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Last updated: 26-Jun-98
REFERENCE FORMAT: Author Lastname; Firstname; Article Number; Article Title; Journal or Book; Year; Volume; Page Numbers
Ashraf ; MS ; 3150* ; Late reversibility of chronic ifosfamide-associated nephrotoxicity in a child. ; Med. Pediatr. Oncol. ; 1997 ; 28(1) ; 62-64
Baerlocher ; KE ; 2225 ; Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndrome. ; Journal of Inherited Metabolic Disease ; 1992 ; 15(3) ; 327-30
Berger ; MM ; 3200* ; Relations between the selenium status and the low T3 syndrome after major trauma. ; Intensive Care Med ; 1996 ; 22(6) ; 575-581
Bernes ; SM ; 1246* ; Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome. ; Journal of Pediatrics ; 1993 ; 123(4) ; 598-602
Bernsen ; RA ; 5714 ; Residual health status after Guillain-Barre syndrome. ; J Neurol Neurosurg Psychiatry ; 1997 ; 62(6) ; 637-40
Blaak ; H ; 5720 ; Temporal relationship between human immunodeficiency virus type 1 RNA levels in serum and cellular infectious load in peripheral blood. ; J Infect Dis ; 1997 ; 176(5) ; 1383-7
Bretscher ; PA ; 3243 ; Towards a strategy of universally efficacious vaccination against pathogens uniquely susceptible to cell-mediated attack. ; J Biotechnol ; 1996 ; 44(1-3) ; 4-Jan
Caballero ; P ; 5747 ; CT in the evaluation of the upper airway in healthy subjects and in patients with obstructive sleep apnea syndrome. ; Chest ; 1998 ; 113(1) ; 111-6
Cursiefen ; C ; 5798 ; Bilateral zonular cataract associated with the mitochondrial cytopathy of Pearson syndrome. ; Am J Ophthalmol ; 1998 ; 125(2) ; 260-1
De Lima ; JJ ; 5809 ; Early elevation of lipoprotein(a) levels in chronic renal insufficiency. ; Ren Fail ; 1997 ; 19(1) ; 145-54
de Vries ; DD ; 2226 ; Detection of extremely low levels of wild-type mitochondrial DNA in the liver of a patient with Pearson syndrome by a sensitive PCR assay. ; Journal of Inherited Metabolic Disease ; 1992 ; 15(3) ; 307-10
Durie ; PR ; 3377 ; Inherited and congenital disorders of the exocrine pancreas ; Gastroenterologist ; 1996 ; 4(3) ; 169-187
Ezra ; E ; 3401* ; Delayed fellow eye involvement in acute retinal necrosis syndrome. ; Am J Ophthalmol ; 1995 ; 120(1) ; 115-117
Farmer ; A ; 3410 ; Screening for psychiatric morbidity in subjects presenting with chronic fatigue syndrome ; Br J Psychiatry ; 1996 ; 168(3) ; 354-358
Feeney ; C ; 3411 ; T-lymphocyte subsets in acute illness. ; Crit Care Med ; 1995 ; 23(10) ; 1680-1685
Fernandez-Real ; JM ; 5848 ; Serum ferritin as a component of the insulin resistance syndrome. ; Diabetes Care ; 1998 ; 21(1) ; 62-8
Fisch ; GS ; 3418* ; Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief report. ; Am J Med Genet ; 1996 ; 64(2) ; 362-364
Frega ; A ; 5864 ; Cervical intraepithelial neoplasia and bacterial vaginosis: correlation or risk factor? ; Eur J Gynaecol Oncol ; 1997 ; 18(1) ; 76-7
Friedlander ; MH ; 5865 ; The relationship of packed cell transfusion to red blood cell deformability in systemic inflammatory response syndrome patients. ; Shock ; 1998 ; 9(2) ; 84-8
Garcia Lerma ; JG ; 5875 ; Measurement of human immunodeficiency virus type 1 plasma virus load based on reverse transcriptase (RT) activity: evidence of variabilities in levels of virion-associated RT. ; J Infect Dis ; 1998 ; 177(5) ; 1221-9
Gibson ; KM ; 979 ; 3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects. ; Journal of Pediatrics ; 1992 ; 121(6) ; 940-2
Gilbert ; RD ; 3451 ; Pearson's syndrome presenting with Fanconi syndrome ; Ultrastruct Pathol ; 1996 ; 20(5) ; 473-475
Gurgey ; A ; 3482 ; A case of Pearson syndrome associated with multiple renal cysts ; Pediatr Nephrol ; 1996 ; 10(5) ; 637-638
Horimoto ; T ; 3532 ; Origin and molecular changes associated with emergence of a highly pathogenic H5N2 influenza virus in Mexico. ; Virology ; 1995 ; 213(1) ; 223-230
Jakobs ; C ; 2229 ; Organic aciduria in Pearson syndrome [letter]. ; European Journal of Pediatrics ; 1991 ; 150(9) ; 684
Johnson ; PA ; 3594* ; Gender differences in the management of acute chest pain. Support for the "Yentl syndrome". ; J Gen Intern Med ; 1996 ; 11(4) ; 209-217
Kapsa ; R ; 2214* ; A novel mtDNA deletion in an infant with Pearson syndrome. ; Journal of Inherited Metabolic Disease ; 1994 ; 17(5) ; 521-6
Kedda ; MA ; 3620 ; Kaposi's sarcoma-associated herpesvirus in Kaposi's sarcoma occurring in immunosuppressed renal transplant recipients ; Clin Transplant ; 1996 ; 10(5) ; 429-431
Kerr ; DS ; 5974 ; Protean manifestations of mitochondrial diseases: a minireview. ; J Pediatr Hematol Oncol ; 1997 ; 19(4) ; 279-86
Kimura ; A ; 3630 ; Serum concentrations of total bile acids in patients with acute Kawasaki syndrome. ; Arch Pediatr Adolesc Med ; 1996 ; 150(3) ; 289-292
Kleinle ; S ; 5989 ; Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR. ; Hum Genet ; 1997 ; 100(5-6) ; 643-50
Kramer ; PR ; 3659 ; Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. ; Human Genetics ; 1996 ; 98(2) ; 151-157
Lacaille ; F ; 3674* ; Magnetic resonance imaging for diagnosis of Shwachman's syndrome ; J Pediatr Gastroenterol Nutr ; 1996 ; 23(5) ; 599-603
Lederer ; SR ; 3684 ; Early renal graft dysfunction. The role of preformed antibodies to DR- typed lymphoblastoid cell lines. ; Transplantation ; 1996 ; 61(2) ; 313-319
Lichter-Konecki ; U ; 2222* ; 3-Methylglutaconic aciduria in a patient with Pearson syndrome [letter]. ; European Journal of Pediatrics ; 1993 ; 152(4) ; 378
Loas ; G ; 3715 ; Anhedonia and negative symptomatology in chronic schizophrenia. ; Compr Psychiatry ; 1996 ; 37(1) ; 11-May
McShane ; MA ; 1376 ; Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. ; American Journal of Human Genetics ; 1991 ; 48(1) ; 39-42
Morikawa ; Y ; 1850 ; Pearson's marrow/pancreas syndrome: a histological and genetic study. ; Virchows Archiv - A, Pathological Anatomy & Histopathology ; 1993 ; 423(3) ; 227-31
Morris ; AA ; 6100 ; Pearson's syndrome without marrow involvement. ; Arch Dis Child ; 1997 ; 77(1) ; 56-7
Muraki ; K ; 6109 ; Severe lactic acidosis and neonatal death in Pearson syndrome. ; J Inherit Metab Dis ; 1997 ; 20(1) ; 43-8
Muraki ; K ; 6108 ; The association between haematological manifestation and mtDNA deletions in Pearson syndrome. ; J Inherit Metab Dis ; 1997 ; 20(5) ; 697-703
Newkirk ; MM ; 3861* ; Rheumatic disease patients, prone to Sjogren's syndrome and/or lymphoma, mount an antibody response to BHRF1, the Epstein-Barr viral homologue of BCL-2. ; Br J Rheumatol ; 1996 ; 35(11) ; 1075-1081
Niaudet ; P ; 1751* ; Deletion of the mitochondrial DNA in a case of de Toni-Debre-Fanconi syndrome and Pearson syndrome. ; Pediatric Nephrology ; 1994 ; 8(2) ; 164-8
Ozsoylu ; S ; 6144 ; Schwachman or Pearson syndrome [letter; comment] ; Am J Hematol ; 1998 ; 57(3) ; 262
Pearson ; HA ; 6154 ; The naming of a syndrome. ; J Pediatr Hematol Oncol ; 1997 ; 19(4) ; 271-3
Pearson ; AC ; 3935* ; Systolic anterior motion of the mitral chordae tendineae: prevalence and clinical and Doppler-echocardiographic features. ; Am Heart J ; 1996 ; 131(4) ; 748-753
Ribes ; A ; 2218* ; Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities. ; J Inherit Metab Dis ; 1993 ; 16(3) ; 537-40
Rotig ; A ; 1048* ; Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome. ; Human Molecular Genetics ; 1995 ; 4(8) ; 1327-30
Rotig ; A ; 2228 ; Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome. ; Genomics ; 1991 ; 10(2) ; 502-4
Rotig ; A ; 2212* ; Phenotypic expression of mitochondrial genotypes in cultured skin fibroblasts and in Epstein-Barr virus-transformed lymphocytes in Pearson syndrome. ; Muscle & Nerve ; 1995 ; Suppl 3 ; S159-64
Santorelli ; FM ; 4026* ; Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletion. ; Neurology ; 1996 ; 47(5) ; 1320-1323
Schanberg ; LE ; 4043 ; Pain coping strategies in children with juvenile primary fibromyalgia syndrome: correlation with pain, physical function, and psychological distress. ; Arthritis Care Res ; 1996 ; 9(2) ; 89-96
Seneca ; S ; 6227 ; Pearson marrow pancreas syndrome: a molecular study and clinical management. ; Clin Genet ; 1997 ; 51(5) ; 338-42
Simonsz ; HJ ; 1325 ; Kearns-Sayre's syndrome developing in a boy who survived pearson's syndrome caused by mitochondrial DNA deletion. ; Documenta Ophthalmologica ; 1992 ; 82(1-2) ; 73-9
Smith ; OP ; 4104* ; Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA. ; Br J Haematol ; 1995 ; 90(2) ; 469-472
Superti-Furga ; A ; 934* ; Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA. ; European Journal of Pediatrics ; 1993 ; 152(1) ; 44-50
Tafas ; T ; 4144 ; An automated image analysis method for the measurement of neutrophil alkaline phosphatase in the prenatal screening of Down syndrome. ; Fetal Diagn Ther ; 1996 ; 11(4) ; 254-259
van de Corput ; MP ; 6339 ; Detection of mitochondrial DNA deletions in human skin fibroblasts of patients with Pearson's syndrome by two-color fluorescence in situ hybridization. ; J Histochem Cytochem ; 1997 ; 45(1) ; 55-61
Wong ; SH ; 4263* ; Totally automated analysis by robotized prepstation and liquid chromatography: direct-sample analysis of felbamate ; Ther Drug Monit ; 1996 ; 18(5) ; 573-580
Yamadori ; I. ; 276* ; Brain lesions of the Leigh-type distribution associated with a mitochondriopathy of Pearson's syndrome: Light and electron microscopic study ; Acta Neuropathologica ; 1992 ; 84(3) ; 337-41