Results 131 to 140 of about 7,234,150 (180)

Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy. [PDF]

Front Pediatr
Sy JAC, Tan PL, Lin JB, Tay SK, Chin HL.
europepmc   +1 more source

Generation and Characterization of Human iPSC-Derived Astrocytes with Potential for Modeling X-Linked Adrenoleukodystrophy Phenotypes. [PDF]

Int J Mol Sci
Kaur N, Singh J.
europepmc   +1 more source

Improving quality of life in rare diseases using disease-specific, multidisciplinary online interventions on the example of rare X-linked adrenoleukodystrophy: a randomized-controlled trial. [PDF]

Ther Adv Neurol Disord
Schäfer L, Unterlauft A, Froebrich-Andreß B, Wollny C, Rößler M, Fischer R, Bähr C, Lier J, Wasmus DT, Bergner CC, Köhler W.   +10 more
europepmc   +1 more source

Pathophysiology of X-Linked Adrenoleukodystrophy: Updates on Molecular Mechanisms. [PDF]

J Biotechnol Biomed
Parasar P, Kaur N, Singh J.
europepmc   +1 more source

Practical Approach to Longitudinal Neurologic Care of Adults With X-Linked Adrenoleukodystrophy and Adrenomyeloneuropathy. [PDF]

Neurol Genet
Kornbluh AB, Baldwin A, Fatemi A, Vanderver A, Adang LA, Van Haren K, Sampson J, Eichler FS, Sadjadi R, Engelen M, Orthmann-Murphy JL.   +10 more
europepmc   +1 more source

From gene to therapy: a review of deciphering the role of ABCD1 in combating X-Linked adrenoleukodystrophy. [PDF]

Lipids Health Dis
Zuo X, Chen Z.
europepmc   +1 more source

X-linked adrenoleukodystrophy

, 2019
openaire   +1 more source