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Journal Abstract Search

135 related items for PubMed ID: 37682370

  • 1. Atypical presentation of Pearson syndrome in an infant with suspected myelodysplastic syndrome.
    Tajan A, Riebel A, Zavala MJ, Quiroz L, Monzón P, Ardiles L, Krall P, Lehmann P.
    Pediatr Nephrol; 2024 Feb; 39(2):447-450. PubMed ID: 37682370
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  • 2. Tubulopathy and pancytopaenia with normal pancreatic function: a variant of Pearson syndrome.
    Atale A, Bonneau-Amati P, Rötig A, Fischer A, Perez-Martin S, de Lonlay P, Niaudet P, De Parscau L, Mousson C, Thauvin-Robinet C, Munnich A, Huet F, Faivre L.
    Eur J Med Genet; 2009 Feb; 52(1):23-6. PubMed ID: 19026771
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  • 4. Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure.
    Yoshimi A, Ishikawa K, Niemeyer C, Grünert SC.
    Orphanet J Rare Dis; 2022 Oct 17; 17(1):379. PubMed ID: 36253820
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  • 6. A Novel Mitochondrial DNA Deletion in Patient with Pearson Syndrome.
    Khasawneh R, Alsokhni H, Alzghoul B, Momani A, Abualsheikh N, Kamal N, Qatawneh M.
    Med Arch; 2018 Apr 17; 72(2):148-150. PubMed ID: 29736106
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  • 10. Pearson marrow pancreas syndrome in patients suspected to have Diamond-Blackfan anemia.
    Gagne KE, Ghazvinian R, Yuan D, Zon RL, Storm K, Mazur-Popinska M, Andolina L, Bubala H, Golebiowska S, Higman MA, Kalwak K, Kurre P, Matysiak M, Niewiadomska E, Pels S, Petruzzi MJ, Pobudejska-Pieniazek A, Szczepanski T, Fleming MD, Gazda HT, Agarwal S.
    Blood; 2014 Jul 17; 124(3):437-40. PubMed ID: 24735966
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  • 12. Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA).
    Pitchon EM, Cachat F, Jacquemont S, Hinard C, Borruat FX, Schorderet DF, Morris MA, Munier FL.
    Klin Monbl Augenheilkd; 2007 Apr 17; 224(4):340-3. PubMed ID: 17458809
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  • 14. [A regenerative anemia in infants: 2 cases of Pearson´s syndrome].
    Martínez de Zabarte Fernández JM, Rodríguez-Vigil Iturrate C, Martínez Faci C, García Jiménez I, Murillo Sanjuan L, Muñoz Mellado A.
    Arch Argent Pediatr; 2017 Feb 01; 115(1):e24-e27. PubMed ID: 28097850
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  • 15. A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression.
    Chen XY, Zhao SY, Wang Y, Wang D, Dong CH, Yang Y, Wang ZH, Wu YM.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul 01; 27(4):2492-5. PubMed ID: 26016877
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  • 16. Early neurological impairment and severe anemia in a newborn with Pearson syndrome.
    Morel AS, Joris N, Meuli R, Jacquemont S, Ballhausen D, Bonafé L, Fattet S, Tolsa JF.
    Eur J Pediatr; 2009 Mar 01; 168(3):311-5. PubMed ID: 18553104
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  • 17. Mitochondrial DNA deletion and duplication in Kearns-Sayre Syndrome (KSS) with initial presentation as Pearson Marrow-Pancreas Syndrome (PMPS): Two case reports in Barranquilla, Colombia.
    Sabella-Jiménez V, Otero-Herrera C, Silvera-Redondo C, Garavito-Galofre P.
    Mol Genet Genomic Med; 2020 Nov 01; 8(11):e1509. PubMed ID: 33030289
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  • 18. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.
    McShane MA, Hammans SR, Sweeney M, Holt IJ, Beattie TJ, Brett EM, Harding AE.
    Am J Hum Genet; 1991 Jan 01; 48(1):39-42. PubMed ID: 1985462
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