lunes, 2 de julio de 2018

Adrenoleukodystrophy AND (genetic OR genomic) AND review - PubMed - NCBI

Adrenoleukodystrophy AND (genetic OR genomic) AND review - PubMed - NCBI

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X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.
Kemp S, Berger J, Aubourg P.
Biochim Biophys Acta. 2012 Sep;1822(9):1465-74. doi: 10.1016/j.bbadis.2012.03.012. Epub 2012 Mar 28. Review.

PMID:
 
22483867
 
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Gene therapy as a new treatment option for inherited monogenic diseases.
Boudes PF.
Eur J Intern Med. 2014 Jan;25(1):31-6. doi: 10.1016/j.ejim.2013.09.009. Epub 2013 Oct 12. Review.

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3.
Hematopoietic stem cell transplantation and hematopoietic stem cell gene therapy in X-linked adrenoleukodystrophy.
Cartier N, Aubourg P.
Brain Pathol. 2010 Jul;20(4):857-62. doi: 10.1111/j.1750-3639.2010.00394.x. Review.

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4.
Pathophysiology of X-linked adrenoleukodystrophy.
Berger J, Forss-Petter S, Eichler FS.
Biochimie. 2014 Mar;98:135-42. doi: 10.1016/j.biochi.2013.11.023. Epub 2013 Dec 4. Review.

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5.
X-linked adrenoleukodystrophy: diagnostic and follow-up system in Japan.
Shimozawa N, Honda A, Kajiwara N, Kozawa S, Nagase T, Takemoto Y, Suzuki Y.
J Hum Genet. 2011 Feb;56(2):106-9. doi: 10.1038/jhg.2010.139. Epub 2010 Nov 11. Review.

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6.
A clinical approach to the diagnosis of patients with leukodystrophies and geneticleukoencephelopathies.
Parikh S, Bernard G, Leventer RJ, van der Knaap MS, van Hove J, Pizzino A, McNeill NH, Helman G, Simons C, Schmidt JL, Rizzo WB, Patterson MC, Taft RJ, Vanderver A; GLIA Consortium.
Mol Genet Metab. 2015 Apr;114(4):501-515. doi: 10.1016/j.ymgme.2014.12.434. Epub 2014 Dec 29. Review.

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7.
Gene therapy for leukodystrophies.
Biffi A, Aubourg P, Cartier N.
Hum Mol Genet. 2011 Apr 15;20(R1):R42-53. doi: 10.1093/hmg/ddr142. Epub 2011 Mar 31. Review.

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8.
Role of family D ATP-binding cassette transporters (ABCD) in cancer.
Hlaváč V, Souček P.
Biochem Soc Trans. 2015 Oct;43(5):937-42. doi: 10.1042/BST20150114. Review.

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9.
Cyclophilin D as a potential target for antioxidants in neurodegeneration: the X-ALD case.
López-Erauskin J, Ferrer I, Galea E, Pujol A.
Biol Chem. 2013 May;394(5):621-9. doi: 10.1515/hsz-2012-0323. Review.

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Persistent hypoglycemia.
Levasseur KA, Tigchelaar H, Kannikeswaran N.
Pediatr Emerg Care. 2013 Jul;29(7):838-41. doi: 10.1097/PEC.0b013e3182989c7d.

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11.
X-linked adrenoleukodystrophy in children: review of genetic, clinical, and MR imaging characteristics.
Melhem ER, Barker PB, Raymond GV, Moser HW.
AJR Am J Roentgenol. 1999 Dec;173(6):1575-81. Review. No abstract available.

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12.
The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis.
Wiesinger C, Eichler FS, Berger J.
Appl Clin Genet. 2015 May 2;8:109-21. doi: 10.2147/TACG.S49590. eCollection 2015. Review.

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13.
Adrenoleukodystrophy.
Moser HW.
Curr Opin Neurol. 1995 Jun;8(3):221-6. Review.

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14.
Adrenoleukodystrophy.
Moser HW, Bergin A, Naidu S, Ladenson PW.
Endocrinol Metab Clin North Am. 1991 Jun;20(2):297-318. Review.

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Hematopoietic stem cell gene therapy in Hurler syndrome, globoid cell leukodystrophy, metachromatic leukodystrophy and X-adrenoleukodystrophy.
Cartier N, Aubourg P.
Curr Opin Mol Ther. 2008 Oct;10(5):471-8. Review.

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Insertional mutagenesis by retroviral vectors: current concepts and methods of analysis.
Knight S, Collins M, Takeuchi Y.
Curr Gene Ther. 2013 Jun 1;13(3):211-27. Review.

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Biosafety challenges for use of lentiviral vectors in gene therapy.
Rothe M, Modlich U, Schambach A.
Curr Gene Ther. 2013 Dec;13(6):453-68. Review.

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18.
Metabolic disorders in children.
Morris AA, Turnbull DM.
Curr Opin Neurol. 1994 Dec;7(6):535-41. Review.

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[Clinical application of gene therapy. Previous experience and the future].
Langer B, Cichutek K.
Pharm Unserer Zeit. 2011 May;40(3):254-62. doi: 10.1002/pauz.201100421. Review. German. No abstract available.

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20.
Gene therapy strategies for X-linked adrenoleukodystrophy.
Cartier N.
Curr Opin Mol Ther. 2001 Aug;3(4):357-61. Review.

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