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The relationship between mitochondrial genotype and mitochondrial phenotype in lymphoblasts with a heteroplasmic mtDNA deletionSPELBRINK, J. N; VAN OOST, B. A; VAN DEN BOGERT, C et al.Human molecular genetics (Print). 1994, Vol 3, Num 11, pp 1989-1997, issn 0964-6906Article

Clinical heterogeneity in mitochondrial DNA deletion disorders : A diagnostic challenge of pearson syndromeLACBAWAN, Felicitas; TIFFT, Cynthia J; LUBAN, Naomi L. C et al.American journal of medical genetics. 2000, Vol 95, Num 3, pp 266-268, issn 0148-7299Article

Tubulopathy and pancytopaenia with normal pancreatic function : A variant of Pearson syndromeATALE, Agnès; BONNEAU-AMATI, Patrizia; MUNNICH, A et al.European journal of medical genetics. 2009, Vol 52, Num 1, pp 23-26, issn 1769-7212, 4 p.Article

Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletionSANTORELLI, F. M; BARMADA, M. A; PONS, R et al.Neurology. 1996, Vol 47, Num 5, pp 1320-1323, issn 0028-3878Article

Pancreatic aspects of cystic fibrosis and other inherited causes of pancreatic dysfunctionDURIE, P. R.The Medical clinics of North America. 2000, Vol 84, Num 3, issn 0025-7125, ix,609-620 [13 p.]Article

Protean manifestations of mitochondrial diseases : A minireviewKERR, D. S.Journal of pediatric hematology/oncology. 1997, Vol 19, Num 4, pp 279-286, issn 1077-4114Conference Paper

A case of Pearson syndrome associated with multiple renal cystsGÜRGEY, A; ÖZALP, I; RÖTIG, A et al.Pediatric nephrology (Berlin, West). 1996, Vol 10, Num 5, pp 637-638, issn 0931-041XArticle

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 DNASUPERTI-FURGA, A; SCHOENLE, E; TUCHSCHMID, P et al.European journal of pediatrics. 1993, Vol 152, Num 1, pp 44-50, issn 0340-6199Article

Pearson's marrow-pancreas syndrome in 2 Turkish childrenGÜRGEY, A; RÖTIG, A; GÜMRÜK, F et al.Acta haematologica. 1992, Vol 87, Num 4, pp 206-209, issn 0001-5792Article

Early neurological impairment and severe anemia in a newborn with Pearson syndromeMOREL, Anne-Sophie; JORIS, Nadia; MEULI, Reto et al.European journal of pediatrics. 2009, Vol 168, Num 3, pp 311-315, issn 0340-6199, 5 p.Article

Diagnosis and management of mitochondrial diseasesGILLIS, Lynette; KAYE, Edward.The Pediatric clinics of North America. 2002, Vol 49, Num 1, pp vii-viii, issn 0031-3955, 18 p.Article

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Pancytopenia and vacuolation of marrow precursors associated with necrotizing encephalopathyBLATT, J; AMMAR KATERJI; MAMDOUHA BARMADA et al.British journal of haematology. 1994, Vol 86, Num 1, pp 207-209, issn 0007-1048Article

ADN mitochondrial et pathologie = Mitochondrial ADN and mitochondrial diseasesNABET-BELLEVILLE, F.Annales médicales de Nancy et de l'Est. 1991, Vol 30, Num 2, pp 173-176, issn 0221-3796, 4 p.Article

Exploration métabolique, enzymologique et moléculaire des cytopathies mitochondrialesMUNNICH, A; ROTIG, A.Pédiatrie (Marseille). 1991, Vol 46, Num 6-7, pp 509-514, issn 0031-4021Article

Pearson marrow-pancreas syndrome with worsening cardiac function caused by pleiotropic rearrangement of mitochondrial DNAKRAUCH, Gabriele; WILICHOWSKI, Ekkehard; SCHMIDT, Klaus G et al.American journal of medical genetics. 2002, Vol 110, Num 1, pp 57-61, issn 0148-7299Article

Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletionBECHER, M. W; WILLS, M. L; NOLL, W. W et al.Human pathology. 1999, Vol 30, Num 5, pp 577-581, issn 0046-8177Article

Bilateral zonular cataract associated with the mitochondrial cytopathy of Pearson syndromeCURSIEFEN, C; KÜCHLE, M; SCHEURLEN, W et al.American journal of ophthalmology. 1998, Vol 125, Num 2, pp 260-261, issn 0002-9394Article

De la myopathie mitochondriale aux cytopathies mitochondriales = From mitochondrial myopathy to mitochondrial cytopathiesLEROY, J. P.Annales de pathologie (Paris). 1994, Vol 14, Num 1, pp 7-10, issn 0242-6498Conference Paper

Molecular and genetic analyses of two patients with Pearson's marrow-pancreas syndromeSANO, T; BAN, K; ICHIKI, T et al.Pediatric research. 1993, Vol 34, Num 1, pp 105-110, issn 0031-3998Article

Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndromeYANAGIHARA, Itaru; INUI, Koji; YANAGIBARA, Keiko et al.The Journal of pediatrics. 2001, Vol 139, Num 3, pp 452-455, issn 0022-3476Article