Back to the Subject ListUnited Mitochondrial Disease Foundation
We welcome any suggested additions to our list.
Last updated: 26-Jun-98
REFERENCE FORMAT: Author Lastname; Firstname; Article Number; Article Title; Journal or Book; Year; Volume; Page Numbers
Adwani ; SS ; 3111* ; Heart transplantation for dilated cardiomyopathy. ; Arch Dis Child ; 1995 ; 73(5) ; 447-452
Anan ; R ; 608* ; Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects [see comments]. ; Circulation ; 1995 ; 91(4) ; 955-61
Angelini ; C ; 743 ; Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect. ; Japanese Heart Journal ; 1993 ; 34(1) ; 63-77
Antozzi ; C ; 5683 ; Cardiomyopathies in disorders of oxidative metabolism. ; Cardiovasc Res ; 1997 ; 35(2) ; 184-99
Aoyama ; T ; 3139 ; Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients. ; J Clinical Investigation ; 1995 ; 95(6) ; 2465-2473
Bakeeva ; LE ; 3161 ; Ultrastructure of intermitochondrial contacts of human cardiomyocytes in alcoholic cardiomyopathy and ischemic heart disease ; Arkh Patol ; 1996 ; 58(2) ; 49-54
Baker ; NS ; 5697 ; D-2-hydroxyglutaric aciduria: hypotonia, cortical blindness, seizures, cardiomyopathy, and cylindrical spirals in skeletal muscle [published erratum appears in J Child Neurol 1997 Apr;12(3):227] ; J Child Neurol ; 1997 ; 12(1) ; 31-6
Bakker ; HD ; 1033 ; Neonatal cardiomyopathy and lactic acidosis responsive to thiamine. ; Journal of Inherited Metabolic Disease ; 1991 ; 14(1) ; 75-9
Belardinelli ; R ; 3189* ; Exercise training improves left ventricular diastolic filling in patients with dilated cardiomyopathy. Clinical and prognostic implications. ; Circulation ; 1995 ; 91(11) ; 2775-2784
Besley ; GT ; 1532* ; Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduria. ; J Inherit Metab Dis ; 1995 ; 18(2) ; 221-3
Bogousslavsky ; J ; 3217* ; Brain ischemia, mitochondrial cardiomyopathy, and rediscovering the wheel ; Stroke ; 1996 ; 27(2) ; 338
Bohlega ; S ; 3218* ; Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy. ; Neurology ; 1996 ; 46(5) ; 1329-1334
Bonne ; G ; 3222* ; The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy ; J Med Genet ; 1995 ; 32(8) ; 670-671
Brackett ; JC ; 586 ; Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency. ; J Clinical Investigation ; 1995 ; 95(5) ; 2076-82
Buchwald ; A ; 2707 ; Alterations of the mitochondrial respiratory chain in human dilated cardiomyopathy. ; Eur Heart J ; 1990 ; 11(6) ; 509-16
D'Adamo ; DP ; 5800 ; The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. ; Am J Hum Genet ; 1997 ; 61(4) ; 862-7
Damian ; MS ; 3330* ; Clinical spectrum of the MELAS mutation in a large pedigree. ; Acta Neurol Scand ; 1995 ; 92(5) ; 409-415
Degoul ; F ; 5813 ; Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene. ; Hum Mol Genet ; 1998 ; 7(3) ; 347-54
Dionisi-Vici ; C ; 5822 ; New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency. ; Ann Neurol ; 1997 ; 42(4) ; 661-5
Dorner ; A ; 5828 ; Adenine nucleotide translocator in dilated cardiomyopathy: pathophysiological alterations in expression and function. ; Mol Cell Biochem ; 1997 ; 174(1-2) ; 261-9
Fabrizi ; GM ; 3404 ; Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defect ; J Neurol Sci ; 1996 ; 137(1) ; 20-27
Gedeon ; AK ; 838* ; X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. ; Journal of Medical Genetics ; 1995 ; 32(5) ; 383-8
Grunnet ; M.L. ; 295* ; Juvenile Leigh's encephalomyelopathy with peripheral neuropathy, myopathy, and cardiomyopathy. ; Journal of Child Neurology ; 1991 ; 6(2) ; 159-63
Guenthard ; J ; 1615* ; Cardiomyopathy in respiratory chain disorders. [Review] ; Archives of Disease in Childhood ; 1995 ; 72(3) ; 223-6
Gvozdjakova ; A ; 3485 ; Metabolic study of mitochondria in myocardial biopsies in patients with cardiopathy of unknown origin ; Bratisl Lek Listy ; 1996 ; 97(6) ; 348-350
Hiruta ; Y ; 3523 ; Mitochondrial encephalomyopathy with A to G transition of mitochondrial transfer RNA(Leu(UUR)) 3,243 presenting hypertrophic cardiomyopathy. ; Internal Medicine ; 1995 ; 34(7) ; 670-673
Ibel ; H ; 931* ; Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria. ; European Journal of Pediatrics ; 1993 ; 152(8) ; 665-70
Ishida ; Y ; 3567 ; Cardiac sympathetic nervous dysfunction in mitochondrial cardiomyopathy and diabetes ; Diabetes Care ; 1995 ; 18(9) ; 1312-1313
Ishikawa ; Y ; 1065 ; Severe mitochondrial cardiomyopathy and extra-neuromuscular abnormalities in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode (MELAS). ; Pathology, Research & Practice ; 1995 ; 191(1) ; 64-75
Ito ; T ; 800 ; Mitochondrial DNA mutations in cardiomyopathy. ; Japanese Circulation Journal ; 1992 ; 56(10) ; 1045-53
Jaksch ; M ; 3581* ; A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus. ; Human Mutation ; 1996 ; 7(4) ; 358-360
Kaido ; M ; 1046* ; Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural study. ; Journal of the Neurological Sciences ; 1995 ; 131(2) ; 170-6
Kim ; Y ; 5978 ; Therapeutic effect of co-enzyme Q10 on idiopathic dilated cardiomyopathy: assessment by iodine-123 labelled 15-(p-iodophenyl)- 3(R,S)-methylpentadecanoic acid myocardial single-photon emission tomography. ; Eur J Nucl Med ; 1997 ; 24(6) ; 629-34
Kitaoka ; H ; 3635 ; A patient with diabetes mellitus, cardiomyopathy, and a mitochondrial gene mutation: confirmation of a gene mutation in cardiac muscle. ; Diabetes Res Clin Pract ; 1995 ; 28(3) ; 207-212
Kovalenko ; SA ; 3655* ; Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathy. ; Biochem Biophys Res Commun ; 1996 ; 222(2) ; 201-207
Li ; YY ; 3703* ; Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy. ; Biochem Biophys Res Commun ; 1995 ; 210(1) ; 211-218
Li ; YY ; 6018 ; Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy. ; J Mol Cell Cardiol ; 1997 ; 29(10) ; 2699-709
Liao ; Y ; 3704* ; Cardiac cytotoxic mechanism mediated by antibodies against myocardial mitochondrial ADP/ATP carrier in patients with dilated cardiomyopathy. ; Chin Med J (Engl) ; 1996 ; 109(3) ; 193-196
Liebes ; R ; 6019 ; Decreased nuclear encoded subunits of cytochrome c oxidase and increased copper, zinc-superoxide dismutase activity are found in cardiomyopathic human hearts. ; Int J Cardiol ; 1997 ; 62(3) ; 259-67
Malcic ; I ; 1795 ; Mitochondrial cardiomyopathy and scapuloperoneal spinal muscular atrophy in a child. ; Acta Medica Croatica ; 1993 ; 47(1) ; 47-50
Manouvrier ; S ; 3752* ; Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. ; J Med Genet ; 1995 ; 32(8) ; 654-656
Marin-Garcia ; J ; 6048 ; A point mutation in the cytb gene of cardiac mtDNA associated with complex III deficiency in ischemic cardiomyopathy. ; Biochem Mol Biol Int ; 1996 ; 40(3) ; 487-95
Marin-Garcia ; J ; 1463* ; Mitochondrial cardiomyopathy. ; Pediatr Cardiol ; 1995 ; 16(1) ; 28-30
Marin-Garcia ; J ; 3756 ; Mitochondrial function in children with idiopathic dilated cardiomyopathy. ; J Inherit Metab Dis ; 1996 ; 19(3) ; 309-312
Marin-Garcia ; J ; 3757* ; Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy ; Cardiovasc Res ; 1996 ; 31(2) ; 306-313
Marin-Garcia ; J ; 6044 ; Mitochondrial cardiomyopathy: molecular and biochemical analysis. ; Pediatr Cardiol ; 1997 ; 18(4) ; 251-60
Marin-Garcia ; J ; 6045 ; Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis. ; J Card Fail ; 1995 ; 1(4) ; 285-91
Marin-Garcia ; J ; 6046 ; Hypertrophic cardiomyopathy with mitochondrial DNA depletion and respiratory enzyme defects. ; Pediatr Cardiol ; 1998 ; 19(3) ; 266-8
Marin-Garcia ; J ; 6047 ; Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy. ; J Inherit Metab Dis ; 1997 ; 20(5) ; 674-80
Mariotti ; C ; 680 ; Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy. ; J Clinical Investigation ; 1994 ; 93(3) ; 1102-7
Maurer ; I ; 6061 ; Carnitine palmitoyltransferase in patients with cardiac ischemia due to atherosclerotic coronary artery disease and in patients with idiopathic dilated cardiomyopathy. ; Cardiology ; 1997 ; 88(3) ; 258-63
Maurer ; I ; 2782 ; Myocardial respiratory chain enzyme activities in idiopathic dilated cardiomyopathy, and comparison with those in atherosclerotic coronary artery disease and valvular aortic stenosis. ; Am J Cardiol ; 1993 ; 72(5) ; 428-33
Medeiros ; DM ; 6068 ; Newer findings on a unified perspective of copper restriction and cardiomyopathy. ; Proc Soc Exp Biol Med ; 1997 ; 215(4) ; 299-313
Melberg ; A ; 3791* ; Autosomal dominant cerebellar ataxia deafness and narcolepsy. ; J Neurol Sci ; 1995 ; 134(1-2) ; 119-129
Melville ; C ; 6076 ; Fatal cardiomyopathy in dystrophic epidermolysis bullosa. ; Br J Dermatol ; 1996 ; 135(4) ; 603-6
Merante ; F. ; 2596* ; Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene. ; American Journal of Human Genetics ; 1994 ; 55 ; 437-446
Mestroni ; L ; 6077 ; Dilated cardiomyopathy: a genetic approach [editorial] ; Heart ; 1997 ; 77(3) ; 185-8
Mestroni ; L ; 3796 ; Molecular genetics of dilated cardiomyopathies. ; Eur Heart J ; 1995 ; 16 ; 5-9
Midro ; AT ; 3799 ; Retinitis pigmentosa in Kearns-Sayre syndrome resulting from mutation of mitochondrial DNA "de novo" ; Klin Oczna ; 1995 ; 97(6) ; 203-206
Morgan ; KG ; 6097 ; Mitochondrial cardiomyopathy [letter] ; Eur Heart J ; 1996 ; 17(10) ; 1600
Muller-Hocker ; J ; 728* ; Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency. ; Archives of Pathology & Laboratory Medicine ; 1993 ; 117(2) ; 202-10
Muller-Hocker ; J ; 1319 ; In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy. ; Human Pathology ; 1992 ; 23(12) ; 1431-7
Muller-Hocker ; J ; 1448 ; Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies. ; Virchows Archiv - A, Pathological Anatomy & Histopathology ; 1991 ; 419(4) ; 355-62
Nagai ; R ; 3846 ; Molecular biology in cardiovascular medicine ; Rinsho Byori ; 1995 ; 43(4) ; 335-336
Nishimura ; T ; 3870 ; Therapeutic effects of coenzyme Q10 on dilated cardiomyopathy: assessment by 123I-BMIPP myocardial single photon emission computed tomography (SPECT): a multicenter trial in Osaka University Medical School Group ; Kaku Igaku ; 1996 ; 33(1) ; 27-32
Ohkubo ; M ; 3890* ; Multicore myopathy associated with multiple pterygium syndrome and hypertrophic cardiomyopathy. ; Pediatr Cardiol ; 1996 ; 17(1) ; 53-56
Orii ; KO ; 3903* ; Genomic DNA organization of human mitochondrial very-long-chain acyl- CoA dehydrogenase and mutation analysis. ; Biochem Biophys Res Commun ; 1995 ; 217(3) ; 987-992
Orstavik ; KH ; 752* ; Possible X linked congenital mitochondrial cardiomyopathy in three families. ; Journal of Medical Genetics ; 1993 ; 30(4) ; 269-72
Otani ; M ; 3907 ; Histiocytoid cardiomyopathy with hypotonia in an infant. ; Pathol Int ; 1995 ; 45(10) ; 774-780
Otto ; A ; 6142 ; Anti-mitochondrial antibodies in patients with dilated cardiomyopathy (anti-M7) are directed against flavoenzymes with covalently bound FAD. ; Clin Exp Immunol ; 1998 ; 111(3) ; 541-7
Ozawa ; T ; 1762* ; Mitochondrial cardiomyopathy. [Review] ; Herz ; 1994 ; 19(2) ; 105-18, 125
Ozawa ; T ; 1633* ; Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic control. ; Biochemical & Biophysical Research Communications ; 1995 ; 207(2) ; 613-20
Ozawa ; T ; 3914 ; Mitochondrial DNA mutations in myocardial diseases. ; Eur Heart J ; 1995 ; 16 ; 10-14
Pastores ; GM ; 461* ; Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G). ; American Journal of Medical Genetics ; 1994 ; 50(3) ; 265-71
Paulson ; DJ ; 6153 ; Carnitine deficiency-induced cardiomyopathy. ; Mol Cell Biochem ; 1998 ; 180(1-2) ; 33-41
Pfeufer ; A ; 3944 ; Angiotensin-converting enzyme and heart chymase gene polymorphisms in hypertrophic cardiomyopathy. ; Am J Cardiol ; 1996 ; 78(3) ;
Pitkanen ; S ; 3947 ; Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase. ; J Clinical Investigation ; 1996 ; 98(2) ; 345-351
Pohlner ; K ; 6167 ; Identification of mitochondrial antigens recognized by antibodies in sera of patients with idiopathic dilated cardiomyopathy by two- dimensional gel electrophoresis and protein sequencing. ; Am J Cardiol ; 1997 ; 80(8) ; 1040-5
Popovich ; M ; 3955* ; Cellular hypertrophy in cardiomyopathic patients is associated with lower creatine-stimulated mitochondrial respiration. ; Molecular & Cellular Biochemistry ; 1995 ; 143(1) ; 1-5
Provenzale ; JM ; 3968* ; Cerebral infarction associated with Kearns-Sayre syndrome-related cardiomyopathy. ; Neurology ; 1996 ; 46(3) ; 826-828
Remes ; A.M. ; 2618* ; Mitochondrial DNA deletions in dilated cardiomyopathy: a clinical study employing endomyocardial sampling. ; J Am Coll Cardiol ; 1994 ; 23 ; 935-942
Robbins ; RC ; 3991* ; Cardiac transplantation for hypertrophic cardiomyopathy associated with Sengers syndrome. ; Ann Thorac Surg ; 1995 ; 60(5) ; 1425-1427
Rodrigues ; B ; 6187 ; Metabolic disturbances in diabetic cardiomyopathy. ; Mol Cell Biochem ; 1998 ; 180(1-2) ; 53-7
Romero ; NB ; 2890 ; Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency. ; Neuromuscul Disord ; 1993 ; 3(1) ; 31-42
Rustin ; P ; 1792* ; Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies. ; Journal of Pediatrics ; 1994 ; 124(2) ; 224-8
Santorelli ; FM ; 4027* ; Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A). ; Am J Hum Genet ; 1996 ; 58(5) ; 933-939
Santorelli ; FM ; 4024* ; A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy. ; Biochem Biophys Res Commun ; 1995 ; 216(3) ; 835-840
Sato ; W ; 641* ; Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. ; American Heart Journal ; 1994 ; 128(4) ; 733-41
Schulze ; K ; 4054 ; The role of the ADP/ATP carrier in the pathogenesis of viral heart disease. ; Eur Heart J ; 1995 ; 16 ; 64-67
Servidei ; S ; 1693* ; Hereditary metabolic cardiomyopathies. [Review] ; Advances in Pediatrics ; 1994 ; 41 ; 1-32
Shevell ; MI ; 4074* ; Glutaric acidemia type II: neuroimaging and spectroscopy evidence for developmental encephalomyopathy. ; Pediatric Neurology ; 1995 ; 12(4) ; 350-353
Silvestri ; G ; 646 ; A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy. ; Human Mutation ; 1994 ; 3(1) ; 37-43
Silvestri ; G ; 6243 ; Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation). ; Muscle Nerve ; 1997 ; 20(2) ; 221-5
Sims ; HF ; 612 ; The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. ; Proc Natl Acad Sci USA ; 1995 ; 92(3) ; 841-5
Skyllouriotis ; ML ; 6248 ; Myoadenylate deaminase deficiency, hypertrophic cardiomyopathy and gigantism syndrome. ; Pediatr Neurol ; 1997 ; 17(1) ; 61-6
Stahl ; J ; 6271 ; Oncocytic cardiomyopathy: a rare cause of unexpected early childhood death associated with fitting. ; Med Sci Law ; 1997 ; 37(1) ; 84-7
Stanley ; CA ; 2682 ; Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake. ; Ann Neurol ; 1991 ; 30(5) ; 709-16
Strauss ; AW ; 4123* ; Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood. ; Proc Natl Acad Sci USA ; 1995 ; 92(23) ; 10496-10500
Sudarikova Yu ; V ; 6278 ; Ultrastructure of mitochondrial reticulum of human cardiomyocytes in alcohol cardiomyopathy. ; Biochemistry (Mosc) ; 1997 ; 62(9) ; 989-1002
Sweeney ; MG ; 717 ; Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathy. ; Quarterly Journal of Medicine ; 1993 ; 86(7) ; 435-8
Takeda ; N ; 6301 ; Cardiomyopathies and mitochondrial DNA mutations. ; Mol Cell Biochem ; 1997 ; 176(1-2) ; 287-90
Takei ; Y ; 1529* ; Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia. ; Muscle & Nerve ; 1995 ; 18(11) ; 1321-5
Taniike ; M ; 814 ; Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy. ; Biochemical & Biophysical Research Communications ; 1992 ; 186(1) ; 47-53
Thompson ; CH ; 6321 ; Abnormal skeletal muscle bioenergetics in familial hypertrophic cardiomyopathy. ; Heart ; 1997 ; 78(2) ; 177-81
Trevi ; G ; 4197 ; Myocardial hypertrophy and arterial hypertension ; G Ital Cardiol ; 1995 ; 25(10) ; 1331-1338
Van Hove ; JL ; 647* ; Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder. ; American Journal of Medical Genetics ; 1994 ; 51(2) ; 114-20
Vilarinho ; L ; 6350 ; The mitochondrial A3243G mutation presenting as severe cardiomyopathy. ; J Med Genet ; 1997 ; 34(7) ; 607-9
Willner ; J ; 305* ; Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G) ; Am J Hum Genet ; 1992 ; 51 ; A110
Winter ; S ; 4258 ; The role of L-carnitine in pediatric cardiomyopathy. ; J Child Neurol ; 1995 ; 10 ; S45-S51
Yano ; S ; 6387 ; A new case of malonyl coenzyme A decarboxylase deficiency presenting with cardiomyopathy. ; Eur J Pediatr ; 1997 ; 156(5) ; 382-3
Yoshida ; R ; 4283 ; Hypertrophic cardiomyopathy in patients with diabetes mellitus associated with mitochondrial tRNA(Leu)(UUR) gene mutation ; Internal Medicine ; 1995 ; 34(10) ; 953-958
Zales ; VR ; 4294* ; Reversible cardiomyopathy due to carnitine deficiency from renal tubular wasting. ; Pediatr Cardiol ; 1995 ; 16(2) ; 76-78
Zeviani ; M ; 1574* ; OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy. ; Muscle & Nerve ; 1995 ; Suppl 3 ; S170-4
Zeviani ; M. ; 61* ; Maternally inherited myopathy and cardiomyopathy: assoiation with mutation in mitochondrial DNA tRNA ; Lancet ; 1991 ; 338 ; 143-47