Allogeneic bone marrow transplantation for Pearson's syndrome

scientific article published on 05 March 2007

Allogeneic bone marrow transplantation for Pearson's syndrome is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1021134952
P356DOI10.1038/SJ.BMT.1705638
P698PubMed publication ID17334378

P50authorAndrea RossiQ56166779
P2093author name stringDini G
Lanino E
Schiaffino MC
Bruno C
Dallorso S
Castagnola E
Cappelli B
Micalizzi C
Morreale G
Faraci M
Cuzzubbo D
P2860cites workMRI of the brain in the Kearns-Sayre syndrome: report of four cases and a reviewQ30583847
Congenital bone marrow failure syndromes associated with protean developmental defects and leukemiaQ34032581
Invasive aspergillosis in a patient with MELAS syndromeQ35457547
Deletion of the mitochondrial DNA in a case of de Toni-Debr�-Fanconi syndrome and Pearson syndromeQ59619375
Kearns-Sayre's syndrome developing in a boy who survived pearson's syndrome caused by mitochondrial DNA deletionQ67483902
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 DNAQ72072128
Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNAQ72343730
P433issue9
P304page(s)563-565
P577publication date2007-03-05
P1433published inBone Marrow TransplantationQ4941523
P1476titleAllogeneic bone marrow transplantation for Pearson's syndrome
P478volume39

Reverse relations

cites work (P2860)
Q42627710Maintenance of therapeutic concentrations of caspofungin after temporary treatment interruption (48 hours) in a child with invasive aspergillosis
Q92861198Pearson syndrome: a rare inborn error of metabolism with bone marrow morphology providing a clue to diagnosis
Q53751980[Advances in genes mutation and pathophysiology of congenital sideroblastic anemia].

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