245 related articles for article (PubMed ID: 2243133)
1. Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.
Rötig A; Cormier V; Blanche S; Bonnefont JP; Ledeist F; Romero N; Schmitz J; Rustin P; Fischer A; Saudubray JM
J Clin Invest; 1990 Nov; 86(5):1601-8. PubMed ID: 2243133
[TBL] [Abstract][Full Text] [Related]
2. [Metabolic, enzymological and molecular assessment of mitochondrial cytopathies].
Munnich A; Rotig A
Pediatrie; 1991; 46(6-7):509-14. PubMed ID: 1664083
[TBL] [Abstract][Full Text] [Related]
3. Molecular and genetic analyses of two patients with Pearson's marrow-pancreas syndrome.
Sano T; Ban K; Ichiki T; Kobayashi M; Tanaka M; Ohno K; Ozawa T
Pediatr Res; 1993 Jul; 34(1):105-10. PubMed ID: 8356010
[TBL] [Abstract][Full Text] [Related]
4. [Pearson's syndrome: a multi-system disorder based on a mt-DNA deletion].
Danse PW; Jakobs C; Rötig A; Munnich A; Veerman AJ
Tijdschr Kindergeneeskd; 1991 Dec; 59(6):196-202. PubMed ID: 1776144
[TBL] [Abstract][Full Text] [Related]
5. [Pearson's syndrome. Pancytopenia with exocrine pancreatic insufficiency: new mitochondrial disease in the first childhood].
Cormier V; Rötig A; Bonnefont JP; Mechinand F; Berthou C; Goulet O; Schmitz J; Blanche S; Vassaut A; Maier M
Arch Fr Pediatr; 1991 Mar; 48(3):171-8. PubMed ID: 2048956
[TBL] [Abstract][Full Text] [Related]
6. Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.
Fischel-Ghodsian N; Bohlman MC; Prezant TR; Graham JM; Cederbaum SD; Edwards MJ
Pediatr Res; 1992 Jun; 31(6):557-60. PubMed ID: 1635816
[TBL] [Abstract][Full Text] [Related]
7. Disorders of the mitochondria.
Treem WR; Sokol RJ
Semin Liver Dis; 1998; 18(3):237-53. PubMed ID: 9773424
[TBL] [Abstract][Full Text] [Related]
8. Widespread multi-tissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.
Cormier V; Rötig A; Quartino AR; Forni GL; Cerone R; Maier M; Saudubray JM; Munnich A
J Pediatr; 1990 Oct; 117(4):599-602. PubMed ID: 2213388
[No Abstract] [Full Text] [Related]
9. Pearson marrow-pancreas syndrome with worsening cardiac function caused by pleiotropic rearrangement of mitochondrial DNA.
Krauch G; Wilichowski E; Schmidt KG; Mayatepek E
Am J Med Genet; 2002 Jun; 110(1):57-61. PubMed ID: 12116272
[TBL] [Abstract][Full Text] [Related]
10. [Pearson syndrome. Case report].
Cammarata-Scalisi F; López-Gallardo E; Emperador S; Ruiz-Pesini E; Da Silva G; Camacho N; Montoya J
Invest Clin; 2011 Sep; 52(3):261-7. PubMed ID: 21950197
[TBL] [Abstract][Full Text] [Related]
11. Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA.
Smith OP; Hann IM; Woodward CE; Brockington M
Br J Haematol; 1995 Jun; 90(2):469-72. PubMed ID: 7794775
[TBL] [Abstract][Full Text] [Related]
12. [Neonatal Pearson syndrome. two case studies].
Collin-Ducasse H; Maillotte AM; Monpoux F; Boutté P; Ferrero-Vacher C; Paquis V
Arch Pediatr; 2010 Jan; 17(1):38-41. PubMed ID: 19914050
[TBL] [Abstract][Full Text] [Related]
13. Pearson's marrow-pancreas syndrome in 2 Turkish children.
Gürgey A; Rötig A; Gümrük F; Cemeroğlu P; Sarialioğlu F; Altay C
Acta Haematol; 1992; 87(4):206-9. PubMed ID: 1519437
[TBL] [Abstract][Full Text] [Related]
14. A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions.
Ayed IB; Chamkha I; Mkaouar-Rebai E; Kammoun T; Mezghani N; Chabchoub I; Aloulou H; Hachicha M; Fakhfakh F
Biochem Biophys Res Commun; 2011 Jul; 411(2):381-6. PubMed ID: 21741369
[TBL] [Abstract][Full Text] [Related]
15. Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome.
Bernes SM; Bacino C; Prezant TR; Pearson MA; Wood TS; Fournier P; Fischel-Ghodsian N
J Pediatr; 1993 Oct; 123(4):598-602. PubMed ID: 8410517
[TBL] [Abstract][Full Text] [Related]
16. [Magnetic resonance imaging and spectroscopy of Pearson syndrome].
Imai T; Kondo M; Ito S; Onishi K; Isobe K; Sotoyama Y
No To Hattatsu; 1992 Jul; 24(4):393-5. PubMed ID: 1520518
[No Abstract] [Full Text] [Related]
17. Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome.
Rotig A; Colonna M; Bonnefont JP; Blanche S; Fischer A; Saudubray JM; Munnich A
Lancet; 1989 Apr; 1(8643):902-3. PubMed ID: 2564980
[No Abstract] [Full Text] [Related]
18. Pearson's marrow/pancreas syndrome: a histological and genetic study.
Morikawa Y; Matsuura N; Kakudo K; Higuchi R; Koike M; Kobayashi Y
Virchows Arch A Pathol Anat Histopathol; 1993; 423(3):227-31. PubMed ID: 8236818
[TBL] [Abstract][Full Text] [Related]
19. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).
Rötig A; Cormier V; Chatelain P; Francois R; Saudubray JM; Rustin P; Munnich A
J Clin Invest; 1993 Mar; 91(3):1095-8. PubMed ID: 8383698
[TBL] [Abstract][Full Text] [Related]
20. Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence.
Remes AM; Peuhkurinen KJ; Herva R; Majamaa K; Hassinen IE
Genomics; 1993 Apr; 16(1):256-8. PubMed ID: 7683627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
