ZACCHINI A; MANCINI R; MONARI L; CEVOLI S; LIGUORI R; SENSI M; LUGARESI E; MONTAGNA P
      LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) WITH 14484 ND6 MUTATION IN A NORTH-AFRICAN PATIENT/

      Journal of the neurological sciences
    89. KATO T; MURASHITA J; SHIOIRI T; TERADA M; INUBUSHI T; KATO N
      PHOTIC STIMULATION-INDUCED ALTERATION OF BRAIN ENERGY-METABOLISM MEASURED BY P-31-MR SPECTROSCOPY IN PATIENTS WITH MELAS

      Journal of the neurological sciences
    90. Kempken, F; Howad, W; Pring, DR
      Mutations at specific atp6 codons which cause human mitochondrial diseasesalso lead to male sterility in a plant

      FEBS LETTERS
    91. SUZUKI S; HINOKIO Y; OHTOMO M; HIRAI M; HIRAI A; CHIBA M; KASUGA S; SATOH Y; AKAI H; TOYOTA T
      THE EFFECTS OF COENZYME Q(10) TREATMENT ON MATERNALLY INHERITED DIABETES-MELLITUS AND DEAFNESS, AND MITOCHONDRIAL-DNA 3243 (A TO G) MUTATION

      Diabetologia
    92. GIAROLA M; WELLS D; MONDINI P; PILOTTI S; SALA P; AZZARELLI A; BERTARIO L; PIEROTTI MA; DELHANTY JDA; RADICE P
      MUTATIONS OF ADENOMATOUS POLYPOSIS-COLI (APC) GENE ARE UNCOMMON IN SPORADIC DESMOID TUMORS

      British Journal of Cancer
    93. ZSURKA G; KALMAN J; JUHASZ A; CSASZAR A; RASKO I; JANKA Z; VENETIANER P
      NO MITOCHONDRIAL HAPLOTYPE WAS FOUND TO INCREASE RISK FOR ALZHEIMERS-DISEASE

      Biological psychiatry
    94. SCHAPIRA AHV
      HUMAN COMPLEX-I DEFECTS IN NEURODEGENERATIVE DISEASES

      Biochimica et biophysica acta. Bioenergetics
    95. LAMONT PJ; SURTEES R; WOODWARD CE; LEONARD JV; WOOD NW; HARDING AE
      CLINICAL AND LABORATORY FINDINGS IN REFERRALS FOR MITOCHONDRIAL-DNA ANALYSIS

      Archives of Disease in Childhood
    96. HOWELL N; BOGOLIN C; JAMIESON R; MARENDA DR; MACKEY DA
      MTDNA MUTATIONS THAT CAUSE OPTIC NEUROPATHY - HOW DO WE KNOW

      American journal of human genetics
    97. Loeffen, J; Smeitink, A; Triepels, R; Smeets, R; Schuelke, M; Sengers, R; Trijbels, F; Hamel, B; Mullaart, R; van den Heuvel, L
      The first nuclear-encoded complex I mutation in a patient with leigh syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    98. HANNA MG; BHATIA KP
      MOVEMENT-DISORDERS AND MITOCHONDRIAL DYSFUNCTION

      Current opinion in neurology
    99. YAMADA K; MASHIMA Y; KIGASAWA K; MIYASHITA K; WAKAKURA M; OGUCHI Y
      HIGH-INCIDENCE OF VISUAL RECOVERY AMONG 4 JAPANESE PATIENTS WITH LEBER HEREDITARY OPTIC NEUROPATHY WITH THE 14484-MUTATION

      Journal of neuro-ophthalmology
    100. KERRISON JB; NEWMAN NJ
      CLINICAL SPECTRUM OF LEBERS HEREDITARY OPTIC NEUROPATHY

      Clinical neuroscience


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/05/20 alle ore 00:37:08